Monday, February 13, 2012

migraines and disability

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Denise Garrett

Denise Garrett

Tue, July 14, 2009

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I have been off work for 2 years now, over that, and waiting on a hearing date. I cannot work now. As of this time, I'm still trying to find a specialist to help me. My next appointment is in 2 days at a new specialist. The last one didn't impress me and didn't remember 2 months later, that "she" had taken me off certain medications, and was asking me why I stopped them.

Well, my question for anyone who is or has been where I am, what kind of chance do I stand with this? Migraines was the reason I stopped working, however, I do have anxiety and depression that I've been treated for in the last 10 years or longer. It's very depressing knowing I worked all my life and now that I can't I'm being told that my age, and the fact that I kept a steady job for the last 10 years and longer has made me not eligible. Ya know, it just ticks me off how people who don't have my body, can tell me what I can do, or not do. For one thing, I was making good money, and good benefits where I was. I climed to the top with hard work and many days of migraines and working hard. I don't know how this will go, and if I could work, I definitely would. Honestly, who would want to stay home in pain almost 90% of the time? The financial burden is enough to make me sick! Oh well, enough whining.thanks to those who read this.

Denise

7/16/09 1:36pm

I have been on disability for 4 years now, and I can tell you that I don't want to be at home 75-80% of the time in pain. Unfortunately, I am and it really sucks. Some of the worst things about it is hearing from friends and family "You are so lucky! You get to stay home all the time." I really want to punch them in the face. It really takes a lot of restraint on my part to patiently explain to them that it is not like a vaction and I get to do all kinds of fun things. That it is actually quite the opposite. It is incredibly boring, frustrating, and a lot of times painful. On top of it all, I get a small income that I am supposed to live off of for a month and because it isn't enough I have to borrow money from my parents, my sister, and my boyfriend. It's quite embarrassing to be 26-years-old without a job and unable to support yourself. I think all of this falls on deaf ears because they still make the "lucky" comment every now and again.

 

I also have depression and I get episodes of anxiety attacks too. I actually have a long line of medical issues. Some are from migraine medications I have taken in the past and some are from stress and depression. It's a horrible cycle really. I have seen many doctors and specialists since I first started my migraines at 13. I just recently changed again to a better doctor because the one I was seeing sounds a bit like the one you had. On top of forgetful she wasn't listening to what I wanted. She wanted me to continue on Botox treatments that just weren't working for me. I was also begining to react negatively to the shots and she claimed I wasn't. Who do you think would know their own body more?

 

I never made it to the top of a career, but I can imagine how horrible it is to work so hard and still not make the disability cut. Social Security claimed I just missed the cut off for the eligibilty and I know I didn't work close to 10 years. I wonder what that is all about?

 

I think everyone has different chances with disability. I had to wait a little less than a year and didn't have to take it to court. Meanwhile I have heard many people who had to fight in court before they got disability and sometimes people took it to court and still lost. I think I was lucky because my father kept excellent documentation of my migraines from when I was 13 until I filed for disability at 21. Every pediatrician, neurologist, ENT, opthamologist, etc. He had records of the visits, receipts, copies of doctors notes, etc. Then we had the same kind of documents for every ER visit for migraines as well as reactions to migraine medications. Some of my current medical issues are causes of medications prescribed from doctors for my migraines. After constinously sending the same documentation and filling out the same paperwork for close to a year I got a letter saying I was accepted for disability.

 

I think if my father hadn't kept records like that we would have had to take it to court. That is just an idea of the road you are headed on. Do not get discouraged!! You deserve disability rights. Migraines are such a serious matter and no one seems to think it is. It is not just a headache and the more people who can prove this the better! Start looking for your past doctors. Even if its just names and numbers, that should do it. 

 

Good luck to you. I hope you can get on disability and I hope your new doctor is better for you.

 

Brianne

 

 

 

 

7/16/09 7:10pm

Brianne,

Yes. Sounds like you feel as I do. I don't like it when people say, "must be nice not to work." It makes me pretty upset too. But now I say, "If you want to have my migraines, you can, and I'll work." They say, "oh no." It's very frustrating and yes it does get boring staying home, and not being able to even go to the grocery store sometimes because of having a bad day. I know it's harder these days, then what it use to be as far as getting disability. But, then I hear some people get it off the bat. I think too, that I will get a pretty good check, since I have worked and earned good money over the years. So, I will have enough to make it, but it won't be like I'm going to be rolling in the money, ya know? But, I'm sure people will think that. And, now, I don't care what they think, I just keep saying well, if you want this body of mine, you will see what it's like. Well, thanks for your feedback, that's great that you at least get something. Hang in there, and keep hope, and faith.

