Fibromyalgia Support Group
You're not alone in your pain. Fibromyalgia is a condition that can be difficult to diagnose and manage. If you're trying to cope with pain throughout your body, sleep problems, general fatigue, or other common fibromyalgia symptoms, you're in the right place. The community is here for you to talk about therapies and share your challenges.
I would just do the best you can. From what I've read, the social security judges don't give these type of evaluations a lot of credit as they are usually only seeing you one time, for a short visit.
I have an appt. to go to a counselor that they are requiring me to visit in my attempt to get SSDI. I also suffer from depression, so I believe that is why they are sending me to her.
I also had a mental evaluation and again one meeting is not going to tell them if I am insane. I guess I passed that test! ha!
I have talked to friends who are SS caseworkers and they say the average for getting approval is 2 yrs. So, don't let the 3 or more rejections get you down. I don't want you to give up.
Hiring a law firm specializing in Disability is an option. I hired one when I was told I would have a hearing and I didn't want to go it alone. Attorney gets 25% of what is owed to you when you are approved. One time payment paid by social security to the lawyer.
Hang in there!
The state of IL has one of the better rates for being approved on initial application. Unfortunately, fibromyalgia, while an approved "blue book" diagnosis for SSI/SSDI, is difficult to get approved for if that's the only basis for application. I don't know if that's the only thing you're applying for, but that's what I discovered. When I applied I mentioned all of my health issues (but I have a lot of them, including over 20 surgeries).
With regard to the CE (Consultative Exam)... the reviewer requests one if s/he feel that your medical records do not provide enough evidence to support your diagnosis OR that you don't have recent enough medical evidence OR that something was mentioned in your medical records that needs to be explored further (for example, if you didn't mention depression, but a doctor mentioned it in your records, then the examiner has to request that it be looked into further in a CE). It's fairly common to be sent on a CE and some claimants are sent on multiple CEs.
What actually happens during the CE varies dramatically depending on the reason why you're being sent for one (the letter should state why) and the individual practitioner who is performing it. These are not state doctors, but doctors who are contracted with the state to perform these exams and you can actually provide feedback to SSA about the doctor's performance.
One thing I did before my CE was google the doctor I had the CE with. Sure enough, I found cases where this doctor's exam reports were cited during hearings and was able to get a feel for the type of reports she did. I also familiarized myself with the doctor's training and background so that I knew what her "bent" was ahead of time. It's the same I would do before I would go to see any doctor actually, so why not? Besides, it also helped me feel less anxious about the process.
Since you're going in for fibromyalgia (and whatever else), be sure to state clearly how you are disabled -- don't make them guess and don't assume that they're going to be able to tell from your exam or state it the way you want it to be said. Remember what you said in your disability application? Be consistent. If you said that you're in pain all the time and exhausted and have trouble getting through your day and this is cause you to be depressed, say it during your CE. Even if the doctor is rude and impolite and may not seem to be the brightest bulb, be polite yourself and just maintain and be sure to point out the things that affect your quality of life. Don't exaggerate or be dramatic or try to appear that you're in more pain or discomfort or whatever than you are because they can tell, but don't be shy about stating what your issues are either.
Good luck!
The visits with the docs, the shrink and the medical doc, were a JOKE!! 5-10 minutes...they will make you mad with their attitude too so don't expect any sympathy from them. It is like something SSDI requires but is a total and complete waste of time and money...hoping you won't show...anything to get you to give up.
DON'T LET THEM DETER YOU WITH THEIR ATTITUDES TOWARD YOUR ILLNESS...THEY ARE WORTHLESS PROFESSIONALLY!!!
Just go to it...IF your lawyer says it's ok (if you have one) and get it over with. Tell them how it is but just don't put much stock into anything they say to you. Mine both said I was ok to work...I got my SSDI though so it didn't matter...it is a weed out tool.
Keep waiting, get a lawyer...your time will come. It takes forever...but it is totally worth the wait. I've had no further communication in the past 5 years regarding my SSDI.
Good luck and remember that MOST OF US HAVE BEEN THROUGH WHAT YOU ARE GOING THROUGH!!!!
xoxoxo
Hang in there take care gentle hugs
I had my appt. yesterday with the state doc...now I am sure it will take forever to hear anything back from SSD...and I have NO IDEA of what the docs diagonsis was. It seemed as if he just asked the same questions that were on the application I had filled out for SSD...was easy to answer....nothing has changed. STILL FEEL LIKE CRAP!!!!.... I also had let ALLSUP know about this appt before going...and as some of you said...is exactly what I told ALLSUP...I think the state is hoping if they put enough pressure on you...you will just give up....AND THAT IS NOT GOING TO HAPPEN!!!.....SO BRING IT ON!!!!. However when one of you said that it had taken 2 yrs....I do get a little discouraged....I have no idea of what to do for income between now and hopefully then!....but that is another story for another day...one day at a time...right?!?
Thanks again to you all,
{{{{HUGS}}}}
Lori