Fibromyligia & Chronic Fatigue Syndrome
Posted , 4 users are following.
Can anyone please give me advice....I am having difficulty in explaining in face to face conversations to health professionals how my Fibro and CFS affects me day to day the pain the fatigue the brain fog the overall bone pain the limitations it impacts on my activities of daily living I just get all stressed and can't explain I waver from one thing to another I have to see an independent doctor to assess my condition as stated by Occi health as I am applying for ill health early medical retirement I will be 56 in June and am dreading this please any advice....thanks HarrietÂ
1 like, 6 replies
trisha87499 Harriet72
Posted
Harriet72 trisha87499
Posted
trisha87499 Harriet72
Posted
Boqer Harriet72
Posted
I found the same thing! Sit down when you are calm and write down how you are and the way things affect you, even write down examples of things that have happened. Then when you go in take the paper with you and read from it. That's what I had to do, and it was fine. It's extremely difficult just to say things normally, never mind when you are under the stress of an assessment or something. You have fibro, we get brain fog and forgetfulness, don't be worried about writing things down, it's the best way.
hope this helps
have a nice day
Boqer
Harriet72 Boqer
Posted
hope4cure Harriet72
Posted
blood test are important to rule out some other issues.
Take careÂ