<?xml version='1.0' encoding='UTF-8'?><rss xmlns:atom='http://www.w3.org/2005/Atom' xmlns:openSearch='http://a9.com/-/spec/opensearchrss/1.0/' xmlns:georss='http://www.georss.org/georss' version='2.0'><channel><atom:id>tag:blogger.com,1999:blog-5905049951798499123</atom:id><lastBuildDate>Sat, 19 Dec 2009 14:00:36 +0000</lastBuildDate><title>livingwithme</title><description>This blog describes my experiences of living and coping with ME / CFS.  Chronic fatigue syndrome (CFS), also known as myalgic encephalomyelitis (ME), post-viral fatigue syndrome (PVFS), and various other names, is a syndrome (or group of syndromes) of unknown and possibly multiple etiologies, affecting the central nervous system (CNS), immune, and many other systems and organs.</description><link>http://livingwithcfs.blogspot.com/</link><managingEditor>noreply@blogger.com (David Elsweiler)</managingEditor><generator>Blogger</generator><openSearch:totalResults>36</openSearch:totalResults><openSearch:startIndex>1</openSearch:startIndex><openSearch:itemsPerPage>25</openSearch:itemsPerPage><item><guid isPermaLink='false'>tag:blogger.com,1999:blog-5905049951798499123.post-4404112504000119947</guid><pubDate>Sat, 22 Mar 2008 09:29:00 +0000</pubDate><atom:updated>2008-03-22T02:40:25.277-07:00</atom:updated><category domain='http://www.blogger.com/atom/ns#'>sugar-free yeast-free diet</category><title>Preparing for the nipper</title><description>Last year, as documented on this blog, I went on a no sugar, no yeast diet for three months to try and sort out my CFS symptoms.  Despite this being quite a challenge, both  physically and of my will power, the diet was a great success.  Three months on and I was feeling more alert and full of life than I had since the onset of my symptoms.  However, after that I gradually slipped into my bad ways.  Starting out with a bit of chocolate each week, which turned into a bar .... you get the idea.&lt;br /&gt;&lt;br /&gt;This year I have been OK health-wise, managing to control the symptoms through no dairy and wheat.  However, I was still having problems especially in the mornings and a bad night's sleep and I was not fun to be with.  Expecting the birth of my first child in June meant that I was also expecting a few (with any luck) sleepless nights, so I wanted to be back in tip-top condition for that.  So, about 3.5 weeks ago I decided to go back on the diet.&lt;br /&gt;&lt;br /&gt;It is funny how it followed almost the same pattern as last year.  Apart from a few cravings for sweet stuff, the first week was pretty easy and I was feeling quite good.  Weeks 2 and 3 were not so pleasant - I started to feel slightly sluggish and concentration was a problem.  This week has been extremely tough.  Stomach cramps, lots of wind, heavy arms and legs, poor concentration.  My insides have been like a war zone.  However, with perseverance I think I am starting to turn the corner.  &lt;br /&gt;&lt;br /&gt;I'll keep you posted on my progress&lt;div class="blogger-post-footer"&gt;&lt;img width='1' height='1' src='https://blogger.googleusercontent.com/tracker/5905049951798499123-4404112504000119947?l=livingwithcfs.blogspot.com' alt='' /&gt;&lt;/div&gt;</description><link>http://livingwithcfs.blogspot.com/2008/03/preparing-for-nipper.html</link><author>noreply@blogger.com (David Elsweiler)</author><thr:total xmlns:thr='http://purl.org/syndication/thread/1.0'>3</thr:total></item><item><guid isPermaLink='false'>tag:blogger.com,1999:blog-5905049951798499123.post-792185947094007107</guid><pubDate>Sat, 23 Feb 2008 15:09:00 +0000</pubDate><atom:updated>2008-02-23T07:19:50.590-08:00</atom:updated><category domain='http://www.blogger.com/atom/ns#'>dairy-free</category><title>So what is a milk-machine anyway?</title><description>Now that I have recovered from the nasty flu/cold bug I reported on last week, I can talk a little about this milk machine I mentioned recently.  So, what exactly is a milk-machine?  No, before you say it, it is not a cow.  Instead it is a kitchen gadget that makes milk from nuts, rice, beans, seeds ... pretty much anything.  It is a rather strange gadget I must admit.  It combines the water heating function of a kettle, with a high powered blender and squeezes the pulp through a filter.  It works a little like this.  You put in the nuts, seeds or rice (after they have soaked), push a button and 20 mins later you have tasty milk.  Well more or less.&lt;br /&gt;&lt;br /&gt;I must admit that it took me quite a while to find a nice recipe.  However, I now have many, but here are the step by step instructions to make milk the way I do at the moment. &lt;br /&gt;&lt;br /&gt;1.  Soak half a beaker (about 20g) of almonds and half a beaker (same volume) of long or short grain brown rice over night.&lt;br /&gt;&lt;br /&gt;2.  Put these in the machine and wait for it to do its job.&lt;br /&gt;&lt;br /&gt;3.  Add 1/2 tsp honey and the seeds from a vanilla pod sliced.&lt;br /&gt;&lt;br /&gt;4.  Wait for it to cool.&lt;br /&gt;&lt;br /&gt;5.  Give it a good shake and you're done.&lt;br /&gt;&lt;br /&gt;This can be used (without the flavourings if you prefer) in soups and hot drinks, in baking etc.  It is also the perfect substitute for milk in cereal. &lt;br /&gt;&lt;br /&gt;Give it a try!&lt;div class="blogger-post-footer"&gt;&lt;img width='1' height='1' src='https://blogger.googleusercontent.com/tracker/5905049951798499123-792185947094007107?l=livingwithcfs.blogspot.com' alt='' /&gt;&lt;/div&gt;</description><link>http://livingwithcfs.blogspot.com/2008/02/so-what-is-milk-machine-anyway.html</link><author>noreply@blogger.com (David Elsweiler)</author><thr:total xmlns:thr='http://purl.org/syndication/thread/1.0'>1</thr:total></item><item><guid isPermaLink='false'>tag:blogger.com,1999:blog-5905049951798499123.post-5889798986957036397</guid><pubDate>Thu, 14 Feb 2008 11:37:00 +0000</pubDate><atom:updated>2008-02-14T03:49:57.463-08:00</atom:updated><title>in from the cold</title><description>It has been over two years since I have had a cold or flu.  It was around New year 2005/ 2007 and it was my first ever experience of a proper achy flu.  Needless to say it wasn't nice.  Three months on I had my first CFS crash.  I don't know if the events were related, but it is possible.  However, I find it very strange that someone with such a poor immune system over the last few years - I have picked up infection after infection - has not had even a sniffle in that time.  It was with a feeling of inevitability then, on Sunday when after my wife had had her fight with a bug, that I would get my turn.  However, by Monday I thought the worst had passed. I was feeling pretty much OK again.  Tuesday was fine, a little achy, but fine.  Wednesday, I kept working away, but by the evening I was dead.  This is where you find me now: an achy, painy, nausea-filled, choked-up feeling sorry for myself mess.  Actually I'm starting to worry that this might lead to a full-circle situation.  I don't even want to think about that!&lt;div class="blogger-post-footer"&gt;&lt;img width='1' height='1' src='https://blogger.googleusercontent.com/tracker/5905049951798499123-5889798986957036397?l=livingwithcfs.blogspot.com' alt='' /&gt;&lt;/div&gt;</description><link>http://livingwithcfs.blogspot.com/2008/02/in-from-cold.html</link><author>noreply@blogger.com (David Elsweiler)</author><thr:total xmlns:thr='http://purl.org/syndication/thread/1.0'>0</thr:total></item><item><guid isPermaLink='false'>tag:blogger.com,1999:blog-5905049951798499123.post-7144884276441513107</guid><pubDate>Tue, 12 Feb 2008 10:39:00 +0000</pubDate><atom:updated>2008-02-12T03:03:46.345-08:00</atom:updated><category domain='http://www.blogger.com/atom/ns#'>dairy-free</category><title>Living Dairy Free</title><description>I've been dairy-free for about a year now.  This has meant removing milk, cheese, cream, and butter from my diet. Considering the number of (favourite) foods that rely on dairy products (pizza, soups, pastas, risottos, hot drinks, cakes, chocolate ...) for many people it is quite a challenge to stay dairy-free.  However, there are options that you can take.  The first is just to bite the bullet and avoid all of these foods. Another option is to try products containing no lactose (milk sugar) such as goat and sheep milk and cheese or even special &lt;a href="http://www.organicvalley.coop/faq/milk-and-cream/lactose-free-milk/"&gt;lactose-free dairy milk&lt;/a&gt;.  A third option is to search for dairy substitutes such as milk made from soya, rice, nuts or oats.  This is my preferred option - these milks can taste great (depending on which brand you choose) and they can be used for any purpose that dairy milk can.  However, there is a downside to some of these milks.  Check the packet for the list of nasty ingredients that are included.  This is not true of all dairy-substitute milks, but it is true of a great many of them.  They are also quite expensive (the good ones at least).  Cue my new toy and ultimate solution.  The milk machine (see picture below). &lt;br /&gt;&lt;br /&gt;&lt;a onblur="try {parent.deselectBloggerImageGracefully();} catch(e) {}" href="http://4.bp.blogspot.com/_M_kiyr6aT3o/R7F87QWjCNI/AAAAAAAAABI/LVDTSMbtgys/s1600-h/milkmachine.JPG"&gt;&lt;img style="display:block; margin:0px auto 10px; text-align:center;cursor:pointer; cursor:hand;" src="http://4.bp.blogspot.com/_M_kiyr6aT3o/R7F87QWjCNI/AAAAAAAAABI/LVDTSMbtgys/s320/milkmachine.JPG" border="0" alt=""id="BLOGGER_PHOTO_ID_5166047605014333650" /&gt;&lt;/a&gt;&lt;br /&gt;&lt;br /&gt; This wonderful device allows me to make my own milk very cheaply, where I have full control of how the milk tastes and what goes in it.  It has taken me a few goes to find recipes that are tasty, but the wait was worthwhile.  In the next few weeks I will share these experiences.&lt;div class="blogger-post-footer"&gt;&lt;img width='1' height='1' src='https://blogger.googleusercontent.com/tracker/5905049951798499123-7144884276441513107?l=livingwithcfs.blogspot.com' alt='' /&gt;&lt;/div&gt;</description><link>http://livingwithcfs.blogspot.com/2008/02/living-dairy-free.html</link><author>noreply@blogger.com (David Elsweiler)</author><media:thumbnail xmlns:media='http://search.yahoo.com/mrss/' url='http://4.bp.blogspot.com/_M_kiyr6aT3o/R7F87QWjCNI/AAAAAAAAABI/LVDTSMbtgys/s72-c/milkmachine.JPG' height='72' width='72'/><thr:total xmlns:thr='http://purl.org/syndication/thread/1.0'>0</thr:total></item><item><guid isPermaLink='false'>tag:blogger.com,1999:blog-5905049951798499123.post-2116895709079381299</guid><pubDate>Fri, 01 Feb 2008 16:54:00 +0000</pubDate><atom:updated>2008-02-01T09:11:22.771-08:00</atom:updated><title>9 months on ....