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Community > 'The Tin Mom' Blog > Tin Mom Blog: Filing for Disability
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Filing for Disability

Have you filed or considered filing a claim for disability?

By Annette Beach

What do you want to be when you grow up? Whatever career or profession you choose and regardless of what it takes to achieve your goal, I am willing to bet it will be easier than being officially labeled, “Disabled.”

In my 45 years of living, I have never heard anyone answer that question, “When I grow up, I want to be disabled.” Nor have I ever known of a person to set their sights on becoming disabled at any point in their life. In fact, of all the people I know who have been diagnosed or have legitimate reasons for qualifying for disability, they deny or avoid the label for as long as possible.

From my earliest years, I was raised with the mentality, if I wanted something, it would not be given to me. Early on, I was taught to set goals then work hard to achieve them.

My work career began at a young age with a paper route, mowing grass, shoveling snow and baby-sitting. At 14, I lied about my age so I could work with my friend in a catering business. When I was able to obtain a work permit, I held typical teenage jobs in restaurants, grocery stores or wherever I could to make a buck. As I worked the non-glamorous jobs, I realized the value of an education or training and seized every opportunity to broaden my mind and skills. Following my high school graduation, doors were opened and I was given the opportunity to expand my future with experiences and further education. When diagnosed with rheumatoid arthritis at the age of 21, I continued to work hard, changing directions whenever necessary to adapt to my abilities.

As my arthritis worsened and the need for medical care increased, I found it harder to maintain fulltime employment. In order to satisfy my employers, I extended my hours to make up for my absence or changed jobs withholding the details of my health. When asked about a limp or noticeable challenge, I often fabricated the truth with little white lies.

Why? I wanted to work to contribute to my family and our lifestyle. Not to mention, I had invested a lifetime of hard work and dedication to become that person and I refused to let a disease rob me from my identity. Being disabled was never on my list and was not something I worked toward. 

When the reality of my limitations and the loss of my abilities began to interfere with activities of daily living, I was forced to re-evaluate my life and make changes. While the physical challenges were painful and overwhelming, the emotional acceptance was even greater! Admitting the truth to myself, let alone out loud, was and continues to be my greatest pain. I am not ashamed of my disabilities, however, there is an unexplained guilt that continues to surface feeling as though I am not living up to my full potential.

Sound familiar?

While reading Valerie’s post on my blog, “Labeled Disabled,” I am reminded of how difficult it is to file a disability claim. The paperwork in itself is exhausting and causes an emotional pain that nobody is prepared to endure. Having to restate the details of what brought a person to this point and having to prove its legitimacy is beyond draining. To experience this, then be denied – again and again.

Nobody wants to be disabled!

If you have filed for disability, what did it take for you to reach that point and take the appropriate steps? Were you approved or denied? How many times have you filed? Was your doctor helpful or a hindrance? Do you have tips or advice that would benefit others?

Annette
10 Feb 2010, 08:41
Has anyone filed for disability and been approved in a relatively short time frame? If so, tell us how you completed the forms, if there's a right way vs. wrong way, or what you did to make your application stand out.

