Food Intolerances
July 7, 2006 by laura
Filed under Diseases & Conditions
Last night, I had a flashback to the early days of my life with CFIDS. I used to have to be so careful with what I ate. It seemed that everything I ate would cause a reaction. A little bit of chicken, would cause a scary high fever, certain fruits would bring on a headache…..and potatoes just forget them – they were completely eliminated from my nutritional menu, if i had even the tiniest bit, i would be doubled over in pain for hours.
But over the years, things have seemed to calm down in that area. That is, until the other night. Two nights ago, a friend from out of town was visiting me. We decided to order in. Our cuisine of choice…..chinese. Huge mistake. Now, chinese food has been not so great to me in the past. Usually I try to avoid it (but I always thought that it was an intimidation thing ~so much food on a table could bring on a mini relapse)…I prefer west coast/asian fusion cuisine better anyway. But this place was close in proximity, and is reputed to have good food.
I probably don’t have to say anything more….but all of the old signs came back full force last night. Strange how the reaction is no longer immediate, but the symptoms were all there. Fever, pain, headaches……and today I just feel wasted.
So the plan is for the next 2 days, is the BRAT diet. For those of you who don’t know this elimination diet; it consists of Bananas, Rice, Applesauce, and Toast, along with clear liquids. After that I will be slowly re-introducing food, so I don’t have another night like last night. Check out this link to learn more about elimination diets. I don’t recommend them for long term use…..but they certainly help for short term trials.
Hopefully I will be back to my old self, soon enough















Morning Laura. As I read your blog today, I wondered how many people have food intolerances with their CFS. I do not, or at least I don’t think I have any. I hope others with this issue will write. I do have a problem with the weather, if it gets to humid or to cold. I get very tired when the weather changes also from one extreme to the other. Do you have issues with the weather?
Karen
Karen….weather does affect ones symptoms with CFIDS and especially Fibromyalgia. Usually symptoms are lessoned if you live or visit a drier climate. I have been told that Arizona is a good place to visit if you are afflicted.
I live in the Pacific Northwest. An area which is known for its mild temperatures, and wet climate.
and so of course I am affected by weather!!!!!
Thank you for reminding me about that. I will be sure to write a post very soon about the climate, and how we deal with these issues.
~Laura