</title><description>It's been a while - over 9 months in fact - since I last posted.  There are a number of reasons why I stopped sharing my views on CFS, although the most important was that I personally was growing tired of whinging about my difficulties.  I didn't (and don't) want to be perceived as someone who thinks the world is against him.  &lt;br /&gt;&lt;br /&gt;When I started blogging my intention was to share my experiences, both positive and negative and I think I did this quite well.  However, after a while I felt like my posts were becoming repetitive: I could only share the same stories, the same problems, the same solutions and the same experiences.  So, I just stopped writing.&lt;br /&gt;&lt;br /&gt;So where am I nine months on ....&lt;br /&gt;&lt;br /&gt;Well a lot has happened in that time and I have achieved a lot too.  I have completed and defended my Ph.D.  I succeeded in persuading my beautiful lady wife to marry me, and I have a baby on the way.  I have also moved permanently to Germany.  So, with all these things happening is CFS no longer a problem and just a bad memory?  Well, in a word, NO.  From the outside it may seem that I am completely healthy and living a full and active life.  However, the truth is that a lot of effort goes in to managing my symptoms and making life liveable.  I have learned that avoiding wheat, dairy and sugar helps.  I have also learned to find my limits, manage my work load and my sleeping patterns.  Despite all this, I still get my bad days where I struggle to get out of bed and do anything productive.  Mornings are usually pretty difficult.  However, I am very confident that I will continue to improve and one day I will rid myself of CFS completely.&lt;br /&gt;&lt;br /&gt;In the mean time however, there are a few topics that I would like to discuss and a few things that I have learned that I would like to share.  So until I run out of words again I have decided to return to blogging - hurray!!!&lt;div class="blogger-post-footer"&gt;&lt;img width='1' height='1' src='https://blogger.googleusercontent.com/tracker/5905049951798499123-2116895709079381299?l=livingwithcfs.blogspot.com' alt='' /&gt;&lt;/div&gt;</description><link>http://livingwithcfs.blogspot.com/2008/02/9-months-on.html</link><author>noreply@blogger.com (David Elsweiler)</author><thr:total xmlns:thr='http://purl.org/syndication/thread/1.0'>1</thr:total></item><item><guid isPermaLink='false'>tag:blogger.com,1999:blog-5905049951798499123.post-6278889989439121234</guid><pubDate>Tue, 03 Apr 2007 12:04:00 +0000</pubDate><atom:updated>2007-04-03T05:17:20.887-07:00</atom:updated><title>Back home</title><description>I have been home now for a few days and all is going well.  I still seem to be stable with a lot more get up and go than I have had over the last year.  I still have a bit of wind, but I am hoping that this will sort itself out if I continue with the diet as I have been.&lt;br /&gt;&lt;br /&gt;On Saturday it was my Grandparent's 55th anniversary celebration.  It was also my first anniversary of becoming ill.  I have read many posts about other CFS sufferers' anniversarys and they all have a familiar pattern.  Before such and such a day I was really health, outgoing person and then bang, without warning, my life was lost.  My post would have followed similar lines, but recently I have been thinking this is not quite true.  Thinking back there were a number of warning signs that I missed.  About a week before I had my first crash, my girlfriend and I enjoyed a well earned holiday weekend in Arran.  Looking at the photos from this break, shows me looking terrible - baggy eyes just looking really tired.  I had been pushing myself really hard that month, both with work and physically competing in a charity fitness event called "move for Malawi".  During the month of March I went to the gym everyday and really pushed it.  Thinking back to a walk in Arran I decided not to climb the extra bit of a hill because I was too tired - not the behaviour of the fit 25 year old as I would have described myself back then.  Also, the other day I spoke to a lecturer in my department who also competed in the move for Malawi.  He said he remembered seeing me in the gym on the 30th of March (the day before the crash) and thinking that I looked awful.&lt;br /&gt;&lt;br /&gt;So the warning signs were there, I just didn't read them.  This is the moral of the story - listen to your body and if you are pushing too hard, stop before you push too much.&lt;div class="blogger-post-footer"&gt;&lt;img width='1' height='1' src='https://blogger.googleusercontent.com/tracker/5905049951798499123-6278889989439121234?l=livingwithcfs.blogspot.com' alt='' /&gt;&lt;/div&gt;</description><link>http://livingwithcfs.blogspot.com/2007/04/back-home.html</link><author>noreply@blogger.com (David Elsweiler)</author><thr:total xmlns:thr='http://purl.org/syndication/thread/1.0'>1</thr:total></item><item><guid isPermaLink='false'>tag:blogger.com,1999:blog-5905049951798499123.post-2357642526170545493</guid><pubDate>Wed, 28 Mar 2007 08:26:00 +0000</pubDate><atom:updated>2007-03-28T01:41:13.800-07:00</atom:updated><title>My last day in Germany</title><description>So this, my friends, is my last day in Germany.  I am really torn about moving back - just as I am torn about many things in my life at the moment.  On the one hand I have enjoyed my time here - albeit it has been an up and down time healthwise.  I have made a good group of friends, have started to familiarise myself with the language once more and Germany has an awful lot going for it.  However, there are so many things I miss about home.  Obviously the main thing is my family - my mum, my dad, my brother and my grandparents, and of course, my friends.  But, there is much more to it than that.  I miss the way people interact with each other in Glasgow.  People smile a lot more - believe it or not.  People talk to others that they do not know.  It is small things like this that I miss.  When you get on the train in Germany everyone sits with a straight face and looks directly ahead.  In Glasgow, whenever you get on a bus or a train you get a friendly comment, a smile or at very least some comical outburst from a ned and this, for me, is enough to brighten up a day.&lt;br /&gt;&lt;br /&gt;I've spoken to Christine's Dad about this and he believes that it would annoy him if people started talking to him on the train - why?&lt;br /&gt;&lt;br /&gt;Don't get me wrong Germany is wonderful and the people here are really friendly.  It is just that serendipitous interaction between the people is somewhat limited and this frustrates me.  I would like to return here and live for longer.  The chances are that, if I am healthy, I will return to Germany in May and finish off the write up of my thesis.  However, long term, I see my future in Scotland.  It is with envy that I read  the events and happenings within my university.  There seems to be so much going on.  Collaboration that has been missing in the past seems to be igniting and I want to be part of this.  However, I want to be with Christine and she is going to be here.  I would really like to be in two places at once.&lt;div class="blogger-post-footer"&gt;&lt;img width='1' height='1' src='https://blogger.googleusercontent.com/tracker/5905049951798499123-2357642526170545493?l=livingwithcfs.blogspot.com' alt='' /&gt;&lt;/div&gt;</description><link>http://livingwithcfs.blogspot.com/2007/03/my-last-day-in-germany.html</link><author>noreply@blogger.com (David Elsweiler)</author><thr:total xmlns:thr='http://purl.org/syndication/thread/1.0'>0</thr:total></item><item><guid isPermaLink='false'>tag:blogger.com,1999:blog-5905049951798499123.post-4267318427041388547</guid><pubDate>Mon, 26 Mar 2007 18:56:00 +0000</pubDate><atom:updated>2007-03-27T02:05:04.848-07:00</atom:updated><category domain='http://www.blogger.com/atom/ns#'>sugar-free yeast-free diet</category><category domain='http://www.blogger.com/atom/ns#'>recipe</category><title>Salmon and Asparagus Risotto</title><description>Now for today's second recipe.  I tried this for the first time tonight and it was delicious.  So delicious in fact that after finishing her plate, Christine decided she would scrape mine. She won't be happy that I shared that with the world, but hey ...&lt;br /&gt;&lt;br /&gt;This is a really easy meal to prepare and it is made with kitchen staples.  &lt;br /&gt;&lt;br /&gt;Ingredients:&lt;br /&gt;&lt;br /&gt;1 filet of salmon (skinned, boned and chopped into small pieces)&lt;br /&gt;8 to 12 cooked asparagus spears cut into 1-inch lengths&lt;br /&gt;1 lemon&lt;br /&gt;500 ml of veggie stock&lt;br /&gt;2 tablespoons of butter&lt;br /&gt;1 medium onion&lt;br /&gt;130g of arborio rice (I used organic short-grain brown rice to correspond to the diet)&lt;br /&gt;dash of cream (optional)&lt;br /&gt;&lt;br /&gt;&lt;br /&gt;- Gently fry the onion in butter over medium heat until soft, then zest the lemon and stir it with the onion.&lt;br /&gt;&lt;br /&gt;- Stir in the rice to coat all the grains of rice with butter.&lt;br /&gt;&lt;br /&gt;- Start adding stock approx. 150 ml at a time.  Have the heat such that the stock just simmers. The stock will reduce and thicken. Every time this happens, add another 150ml. Stir frequently and continue until the rice is just about done. Meanwhile, squeeze the lemon and add a couple tablespoons along with some broth. &lt;br /&gt;(Save the last bit of lemon juice to season the dish with at the end.)&lt;br /&gt;&lt;br /&gt;- When the rice is just a tad underdone, stir in the asparagus and salmon. Season with salt, pepper, and lemon juice.&lt;br /&gt;&lt;br /&gt;- Cover the pot and let it sit for 5 minutes. By then the salmon is usually cooked, but it may need a minute more. If you wish add a dash of cream now.