When You’re Not Sick Enough

 

Before I even get started with this article, let me state for the record, that for those who have been approved for short or long term disability, you deserve it. You’ve suffered just as much, if not more than any of the rest of us and I do not begrudge you a thing. In fact, I understand that it’s a double edged sword. You aren’t happy about the fact that you need disability, but to simply survive, it is much needed and warranted.

Now, that being said, I wonder sometimes exactly where and when I fell through the proverbial cracks. I have a diagnosis. I actually have five diagnoses. I have the MRIs and CT scans to prove the 90 year old woman inside is cleverly disguised as a 37 year old female powerhouse on the outside. I most definitely have the monthly medical bills, which probably will be finally paid off by my great-great grandchildren, to validate my repetitive emergency room visits. I have all of this and more, so why do I keep getting denied disability?

Simple.

I’m not sick enough.

That statement is quite an emotional conundrum to me, as I don’t know whether to laugh till I cry or cry till I laugh. How in the world can I not be sick enough? How can the tears I cry alone in the early hours of the morning because I know it’s going to be a struggle to even get out of bed, be belittled to the point of humiliation? I had so many questions swirling around in my head that it was making me dizzy until a former rheumatologist of mine, let’s just call him Dr. HeadUpMyOwnHiney, gave me the cold hard truth as apparently others saw it. I didn’t look the part.

Thus befalls the curse of the invisible illness.

I have been turned down for disability more times than I even care to share with you all. I have begged, pleaded, cried and would have gladly paid someone off, but the answer is always the same. “You are still able to work a full time job.” Yeah, I can. I can most definitely work a full time job. I can even get up at dark-thirty and drive an hour to said full time job, where I end up putting in a 10 hour day fueled solely on caffeine and Skittles. I can also come home, never cook for my family, never play with my children never put my son to bed and say his prayers with him as I kiss him goodnight. I can’t do that because I can’t climb the stairs at the end of the day. I come home and go to bed. I stay there until the entire process starts anew the next day. And weekends? Forget about it. Very rarely do I even get out of pajamas for the entire 48 hours of the “weekend”. (If you could see me, I would be doing air quotes as I show off my perfected eye roll). My body is broken, I’m sick more than I’m not and until recently the “Sunday” part of my “weekend” was spent with my head in the toilet due to one gnarly shot of chemo.

No, I absolutely am capable of working. I work my rear end off for the craptastic insurance I have that left me with thousands of dollars of medical bills and a penchant for passing on much needed testing because I can’t afford the out of pocket part of my deductible.

Here’s the stripped down truth: That healthy glow I have is self-tanner. It’s a nice orange color that makes me look like I’ve been rolling around in an open bag of Doritos because the rash underneath mixes with the tanner. I’m thrilled that my skin shade of “Oompa Loompa” impresses you. The bouncy volume in what’s left of my hair is a direct result of 45 minutes of teasing it with a fine tooth comb so much that Peg Bundy would be jealous of the height. The sharp business suit I wear to the doctor’s office is because apparently it is frowned upon to wear sweats, t-shirt and flip flops to work. You know…because of that “fired” thing that I try to avoid. And finally, that strong put-together exterior that just stares intently at you (I’m talking to YOU here, Dr. HeadUpMyOwnHiney) as you tell me you will NOT agree to support me in any litigation for disability, is because I won’t give you the satisfaction of using tears to prove my pain. I save those tears for when I’m alone in my car outside your office, where you can’t see me…where no one can see me.

I’m constantly reminded of the phrase “looks can be deceiving” because I live it everyday. I will continue to push myself until something gives, whether that be THE system or MY system, because I just don’t have any other choice right now.

Because I don’t look sick.

 

Article written by Senior Editor, Stephanie Kennedy.

Stephanie lives in Fayetteville, NC and is the mother of 3 always hyperactive and occasionally adorable children. She was diagnosed with Systemic Lupus Erythematosus in 2001 and in the time since, has added Scleroderma, Hashimotos and Celiac diseases. In her day-to-day life she is a Community Relations Specialist (aka, marketing and creative hodgepodge facilitator) and a part-time blogging snarkzilla. She can always be found somewhere in social media-land causing some sort of trouble. Find her on twitter at @steph_in_nc or on facebook at Stephanie Welborn Kennedy.

©2024butyoudontlooksick.com
  • Amik

    I can relate so much to your article. I have severe invisible chronic illnesses too, but I don’t look sick enough on the outside to be taken seriously.

    I work full time, but I’ve struggled with that for years and things have been getting a lot worse over the last six months, so I don’t know for how much longer I can take it. My health is deteriorating rapidly and I don’t have the spoons to do anything else than work. I can barely sleep either out of pain, so when I come home I lie down and my next 13 hours of existance feel empty and numb and I can neither get good rest/sleep to recharge my batteries nor can I do anything for myself or my family.

    It took me countless years to get as much as a diagnosis. I was finally diagnosed a year ago and started treatment then, but my rheymy says there are limited treatment options for my illnesses and I’m still awaiting diagnosis for some of my other health issues. I no longer have the energy needed for the physical therapy that I desperately need, because work soaks up all of my limited spoon supply.

    I don’t know how sick I have to get to be “sick enough”, nor do I know how I can convince anyone of just how sick I really am, since my illnesses are invisible. I’ve stopped putting on a brave face and started talking more about my illnesses (like someone said, a squeaky wheel gets oiled), but I’m young and I “look normal”, so people assume I’ll be fine and am just going through a phase or looking for attention.

    The hardest part is that I’m going through this alone. My family has been very unsupportive and I have practically no friends. The only friend I do have is supportive, but she lives very far away and is very sick herself, so I don’t often have the chance to speak with her. Being as sick as I am is making me more and more isolated, but ironically people don’t believe I’m actually this sick because I don’t look like it.

    All of you who are struggling with invisible illnesses have my sympathy. I hope that you’ll get the help and support you need and deserve soon.

  • Terri

    I work because my government says I am capable of working between 1 and 8 hours a week … have they tried getting a job where you only have to work 8 hours a week that doesn’t involve some sort of lifting, pulling, pushing heavy work because it’s a dead end job anyway? For 12 months I worked 15 hours a week but I recently managed to reduce my working hours to 12 because I wasn’t coping well. One of my delightful co-workers informed me that she had a friend who had the same illness as I have but he manages to hold down a full time job. I jumped on her, pushed her over and banged her head up and down on the floor!!!!!! No I didn’t .. that’s just what I felt like doing, but I don’t have the strength or the energy … after all she’s as healthy as a horse, gets up at 5am everyday and cleans her house and her daughter’s house and takes her grandkids to school before coming to work and doing an 8 hour day while going home during her lunch break to put dinner for herself and her husband in the slow cooker. What I actually did was smile sweetly and ask her if her friend was married and had a wife that cleaned the house and cooked the meals. Why did I even bother??? I don’t know. She made me soooo MAD!!!! I know I shouldn’t get upset. After 22 years I should be used to the ‘but you don’t look sick’ comments, but I’m not. Will I ever get used to it? Probably not. It the meantime … just keep smiling, just keep smiling. Hugs to you all for listening and I hope you all get the help you deserve.

