Arthritis Patients Share How It Hurts
Reading Time: 2 MinutesLast Updated: September 30, 2021
At the Arthritis Foundation, we focus on alleviating the pain and disability caused by arthritis. We have a wealth of resources and initiatives to help you navigate your specific arthritis-related issues.
Our How It Hurts report summarizes our latest findings on the impact of arthritis pain. This year’s report concentrates on three core areas: physical health, emotional and social health, and experience of care. We found that almost 90% of arthritis patients surveyed have pain that interferes with their daily lives and activities. More than two-thirds experience higher levels of fatigue than the general population.
We’re working to improve the lives of those with arthritis – both now and for future generations. Addressing chronic pain is our top priority. We encourage you to check out the following resources to help with your specific situation:
- Our current pain initiative led us to develop a new pain management app called Vim. This app helps people with arthritis gain power over their pain by setting attainable goals. We encourage you to review our Privacy Notice to understand how we collect and use your personal information.
- You’ll also want to use our Rx for Access center to help you choose the right insurance coverage, learn your rights, and appeal denials.
- Our Take Control of Pain page offers pain management webinars, podcasts, and e-books to help you along as well.
We also want you to know that Social Security is here for you if your arthritis is debilitating enough. Please check out their Disability Benefits page for information about their Social Security Disability Insurance and Supplemental Security Income programs. These programs could help you if your arthritis is disabling and you can’t do any type of work. If you think you may qualify for disability, please visit their website today.
Please share this information with your friends and family – and post it on social media.
Social Security’s posting of this blog does not constitute an endorsement or recommendation of any non-Social Security organization, author, or product. The websites available within this posting are not within Social Security’s control and may not follow the same privacy, security, or accessibility policies. Once you visit such a website, you are subject to the policies of that site.
Tags: Disability, social security disability benefits, SSI, supplemental security income
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Geohomecorfu
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Florence ".
What I’ve found out over a couple decades is that a mass number of people including my elderly and not so elderly family members would be walking slowly every other day for years this was happening & they would say “Old Arthritis” got me today. I myself was told by a rheumatologist around yr 05 that i was suffering from Rheumatoid Arthritis and was given medications for, but no relief would come. I found a new Rheumatologist and after our consultation and quite a order for the lab to check my ANA along with 13 other test, well after all these years i was taking arthritis when all this time i had Lupus SLE because Lupus is what they call a copycat disease and tends to mimic other illnesses and that was the case with quite a few relatives friends and neighbors too. You just have to ask them to go a little above and beyond to make sure it can be ruled out, because when you tell your doctor about all the joint pain and swelling they are going to automatically say it Arthritis because those are the exact symptoms & guess what? Lupus will imitate those exact symptoms as well but it won’t be any form of Arthritis at all, it’s so easy to be misdiagnosed because not a lot of Dr’s are familiar with Lupus but there is specific lab work that can differentiate to let you know for sure. It’s true there’s no cure but you can finally be treated for what you actually have so when choosing a Rheumatologist please ask him/her if they are knowledgeable of the disease Lupus because i found out myself that a lot of them were not & Lupus kills like any other disease and tons of people just simply don’t know they have it. Quite a few celebrities has it and let their fans know, but sadly Lupus had the chance to attack 1 or more major organs so if they have a flare up they will be admitted into the hospital due to the damage Lupus has caused. Now we have had many who has/ had Lupus live through the ripe age of 90 and beyond, it’s all about being tested for it and treated correctly. I may have Lupus but Lupus doesn’t have me!!! Lupus Warrior👊
Karan
Nice post
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David G.
Good one. Arthritis is not easy to live with but there is much you can do to change, overcome, or cope with the problems it presents. Your doctor and other members of your health care team can recommend medications, special exercises, joint protection techniques and devices and other self-care activities.
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Charles C.
Informative Article. Thank you for sharing this great information about Arthritis diseases also shared how it works by this patient. We all know that Arthritis is a disease that affects your joints that causes chronic pain, inability to do daily activities, and makes it difficult to walk. Actually, I am a medical student Recently I have read about the cardiovascular system from this resource, you can check more info where they have shared lots of effective information and essay ideas about it that can help me to write my academic research paper on this topic. So I am also very glad to read this good information about Arthritis diseases. Appreciated the author.
Brenda L.
I have bursitis. Is that some type of arthritis ? It’s the worse pain I ever felt.
Debbie
I’m so sorry for all of you. I suffer with Rheumatoid, Osteo Arthritis and Fibromyalgia also sjogrens disease and Lymphodemia. I’m have degenerative spine disease with 3 blown disc in my lower back. I’m thankful for my Great Doctors I keep going to make sure I don’t loose the ability to walk I still have Pain, but I know it’s going to get worse some day.