&lt;div class="blogger-post-footer"&gt;&lt;img width='1' height='1' src='https://blogger.googleusercontent.com/tracker/5905049951798499123-4267318427041388547?l=livingwithcfs.blogspot.com' alt='' /&gt;&lt;/div&gt;</description><link>http://livingwithcfs.blogspot.com/2007/03/salmon-and-asparagus-risotto.html</link><author>noreply@blogger.com (David Elsweiler)</author><thr:total xmlns:thr='http://purl.org/syndication/thread/1.0'>0</thr:total></item><item><guid isPermaLink='false'>tag:blogger.com,1999:blog-5905049951798499123.post-6573790057550002894</guid><pubDate>Mon, 26 Mar 2007 18:26:00 +0000</pubDate><atom:updated>2007-03-26T12:13:20.039-07:00</atom:updated><category domain='http://www.blogger.com/atom/ns#'>sugar-free yeast-free diet</category><category domain='http://www.blogger.com/atom/ns#'>recipe</category><title>Soup da loop</title><description>Time for the next recipe.  I think today I will post two - just cause!&lt;br /&gt;&lt;br /&gt;The first is a soup.  When on a candida diet you are not allowed fruit so you have to make up for this with numerous portions of veggies.  One way of doing this that never gets tiresome is soup.  One of my new favourite soup recipes is creamy Kale - it is wholesome, filling, delicious, not to mention full of fibre, nutrients and flavour.  I adapted the recipe from one I found at &lt;a href="http://franlife.blogspot.com/2006/10/recipe-creamy-kale-soup.html"&gt;Fran's house of Ayurveda&lt;/a&gt;.  I know nothing about Asian life philosophies, but Fran's website has a great collection of recipes.&lt;br /&gt;&lt;br /&gt;Ingredients:&lt;br /&gt;&lt;br /&gt;1/2 cup Green lentils (or lentils of your preference)&lt;br /&gt;1/4 cup brown rice &lt;br /&gt;1/4 cup quinoa &lt;br /&gt;1/2 medium onion, finely chopped&lt;br /&gt;1 clove of garlic&lt;br /&gt;4 tbsp olive oil&lt;br /&gt;1/2 bunch of kale&lt;br /&gt;5 cups water&lt;br /&gt;1 tsp veggie stock&lt;br /&gt;&lt;br /&gt;SPICES&lt;br /&gt;1 tsp of cumin powder (heaping, or as desired)&lt;br /&gt;1 1/2 tsp of curry powder&lt;br /&gt;1 tsp of sea salt, to taste&lt;br /&gt;&lt;br /&gt;TAHINI DRESSING&lt;br /&gt;1 Tbsp tahini (heaping, or as desired)&lt;br /&gt;2 Tbsp flax / olive oil&lt;br /&gt;&lt;br /&gt;Before you start to cook, add all spices together in a small bowl and mix well (prevents clumping when added to the cooking pot later). Wash kale and chop finely.&lt;br /&gt;&lt;br /&gt;Add olive oil to a pre-heated cooking pot on medium temperature. When the oil is hot, add onions and garlic and cook until soft. Add the spices, being careful to blend well. Then add lentils, brown rice and quinoa right away and stir well. When that is done, add chopped kale and mix.&lt;br /&gt;&lt;br /&gt;At this stage, take a moment to appreciate how beautiful the mixture looks -- but not too long, because the water must now be added. Cover the pot and bring to a boil. Simmer on low for 45 minutes.&lt;br /&gt;&lt;br /&gt;With about 10 minutes to go add the Tahini mix.&lt;div class="blogger-post-footer"&gt;&lt;img width='1' height='1' src='https://blogger.googleusercontent.com/tracker/5905049951798499123-6573790057550002894?l=livingwithcfs.blogspot.com' alt='' /&gt;&lt;/div&gt;</description><link>http://livingwithcfs.blogspot.com/2007/03/soup-da-loop.html</link><author>noreply@blogger.com (David Elsweiler)</author><thr:total xmlns:thr='http://purl.org/syndication/thread/1.0'>0</thr:total></item><item><guid isPermaLink='false'>tag:blogger.com,1999:blog-5905049951798499123.post-6663874726974803707</guid><pubDate>Thu, 22 Mar 2007 20:46:00 +0000</pubDate><atom:updated>2007-03-22T13:55:34.197-07:00</atom:updated><category domain='http://www.blogger.com/atom/ns#'>sugar-free yeast-free diet</category><category domain='http://www.blogger.com/atom/ns#'>recipe</category><title>Potato, fennel and basil salad</title><description>The first post from my promised series on Candida diet tips and recipes.  This has become of one of my favourites - in fact Christine and I ate it tonight for dinner.  The fennel and lemon juice go together wonderfully.  &lt;br /&gt;&lt;br /&gt;The recipe is adapted from one by &lt;a href="http://www.bbc.co.uk/food/recipes/database/potatofennelandbasil_85513.shtml"&gt;James Tanner&lt;/a&gt; and is extremely quick and easy to prepare. Perfect for those on the Candida diet who have to prepare everything from scratch.&lt;br /&gt;&lt;br /&gt;Serves 2&lt;br /&gt;&lt;br /&gt;Ingredients&lt;br /&gt;1 tbsp olive oil&lt;br /&gt;300g of potatoes sliced&lt;br /&gt;1 fennel bulb, finely sliced&lt;br /&gt;1 lemon, juice only&lt;br /&gt;&lt;br /&gt;salt and freshly ground black pepper&lt;br /&gt;small handful fresh basil leaves, to garnish&lt;br /&gt;&lt;br /&gt;Method&lt;br /&gt;1. Heat the oil in a frying pan over a medium heat and fry the potatoes until golden-brown. (I prefer to par-boil the potatoes)&lt;br /&gt;2. Add the fennel and lemon juice and stir well. Season with salt and freshly ground black pepper and cook until the fennel is tender.&lt;br /&gt;3. To serve, place the warm salad onto a plate and garnish with basil leaves.&lt;br /&gt;&lt;br /&gt;Enjoy! More to come&lt;div class="blogger-post-footer"&gt;&lt;img width='1' height='1' src='https://blogger.googleusercontent.com/tracker/5905049951798499123-6663874726974803707?l=livingwithcfs.blogspot.com' alt='' /&gt;&lt;/div&gt;</description><link>http://livingwithcfs.blogspot.com/2007/03/potato-fennel-and-basil-salad.html</link><author>noreply@blogger.com (David Elsweiler)</author><thr:total xmlns:thr='http://purl.org/syndication/thread/1.0'>0</thr:total></item><item><guid isPermaLink='false'>tag:blogger.com,1999:blog-5905049951798499123.post-2987915594093584782</guid><pubDate>Thu, 22 Mar 2007 20:23:00 +0000</pubDate><atom:updated>2007-03-22T13:44:09.867-07:00</atom:updated><title>The first of two posts for today</title><description>I've been a little slack with my blogging lately.  This is probably because I have been feeling better - it is amazing how when you feel healthy the number of things to do just multiplies.  This is a great feeling!&lt;br /&gt;&lt;br /&gt;A quick update on the diet and the capryllic acid.  I think it is going well.  After the second day on the acid I thought I was going to get a reaction similar to the replete, the wind came back etc.  However, it has not worked out like that.  I started to drink lots of water and this may have helped my body deal with things.  I read that the capryllic acid finds its way into the liver and plenty of fluids help to flush it out of the system - hopefully along with any toxins from the candida growth.&lt;br /&gt;&lt;br /&gt;I have uncovered, in the last few days, some evidence that I think points towards a milk intolerance (apologies to those who suggested this before for my prompt dismissal of the idea).  After visiting the German doctor the other week, on the advice of the doctor, I started to drink lots of milk.  He recommended a litre of milk per day.  I love milk so I happily indulged in this.  I have since learned that milk is a big no no for the candida diet (oops).  Anyway, after over a week of enjoyable but heavy milk drinking, I noticed that the dermititus on my pinky (I have posted before about how this disappeared when I started the diet) returned and was worsening on a day by day basis.  The only change I had made was the milk so I cut this out straight away.  After only a few days the redness lessened and the pinky seemed to be healing.  I can only think of two explanations.  The first is that I have a milk intolerence.  The second is that the lactose (milk sugar) had influenced the candida.  Yoghurt and cream do not seem to be a problem, so it could be the latter.  However, I have read that the fermintation process involved in yoghurt and cream lessens the quantities of lactose.  I think the only thing for me to do is to stop milk for 2-3 months.  Hopefully I will be healthy at this point and then try to re-introduce it.&lt;div class="blogger-post-footer"&gt;&lt;img width='1' height='1' src='https://blogger.googleusercontent.com/tracker/5905049951798499123-2987915594093584782?l=livingwithcfs.blogspot.com' alt='' /&gt;&lt;/div&gt;</description><link>http://livingwithcfs.blogspot.com/2007/03/first-of-two-posts-for-today.html</link><author>noreply@blogger.com (David Elsweiler)</author><thr:total xmlns:thr='http://purl.org/syndication/thread/1.0'>0</thr:total></item><item><guid isPermaLink='false'>tag:blogger.com,1999:blog-5905049951798499123.post-6782317324875779360</guid><pubDate>Mon, 19 Mar 2007 19:49:00 +0000</pubDate><atom:updated>2007-03-19T13:01:53.414-07:00</atom:updated><title>Lamenting a wasted day</title><description>I'm pretty angry with myself at the moment.  Despite a good day healthwise I just could not get into gear and do some work today.  When I think of all those days wasted when all I wanted was to work but wasn't well enough to manage it, it makes my blood boil when I waste away days like today.  However, it wasn't all my fault.  I spent most of the morning fiddling with my computer, which over the last day or so had more or less ground to a halt.  Closer inspection revealed a trojan had sneaked its way through my defenses.  It took 5.5 hrs to run the virus check completely, while I struggled to work along side.  After removing the virus, the machine still required over 12 minutes to boot.  I couldn't believe it - the machine is not even 1 yr old.  So, I cleaned the registry, deleted all temporary files and cookies etc. and made a few tweaks.  This appears to have improved the performance somewhat, but not enough for my liking.  Top of my priority list for when I get home is a fresh install of windows.  It is times like this that I wish I had splashed out for a mac.&lt;div class="blogger-post-footer"&gt;&lt;img width='1' height='1' src='https://blogger.googleusercontent.com/tracker/5905049951798499123-6782317324875779360?l=livingwithcfs.blogspot.com' alt='' /&gt;&lt;/div&gt;</description><link>http://livingwithcfs.blogspot.com/2007/03/lamenting-wasted-day.html</link><author>noreply@blogger.com (David Elsweiler)</author><thr:total xmlns:thr='http://purl.org/syndication/thread/1.0'>0</thr:total></item><item><guid isPermaLink='false'>tag:blogger.com,1999:blog-5905049951798499123.post-5442093079377941043</guid><pubDate>Sun, 18 Mar 2007 17:15:00 +0000</pubDate><atom:updated>2007-03-19T05:57:19.902-07:00</atom:updated><category domain='http://www.blogger.com/atom/ns#'>sugar-free yeast-free diet</category><title>The sugar and yeast free diet - a 3 week update</title><description>It is now 3 and a half weeks since I started my diet.  