  • nikki

    Remember to use your resources Your State Rep’s they have liasons that will help you and keep you updated I was approved in 11 mo but I didnt have to pay anyone. I got the full back pay.

    I have had attorneys for other things and they failed, my State Rep helped with disabiity medicaid and my disability.

  • I know where you are. I got turned down three times, all the while trying to work as a waitress in a three story building, or as a gardener for a landscaper. Didn’t know what the heck was wrong. Just thought I had a blown back from a work injury in 2006. Ended my work life at the end of 2007, got diagnosed two months later, and have been diagnosed with more fun as the years have worn on. Husband got fired at end of 2008, and REFUSED to work for almost two years – hence no insurance. Still refuses to get employment; just barely works odd jobs. Have had to fight foreclosure for three years, going on four, had to file HIS unemployment claims because he played on the computer for a couple of years. Moved 5 times, moved back to house fighting foreclosure on and am still fighting. HE says that I’m lazy; I don’t work. The stress of HIM alone is killing me. I did finally get SSDI in June 2009. But, I went untreated for a couple of years until I got Medicare (24 month waiting period). Have borrowed more money than I can account for, because my paultry amount of 1400.00 per month doesn’t go far anywhere in the metro Washington D.C. area. I am determined to get rid of spousal problem, because it has occurred to me that he could care less if I live or die. Have started a career program at the local community college for medical billing/coding. I figure the few days I will be able to work, I can do it at home. State I live in is “Right to Work” state. This just means that an employer can tell you he’s firing you for excessive illness, and can get away with it as long as your firing is recorded as “no cause.” If I’m at home, no one sees how bad I may feel one day to the next. School is part-time, and, although I have gone to class feeling really crappy, I still can make it. NO ONE who isn’t a proud owner of a chronic and debilitating disease or two (or more), understands the pain, fatigue and depression. No one gets that it is embarrassing to walk around in public with NO EYEBROWS, NO LASHES, BARELY-THERE HAIR, and, rashes. No one gets it that I’m slowly going blind, with no diagnosis because the out-of-pocket is too high right now to see an opthamologist. I’ve had rheumatologists just stare at me as my mouth goes so dry that I’m in PAIN trying to talk to them. No offer of water. No medication to be tried for the drymouth. I will never recover financially as I’m fifty years old, and I can’t even touch my medical bills until I get a little something additional coming in. But, at the same time, there’s this little voice in me that keeps chanting “remission”. I keep hoping for a cure. Some days, I don’t see myself as old and sick. Most days, I still feel there is a purpose to my life, and I just have to keep looking for it.

  • Sandy Cooper

    Hi there I know how you feel, I am ill from silicone implants , you know the “safe” PIP ones….

  • Catherine

    Today, after a 3 month break from all things physical during the 2-year period of trying to get my RA (20 yrs) under control, amidst liver infections, side effects and months of prednisone, I made my first attempt to go back to the gym, where I jumped some rope and took it easy. Upon leaving, there was a note on my car, which was parked in one of 4 handicapped spaces, visibly displaying my legal placard, which read “you didn’t look handicapped jumping rope today”.
    Struggling with the patience to deal with such rude, entitled, invasive, judgemental people. Maybe I should keep it up at the gym so I can kick someone’s ass. My feet work better than my hands anyway.

  • Jean

    I understand completely. I’m in the same place –

    I can live to go to work and with days of pre-planning, can even plan to do something fun outside of work — like go to a movie. And keep the insurance that pays for my expensive Remicaide treatments

    Or I can stop working an have a little bit of energy to actually enjoy my life — but lose the Remicaide, and end up back taking 6-8 vicodins a day and perhaps my mobility.

  • Mary M Davis

    I could have written any and almost all of the comments above except chemo thankfully, (knocking on wood). My health insurance has my medical record lab results and diagnosis’s online now but only 25 show up, unfortunately I have 56. Obviously the 25 that are listed are the early not so bad issues and doesn’t even touch on the kidneys down to 44% or Congestive Heart Failure (Enlarged Heart), Familial tremors where I can only type and even then have to erase about every 5th character to re-spell correctly because I hit 2-3 letters at a time. When still working I had 7 different doctors who said any 2 would qualify me but none would put me out on medical leave so I could start the disability process they would only put me off 1/2 time and my work wanted me to work so bad they would put them together and force me to work the other 1/2 time and hassled me when I would call in sick even if I was praying to the porcelain god but had to use the cell phone because I HAD to call within so many minutes before 8.

    I filed was denied, appealed was denied was so humiliated and demoralized by the process when they told me my problems were a nuisance and nothing more and as long as I could move my hands, arms, feet, and legs, I wouldn’t qualify. I gave up but have been in lots of therapy as my health has gotten better in some ways and seriously deteriorated in others.

    I’m not the scared little girl they messed with in 2007. I found a group online disabilitydigest.com even if they aren’t able to get my claim approved becaused I waited to long it is an EXCELLENT resource site and they email you weekly information to help you know what to say and when so you improve your chances of being approved.

    Now, not only am I fighting for MY claim to the finish, as I told the advocates and social security I will get the media, congress, and President of the United States of America involved if I have to. Their behavior is deplorable. I used to work on the other side of the social services counter and made sure EVERYONE knew that all of us are one illness, one injury, one paycheck away from the other side of the counter, so treat them the way you would want them to treat you.

  • HypoGal

    Having a chronic illness is a full time job. The juggling of doctors and medication just to stay alive.
    If you saw me you would think I look great but after numerous blood clots, perforated colon and the rare disease Sheehan’s Syndrome my doctors finally take me seriously. However, I did have to almost die at least a dozen times.
    I think you should be very candid with your doctor and show up looking how you feel. If your doctor can’t relate to your pain and low energy then I would choose another doctor. My Best

  • toosicktowork

    I know how that is. So what if you’ve gained 50 pounds in a matter of months, your hands swell up, you can’t stand for the vertigo and general sense of dizziness. Was told to ignore my symptoms by my doctor. Been called crazy. Been accused of doing drugs. That last one really insulted me. I have chosen to adorn my body as I see fit, with a few tattoos and plentiful body piercing. This does not mean I snort, inject, smoke, pop, quaff, or whatever the heck it is that people do. I haven’t bothered to apply for disability, because I know I won’t get it. All of this started up a little over a year ago. Still no real diagnosis, and I know why. To give a diagnosis would mean that they would have to own up to their earlier negligence, and that would put them at risk for a lawsuit. I just wanna be better, and I’m going to need something to eat in the meantime. I paid my taxes for just such an occasion. Pamphlet from the Social Security says I’ll get x amount of MY OWN MONEY back if I become too sick to work. So what gives?