Thanks!
Valerie
07 Feb 2010, 20:14
Oops! I meant to say we spent almost $1500 not $2500 a month purchasing insurance. My typo, sorry.
Valerie
07 Feb 2010, 14:17
I applied for disability years ago as is mentioned in Annette's intro above and it was exhausting and extremely painful reliving everything I so readily forget. Who among us hangs on to the memory of the pain and difficulties. I of course was denied and did not go on to fight it, although I was told to keep fighting as eventually I would be approved. I feel extremely guilty even asking for help even though everyone says you payed into the system so it isn't getting something for nothing. I did not think things through, my husband got a good paying job and we could get by so instead of continuing the fight to get disability, an intensely draining process I let it go. Of course with the economy my husband was laid off again I couldn't hold down a job, couldn't even keep up with the day to day chores of daily living. By then I had not worked in a few years and was totally locked out of the system. I look around and often think that the way the 'system' is set up many people who get accepted are those who don't need it. I think that often those who need it just plain don't have the energy or bandwidth to fill out the forms and fight the fight. It has gotten to the point I even hate to read articles of people who have some sort of arthritis and are running marathons, climbing mountains and God know what else. It all just makes me think if I would only do something I don't know quite what differently I too could be doing all these wonderful things, that my difficulties are a personality flaw. I am so happy for and inspired by these people doing these wonderful things even though they have disabilities. Yet the end result is always me beating myself up because I have trouble making a simple meal for my family. I seem to be always negative on these blogs but they hit a sore spot and I guess I need to vent. We have kept insurance through all these years, paying close to $2500 a month and then having little coverage until we meet the $6000 deductible. Is it any wonder I am now filing for bankruptcy. Should I have let the insurance go? I am now reevaluating all my meds, trying to figure out what I can do without and still function enough to be a mother to by children. My visits to the docs are fewer and far between, as it is $40 to walk in the door. Thank goodness for my wonderful Physical therapist who is helping me get range of motion back after my recent shoulder replacement all on her own time and charging me nothing. Bless her. Something I may have rushed into because we had coverage but I did not know for how long. The saddest thing of all is I see so many others not only with arthritis but other diseases with even worse choices than I have regarding medical care. I hope something is done and done soon that will allow everyone to have good medical care. Unfortunately, greed seems to be winning out and the insurance companies and pharmacuetical companies seem to be carrying the day. We may have the best medical care in the world but only the rich can access it. At least that is what it looks like from my corner of the world.
connie muir
03 Feb 2010, 07:30
I supported my family with a decent paying job. I was proud of working despite my disabiliy. I got fired last year.They didn't want to cope with my defects of character that were a direct result of arthritis and depression. I gave all that I had but they wanted more. I've lost the ability to work unless I find a compatriot who will work with me not against me.
I applied for diability my self. It was an excruciating experience. All my life I've minimized my weakness, trying to prove how capable I am. Now on the paperwork, I had to whine about the smallest stuff. Then to have them deny me and tell me I can work low skilled work that wont support my family? It really hurt to have someone tell me I wasn't suffering enough. I feel like the dregs of society
Debbie
02 Feb 2010, 18:15
I have been trying for 2 years to get on disability. It is a long process and I find it so hard to say I need it. It has taken me a long time to realize that I can no longer work. I need to take an afternoon rest and just put my head down. The weight of my head makes my neck hurt after a while, the pain is so unbearable these days that I do as little as possible. It would help my family greatly if I could get a little help I know it won't be much but it will pay a bill or two. I feel helpless and as if this disease is not bad enough and we feel bad to have to ask for help the process is humiliating. I have been denied twice and go up in front of a judge in March. Friends say that I look fine so it will be hard for a judge to give it to me. So I fear I may be denied again. It is so frustrating.
Mellanie
23 Jan 2010, 00:12
I am 23 years old and I was diagnosed with RA at the age of 18. That news was hard to accept. At that time my mom had medicaid to get my injections. Then we lost it. I have not taken anything for 2 years. I am a full time student, with a part time job and cannot afford medication. Insurance companies either wont take me or are too expensive because of my condition. At times I get depressed because I cannot open a soda bottle, or bend down because of the severe pain. I can not wear sneakers because my feet swell so much. I believe that this disease should be considered a disability. I have called out of work so many times because the pain is unbearable.
Linda
21 Jan 2010, 18:46
I never wanted to be considered disabled. At the age of 53 my body just can't keep up with the pace I once enjoyed.
I can't stand up for along time like I used to. My knees and feet hurt too much. Sitting hurts too. My family needs me to keep working. My family Dr. is a DO and says the bumps on my fingers are just a sign of old age.
If it were possible to be considered legally disabled I could at least work part time to help with the bills. I need to keep active but not working 12 hour shifts 7 days a week.

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