For those readers new to this blog, I am following a sugar and yeast free diet after &lt;a href="http://livingwithcfs.blogspot.com/2007/03/diagnosing-candida.html"&gt;self-diagnosing Candida-Albicans&lt;/a&gt;.  With the help of my herbalist and a lot of reading, I designed a diet designed to kill off any yeast growth in my digestive system.  The basic rules of the diet and information about candida are given in a &lt;a href="http://livingwithcfs.blogspot.com/2007/02/bug-in-system-candida-albicans.html"&gt;previous post&lt;/a&gt;.&lt;br /&gt;&lt;br /&gt;The diet has taken quite a lot of thought and preparation in terms of what I can eat and how I can maintain a balanced diet with all of the nutrients that I need.  I have spent a lot of time looking at labels to see if any nasty extras have been sneaked into food products that would make them unsuitable for me and a lot of time searching for recipes.  When following such a diet, most meals have to be prepared completely from scratch.  I have made my own mustard without sugar or vinegar, my own mayonaise and my own bread spreads.  Bread spreads are important even though I am not allowed bread.  Staple snacks have been oatcakes (homemade), rye crackers and rice waffles and after a while the same spreads become tiresome.  &lt;br /&gt;&lt;br /&gt;As you can imagine it has been quite a challenge to keep an interesting and varied diet while following the rules of the sugar and yeast free diet, but my girlfriend and I have managed it.  Actually it has been an opportunity for us both to search for new recipes and some of the ones we have found are delicious.  I plan to post a selection of candida diet friendly recipes and guidelines over the coming weeks to perhaps ease the workload of others following a similar path.  &lt;br /&gt;&lt;br /&gt;The diet itself has not been the main challenge for me, the problem has been how I have been feeling healthwise as I have been following the diet.  The first week was so easy because I could see that I was improving healthwise.  There was an almost immediate effect.  My eyes were clearer, I had more energy and the wind that I had been suffering from died back somewhat.  This made it easy to continue with the diet because I felt it was doing me good.  &lt;br /&gt;&lt;br /&gt;The second week was not so easy however.  I had problems with low blood pressure and was panicky about this even though I don't think this was anything to do with the diet.  On top of this I had increased wind which worsened as the week went on.  I also had increasing tiredness towards the end of the second week.  I attributed these  second symptoms to two things: 1)the relete acidophilus that I was taking along with the diet to rebuild my gut flora and 2) some kind of die of reaction from the candida.  &lt;br /&gt;&lt;br /&gt;Sure enough, at the start of the third week, when the course of replete was complete, I came to a turning point.  I started to feel much better, both mentally and physically and this continued for the whole of week 3.  I've been able to work effectively, get out and about more and generally enjoy my life.  Christine and I have been able to do things together; we've been to museums, out with friends, and to watch her nephew play football.  So this week has been great.  Hopefully, it continues this way.&lt;br /&gt;&lt;br /&gt;Now, I am moving on to the next phase of the diet, where I take capryllic acid, which should take care of the remaining candida.  I have been warned during this phase that I may experience some discomfort due to the yeast dying off, but hopefully because I experienced these symptoms earlier this final phase of the diet will become easier.  Wish me luck!&lt;div class="blogger-post-footer"&gt;&lt;img width='1' height='1' src='https://blogger.googleusercontent.com/tracker/5905049951798499123-5442093079377941043?l=livingwithcfs.blogspot.com' alt='' /&gt;&lt;/div&gt;</description><link>http://livingwithcfs.blogspot.com/2007/03/sugar-and-yeast-free-diet-3-week-update.html</link><author>noreply@blogger.com (David Elsweiler)</author><thr:total xmlns:thr='http://purl.org/syndication/thread/1.0'>2</thr:total></item><item><guid isPermaLink='false'>tag:blogger.com,1999:blog-5905049951798499123.post-5893836564146904977</guid><pubDate>Thu, 15 Mar 2007 08:49:00 +0000</pubDate><atom:updated>2007-03-15T13:30:44.534-07:00</atom:updated><category domain='http://www.blogger.com/atom/ns#'>symptoms</category><title>Brain fog and its many guises</title><description>&lt;span style="font-family:arial;"&gt;There are a few CFS topics that I have wanted to write about for some time and brain fog is one of these.   Brain fog, described as  "a state of confusion or lack of clarity" [&lt;a href="#ref1"&gt;1&lt;/a&gt;], is a symptom suffered by many people diagnosed with CFS.  It is something that I too have experienced regularly over the last 11 months.  For me, however, brain fog is more than the inability to think because of a muddled head.  I have had a range of symptoms relating to my cognitive abilities, each of which I associate with the term brain fog.  Many of these are experienced by healthy people and I too had some of these before I became ill, but since I have been diagnosed I have noticed them happening more and more, especially when I am tired.  I wondered if anyone else with or without CFS had suffered these scenarios.  What are your thoughts on the subject?  Here are a few of the things that i relate to brain fog:&lt;br /&gt;&lt;br /&gt;&lt;/span&gt;&lt;ol&gt;&lt;li&gt;&lt;span style="font-family:arial;"&gt;When I read signs, adverts or newspaper billboards, the words that i read are often not the words printed, but words that look similar, relating to something that I have been recently thinking about.  After a second look the real word comes to me.&lt;br /&gt;&lt;/span&gt;&lt;/li&gt;&lt;li&gt;&lt;span style="font-family:arial;"&gt;A similar thing happens with people.  Often, when I walk past people in the street, for the first few seconds I see a person that i recognise.   Again, a second or closer look makes it obvious that the person is not who I am thinking and often looks nothing like that person.  This has been happening a lot to me in Germany.&lt;/span&gt;&lt;/li&gt;&lt;li&gt;&lt;span style="font-family:arial;"&gt;My memory for names has become apalling.  I find that when I am introduced to someone their name never sticks in my head.  This never used to happen.&lt;/span&gt;&lt;/li&gt;&lt;li&gt;&lt;span style="font-family:arial;"&gt;Also, I don't really pay attention to what I'm doing.  I often find myself asking - did I lock the door? Did I take my tablets?&lt;/span&gt;&lt;/li&gt;&lt;li&gt;&lt;span style="font-family:arial;"&gt;Again, relating to attention, my concentration span is terrible.  I cannot concentrate on anything for any length of time before my mind wanders off elsewhere.&lt;/span&gt;&lt;/li&gt;&lt;/ol&gt;My research is associated with memory and I know quite a lot about it.  Indeed, I have even studied everyday memory lapses [&lt;a href="#ref2"&gt;2&lt;/a&gt;].   So, I know that these are all fairly common memory lapses and in themselves don't merit any worry.  The point I want to emphasize is the frequency with which they now happen to me.  I'd really like to hear other peoples' thoughts and experiences.&lt;br /&gt;&lt;br /&gt;References:&lt;br /&gt;&lt;br /&gt;&lt;div id="ref1"&gt;1. &lt;a href="http://www.drlwilson.com/articles/brain_fog.htm"&gt;http://www.drlwilson.com/articles/brain_fog.htm&lt;/a&gt;&lt;/div&gt;&lt;br /&gt;&lt;div id="ref2"&gt;2.  Elsweiler, D., Ruthven, I., and Jones, C. "Towards Memory Supporting Personal Information Management Tools"  Journal of the American Society for Information Science and Technology 2007 (&lt;a href="http://www.free-conversant.com/tipster/504/enclosure/jasist%20paper_revised2_after_ian.pdf"&gt;pdf&lt;/a&gt;)&lt;/div&gt;&lt;br /&gt;&lt;span style="font-family:arial;"&gt;&lt;br /&gt;&lt;/span&gt;&lt;span style="letter-spacing: -0.15pt;font-family:arial;font-size:16;"  &gt;&lt;/span&gt;&lt;div class="blogger-post-footer"&gt;&lt;img width='1' height='1' src='https://blogger.googleusercontent.com/tracker/5905049951798499123-5893836564146904977?l=livingwithcfs.blogspot.com' alt='' /&gt;&lt;/div&gt;</description><link>http://livingwithcfs.blogspot.com/2007/03/brain-fog-and-its-many-guises.html</link><author>noreply@blogger.com (David Elsweiler)</author><thr:total xmlns:thr='http://purl.org/syndication/thread/1.0'>0</thr:total></item><item><guid isPermaLink='false'>tag:blogger.com,1999:blog-5905049951798499123.post-757250245974558990</guid><pubDate>Tue, 13 Mar 2007 19:41:00 +0000</pubDate><atom:updated>2007-03-13T13:07:53.033-07:00</atom:updated><title>A new day a new frame of mind</title><description>I felt wonderfully positive today.  It makes a nice change to write like this rather than the negative claptrap I have been blogging recently.  I really did notice a difference.  I woke up without the heavy legs and arms that I have become accustomed to, without the blurry brain, and without the wind - well I had reduced wind anyway.  This has continued throughout the day without the hangover that I was expecting from the doctor's appointment yesterday (I will explain in a minute).  So all in all a good day all round - positive mentally and physically.  Lets hope it continues.&lt;br /&gt;&lt;br /&gt;As far as I can tell there are two reasons for this - well three if you count the glorious sunshine we had today.&lt;br /&gt;&lt;br /&gt;The first is that I never had to take the replete today.  While my herbalist is convinced that the stuff will restore my gut flora to a healthy state, I never did feel comfortable taking it.  It really is so strong and upset my entire digestive rythmn and latterly I believe my energy levels too.  So, not having to take a sachet this morning, I believe, has made me feel so much better in myself.&lt;br /&gt;&lt;br /&gt;The second reason that I believe I am feeling better is the thorough examination I received yesterday at the heart specialist.  I never believed that there was anything wrong with my heart or my CV system, I've had it checked out before, but the low pressure mystery and the fact that someone felt it needed to be checked starts to eat away at you.