  • Sad to say that sometimes I thank my lucky stars that I have an observable phenomenon (discoid lesions), otherwise my doctors would have shrugged me off completely years ago as my labs are not pointing to anything specific.

    I too spend every last bit of my waning energy pool working during the week for the insurance that keeps my family healthy. I too sometimes feel the guilt of having to nap rather than have the energy to play with my children as using my energy to attend to their core needs like feeding them dinner, etc are more important. My 9 yo daughter has been a pillar of strength throughout this, helping me with her 6 yo brother for the times I can barely move. My husband works an opposite shift to me, so during the week, I am left to handle it all on my own.

    I feel guilty leaving most of the housework to my husband, though I help out where I can, even if it’s just sitting and folding piles of laundry for the kids to run up the stairs and put away for me. I know he understands that I am ill, but a piece of him can’t help but resent me. Well, perhaps not me, but the cards we’ve been dealt. I love him for his strength through this.

    I look the part, but only to those who know what they’re looking at.

  • Teri Miller

    Hi, Hire one of the Social Security attornys. They geet a portion of your first award but, it goes back to the first time you applied. We all had to do this and it works. Social Security is like insurance companies, they automatically turn you down 2 times as a matter of regular policy. Believe me attornys get their attention. And, don’t let them send you to any of their lame doctors for asessment. Good luck

  • Nancy l

    To Salied,
    In California you can go on state disability for up to a year while applying for your permanent disability. I would check in your state what benefits they have. I would also talk to your manager and the HR department to see if they could accommodate you working at home. Look at the disability rights both in your State and the Federal laws to see what your rights are. Talk with your doctor and see what advice they have for you, it sounds to me like you need to stay home if you are ever going to have any quality of life. Good luck and hope I helped some. Don’t give up as their has to be an answer to your situation. Nan

  • Nancy l

    I feel so bad for you and everyone that has to deal with this when you are so sick. I have been there and was denied too because I had a terrible company representing me. I was so sick and could barely get out of bed. I too worked for 10 years while trying to hide my illness and I worked at a hospital. I would get epidurals at lunch and return back to work. They set me up at home so i could get my job done. Then after one last surgery I was done, could barely walk. But they still denied me….then I got the best man around and he knew I had a solid case with metal plates in my neck, screws all over my body, all my surgeries, MRI’s, hospitalizations for pain control. He told me on day of court wear no make up do not wash your hair or do it. Wear a black shirt and pants…he know his job as he once worked for the other side. I won and got retroactive but i had a LTD policy so it was no so much for the money but I needed Medicare as no one would insure me…now that alone should tell you how sick I was. It was an inhumane treatment of the disabled and the fight I had to go through was unacceptable. I would love to see the laws changed. If I was an illegal citizen I could of gotten emergency Medi-Cal within 24 hours, I seen it everyday at work they cross the borders to have their babies here and yet the American citizens who have paid into the system get treated like we are trying to abuse the system! We need reform again for the disabled as it borders on our civil rights!

  • sailead

    My name is Karen. I posted this earlier, but I didn’t know that I had to register first. So here it goes again….(glad I saved a copy to my pc in case of failure. 🙂

    I’m now 63 years old and have been suffering with multiple symptoms since I was 17years old. Of course, no one could figure out why I was always so sickly and came down with the oddest conditions. So here’s my story…

    Thanks for the comforting and encouraging information you all provide at this website. I am age 63 and have been dealing with multiple issues since I was a teenager.

    17 years ago I moved to FL from the NE after being diagnosed with RA, OA and Depression since I was 17yrs. Old, and coming to the point of being disabled. I went through all kinds of meds over the years that were killing my insides, and I finally decided that it might help to change my location when I could no longer function in the cold weather.

    The move helped; and since my husband was retired and financially stable, I didn’t have to seek a job when we located there. I felt so good in the warm and sunny environment that I was able to get involved in many activities in my 55+ active community. I even biked! The pain and depression was still there, but I was able to deal with it so much better with this kind of environment. Not working brought its benefits….I didn’t have to worry about calling in sick when I was having a bad day, Still, more days were bad than good, but I managed to deal with it since I had a high pain tolerance like many who suffer pain the bulk of their lifetime.

    Time brought change, and change brought divorce…and divorce brought me to a point at age 52 where I had to go back to work. The added stress was more than my body could handle. The job was one that brought me into the public light and I was considered to be a very happy and vibrant person, and I enjoyed the work I was doing. Things were going well for me…I found a place to live and a new beau. I was still suffering from the RA, OA, and depression but not as bad. Then, one weekend I woke up from a nap with double vision. After seeing a specialist, I was diagnosed with Diplopia which would probably correct itself. My vision returned to normal after 2 weeks of wearing a patch over one eye.

    A year later, after surgery, I ended up getting a severe case of Shingles which was explained to me: my immune system being so low. It took months to clear up and there is still a damaged nerve area where it occurred. Then, my new husband and I were in a near fatal hit and run accident which ended up with my having back surgery a year later from the trauma of the accident affecting my body. I woke up from that surgery, once again with double vision, and also Horner’s and Dwayne’s syndrome. While in the hospital, I was treated by a neurologist on duty who specialized in MS and FM, and she diagnosed me with MS after viewing the results of my brain scans. It took 3 ½ months till my vision was back to ‘normal’, wearing a patch again, and body cast/brace. I was only out of work for 2 weeks, and was able to continue to function at my job. I was referred to another specialist who did numerous tests and said that my results did not conclusively indicate MS, so he diagnosed it as Fibromyalgia. Then, 3 years ago I ended up with ‘sudden hearing loss’ in my left ear which I’m told the nerve died from the ear to the brain.

    I intently researched MS and FM and realized that they were very similar….yes, I had all the indications that were mentioned… fatigue, pain, sensitivity when touched, chronic headaches, depression….and on and on, along with RA and OA symptoms being similar. During the past 10 years since the first episode of double vision, I have had more time off because of symptoms than ever. And, I’ve been late many, many times because I can’t wake up or get out of the ‘fog’ some mornings. Of course, I’m older now and I expect more aches and pains.
    My dilemma is:
    • I use up all my sick time (40hrs) if I get a cold or virus and then don’t have any time for ‘down time’
    • So tired of people saying, ’You don’t look sick!’
    • Get through my days on adrenaline and caffeine (my meds side effects are drowsy)
    • Have to take ‘power naps’ to make it through the afternoons because of exhaustion
    • Life consists of waking….working…eating….sleeping

    I tried returning to one of my passions….singing with Sweet Adeline’s International…thought I’d never be able to sing again because of my hearing impairment, but tried anyway. Then, after suffering from bronchitis, my voice changed drastically and I had to switch to a different harmony part…bass, and am limited to do the choreography. When I mention my discomfort, my friends think I am whining! I am now very depressed and angry that all these dysfunctions are keeping me from doing anything. But, like most of you….I hide it because everyone tells me: “You look so good!”

