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#1 | |||
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Member
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I was surprised that I was accepted after the first denial, but my LTD company hired a firm to advocate for SSD for me. It doesn't hurt to let your physicians know that you are applying, so they can be ready to advocate if necessary.
That said, I think my doctor listing my prognosis as "poor" went a long way in my fairly quick acceptance. I have to admit, seeing "prognosis: poor" in my medical records shook me up a bit. I guess with all the body parts I have had removed, and all the interactions, side-effects and restrictions I have on my diet, my prognosis for improving is, in fact, rather poor! If you will never improve, medically, make sure your doctor documents that clearly in your records. BTW, I was accepted for Crohn's, complicated by having had my entire colon removed, and a less than good result with my j-pouch (recurring complications.) I didn't even have to list my growing neurological complaints, which at the time were diagnosed as just peripheral neuropathy.
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We live in a rainbow of chaos. ~Paul Cezanne . |
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#2 | ||
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n/a
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#3 | ||
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Senior Member
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Most disabled people haven't actually lost body parts. Being disabled doesn't mean you are ill.
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. Gee, this looks like a great place to sit and have a picnic with my yummy bone ! |
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#4 | ||
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#5 | ||
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New Member
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I have osteo arthritis (OA) in my hips, knees, ankles, lower cack and cervical spine. I have been offered a full knee replacement but refused. I am in constant pain and on most days I walk very awkwardly. However, when I manic I can overcome the pain or should I say disregard it. Unfortunately I pay the price when I get down. Usually it warrants a week in the house with a very low mood and aching body.
Has anyone else experienced this which one could say it mimics "mind over matter" ![]() |
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#6 | ||
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Senior Member
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You might get more responses if you start your own thread in the main section below. If your concern is how to explain to SSA that at times you are able to be more active despite the pain, I would focus on the fact the you pay the price with increased pain afterwards, that your manic periods are unpredictable so you cannot schedule work when they occur, and the aspects of bipolar that contribute to and complicate your disability, like the poor impulse control, poor judgement, tendency to spend money that you can't afford, and inability to concentrate. Increased physical activity during periods of mania is a symptom of that disorder, not a sign that your physical limitations aren't valid.
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. Gee, this looks like a great place to sit and have a picnic with my yummy bone ! |
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#7 | ||
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Junior Member
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Glad I read this post. I was going to the SS office this morning with exactly the way you mention not to. Well now i will take my time and get all the medical info of my medical conditions from my doctor. I also suffer from diabetes as well as having MG. The one main concern I do have is that I do work P/T which my doctor's recommend me doing as long as i don't put myself in stressful situations that may cause severe fatigue. So I wonder if this will be an issue with the SSI claim? I guess I will find out. Thanks for the heads up.
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#8 | ||
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Magnate
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It is also important to analyze and document your functional limitations.
Personally, I have a tendancy to not clue my docs in about all the ways I've adapted to daily life and put a smile on when in public and hide away when I'm at my worst. For those that you see infrequently, and only for shorts periods of time, the hundreds of adaptions you might have to make in order to cope with your disability, might not be readily apparent. So, first, you must be brutally honest with yourself. Keeping a journal will likely help. Then ask your doc for some extra time to discuss your limitations with you in preparation for your SSD application. (Relating the realities of your life isn't tantamount to whining.) Even if your doc is supportive of your application, and believes your disability is severe, he might not have an understanding of your daily functional limitations. And honestly, for the "suck it up and bear it" patients, you might be surprised how much of your life has changed... This link explaining Residual Function Capacity is a must read IMHO: http://disabilityblogger.blogspot.co...-residual.html If you have legal representation ask them if they have their own Residual Functional Capacity forms, or if they use a different way to document your functional limitations. If your filing without representation these forms might work for you. You doc might charge you a fee for his extra time since this is a special request.: http://www.disabilitysecrets.com/rfcdownloadhome.html The earlier in the process that you supply this type of indepth look at your disability, the better. But, if you're going to have an ALJ hearing, this info is extremely important so that the Voc Counselor and the ALJ can accurately determine if you might be able to perform "other work." Regarding medications, document the effects and side effects. It's great for you that a med might reduce your pain, but if it causes you to sleep 12 hours a night and nap for another couple, that will effect your ability to work, and don't assume that this is just common sense. If more break through meds are required from activity, which again starts the cycle of additional drowsiness, this is important to address. It is also a good thing to supply a brief explanation of your meds. For example, if you take MSIR--write out Morphine Sulphate Instant Release. Or with a designer drug, such as Avinza or Kadian, include "Time Release Morphine." |
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"Thanks for this!" says: | lefthanded (10-13-2011) |
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#9 | ||
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Junior Member
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flat broke .went to social services to get help to see doctors for my condition
sent me to ssi office filed claim denied. there was another program that soc serv signed me up for. disability determination services. have two appointments 14th and 18th this month to see two different doctors one is a phd? and the other I don't know what they do... a group of some sort. just received a personal function report that asks a lot of weird questions... sorry really foggy this morning... has any one delt with this and know what is expected from them and where I go now what I should do Still dont have a diagnosis as to my condition but am convinced that this TBI is a perfect match? |
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#10 | ||
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Member
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Why was your SSI claim denied?
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