&lt;br /&gt;&lt;br /&gt;So, to the examination.  Firstly, I had a full ultrasound.  Starting with the heart, the doctor proceeded to check all of my major organs.  All of which were healthy and normal.  Then, I had a "belastungs EKG" or to you and I, a heart test while going through a full workout.&lt;br /&gt;&lt;br /&gt;I did more exercise in this one session than I have in one go since I became ill.  While hooked up to the heart monitor I had a 12 minute session on the exercise bike, starting from a moderate pace, building up to 250 watts (so the doctor told me) or in laymans terms, a pretty high level.  My pulse and blood pressure reacted as they should and after the session was complete,  returned to a normal level reasonably quickly.  I was really proud of my efforts, especially considering it was only 2 days ago that I needed to find a seat while shopping.  However, as everyone who has experienced CFS will know, at the back of mind I was expecting a crash today.  It did not happen!  I know that it could still happen tomorrow, or at somepoint later this week, but at the moment I just don't believe that it will. &lt;br /&gt;&lt;br /&gt;I don't believe for one minute that I have been magically cured, but I am determined to keep this positive outlook, continue this diet and look after myself.   With hard work and a happy face I will beat this thing!&lt;div class="blogger-post-footer"&gt;&lt;img width='1' height='1' src='https://blogger.googleusercontent.com/tracker/5905049951798499123-757250245974558990?l=livingwithcfs.blogspot.com' alt='' /&gt;&lt;/div&gt;</description><link>http://livingwithcfs.blogspot.com/2007/03/new-day-new-frame-of-mind.html</link><author>noreply@blogger.com (David Elsweiler)</author><thr:total xmlns:thr='http://purl.org/syndication/thread/1.0'>0</thr:total></item><item><guid isPermaLink='false'>tag:blogger.com,1999:blog-5905049951798499123.post-325722043504903003</guid><pubDate>Sun, 11 Mar 2007 10:55:00 +0000</pubDate><atom:updated>2007-03-11T04:10:02.444-07:00</atom:updated><title>A step back in time</title><description>I've definately regressed over the last few days.  It is not the wind that is bothering me, although this too has been pretty severe.  The main problem has been my energy levels.  Christine and I went food shopping yesterday and I had to find a seat twice within an hour.  I have not been in this situation for months.  When we got home I was completely knackered.  We had planned to go to an art gallery yesterday, but I just didn't have the get up and go needed.  Instead I sat in an easy chair and tried to recharge the batteries.   Three hours or so later I felt a bit better and we went out for a short walk - 20 mins or so at a slow pace.  Again, when I returned the batteries were completely flat.&lt;br /&gt;&lt;br /&gt;Strangely, I have been able to concentrate ok.  My work has progressed over the last week, despite my overall health going the other way. This has been my shining light.   My other positive is that I believe that this replete, that I have mentioned a few times, is the root cause of my lack of energy.  It is only since I started taking it that my energy-levels have suffered.   I hope, I really hope, that after I take the last sachet tomorrow that my system will return into its natural flow and my energy will return.&lt;br /&gt;&lt;br /&gt;Tonight I am meant to be going to a concert.  &lt;span style="font-size:-1;"&gt;Fanfare Ciocarlia - the fastest brass band in the world and one of Christine's favourite bands - are playing in Nuremberg.  I bought the tickets as a treat for us both and a thank you to Christine for putting up with me.  However, I was feeling somewhat better when I bought them and now I am really dreading it.  At the same time though I do not want this illness to define who I am and I am determined to go.  I will take a nap this afternoon and hopefully this will leave me in a fit state to enjoy myself this evening.&lt;br /&gt;&lt;/span&gt;&lt;a onblur="try {parent.deselectBloggerImageGracefully();} catch(e) {}" href="http://bloguedeumaloura.weblog.com.pt/arquivo/fanfare.jpg"&gt;&lt;img style="margin: 0px auto 10px; display: block; text-align: center; cursor: pointer; width: 320px;" src="http://bloguedeumaloura.weblog.com.pt/arquivo/fanfare.jpg" alt="" border="0" /&gt;&lt;/a&gt;&lt;br /&gt;&lt;span style="font-size:-1;"&gt;&lt;br /&gt;&lt;/span&gt;&lt;div class="blogger-post-footer"&gt;&lt;img width='1' height='1' src='https://blogger.googleusercontent.com/tracker/5905049951798499123-325722043504903003?l=livingwithcfs.blogspot.com' alt='' /&gt;&lt;/div&gt;</description><link>http://livingwithcfs.blogspot.com/2007/03/step-back-in-time.html</link><author>noreply@blogger.com (David Elsweiler)</author><thr:total xmlns:thr='http://purl.org/syndication/thread/1.0'>0</thr:total></item><item><guid isPermaLink='false'>tag:blogger.com,1999:blog-5905049951798499123.post-5401515642592555205</guid><pubDate>Thu, 08 Mar 2007 13:58:00 +0000</pubDate><atom:updated>2007-03-08T06:22:06.038-08:00</atom:updated><title>The german specialist</title><description>So what was the verdict of the specialist I went to see about my blood pressure mystery?  "Oh dear you don't look good at all!".  This is unfair.  In fact, the doctor was very supportive of my cause and told me that in cases like this.  When I am not 65, but 25 and I look so unwell, we must search and search and search until we find the answer.  He even said that if he could allocate it he would sanction a hospital trip where they could do tests for 2 weeks without time to do anything else.  This wont happen of course, but only the other day I turned down the opportunity to go into hospital for checks - 2 days in a foreign hospital does not sound appealling to me.&lt;br /&gt;&lt;br /&gt;However, the tests begin tomorrow.  I have had most of these tests before, but I was not about to turn down this man's help.  I am scheduled for "ein grosses Blutbild" (full range of blood tests), ecg, blood pressure tomorrow with the results coming on Monday.&lt;br /&gt;&lt;br /&gt;The doctor was not too supportive of my diet.  He said that at the moment I should eat anything that takes my fancy.  This way I will not become deficient in anything on top of CFS.  However, I want to continue with this.  I have put a lot into this diet and do not want to give up now before I potentially reap the rewards.  There are a few things worrying me however.  The first is having blood tests without any sugar afterwards.  I am not the greatest when it comes to giving blood and usually, to keep me from collapsing in a heap, I take a supply of chocolate with me.  The other thing that is worrying me is the replete.  It has really changed my digestive pattern and I am not comfortable taking it at all.  I will have to chat over all of these issues with my herbalist.&lt;br /&gt;&lt;br /&gt;So, we shall see what the tests bring.  I am pretty sure they will all come back normal but we shall wait and see.&lt;div class="blogger-post-footer"&gt;&lt;img width='1' height='1' src='https://blogger.googleusercontent.com/tracker/5905049951798499123-5401515642592555205?l=livingwithcfs.blogspot.com' alt='' /&gt;&lt;/div&gt;</description><link>http://livingwithcfs.blogspot.com/2007/03/german-specialist.html</link><author>noreply@blogger.com (David Elsweiler)</author><thr:total xmlns:thr='http://purl.org/syndication/thread/1.0'>2</thr:total></item><item><guid isPermaLink='false'>tag:blogger.com,1999:blog-5905049951798499123.post-1802394544430643088</guid><pubDate>Wed, 07 Mar 2007 09:48:00 +0000</pubDate><atom:updated>2007-03-08T05:58:37.195-08:00</atom:updated><category domain='http://www.blogger.com/atom/ns#'>symptoms</category><category domain='http://www.blogger.com/atom/ns#'>setback</category><title>The events of the last few days</title><description>Wow it has been a hectic week.  This is the reason that it has been nearly a week since my last post.  Since I first became ill I have had many ups and downs, false dawns and setbacks.  I think this week has been the perfect example of this.  When I last posted I wrote about my niggling doubts about the candida diet because of the wind and disappearing energy etc.  However, I continued on and after a few days started to reap the rewards (ish).  My energy came back and the wind died back somewhat.  However, as there always seems to be, there was a sting in the tail.  My blood pressure was low at the start of the week and continued to drop almost daily to worrying lows (I had one reading of 87/38).  My hands and feet were freezing, my head was dizzy and I had pains in my hands  where the veins embossed.    The blood pressure raised when I did some exercise, a little dancing (don't tell anyone) or a brisk walk, but soon fell again as soon as I sat down for any length of time. Naturally I was worried.  Although, on the other hand, it was reassuring to find that I was able to do all this exercise without any problems.  I did more exercise in one day on Monday than I had done in months before.  However, on Tuesday it came to a head, perhaps as a result of the exercise - who knows?&lt;br /&gt;&lt;br /&gt;Tuesday morning, after a hot and cold shower and a few stretches, the b.p was on the verge of normal (105/59), but by lunch time this had lowered to (100/41).  Desparate for it not to fall any more I went for a short, brisk walk.  When I returned I had lunch but I wasn't feeling great.  I thought a short 30 min nap would sort me out.   I woke up 2 hrs later, panic stricken, heart pounding, sweating and disorientated.   I lay in bed not knowing exactly what to do, but I tried to go back to sleep.  A few hours later I woke up, felt ok (ish).  I took my b.p, which was normal (something like 115 / 70 - the highest it had been in a week).  I found this bizarre.  I went to the doctors to check it out anyway.  Again the doctor read my b.p as normal, but recommend I see a specialist to get my C.V system checked out properly.  This is what I am doing tomorrow.  However, since then my readings have been fine and I have had no other symptoms etc. This seemed truelly bizarre until I discovered that the readings my girl friend's parents' b.p measure varies depending on the position of your arm.  