    I would like to file for disability but I can’t quit my job to prove that I can’t work. When I go to work, I can hardly make it through some days! What I would like to do is work from home where I can pace myself to do the work when I am feeling good during the day. It is possible to do my job remotely) Today I went to work and the temp was so cold, I could not function or concentrate because of the discomfort.

    Please…..feedback welcomed…. sorry it was a long post! I feel like I am going nowhere with these years of my life

  • Lymelin

    I can’t believe I’m hearing my own angst echoed in your posts. I was “blessed” by being raised in a dysfunctional family where I grew up way too fast to become caretaker for everyone else and their dysfunctions. Hence, my modus operandi was all about “looking good” because I was the “healthy” in my family so having a bang up awesome appearance in public became a game and I had to win. I’ve literally spent thousands of dollars on clothes, makeup, and shoes for which I became the envy of everyone where I worked. The sicker I got, the more clothes and shoes I bought because I was too tired to do the laundry and with more “stuff”, it was easier to put together a nifty outfit complete with 4″ heels. Underwear? Why wash it when you can just go to Walmart and get more? I live alone so there is no help- a blessing when everything you own is spread out on the floor because you just don’t have the energy to put anything away. In fact, the notion of organizing things or making a task list and executing it are mere fantasies.

    My boss adored me while I worked 16 hour days (basically doing everyone else’s job to be sure it got done right) but as soon as I told him I had a medical issue and would need some time for doctor’s appointments, I became the bastard child. I tried to work a reduced hour schedule to attenuate the chronic fatigue and do doctor’s appointments on my “day off.” However, after working 14 hours a day on my reduced schedule simply trying to keep up with the paperwork it required, not to mention responsibilities piling up on my desk undone, I went to several coworkers, as my boss was out, and said I didn’t feel well and I was going home early. I knew it was the end. At 5 pm still fully decked out in work clothes, I lay down on the couch and slept 20 hours straight. I haven’t been back.

    So I’m doing a dance with my employer’s disability insurance company and even though they can’t physically see me, they can’t see the virtual me in all the doctor’s reports and tests and squeaky clean absolutely incontrovertable diagnosis in a what can be a controversial illness. FYI there’s a great (well best in a bleak class) iPhone app called My Medical that has let me enter in all the info related to this illness and I have something like 19 doctors and I’m on something like 15 medications (and oh by the way MedScape for iPhone has an interaction checker for you to enter all your meds to be sure they’re all ok).

    I don’t have FMLA. I don’t know if I even could go back to that job with all the bad blood and it’s clear the insurance company is trying to wear me down and in the process is harrassing the very kind doctors I am blessed to have found hoping I will go away. My employer endorsed another month off to rest but doesn’t understand that I rarely have a day to myself. I usually have 1-2 appts a day that either take away my lunch time or conflict with my nap time. So when I do get a day to myself I usually stay in my PJ’s and sleep through it. So much for the foot high stack of books I was going to read in leisure.

    So I don’t know what my financial future holds but until someone cuts the faucet off I have been living on line (too tired to go to actual stores) and buying any and everything I can think of that would simplify my life (I’m on a very special diet so I bought all the cooking gadgets though unfortunately all the produce is growing mold). The thought of following a recipe is beyond me; hence I’ve lost 15 lbs in two months which totally freaked me out, not to mention my doctor.

    My “back door” is a former SSD claim that runs for 5 years for which I would have to somehow convince them that that diagnosis still holds. It’s for PTSD – Lyme/PTSD – at this point I’m not sure the name of the invisible disease matters. I did here that Social Security’s new case load at least in my area is so backed up that it would be nearly impossible to file a new application and get any action whatsoever in at least a year. First time around was a miracle – fantastic lawyer (who kept saying how good I looked) and claim granted in a month with no hearing, exam, or appeal.

    After whining, LET ME EXPRESS MY GRATITUDE in finding all of you and this website! Bless you all.

  • Mrs. Brown

    Wow. I am so glad I stumbled across this. I was actually beginning to think I was a whiner.

  • Kathy Newman

    Wow, what a website! I have been diagnosed with Fibromyalgia, degenerative discs and have recently had both hips replaced. I have wonderful doctors and apparently a good attorney because I was awarded SSDI within 9 months of leaving my job. So, why do I still get snide comments and looks of disbelief from friends and family members when I say I am disabled and can’t do things????????? Don’t they realize I would like to do more than spend 4 hours getting ready to leave the house to go to physical therapy and doctor appts, come home, eat, try to get comfortable to watch some TV and then try to get some sleep so I can do it all again tomorrow? I am in constant pain – get it? Be grateful you’re not and don’t tell me things like – “oh, just take a hot shower and have a cup of tea”
    WOW I NEVER THOUGHT OF THAT – I’ll stop taking my meds and cancel my appt because YOU figured it out! Am I bitter? Yeah, sometimes because I’m only 52. I just have to keep in mind that it could always be worse.

  • Amen, sister!

    Sorry you are still “draggin’ yourself around by the scruff of your neck”.

    I have come through the fire (somewhat), to having more good days than bad. I feel your pain.

  • Eva

    Yeah, it stinks, not being “really” sick because you still function, sometimes. Because you don’t complain to anyone who will listen about what a crappy day you are having, because your nerve endings are so sensitive that your clothes feel like sandpaper.

    But if anyone ask how you feel, you say “Oh, fine” because they don’t really care. I have taken to answering “I feel like crap today, I could detail it for you but you don’t have time. And how are you?” With a smile but not a real “oh I’m joking” smile. And if they don’t get it I will tell them more until their eyes glaze over and they wander off in a daze.

    I usually only do this when I feel, oh yeah, like crap! Which is 80% of the time, but that’s okay. 20 % of the time, “I’m not sick.” Right?

  • Gail

    I just run across this site. I completely understand the comment Joan made about the concrete wall. I have fibro, I’ve lived with it for nearly 20 years and just can’t deal anymore. In the last year, the pain and fatigue have gotten so much worse. I eat, sleep, and work. That’s it and that’s not living. I’m just so tired of it. I have been to a neurologist recently, with some testing I had never had before, and so far have a clean bill of health. That should make me happy, I have nothing wrong with me. Why do I feel so bad? I don’t know how much longer I can work, I feel I’m barely hanging on.

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  • I got SSDI because my doctor kept adding on more & more tests showing I was UNABLE to work an 8 hour day… UNABLE…

    and my SSDI attorney kept reapplying EACH & EVERY TIME…

    I believe the SSA plays a numbers game, they hope you will give up – when you don’t eventually they have to pay you right back to when you applied (minus 6 months I believe)

    DO NOT GIVE UP!!

  • Irene

    I have never been a “needy” person. Strictly type “A” personality. When I lost my health at age 31 I was in shock.. We feel the pain and other symptoms of Systemic Lupus, but others do not see it. I finally realized that if I tell my friends how I feel all the time, I probably won’t have any friends left. They can get tired of hearing about it and also get tired of my cancelling lunch dates, etc. When you get sick you find out who your friends really are.