Denise

7/16/09 4:39pm

With doctors support, great documentation and a lawyer is a way to go if you are denied the first time.

 

Have you looked at this article? Disability Benefits - SSI and SSDI it has a wealth of information in it and I found very helpful. The social security site was helpful too.

 

Let us know how you make out at your new doctor, ok?

7/16/09 7:14pm

Nancy,

Well, he seems like he knows what he's talking about. He asked me questions about what I'm on, and have tried. He wanted to get lab work first, so, then I go back next month. I hope he can help me. So far he seems nicer than the ones here in town, that I went to, so he's worth the drive. He's about 1 and half hour away, so that's not bad. But, I can't hardly drive it. My neck is stiff and killing me. I just had a massage 2 days ago. Hopefully, my husband can take off work early, and take me next month. I'll keep in touch.  So far I think he wants to check my labs. He did mention a sleep study test. Which, I've never had done.

Take care. Thanks for thinking of me.

DeniseWink

7/18/09 1:32pm

When I first thought of filing for SSD for cluster migraines, I thought this condition wa snot approved but fortunately found out I was misinformed.

 

I do want to let everyone know who is thinking of filing that your first attempt is 95% of the time DENIED automatically.

 

Who knows why?  I think it's a way to weed out those who are not seriously affected but I have no proof of this.

 

Get your claim in and get it denied asap, then go straight to an attorney who deals with this process and has had great results.

 

You pay nothing upfront and the attorney usually gets about 25% of the settlement, not of your monthly benefit but others might have a different experience.

 

In 2003 when I was approved after about 9 months (I got lucky and was allowed to work p/t while waiting), I got a check and had the choice to send it back into SS (not sure why) or keep it and have it deducted from my monthly benefit.  The interest rate was so low I chose to keep it since I needed to pay off many bills.

 

I lose $150. per month for about 10 years but couldn't have qualified for such a loan after missing so much work so I took it and have never regretted it.

 

Lately, a friend filed and was approved but just go to keep the check sent to him.  I don't know why the change in policy but everyone might be different according to some State rules or something.

 

I just wnat you to know, FILE, be prepared for automatic denial, then get an attorney asap.

 

GBU all,

pat

7/25/09 11:43pm

Thanks for your feedback. I was told SS does reject many claims the first time. I thought when they saw all my records, they may reconsider. But, my attorney is working the case, and I should get a hearing date soon. I will hear in a few months, according to a letter I wrote to congress. I'm still getting them daily. Every once in awhile, I have a good day without one, and it shocks me. I've taken 2 Vicodin 2 Aleive 1 800 Ibuprofen and other meds to try to get rid of the pain. It's finally better now. I'm tired and going to bed though. No one except people on this forum really know what it's like. WE can't control it. I'm still working on getting a regimen with a new doctor I found. I hope and pray he is the one to help me. 

I think this needs to be talked about more as a "real" disease, and not something that everyone can just get drugs for and be okay. Well, thanks again. I'm glad you had success. I feel like I will have a strong case.

 

Denise

Anonymous
Deborah delaBruere
8/29/09 8:33pm

Hi my name is Deborah.  I have been suffering with chronic migraines for 4 years now.  I moved 2 years ago and everytime I think I will go look for a job today I have a migraine.  I gave up about 7 monthes ago with my neuroligist and just go my reg doc to get shots of demeral when needed and she keeps me supplied with promethize for nausia and vicodan for pain.  My neuroligist just dept trying drugs like Topamax and anti depressants that don't work.  I am looking at going for Social Security any advice I would apprciate.  Do I need to go back to the neuroligist or can I just go?

8/30/09 1:33pm

They like to see you going to a neurologists for treatment.   You can google or look up any attorney who specializes in SSDI. They will let you know what chance you have on getting it approved. It will take awhile to even get a hearing date.

That's because, there is so many people in the system, (some who shouldn't be) For example, I read that many mothers try to get them for their children have ADD. Well ADD is not a disability. It's a disorder. I know about it, because my husband and step-son have this. They have medicines for this. Migrianes are invisable, and there's not really a specific prevention medicine made, just for migraines. Yet. Well, good luck. Take care. I know how you feel. I really do.

Denise

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