When I hold it in the position I was instructed by the doctor I get a low reading (altho everyone else seems to get a normal reading this way) and when you hold it as instructed in the manual, you get a normal reading.  This means that the chances are my bp had never actually been as low as I thought.  However, how do you explain the dizzy headaches, cold hands and feet, embossed veins and pains?  All of these disappeared on Tuesday afternoon so were they all manifested by panic? Hopefully the specialist will get to the bottom of my little mystery.&lt;br /&gt;&lt;br /&gt;During all of this I entered the next phase of the diet.  On Monday I started taking the replete that I was actually meant to take along with starting the diet, but found difficult to source in Germany.  So I have started 2 weeks late.  Biocare Replete is high strength acidophilus recommended to me by my herbalist.  It contains 100 billion bacteria per sachet (50 times the strength of my quest acidophilus) and you take 1 sachet per day for 7 days.  You take each sachet dissolved in water and with your first sip you can feel the effect.  Actually, it is not a particularly pleasant sensation, bringing about wind (not disimilar to what I have been experiencing).  The tub notes this as a possible side effect, so I will keep an eye on it and consult my herbalist if it continues.&lt;br /&gt;&lt;br /&gt;Well that was my week.  I hope this post makes sense.   I feel as if I have just blurted out everything in one incoherant rambling.  Maybe this is the best way to blog.  Let me know what you think.&lt;div class="blogger-post-footer"&gt;&lt;img width='1' height='1' src='https://blogger.googleusercontent.com/tracker/5905049951798499123-1802394544430643088?l=livingwithcfs.blogspot.com' alt='' /&gt;&lt;/div&gt;</description><link>http://livingwithcfs.blogspot.com/2007/03/last-events-of-last-few-days.html</link><author>noreply@blogger.com (David Elsweiler)</author><thr:total xmlns:thr='http://purl.org/syndication/thread/1.0'>1</thr:total></item><item><guid isPermaLink='false'>tag:blogger.com,1999:blog-5905049951798499123.post-4827815776460570855</guid><pubDate>Fri, 02 Mar 2007 12:56:00 +0000</pubDate><atom:updated>2007-03-02T05:52:51.592-08:00</atom:updated><category domain='http://www.blogger.com/atom/ns#'>sugar-free yeast-free diet</category><title>Diagnosing Candida</title><description>Over the past few days, my (candida) symptoms have progressively worsened.  My eyes have once again become cloudy, my energy levels decreased and the wind problem has returned to almost as bad as it has ever been.  Interestingly though, brain fog hasn't been a problem and I have been able to be  (&lt;span class="blsp-spelling-corrected" id="SPELLING_ERROR_0"&gt;comparatively&lt;/span&gt;) quite productive.&lt;br /&gt;&lt;br /&gt;The worsening symptoms have really caused me to question whether or not the problem is candida.  I have been searching for ways to diagnose Candida and here is what I have found.&lt;br /&gt;&lt;br /&gt;Generally, diagnosis comes from symptoms.  Several websites / books provide a list of symptoms that candida can cause and suggest that if a person has one or many of these symptoms Candida could be the answer.  The most complete list I found was by &lt;a href="http://www.afpafitness.com/articles/Candida.htm"&gt;Lindsey Duncan CN&lt;/a&gt;, a nutritionalist  and founder of the Home Nutrition Clinc in California.  A similar list is given in &lt;a href="http://www.amazon.co.uk/Complete-Guide-Food-Allergy-Intolerance/dp/0747534306/ref=pd_ka_1/202-2889996-6691002?ie=UTF8&amp;s=books&amp;amp;qid=1172841090&amp;sr=8-1"&gt;&lt;span class="srTitle"&gt;The Complete Guide to Food Allergy and Intolerance&lt;/span&gt;&lt;/a&gt;      by Jonathan Brostoff and Linda Gamlin.  However, I have misplaced my copy so I will need to refer to Lindsey Duncan's list.&lt;br /&gt;&lt;i&gt;&lt;span style=";font-family:Arial;font-size:85%;"  &gt;&lt;br /&gt;Ask yourself the following questions. One or more "yes" answers is a strong indication you have Candidiasis.&lt;/span&gt;&lt;/i&gt;  &lt;p class="article-text"&gt;&lt;span style=";font-family:Arial;font-size:85%;"  &gt;1. Have you ever taken cortico-steroid drugs or antibiotics, or been on antibiotics for an extended length of time?&lt;/span&gt;&lt;/p&gt;&lt;p class="article-text"&gt;&lt;span style=";font-family:Arial;font-size:85%;"  &gt;&lt;span style="font-weight: bold;"&gt;Yes, when I was in my teenage years I took several courses of antibiotics for acne.  One period lasted over 2 and 1/2 years.  I am convinced this is the reason for my illn&lt;/span&gt;&lt;/span&gt;&lt;span style=";font-family:Arial;font-size:85%;"  &gt;&lt;span style="font-weight: bold;"&gt;ess.  Since becoming ill, I have reluctantly had to take 3 more short courses of antibiotics for infections that could not have been controlled in any other way.&lt;/span&gt;&lt;br /&gt;&lt;/span&gt;&lt;/p&gt;&lt;p class="article-text"&gt;&lt;span style=";font-family:Arial;font-size:85%;"  &gt;2. Are you currently on birth control pills or ever taken them for a period of two years or more?&lt;br /&gt;&lt;/span&gt;&lt;/p&gt;&lt;p class="article-text"&gt;&lt;span style=";font-family:Arial;font-size:85%;"  &gt;&lt;span style="font-weight: bold;"&gt;(n/a)&lt;/span&gt;&lt;br /&gt;&lt;/span&gt;&lt;/p&gt;&lt;p class="article-text"&gt;&lt;span style=";font-family:Arial;font-size:85%;"  &gt;3. Have you ever been plagued with vaginal yeast infections, vaginitis, PMS, menstrual pain, endometriosis, prostatitis, or loss of sexual interest? &lt;span style="font-weight: bold;"&gt;&lt;br /&gt;&lt;/span&gt;&lt;/span&gt;&lt;/p&gt;&lt;p class="article-text"&gt;&lt;span style=";font-family:Arial;font-size:85%;"  &gt;&lt;span style="font-weight: bold;"&gt;(n/a)&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;4. Do you crave sweets, bread or alcoholic beverages?&lt;/span&gt;&lt;/p&gt;&lt;p class="article-text"&gt;&lt;span style=";font-family:Arial;font-size:85%;"  &gt;&lt;span style="font-weight: bold;"&gt;Yes, I have often craved chocolate and other sweet goodies.  Never alcohol though&lt;/span&gt;&lt;br /&gt;&lt;/span&gt;&lt;/p&gt;&lt;p class="article-text"&gt;&lt;span style=";font-family:Arial;font-size:85%;"  &gt;5. Do you suffer from unexplained aches and pains or headaches?&lt;/span&gt;&lt;/p&gt;&lt;p class="article-text"&gt;&lt;span style=";font-family:Arial;font-size:85%;"  &gt;&lt;span style="font-weight: bold;"&gt;Yes, I have had various unexplained aches and pains including headaches since my illness started&lt;/span&gt;&lt;br /&gt;&lt;/span&gt;&lt;/p&gt;&lt;p class="article-text"&gt;&lt;span style=";font-family:Arial;font-size:85%;"  &gt;6. Have you been pregnant more than twice? (Hormonal changes contribute to candidiasis susceptibility.)&lt;br /&gt;&lt;/span&gt;&lt;/p&gt;&lt;p class="article-text"&gt;&lt;span style=";font-family:Arial;font-size:85%;"  &gt;&lt;span style="font-weight: bold;"&gt;(n/a)&lt;/span&gt;&lt;/span&gt;&lt;/p&gt;&lt;p class="article-text"&gt;&lt;span style=";font-family:Arial;font-size:85%;"  &gt;&lt;br /&gt;7. Are you overly sensitive to chemicals including perfumes, tobacco smo&lt;/span&gt;&lt;span style=";font-family:Arial;font-size:85%;"  &gt;ke, paint, insecticides, etc.?&lt;/span&gt;&lt;/p&gt;&lt;p class="article-text"&gt;&lt;span style=";font-family:Arial;font-size:85%;"  &gt;&lt;span style="font-weight: bold;"&gt;Not that I know of&lt;/span&gt;&lt;br /&gt;&lt;/span&gt;&lt;/p&gt;&lt;p class="article-text"&gt;&lt;span style=";font-family:Arial;font-size:85%;"  &gt;8. Are you bothered by chronic digestive complaints such as bloating, gas? Do you have constipation or diarrhea?&lt;/span&gt;&lt;/p&gt;&lt;p class="article-text"&gt;&lt;span style=";font-family:Arial;font-size:85%;"  &gt;&lt;span style="font-weight: bold;"&gt;Yes, I have suffered wind for some time.  Chronically over the last few months.&lt;/span&gt;&lt;br /&gt;&lt;/span&gt;&lt;/p&gt;&lt;p class="article-text"&gt;&lt;span style=";font-family:Arial;font-size:85%;"  &gt;9. Do you find yourself having to deal with problems like athlete's foot, jock itch, nail fungus, ring worm? Do you have bouts with psoriasis, eczema, hives or chronic dermatitis?&lt;/span&gt;&lt;/p&gt;&lt;p class="article-text"&gt;&lt;span style=";font-family:Arial;font-size:85%;"  &gt;&lt;span style="font-weight: bold;"&gt;Yes, I have had several fungal infections over the period of my illness in various parts of my body including my toes.  I have also had dermatitis on my pinky for some time, although this has cleared up significantly since starting this new diet.&lt;/span&gt;&lt;br /&gt;&lt;/span&gt;&lt;/p&gt;&lt;p class="article-text"&gt;&lt;span style=";font-family:Arial;font-size:85%;"  &gt;10. Are you chronically fatigued? Do you suffer from memory loss ("brain fog"), erratic vision, spots or  "floaters" in front of your eyes, nervous tension?&lt;/span&gt;&lt;/p&gt;&lt;p class="article-text"&gt;&lt;span style=";font-family:Arial;font-size:85%;"  &gt;&lt;span style="font-weight: bold;"&gt;Yes, I have been diagnosed formally with CFS.  I have sometimes, since my illness began, suffered from tip-of-the-tongue situations and I have often referred to "brain fog" although this is not a permanent thing.  My eyes are often yellow, blood shot and glased.  Further, I h&lt;/span&gt;&lt;/span&gt;&lt;span style=";font-family:Arial;font-size:85%;"  &gt;&lt;span style="font-weight: bold;"&gt;ave (uncharacteristically) been nervous and panicy many times since I became ill.&lt;/span&gt;&lt;br /&gt;&lt;/span&gt;&lt;/p&gt;&lt;p class="article-text"&gt;&lt;span style=";font-family:Arial;font-size:85%;"  &gt;11. Do you feel depressed or ill for no known reason? Do you feel worse on damp days?&lt;/span&gt;&lt;/p&gt;&lt;p class="article-text"&gt;&lt;span style=";font-family:Arial;font-size:85%;"  &gt;&lt;span style="font-weight: bold;"&gt;I have had many down days in the last year.  However, mostly I remain a very positive person. I'm not sure about damp days that is something to look out for.&lt;/span&gt;&lt;br /&gt;&lt;/span&gt;&lt;/p&gt;&lt;p class="article-text"&gt;&lt;span style=";font-family:Arial;font-size:85%;"  &gt;12. Do you often have cold hands and feet?