    We also spend a lot of time alone, which can be difficult and emotionally painful. After the shock of my diagnosis I started a Lupus support group in my town. It amazed me that there were 4 women who lived within 5 blocks of my house that were also suffering..

    I remember my dad telling me one day , “Irene, how come all of your friends are sick?” My answer was “because they understand how I feel Dad.” Finding these women was truly a gift, and they became my lifeline.
    After my diagnosis and when I got out of the hospital I had to quit my job. The thought of staying home all day was traumatic, but as time went by I realized that I had days where I could just hang out with my kids. I didn’t have to spend my evening lying in bed listening to my family downstairs laughing. My finally getting disability was a blessing…

  • Nadia

    “But you don’t seem depressed…”

    Can’t get out of bed, brush my teeth, take my meds without my boyfriend making sure that I do and reminding me when these things constantly fall out of the ‘important box’ in my head, replaced by things like ‘stare at that wall and wonder why my wrists feel like they’re burning’. But no, I should totally be in full time work, hiding in the toilets because someone just corrected my work and suddenly I’m having a panic attack.

    I spent a very long time being really hard on myself because “being depressed isn’t like a real illness”. I pushed myself into a suicide attempt in my second year of university and a mental breakdown during my third because I couldn’t accept that I maybe needed more allowances made for me than I was allowing. Then after a lot of discussion with counsellors, doctors and friends I finally accepted that depression and anxiety disorder were ‘real’ illnesses. Only to find that, having spent so many years being ashamed of how broken I was, I couldn’t let it out any more. The council workers I see ‘know’ I’m depressed, but I can tell they don’t really believe it because I force myself without thinking about it not to show up in tears or panicking or wearing short sleeves.

  • Rach

    I can relate to every person on here and my heart and love goes out to you all. I have been suffering with chronic pain for the last 13 years and it has only been in the last 6 months that I have stopped hiding my pain and being strong!!! I now feel like a massive weight has been lifted off my shoulders as I can now tell people how I feel and the effect the pain has on my life and how at times if it weren’t for my son, my husband and lovely family I would no longer be here!!! However there are people out there who show little understanding especially my employers ( a police force) who make matters worse and just because I wear make up and nice clothes and present with a smile on my face think i am ok. It’s so lovely to read that I am not alone however so disturbing to think that chronic pain is so vastly misunderstood with a severe lack of understanding and education.
    I wish everyone luck in their mission to achieve what they want and need and to manage their pain/illness the best they can.
    Some days I really feel like knocking on Number 10 and having a rant!!!….maybe we could achieve something then!!!

  • Anne

    I let myself fall apart at my former Dr.”headyuphishinney”. He finally told me that I was obviously “not trying hard enough” not “doing what you have to do”. He also stated categorically that he would never write a letter for SSI/SSDI, parking tag, or any other requests. “I never do” Due to many other factors, I kicked the guy to the curb.
    I’m still recovering from one year of heck-in-a-handbasket. Former Dr’s actions had a lot to do with it all. My lawyers are always asking me to refile. One “lawyer” aka legal professional says one thing then six months later a new one says “ohthat – no that wasn’t true”. Begin again Finnegan.

    Oh and to top it all off? in my community, only one Rhuemy sees Fibros. That is the dude i kicked to the curb. I could go on and on. However, I won’t.

  • pam egger

    wow. you said it all. and people still don’t understand. I keep alot to myself too. no point in complaining. besides no one wants to hear it.

  • unicorn

    Yep… do we struggle on, being active, pro-active and creative when we can, because hey, we are awesome at getting lots done with a tiny spoon supply, or do we grab ourselves with both hands and give ourselves a good shake and force orselves to see us as others do?

    I live alone so folk only see me when I am out and about and being active…and if I can get out of bed I am out and about. Siiiiigh! This means that the stuff that doen’t get done is house type chores etc. No one knows as I always visit others rather than vice versa and I never stay home to do the basics if there is something else on offer.

    I am a Job Seeker so my subsistance benefit depends on me continually demonstrating my job search activity, participatig in training courses and schemes etc. In reality, any job I would do would be liiely to impact upon my health negatively…but how do I demonstrate this whilst unemployed and using spoons to manage my health, spoons that would be sucked up by a job?

    Experience shows that I give 110% to ‘work’ and that I have held two jobs at the same time, worked very unsociable hours at different sites etc so I have a strong work ethic. Hmmm what am I trying to say? I think I am saying that for most spoonies,the acknowledgement that work is no longer the appropriate option has been a long hard won position to reach, we really don’t then need outside bureaucrats and ‘experts’ questioning and disputing our emplyability. Pain and fatigue… just how are these supposed to measured in terms of how much a person can cope with alongside a job, self-care, child-care, depenedent care and house-care?

    A job can involve all sorts of activity that most folk do without much thought, such as having laundered and ironed work clothes available for every shift, a lunch to take with you, perhaps personal equipment to transport, it may mean getting up an hour before others if mornings are difficult, travel, especially on public transport can be an hour and a half one way with changes… umm I already feel like a lie down just typing this. Add 7 and a half hours work and an hour and half travel home and err… yeah I reckon we all would be ready then to get kids to their activities, walk the dog, cook a meal, hoover, visit, rush to a training course or hobby class, doctor appointment etc… Unfortunately, despite recent dabblings in the importance of work/life balance, the tide has turned, very noticeably in the UK, to squeezing the ‘undeserving’ poor/jobless. I feel it wouldn’t matter if the only way to manage your job was to sleep under your desk overnight so you were there the next day… you can work. Lots has been said about the failings of our Work Capability Assessment so I will just say being able to do something once isn’t the same thing a being able to do it many times (as would be requred in a job) being able to do it having done things before it, being able to do stuff after it, or being able to do it pain free or without disproportionate or unrecoverable fatigue.

    Whipo off our coping mask?? First we have to look at unmasked selves in the mirror, then acept there is no better use of our skills than applying them to manage our health with any other work being a bonus. Pity we can’t be funded as our own health managers : )

    Take care… and time for your self… kuz no-one is going to give it to you.

  • Wow! I identify so much with your article.

  • Linda Cahill

    I am one of the “lucky” ones. I was approved for SSD after filing the first appeal. As a long haul truck driver, having severe balance and disequilibrium issues, as well as double vision and depth perception issues, I had no business remaining as a driver on the road. Financially, I had to. Commercial drivers are required to pass a D.O.T. physical exam every two years and when time came for mine to be renewed, the Doctor I went to not only failed me, but he pulled my medical certificate, told me to go home and park it. But he also referred me to a specialist at a well known teaching hospital who knows more about my disease than I do, which was unique for me. Having had Ramsay Hunt Syndrome (shingles of the ear), I was informed that I would never be able to drive truck at night again (it is still extremely difficult to drive my car at night, so I don’t if I can avoid it). I had found two Doctors that supported my claim. Two out of twelve, my oh my. As my facial paralysis continued to improve, my life with an invisible illness came to the forefront. I still have to plan my activities day by day. Most days I am just too off balanced to do much more than get out of bed. Because I live alone, the chores pile up, the house isn’t kept free of dust bunnies, there are weeds in the garden, the broken screen window is still broken. But I am one of the lucky ones. I receive monthly social security disability, I am on Medicare, I have permanent handicapped license plates on my car and I get by. This is not the “retirement” I had in mind, but it is what it it is.

