I am just curious as to how many people get a flu shot who have ME CFS. I haven't had a cold in eight years and I think the last time I got a flu shot before I knew what I had and it made me crash. What is anybody's experience with Flu shots out. I believe my immune system is too shot to deal with a shot. When I tell my local non ME CFS GP that I don't want a FLU shot I get the eye roll. Basically half of my immune system (TH-1) is shut down and TH-2 part of my immune system (fights bacteria) is going a hundred miles an hour, maybe 99 mph.
What say you, flu shot or no flu shot????? Reactions...no reactions????
DID YOU GET A FLU SHOT THIS YEAR WITH ME CFS?
Blog entry posted by Xandoff, Jan 13, 2013.
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