&lt;/span&gt;&lt;/p&gt;&lt;p class="article-text"&gt;&lt;span style=";font-family:Arial;font-size:85%;"  &gt;&lt;span style="font-weight: bold;"&gt;Yes&lt;/span&gt;&lt;/span&gt;&lt;span style=";font-family:Arial;font-size:85%;"  &gt;&lt;br /&gt;&lt;/span&gt;&lt;/p&gt;&lt;p class="article-text"&gt;&lt;span style=";font-family:Arial;font-size:85%;"  &gt;13. Is your tongue coated?&lt;/span&gt;&lt;/p&gt;&lt;p class="article-text"&gt;&lt;span style=";font-family:Arial;font-size:85%;"  &gt;&lt;span style="font-weight: bold;"&gt;It has been but in the last few days I have noticed that it is less so - good sign?&lt;/span&gt;&lt;br /&gt;&lt;/span&gt;&lt;/p&gt;&lt;p class="article-text"&gt;So I scored high on most of these questions.  In addition to taking this test I have taken the "Candida Spit test" that was first recommended to me by &lt;a href="http://copingwithme.blogspot.com/"&gt;Sarah&lt;/a&gt;.  I have since read about this test in a number of places.  Including &lt;a href="http://www.adhdrelief.com/CandidaTest.html"&gt;this site.&lt;/a&gt; who recommend the following:&lt;br /&gt;&lt;/p&gt;&lt;p align="left"&gt;        &lt;/p&gt;&lt;blockquote&gt;&lt;p align="left"&gt;&lt;span style=";font-family:Verdana,Arial,Helvetica,sans-serif;font-size:85%;"  &gt;First thing in        the morning, before you put &lt;b&gt;ANYTHING &lt;/b&gt;in your mouth, fill a clear glass        with room temperature &lt;b&gt;Bottled Water.&lt;/b&gt; &lt;/span&gt;        &lt;/p&gt;&lt;p align="left"&gt;        &lt;span style=";font-family:Verdana,Arial,Helvetica,sans-serif;font-size:85%;"  &gt;Work up a bit        of saliva, then spit it into the glass of water. Check the water every 15        minutes or so for up to one hour. &lt;/span&gt;        &lt;/p&gt;&lt;p align="left"&gt;        &lt;span style=";font-family:Verdana,Arial,Helvetica,sans-serif;font-size:85%;"  &gt;If you have a        &lt;b&gt;potential problem&lt;/b&gt;, you will see &lt;b&gt;strings&lt;/b&gt; (lik&lt;/span&gt;&lt;span style=";font-family:Verdana,Arial,Helvetica,sans-serif;font-size:85%;"  &gt;e legs) traveling        down into the water from the saliva floating on the top, or &lt;b&gt;"cloudy"        saliva&lt;/b&gt; will sink to the bottom of the glass, or &lt;b&gt;cloudy specks&lt;/b&gt;        will seem to be suspended in the water. &lt;/span&gt;        &lt;/p&gt;&lt;p align="left"&gt;        &lt;span style=";font-family:Verdana,Arial,Helvetica,sans-serif;font-size:85%;"  &gt;If there are        no strings and the saliva is still floating after at least one hour, you        probably have Candida under control, and have nothing to worr&lt;/span&gt;&lt;span style=";font-family:Verdana,Arial,Helvetica,sans-serif;font-size:85%;"  &gt;y about.         &lt;b&gt;Congratulations.&lt;/b&gt;&lt;/span&gt;&lt;/p&gt;&lt;p align="left"&gt;&lt;a onblur="try {parent.deselectBloggerImageGracefully();} catch(e) {}" href="http://www.adhdrelief.com/images/testglass.jpg"&gt;&lt;img style="margin: 0px auto 10px; display: block; text-align: center; cursor: pointer; width: 227px; height: 179px;" src="http://www.adhdrelief.com/images/testglass.jpg" alt="" border="0" /&gt;&lt;/a&gt;&lt;/p&gt;   I took this test and my saliva was stringy.  More evidence for the candida problem.  So what does this mean?  According to these tests (how reliable they are I have no idea) the evidence points to a candida problem.  So why am I getting worse again despite being on this diet?  This has been puzzling me.  One explanation is that I am suffering Herxheimer                or "die-off" reaction. According to some websites such as &lt;a href="http://www.ei-resource.org/anti-fungal.asp"&gt;this one&lt;/a&gt;, this is said to occur as a result                of the yeast being killed too rapidly which overwhelms the body                with yeast cells and their toxins. Any number of nasty symptoms                can arise as a result, most frequently a flu-like feeling or worsening                of symptoms already present. The solution to this may be to take                a lower dose of anti-fungal for a while or take extra fibre or a                product like bentonite clay to help carry the toxins out of the                body before they are absorbed.  My herbalist never mentioned this when he recommended the special diet, nor did the food allergy book, but it is certainly something I will ask him about.&lt;br /&gt;&lt;br /&gt;So what do I do in the mean time?  I think all that I can do is continue with my diet and perhaps try and increase my fibre intake.&lt;br /&gt;&lt;br /&gt;&lt;p align="left"&gt;&lt;br /&gt;&lt;/p&gt;&lt;p align="left"&gt;&lt;br /&gt;&lt;/p&gt;&lt;/blockquote&gt;&lt;p align="left"&gt;&lt;span style=";font-family:Verdana,Arial,Helvetica,sans-serif;font-size:85%;"  &gt;&lt;b&gt;&lt;/b&gt;&lt;/span&gt;&lt;/p&gt;&lt;p align="left"&gt;&lt;br /&gt;&lt;/p&gt;&lt;p align="left"&gt;&lt;span style=";font-family:Verdana,Arial,Helvetica,sans-serif;font-size:85%;"  &gt;&lt;b&gt;&lt;br /&gt;&lt;/b&gt;&lt;/span&gt;        &lt;/p&gt;&lt;div class="blogger-post-footer"&gt;&lt;img width='1' height='1' src='https://blogger.googleusercontent.com/tracker/5905049951798499123-4827815776460570855?l=livingwithcfs.blogspot.com' alt='' /&gt;&lt;/div&gt;</description><link>http://livingwithcfs.blogspot.com/2007/03/diagnosing-candida.html</link><author>noreply@blogger.com (David Elsweiler)</author><thr:total xmlns:thr='http://purl.org/syndication/thread/1.0'>9</thr:total></item><item><guid isPermaLink='false'>tag:blogger.com,1999:blog-5905049951798499123.post-2253565115291260124</guid><pubDate>Tue, 27 Feb 2007 09:39:00 +0000</pubDate><atom:updated>2007-02-27T01:59:41.477-08:00</atom:updated><category domain='http://www.blogger.com/atom/ns#'>sugar-free yeast-free diet</category><title>A wee bit confused ...</title><description>The last few days have been a bit of a puzzler for me.  The first week or so of this diet had been so profitable.  The progress I had made in a short period of time made it easy to avoid eating foods that normally would challenge my will power.  My eyes were clearer, my mind was clearer and my energy levels were continuously improving.  Then, on Sunday I had a wee dip in energy that got me down a little, but in the evening it came back and I was fine.  Yesterday I was feeling ok in the morning, but the wind was quite bad mid-afternoon (albeit not as bad as it once had been) and continued until bed time.  Today, I just feel terrible.  My eyes are bloodshot, my arms and legs are heavy and I have the brain fog again.  I have not had any of the foods I am meant to avoid so what does this mean?  Does it mean that Candida is not the (main) problem?  Is it just another period of adjustment that my body needs to get used to this diet?  Is it perhaps that the problem is a food intolerance - I have been avoiding a particular food for a week and then inadvertently consumed it in the last few days?&lt;br /&gt;&lt;br /&gt;These are challenging questions and the setbacks - I say setbacks because they are not full blown crashes, no where near - have thrown niggling doubts into my will power.  Am I avoiding these goodies, things that give me pleasure for no reason?  Is it sheer coincidence that I felt better for the first week? &lt;br /&gt;&lt;br /&gt;I have to be strong and give this diet the full month to do its job.  I have also finally been able to order the high strength acidophilus (&lt;a href="http://www.ventris.org.uk/health_supplements_biocare_replete_b305-20.htm"&gt;biocare replete&lt;/a&gt;) that is meant to complement this diet. &lt;br /&gt;&lt;br /&gt;I will also make a note of what I have eaten in the last few days incase I need to find patterns for a food allergy later.  For now, though, keep the chocolate away from me....&lt;br /&gt;&lt;br /&gt;&lt;span style="font-style: italic; font-weight: bold;"&gt;Sunday&lt;/span&gt;&lt;span style="font-weight: bold;"&gt; &lt;/span&gt;&lt;br /&gt;&lt;br /&gt;breakfast: Live yoghurt with oats&lt;br /&gt;Lunch: Russian savoury mince with leak and potatoes&lt;br /&gt;Dinner: Red lentil and coconut soup with rye crackers and oat cakes.&lt;br /&gt;&lt;br /&gt;&lt;span style="font-weight: bold; font-style: italic;"&gt;Monday&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;breakfast: Live yoghurt with oats&lt;br /&gt;Lunch: Red lentil and coconut soup with rye crackers and oat cakes with walnut, tofu and aubergine spread&lt;br /&gt;Dinner: short-grain brown rice and pepper stir-fry with pork&lt;div class="blogger-post-footer"&gt;&lt;img width='1' height='1' src='https://blogger.googleusercontent.com/tracker/5905049951798499123-2253565115291260124?l=livingwithcfs.blogspot.com' alt='' /&gt;&lt;/div&gt;</description><link>http://livingwithcfs.blogspot.com/2007/02/wee-bit-confused.html</link><author>noreply@blogger.com (David Elsweiler)</author><thr:total xmlns:thr='http://purl.org/syndication/thread/1.0'>2</thr:total></item><item><guid isPermaLink='false'>tag:blogger.com,1999:blog-5905049951798499123.post-7889924165462475670</guid><pubDate>Sun, 25 Feb 2007 16:41:00 +0000</pubDate><atom:updated>2007-02-25T08:47:42.140-08:00</atom:updated><title>A wee bit down</title><description>I'm feeling a wee bit low at the moment.  I knew that I was probably setting myself up for a fall by believing that I had found a miracle cure and it is still possible that it may be the help that I need.  However, it is mid-afternoon and I am feeling really worn out and its enough to lower my spirits again.  It's not like a crash - the tiredness didn't come on suddenly.  Rather it crept up and gradually this afternoon I have just got more and more lackluster.&lt;br /&gt;&lt;br /&gt;So what I'm going to do now is have a wee meditation then listen to &lt;a href="http://www.bbc.co.uk/radio2/shows/parkinson/"&gt;Parky&lt;/a&gt;, which usually cheers me up.&lt;div class="blogger-post-footer"&gt;&lt;img width='1' height='1' src='https://blogger.googleusercontent.com/tracker/5905049951798499123-7889924165462475670?l=livingwithcfs.blogspot.com' alt='' /&gt;&lt;/div&gt;</description><link>http://livingwithcfs.blogspot.com/2007/02/wee-bit-down.html</link><author>noreply@blogger.com (David Elsweiler)</author><thr:total xmlns:thr='http://purl.org/syndication/thread/1.0'>1</thr:total></item><item><guid isPermaLink='false'>tag:blogger.com,1999:blog-5905049951798499123.post-3712207665479129910</guid><pubDate>Sun, 25 Feb 2007 13:14:00 +0000</pubDate><atom:updated>2007-02-25T06:01:02.786-08:00</atom:updated><title>Dealing with those heavy legs</title><description>One symptom common to most sufferers of chronic fatigue syndrome / ME is the "heavy legs".