  • RedCat

    After years of going to doctor after doctor, enduring endless tests and surgeries, with no one able to tell me definitively why I still struggle to get through a day, I’ve finally decided that my epitaph will read, “Hey, I TOLD you I was sick.”

  • I am Epileptic, and also have Fibro, as well as a few other health issues. After working full-time for nearly 30 years, I was denied SSI/SSD in both New Mexico (where my case never even got to the appeal before I left the state, 4 years later!), and in Oregon, where I was denied twice in a 6 year period. My younger sister, who worked in Social Services Vancouver WA, kept telling me I should move to Vancouver & apply there, that everything went faster in Washington. I did move to Vancouver (because my fiancée lives here) two years ago; I applied in June of 2009, and had my benefits by September.
    It was amazing! I’ve been truly grateful for this heathcare. For years I never had any benefits at all (I was a preschool teacher), and seeing a doctor or paying for my meds was nearly impossible.
    I have family members who question why I don’t work anymore (one brother constantly asks why I’m “being a bum”) but they’re the ones who have never been around when I’ve had a seizure, or seen the aftermath. To them, I say “Screw you.”

  • Kayla

    I have said it to friends many, many, many times… when you are dealing with the bureaucracy that is any government medical review or assessment for disability/illness payments (no matter what country) DO NOT wear make-up; DO NOT “do your hair”; DO wear creased and crumpled clothes that are obviously easy to put on (bonus pints for mis-matched buttons). Simply… DO NOT try to look as good as you can. Those appointments are not the time to take any pride in your appearance or in what you are still capable of doing alone. Even if it is on one of your best days, you MUST behave as if it is one of your worst. Use your walking sticks/wheelchair/crutches. Make sure someone takes you there and sits with you “because you cannot cope alone” and so on.

    When you are filling in the forms that ask you what you can do? Don’t think about what you do when you’re on a good day. Write down what you can do on a bad day. Think about those days when rolling over in bed is too bloody hard and someone has to help you. Always, always, use those days as your guideline. Because, if you use your best day, the person doing the assessing assumes that you’ve just told them what your worst days are like.

    I am lucky in one respect, despite having fibro, my husband is on a good income and we have been able to make the decision not to put ourselves through the additional hassle of claiming any government money – but the above applies for those non-financial benefits (disabled parking permit) that I have applied for. When we have invisible illnesses we have to actually make an effort to look sick for those who are too blind to see beyond the masks we routinely wear.

    So, as much as we all hate to do it, we have to hide the mask away at these times and show the world exactly how sick we really are.

  • FibroLimeyMommy

    This article really struck home for me. It’s the reason I have hesitated about trying to file for disability, because even though I am having difficulty caring for my kids and am in chronic pain every day….. I know they are going to say I’m not sick enough.

  • To kfunk,
    Drop me a message through my blog… I would really like to talk to you about your experience with med school. I had to take medical leave last year due to Lyme, and am gearing up to fight them for continuing as I had antibiotic issues throughout the year (not paying enough attention to how I was feeling, i.e. am I regressing? just tired? plateauing? etc.).

    And beyond that, this site rocks. This article hit the nail right on the head–when I see people at school I do NOT LOOK SICK, because I am having a dang good day if I am there! Sorry that my hair is not falling out, my skin and eyes aren’t yellow, and I don’t have oozing sores to stare at, man. That would make everything so much easier wouldn’t it? 🙁

  • I have CP, I was born with it & I’m honestly not sure whether my mom still gets disability for me. God knows she would never let me know how hard it is having a disabled kid……& 5 other “normal” ones. My most recent surgery wasn’t fully covered by my insurance so we’ll be paying it until I’m 507 years old (I’m 16 now). So to all my invisibly & visibly sick friends GOOD LUCK & GOD BLESS!!!!!!!

  • Melany

    Hi,

    You sound just like me. I am 37 and have two small kids. I work full time, go to school part time and take care of the house. My husband helps alot, but often times I have the kids and the house to myself. He works two jobs, one is as a firefighter so he is gone for 24hrs. I have to make myself get up and go every day and continue to go at night. I spend most weekends trying to rest and not doing much. I am so tired of being tired! I cry alot at night when I am alone and wish others new what it was like to live with the pain. I also look put toghether on the outside and hide my pain all day at work. I happen to work in a dr’s office on the nursing staff, so I am on my feet all day, ironically, most of my pain is in my feet and legs. I hope to find a good way to control my pain. I know it’s going to be tuff, but sometimes I am reminded that tuff is my middle name.

  • Robby

    At 28 I had to quit work for the third time, and it was the worst time. Finally after 10 years of major on/off problems, and a lifetime of being called a hypochondriac, the biggest quack dr. in town found the problem, a cracked spine (L5-S1), of course Fibro was already DX’d, we then added Reynauds, Involuntary Muscle Movment, asteo, Insomnia and what was that, oh yea, Degenerative Bone Disease. (What do you think caused the broken spine?) Of course I was denied my SSD, because “I could still work”. And yet, I had to have my 18 y/o step-son (my wife is older) carry me to bed at night, from bed to couch in the morning, and to the restroom whenever. Have you ever had to have your son take you to the restroom, or bathe you? That is humiliating. But I was not sick enough. Luckily two days before going before the judge, I had some test done, including a sleep study. Which showed pain response within the brain, as I was sleeping, which is also what woke me up 8 times that night. This was key in me getting approved.
    On a side note, my step-son, had a stroke at birth, and has some brain damage, so his IQ is two points above mentally challenged, we can not get him approved because of those two points. He is not able to hold down a job, the medical dr said he could not hold a job, the SSA psych said he could not hold a job, the court appointed “job {specialist}” said he could not hold a job, and yet the judge said he could. We can’t get him approved without two years of dr’s note’s, but we can’t get him the dr’s without getting him approved. A rock and a hard place.

  • Melanie

    I highly recommend using an advocate to file your disability papers and be your liaison with Social Security Disability. I used a company called Allsup, which was paid for by my employer. My disability claim was approved the first time it was submitted. They handled the huge amount of paperwork. I didn’t have to do anything at all. Allsup reps told me the statistics for people filing on their own. A huge percentage of claims are denied the first, second, and third times around and most of the time it is a paperwork issue. Like others who have posted here, I, too, worked years beyond what I should have. I was in constant, severe pain. I worked from home, so no one at the office knew what I was dealing with every day. I pushed myself to keep working to support my children. I don’t know how I got through those last two years. They were horrible. My life consisted of working and sleeping and that’s it. My heart goes out to everyone who is struggling to work with a disability.

