Nothing about my condition has changed and if anything it's gotten worse! Come to find out they only revised part of my medical records and only had 3 of my 16 yes I said 16 total medications listed! Now I have to stress about this issue for months till I get a date for a case review. Their incompetence should be held accountable!
Just wondering how things have gone since your post of 9 months ago when you were having huge issues with tests vs your condition. Haven't seen anything from you since then, but I'm not on here regularly--wish I were, but, as you know, every day is a challenge. Wishing you the very best for the right outcome!! Waiting to hear! Hugs--Jude
Please tell me you have an attorney!
Good question!!! Would greatly appreciate any help you could give me! My pcp is helping me also.
GRRRRR! You would think that the disablitiy checks came straight from the accounts of the people working the cases. We MUST make FM more understood by all. I am working diligently on a pilot program to help raise awareness. May 12 in National Fibromyalgia Awareness Day (in the U.S. at least) and I am trying to come up with ideas to spread the word, to educate, etc. These folks you are talking about really don't get it. How can we get them to understand and care?
I got refused disability as they said I can have a face to face conversation and plan a journey to work. I'm only 5 minutes from my work by car and 10 by bus. Also because I turned to pick my bag up and take my medication. My chemist make my tablet box up every week. At times I really struggle to walk at times and fall over. J think it's a disgrace how they mark you for it. 😞