&lt;br /&gt;I know that other suffers refer to these  by other names such as &lt;a href="http://www.liverpool-leftovers.blogspot.com/"&gt;"lead-legs"&lt;/a&gt; or "&lt;a href="http://velo-gubbed-legs.blogspot.com/"&gt;&lt;span class="blsp-spelling-error" id="SPELLING_ERROR_0"&gt;velo&lt;/span&gt;-&lt;span class="blsp-spelling-error" id="SPELLING_ERROR_1"&gt;gubbed&lt;/span&gt; legs&lt;/a&gt;".&lt;br /&gt;&lt;br /&gt;From my experience this is not always the same feeling, but a spectrum of feelings.  At one end the problem is "chronic" with me not being able to move my legs at all, feeling as though they are lumps of metal, at the other end it is a mild heaviness that means I cannot walk as fast or as far as normal.   When I was first diagnosed with ME I often experienced heavy legs (and arms) at the chronic end of the spectrum.  If I was lying in bed it actually felt as though I had an invisible man lying on top of me who was pushing my body into the bed.  I can assure you that this is a very disturbing feeling.  I still experience heavy legs and arms from time to time, but usually the feeling is on the milder side of the scale.  I have found mild stretches in the morning and evening reduce the problem considerably.&lt;br /&gt;&lt;br /&gt;I don't recommend these if the problem is at the "chronic" side of the spectrum, but if the problem is on the milder side give them a go.  Don't over do it - if your muscles are not used to being stretched then break them in gently.  My physio recommended the following stretches when to aid my route to recovery.&lt;br /&gt;&lt;br /&gt;&lt;a onblur="try {parent.deselectBloggerImageGracefully();} catch(e) {}" href="http://3.bp.blogspot.com/_M_kiyr6aT3o/ReGTLtu5E3I/AAAAAAAAAAY/yRl1CN4Po5U/s1600-h/hamstring_Stretch.JPG"&gt;&lt;img style="margin: 0pt 10px 10px 0pt; float: left; cursor: pointer;" src="http://3.bp.blogspot.com/_M_kiyr6aT3o/ReGTLtu5E3I/AAAAAAAAAAY/yRl1CN4Po5U/s320/hamstring_Stretch.JPG" alt="" id="BLOGGER_PHOTO_ID_5035467687841043314" border="0" /&gt;&lt;/a&gt;&lt;br /&gt;1) The hamstring stretch (figure: left)&lt;br /&gt;&lt;br /&gt;lying flat on the floor with knees stretched to 90 degrees and back flat on the floor.   Slowly raise and straighten one leg, grasping it loosely with behind the thigh with both hands.&lt;br /&gt;&lt;br /&gt;&lt;br /&gt;&lt;br /&gt;&lt;a onblur="try {parent.deselectBloggerImageGracefully();} catch(e) {}" href="http://1.bp.blogspot.com/_M_kiyr6aT3o/ReGUINu5E4I/AAAAAAAAAAg/KDsd7btu-FE/s1600-h/calf_stretch.JPG"&gt;&lt;img style="margin: 0pt 0pt 10px 10px; float: right; cursor: pointer;" src="http://1.bp.blogspot.com/_M_kiyr6aT3o/ReGUINu5E4I/AAAAAAAAAAg/KDsd7btu-FE/s320/calf_stretch.JPG" alt="" id="BLOGGER_PHOTO_ID_5035468727223128962" border="0" /&gt;&lt;/a&gt;&lt;br /&gt;&lt;br /&gt;2)  The calf stretch (figure:right)&lt;br /&gt;&lt;br /&gt;Standing 3-4 feet from a wall with feet in position shown &lt;span class="blsp-spelling-error" id="SPELLING_ERROR_2"&gt;perpindicular&lt;/span&gt; to the wall.  Lean against your forearms while maintaining a straight line through the spine and your back heel firmly on the floor.&lt;br /&gt;&lt;br /&gt;&lt;br /&gt;&lt;br /&gt;&lt;br /&gt;&lt;a onblur="try {parent.deselectBloggerImageGracefully();} catch(e) {}" href="http://3.bp.blogspot.com/_M_kiyr6aT3o/ReGVgtu5E5I/AAAAAAAAAAw/VcwG0yL619s/s1600-h/quad_stretch.JPG"&gt;&lt;img style="margin: 0pt 10px 10px 0pt; float: left; cursor: pointer;" src="http://3.bp.blogspot.com/_M_kiyr6aT3o/ReGVgtu5E5I/AAAAAAAAAAw/VcwG0yL619s/s320/quad_stretch.JPG" alt="" id="BLOGGER_PHOTO_ID_5035470247641551762" border="0" /&gt;&lt;/a&gt;&lt;br /&gt; 3) The quad stretch (figure:left)&lt;br /&gt;&lt;br /&gt;Stand with one hand against the wall for balance.  Bring the foot up to the hand and grasp around the ankle.  Pull gently upwards until the stretch is felt.  Remember to keep the knees side by side.&lt;br /&gt;&lt;br /&gt;&lt;br /&gt;&lt;br /&gt;Thank you to the&lt;a href="http://www.city.saskatoon.sk.ca/org/leisure/programs/smartstart/stretch/design_plan.asp"&gt; city of Saskatoon leisure programme&lt;/a&gt; for the images and text.&lt;div class="blogger-post-footer"&gt;&lt;img width='1' height='1' src='https://blogger.googleusercontent.com/tracker/5905049951798499123-3712207665479129910?l=livingwithcfs.blogspot.com' alt='' /&gt;&lt;/div&gt;</description><link>http://livingwithcfs.blogspot.com/2007/02/dealing-with-those-heavy-legs.html</link><author>noreply@blogger.com (David Elsweiler)</author><media:thumbnail xmlns:media='http://search.yahoo.com/mrss/' url='http://3.bp.blogspot.com/_M_kiyr6aT3o/ReGTLtu5E3I/AAAAAAAAAAY/yRl1CN4Po5U/s72-c/hamstring_Stretch.JPG' height='72' width='72'/><thr:total xmlns:thr='http://purl.org/syndication/thread/1.0'>0</thr:total></item><item><guid isPermaLink='false'>tag:blogger.com,1999:blog-5905049951798499123.post-591006993783291776</guid><pubDate>Sat, 24 Feb 2007 15:50:00 +0000</pubDate><atom:updated>2007-02-24T08:01:04.349-08:00</atom:updated><category domain='http://www.blogger.com/atom/ns#'>sugar-free yeast-free diet</category><title>Killing 2 birds ...</title><description>Two problems I have had with the sugar and yeast free diet are 1) I am worried about my vitamin C intake because of my lack of fruit and 2) I cannot find anything interesting to put on my bread &lt;span class="blsp-spelling-corrected" id="SPELLING_ERROR_0"&gt;substitutes (rye crackers, rice cakes, and oat cakes).&lt;br /&gt;&lt;br /&gt;I have been exploring different ways of tackling these problems.  I thought about vitamin c supplements, but these are loaded with nasty extras including sugar and various E numbers so that is out.  I thought about veggie spreads that Christine loves so much and are freely available here in Germany.   However, these also seem to have one or more of the things that I cannot have: sugar, yeast-extract or lemon juice.&lt;br /&gt;&lt;br /&gt;Then I found a solution to both problems in one go.  A recipe for walnut, aubergine and tofu pate.  Walnuts are rich in vitamins C and E, as well as zinc.  Aubergines are full of calcium, phosphorus and beta-carotene, which help clean the blood and protect arteries.  Tofu is a great source of protein and iron.&lt;br /&gt;&lt;br /&gt;So all in all a healthy snack.  When I get a chance I will post the recipe to &lt;a href="http://www.snacksby.com"&gt;snacksby.&lt;/a&gt;&lt;br /&gt;&lt;/span&gt;&lt;div class="blogger-post-footer"&gt;&lt;img width='1' height='1' src='https://blogger.googleusercontent.com/tracker/5905049951798499123-591006993783291776?l=livingwithcfs.blogspot.com' alt='' /&gt;&lt;/div&gt;</description><link>http://livingwithcfs.blogspot.com/2007/02/killing-2-birds.html</link><author>noreply@blogger.com (David Elsweiler)</author><thr:total xmlns:thr='http://purl.org/syndication/thread/1.0'>0</thr:total></item><item><guid isPermaLink='false'>tag:blogger.com,1999:blog-5905049951798499123.post-7073994862804729233</guid><pubDate>Sat, 24 Feb 2007 13:48:00 +0000</pubDate><atom:updated>2007-02-24T05:59:08.626-08:00</atom:updated><title>A strange thing happened last night ...</title><description>For the first time in over 10 months, Christine, my girlfriend was more tired than I was on a Friday evening.  We visited friends to watch a DVD and returned home unusually late for me - around 1 am.  I felt strangely fit, whereas Christine was dead on her feet.&lt;br /&gt;&lt;br /&gt;Perhaps I am getting my hopes up; setting myself up for a fall, but half of me firmly believes that this diet free of sugars and yeasts may be the answer to my problems.   I have now been avoiding sugars for nearly two weeks (strictly without fruit and yeast for 5 days) and an increase in energy has not been the only change.  The amount of wind that I have experienced as dropped  by a huge amount and the dermatitis in my finger - something that has been with me for 8 months - has cleared up considerably too.  Are these all coincidences?  Only time will tell, but for the moment at least, I am remaining cautiously positive.&lt;div class="blogger-post-footer"&gt;&lt;img width='1' height='1' src='https://blogger.googleusercontent.com/tracker/5905049951798499123-7073994862804729233?l=livingwithcfs.blogspot.com' alt='' /&gt;&lt;/div&gt;</description><link>http://livingwithcfs.blogspot.com/2007/02/strange-thing-happened-last-night.html</link><author>noreply@blogger.com (David Elsweiler)</author><thr:total xmlns:thr='http://purl.org/syndication/thread/1.0'>0</thr:total></item><item><guid isPermaLink='false'>tag:blogger.com,1999:blog-5905049951798499123.post-5919555302116865551</guid><pubDate>Fri, 23 Feb 2007 08:43:00 +0000</pubDate><atom:updated>2007-02-23T00:43:20.698-08:00</atom:updated><title>Getting enough veggies</title><description>One problem that I have found with this new diet is getting enough vegetables into my &lt;span class="blsp-spelling-corrected" id="SPELLING_ERROR_0"&gt;daily&lt;/span&gt; intake.  I never used to have problems with this because I ate lots of fruit and drank fruit juice.  However these are all no nos now.  Yesterday I resorted to steaming myself an extra portion of veggies before dinner to satisfy the need.  I have also thought about nibbling raw carrots or peppers, but these may be difficult to digest.&lt;br /&gt;&lt;br /&gt;Does anyone have any ideas on how I can sneak more veggies into my diet?  All thoughts appreciated!&lt;br /&gt;&lt;br /&gt;Yesterday's diet was the following:&lt;br /&gt;&lt;br /&gt;breakfast: porridge (no sugar or fruit, but plenty of milk)&lt;br /&gt;lunch: rye crackers with smoked salmon and ham&lt;br /&gt;snacks: cashew and brasil nuts and a portion of steamed veggies&lt;br /&gt;dinner:salmon pasta, cooked in onion, garlic and cream with spinach&lt;div class="blogger-post-footer"&gt;&lt;img width='1' height='1' src='https://blogger.googleusercontent.com/tracker/5905049951798499123-5919555302116865551?l=livingwithcfs.blogspot.com' alt='' /&gt;&lt;/div&gt;</description><link>http://livingwithcfs.blogspot.com/2007/02/getting-enough-veggies.html</link><author>noreply@blogger.com (David Elsweiler)</author><thr:total xmlns:thr='http://purl.org/syndication/thread/1.0'>2</thr:total></item></channel></rss>