  • DoreenBSkipper

    I’ve read all of the above, and agree with the comment “A squeaky wheel gets oiled”. To keep this short and not so simple but hope to encourage those that think they are at their ropes end….Always use your appeal rights until they have been exhausted! Including civil court.

  • Suzi Paullin

    Stephanie
    I want you to knowt that I spoke with you today at the Dogwood Festival and you truly have inspired me. We shared the same Dr. with his head up his rear and I know now that I can try to find that light at the end of the tunnel. I hate waking up in the mornings and even moving around. From the constant migranes and horrible body aches and pains everyday……..It gets to you beyond what your loved ones and people around you know. There are people out there that do know, this makes me smile a bit. I thank you for talking to me and you have truly helped me feel better just by sharing. Thank you so much.

  • stella

    I’m so sorry you’re in that horrible middle… I was there for soooo long… It took almost 20 years for them to finally give me the diagnosis of Addison’s Disease… the doctor who told me, had me come in to his office the very same day he got the results, was shocked that I was not devastated… I was happy, as I’d always known SOMETHING was wrong… and now I finally had a word for it, and I didn’t have to hear doctors tell me it’s all in my head or that I just need antidepressants or just needed to suck it up and get on with my life… and I was finally “sick enough” for Disability, after dealing with denials and appeals for years… what’s extra-f*ed up is that the symptoms were always the same, but with 2 words all of a sudden I scored high enough for them to finally approve me… weighing 82 lbs was not enough… suicide attempts were not enough… all the 911 calls my friends had to make when I couldn’t stop throwing up and passing out were not enough… all the pain and misery meant nothing to them without those 2 magic words… and then the judge and their doctor actually HELPED me get disability without a lawyer…

    So I’m sorry your words don’t score high enough and mine do, when we clearly feel similar on a daily basis…

    xoxoxo, Stella

  • Britne

    This Article Meant allot to me, I am often troubled of weather to let it show when I am flaring up. I know if I do some people in my life would be allot easier on me but I also know there is a down side to that… PITY I dont want people to pitty me but I want them to care…. is that possible??. I often to ousiders and even sometimes good friends put on a front that I have lupus and I get sick sometimes but look how normal I am or look how good I can look and how Happy I am… that is exhausting.
    The truth is most days I survive till its time to go to sleep. I feel like my sickness shouldnt ruin anyone elses day so unless I physically cant I am faking it even when in severe pain. When I do need help and I reach out to family and I tell them how bad I am feeling its almost like they have no feelings at all about it. I dont look like it hurts to even walk so I must just be “whiney”
    I am sooo struggling here and I dont know which way to turn

  • Joan

    I worked a full time job that frequently turned into 60-65 hour weeks. I struggled to keep a normal front..I would take time to “collect” myself so that I could maintain a cheerful exterior. When I became desperate becauseI knew I couldn’t do it anymore I made a decision to drive my car into a concrete wall. I didn’t really want to die but I knew I could at least get some time off work. That really scared me and I called my Doctor (a General Practicioner) and told him what was going on. After that I saw a Rheumatologist, Pain Specialist and a phycologist. All four Doctors agreed that I should stop working. SS approved my claim within one month. I am now on Disability and getting treatment for my illness. I don’t know how I managed to keep working those (five) last years.

  • RichardFelyne

    Wow.

    Reading about all these things makes me choke up a little. I know it’s strange, because I myself am not afflicted with any invisible disease.

    My mother is.

    All my life, I’ve watched her put on a brave face, and try to hide how hard it is for her. I’ve watched her go to work every day to feed me and keep me in clothes and keep a roof over my head, and I’ve watched it nearly kill her. She can hide it from other people, she’s very good at hiding it with makeup and a cheery demeanor, but I can always see through it. I’m her daughter, of course I can see through it. I’ve known the woman since before I was born, after all!

    It’s… Different to watch someone try to hide something from you while it’s painfully obvious. Struggling through something yourself is one thing. Watching someone you love do it is another. It’s a situation where you don’t know whether to call them out, and make them rest, or let them keep their pride and damage themselves. I’ve found that many people with lupus and so on are somewhat prideful, and don’t want anyone to see their illness. I guess they have to be tough to live through it. They don’t WANT to be on disability (or, at least, the ones that I know don’t) because keeping a job with it is near-impossible. The don’t WANT to “give up”. (I’m not saying disability is giving up, that’s just how my mother feels. I wish she wouldn’t feel that way- after all, that’s what disability is for, helping people with debilitating illnesses and conditions.)

    I’m not sure what I’m trying to say.

    I hate that she’s sick. I’d rather be sick or feel pain myself than watch her feel bad.

    I guess what I’m trying to say is to not hide it from your families, please. We will be there to take care of you. Even though I’m so far away, I’ll be there to take care of my mother.

    I think that’s what I was trying to say.

  • Sarah Phelps

    My Mum has a saying:

    “Only a squeaky wheel gets oiled”

    I have an abnormally extremely high pain threshold. Which is great, because I have to cope with large amounts of pain every day. It’s not so great, however, when you’re:

    a) sitting in the hospital emergency room struggling to stay conscious, but being continually passed over for screaming toddlers with scraped knees

    b) applying for a disability pension at age 20

    c) trying to explain to friends why you can’t come out today, even though you “look fine”.

    That’s the thing about invisible illnesses. They’re INVISIBLE!

    It’s our job to make doctors, pension officers, friends etc understand what’s REALLY going on. This may include taking off the “I’m fine” mask, instead of looking at them with your “I’m so normal” face. It may include crying, even though it’s humiliating, instead of holding back the tears until in private. It may include going in your pj’s, instead of calling your husband to help you get dressed, because you’re too tired to dress yourself. Because unfortunately, how sick you are is judged by OUTWARD appearances. I am NOT advocating pretending to be sick. What I AM advocating is showing how sick you really are – not showing the face you put on every day to survive. That’s not what they need to see.

    Only a squeaky wheel gets oiled. If you need something… don’t be afraid to make a little noise! 🙂

  • Tammie

    you know…this is the reason that I just stopped hiding what I really felt and allowed myself to fall apart on the outside just as I was on the inside for a while.
    I was tired of just getting through my day…surviving. So…I started to show people what I really thought and felt. I did however quite literally have to crawl out of my job to go to the doctor to get my release from work.
    I just had to let myself fall apart in front of everyone. It was definitely not my proudest point in life…and the aftermath was less then pleasant, but has in the long run been worth it. More of my time is mine now, and I have time to take care of myself properly.
    That in itself is a full time job.
    I pretty much told my doctor that I wasn’t going back to work and that was that. It wasn’t a discussion. It just was that I was done…
    I could have worked. If I wanted to blow my kidneys with pain meds and do nothing else other then sleep…and then it was still a push. I know exactly where you are…and it is ok to be there.
    I hope you get relief soon!

  • kfunk937

    Should my rather lengthy comment be to a more appropriate spot? Sorry, it was my first time saying anything . . .

  • kfunk937

    Advice for others re: SSDI – appears in context later, learned AFTER I lost SSDI case: Hope that others may find beneficial. Oh, and DO check the max allowable earnings, which change from time to time
    Maybe check at your county/state: some have “benefits banks” Aso United Way and other referrals agencies, and churches etc. even tho’ it’s ung_dly hard to ask for help, and costs a lot of spoons to follow through with paperwork they all seem to require for available assistance. To the SSA-specific stuff:
    (1) I should have filed to “protect my benefits” – the crucial earned quarters allowing SSDI – while waiting for my claim to be processed. No one volunteered this information. Doing this may also carry forward to subsequent re-filings, if turned down all the way thru Hearing and Court appeals.
    (2) I should have immediately refiled a new claim, “attaching” it to the “decision date” from the hearing, once the law firm screwed up the court date deadline; this would have also protected my many years of earned work quarters, and essentially kept the original claim open. BTW, no attorneys are eager to pursue other law firms for screwing up.
    (3) I should have immediately filed another claim, anyway, even if SSA wouldn’t let me attach to the decision date (I still had earned quarters earned available); since my health NEVER re-stabilized enough to return to work; in fact, I got worse, and developed new illenesses with additional diagnoses, even while the primary caregiver for disabled spouse, whose health continued to seriously decline. I had no advice, little to no support network, and my hands were way too full, just trying to keep up. My benefits expired. Twenty-plus years of paid-in taxes: apparently gone for good.

    In context, details follow. If anyone has feedback, I’d welcome.
    I lost my SSDI case (filed Feb. ’03, went to Hearing, with -poor- representation, in Dec. ’05, just after nine month’s part-time trial work job loss due to disability – info not introduced at hearing, nor afterward, altho allowed -an unusual judgement- and diligently provided by me – hearing decision by Summer ’06). Filed for disability after withdrew from medical school, while out on med LOA. Prior to that worked as researcher, was in college, worked PT & FT when possible in school, and before that, pretty much worked continuously, altho w/ some health-related job changes – often multiple jobs at once, for over 20 (taxable) yrs. Engaged big Cleveland law firm, adverts as mondo disability advocate, whose named partner informed me that I’d (they’d) missed critical court filing deadline by one day, thusly, “Guess ya don’t wanna work with us,” and then charged me to return my original evidentiary paperwork and other documents . . . Later learned important facts that may help others, but too late, probably for me now, in 2010-11. Am currently pending mandatory SSI, Medicaid disability re-determination, state disability assistance (a cash benefit I should have been told to apply for last Fall, but was told not to); food stamps depend on this also. Now separated from disabled spouse, whose income was sole source.
    (1) I should have filed to “protect my benefits” – the crucial earned quarters allowing SSDI – while waiting for my claim to be processed. No one volunteered this information. This may also carry forward to subsequent re-filings.
    (2) I should have immediately refiled a new claim, “attaching” to the “decision date” from the hearing, once the law firm screwed up the court date deadline; this would have also protected my many years of earned work quarters, and essentially kept the original claim open. BTW, no attorneys are eager to pursue other law firms for screwing up.
    (3) I should have immediately filed another claim, anyway, even if SSA wouldn’t let me attach to the decision date (I still had quarters earned and available); since my health NEVER re-stabilized enough to return to work; in fact, I got worse, and developed new illenesses with additional diagnoses, even while the primary caregiver for disabled spouse, whose health continued to seriously decline. I had no advice, little to no support network, and my hands were way too full, just trying to keep up.
    Because I was sucessful winning SSDI for my spouse (1st app), household income was too high for me to apply for SSI (once I’d lost my crucial quarters), while he was in the home. Among other disabilities, he eventually developed, tho unDx’d, diagnosable dementia, with paranoia & violent outbursts directed mostly at me. As we became more isolated, most events went unwitnessed; many happened at night as is common with “sundowners.” My many attempts to get help to care for him, safely, at home, failed. He only turned 60 in Apr 2010; I just passed 50 last June: elders get better attention and the cut off ages are somewhat arbitrary; this hampered my attempts to get help for us. I was actually told that in our county (Portage) he’d be better off in the legal system, than in mental health or social service networks (bad advice, save for the not hurting or killing me part). On second DV arrest, he was effectively, removed from home. About a month later, I suddenly lost regular Medicaid, forced into a managed care program (that took 2 months to return my calls, during which I got no care at all) with new docs – turns out disability determination had expired some time ago. Was suddenly forced to apply for SSI, as was now ineligible for SSDI (at least the field office b*&*^ wouldn’t permit me to specify a date, and as it turned out, she didn’t enter most of the information I did give her, like physician info, hospitalizations, diagnoses, etc.). The local county worker was hostile & misinformed me initially, lost paperwork submitted by the one physician who actually sent anything (and denied it), has since been replaced by someone else, and the doctor’s office won’t resend the file, or expanded information requested by the replacement county worker. Have a very bad feeling about this. Was already reemed in the first case where the SSA hearing’s medical expert threw out the medical evidence, saying the physicians were biased (one had treated me for about 10 years, several others were faculty members) but he obviously was unable to make out the writing in the charts – very old – could not even read the writing, which I had memorized in some cases; the occupational specialist didn’t have to refer to the medical evidence, which specifically refuted his own conclusion(s) directly; and the attorney didn’t introduce my job loss due to disability, or allow me to do so. The lawyers, as near as I cld tell, never introduced any additional evidence, tho’ SSA hasn’t responded to my written request for case records made almost eight months ago, shortly after consulting a local disability attorney (before I was forced to apply for SSI when my personal life fell apart so suddenly), who told me “no one would help me until I was turned down again.” If I’m turned down again, I’m DOA. I have no income, no assets, and unlikely to be able to find work or keep it. I’m now overaged, haven’t anytime recently, have no references, am too ill (according to my doctors), am advised not to drive, and live in a poor rural county with limited transport options. Wasn’t thinking about building a case so much as getting necessary care – had typically under-utilized medical services, or at least not used as well as I might, without prior disruptions and tendency to ignore or downplay own health issues. Recent events caused many lost and changed doctors, insurance carriers (and will lose coverage entirely if denied, affecting this disability determination, as well as making reapp more difficult, not to mention continuity of care while homeless and uninsured. lol). Am intimidated, overwhelmed, in despair; the bright face is capable of denial at most, but am not sure that’s in my best interests. Any thoughts? Someone mentioned advocates in Canada – but I remember when applying to med school they made me promise to move back to the states if accepted there haha. Are there such things as real advocates, not BS ones, near or in Portage County, OH?