Gloria M.
i have arthitis–painful–and can’t walk–hurts-on my right—I am 61 years–old–‘why now–to–have–arthistis–‘why’–i don’t eat–bad–food–it just happen–wow—-numb ness–right leg–won’t–move–i-can’t–even–clean–the–living-room–bathroom–or–car-wash–or–standing–cleaning–up–wash–outside–“i need-to–know–why –now–
Mj
God bless Signature Health Care in Boston I have chronic arthritis pain in my knee could not walk and because of your excellent therapist I can move Arthritis is a very dangerous disease God bless excellent staff
John
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Shannon H.
How do you think you can talk the pain away. You’ve taken us off our pain meds. Because of the war on drugs. But all y’all did was take away our quality of life. Which shortens out lives. And NO ONE CARES. Do you know the number of chronic pain patients who have committed suicide? Over the pain that wasn’t being treated. Or the staggering number that will be by the end of this year? Or about the number of people have turned to herion or meth? Or even alcohol just to dull the pain. I know before I ever become dependent on some one I’ll take my self out first. I’ve live with RA and Fibromyligia for 52 years and I’m just so tired of seeing doctors and getting no help. Give the doctors the right to give us our medications back. Because whatever life we have left ain’t worth living constant pain. How would you feel to watch your family member to die slowly from an inherited disease. Ask my children.
Debra M.
U r million % right!! I was prescribed in VA on disability for rare bladder disease back neck kidney ailments u name it I had it.. prescribed high dosages pain meds for 10yrs then moved to ny cuz dot disability and that whole 703 month didn’t put roof over me and my boys head. Back to parents yucca! NY decided my Ulcers in my bladder aren’t painful when my urine fills with toxins and hits these opens sores. Rare disease ny drs never heard of it vut off cold turkey.. suboxkne no help for pain.. street pills all pressed with fentynal killed 2 my son’s last year.. wtf 1. To do in pain. Street chance lol with the 750 month disabikity pay check lol or kratom which I just found out about.. many don’t no bout this or how to take it
red kratom for pain don’t get smoke stores. Fda tryn make this illegal too.. wat u want everybody miserable in pain and either gonna snap hurt themselves,, somebody else,, maybe the pharmacist or dr who says oh deal with ur pain…no u deal with this.. we want our lives back.. we don’t want this!!!! No only physically it sucks but mentally emotionally and financially. Pain disease thst who we were away no self esteem no laughter no hope and we can’t deal with people who abused system and hurt those in rwal need. My sisters buddy today goes pain mgnt sold her every psin pill he got today 90 pills 520.00 psid 0 medicaid paid and he qualifies for medicaid on disability and I don’t he makes more money than me wtf is wrong this is gone wrong for us NOT scamming the system and I’m done. Kratom works for opiate withdrawls if u know how to take it u won’t have any craving no sweats no sickness no withdrawls at all most ull have is afterc4cweeks hard time Sleeping sets in. Red hulu 6grsms mixed 2oz og approx shoot down like a shot yucchy tasting but works every 4 hours.
Fran
My 75 year old friend suffers with arthritis in the hip/back area. We are trying our best to find him relief by getting stem cell injections, physical therapy, supplements for inflammation, …There is a crack down on pain meds and we understand because people abuse them but people need help in paying for the stem cell route. $900 co-pay needs to be addressed for people on fixed incomes.
Mary
You are so right. It’s awful. And if I do ask for a pain med they treat me like I am a junkie. I live in a state that does not even hav medical MJ which does help with pain for a while. Since I had a transplant I can’t even take Ibuprofen so that leaves me with nothing. I did find an herb called Kratom that does help with the pain but the FDA is trying to ban it. I am like you, I don’t want to hear the BS about “ talking the pain away”
Lisa M.
Social Security has nothing to do with pain-control medicine..Call your Senator,,or the CDC..I agree it isn’t right to punish the people who really need pain meds..I have RA-Fibromyalgia-Lupus with other ailments..Chronic pain is no fun,,and affects your life-family in many ways…Best of Luck…
Warren
Wow you hit it on the head…the medical community seems to feel that they know our pain better then we do… Being tired, weak, and in pain is not really a life, it is just being here. Forty years of this crap and I am burnt. I did get disability but now argue with the wife about being home now… Can’t win… I pray all of you find some sort of relief with the pains of life…
Jen
I 1000% agree. I just turned 43 last month and I feel like I am 80. I live in a Queen sized island 95% of my life because of the pain. I have fibromyalgia and arthritis (arguments that it’s RA vs. OA – Doctors are assholes) and I am a Cancer Survivor with massive nerve damage from the surgery and radiation treatments. Degenerative disks in my spine, I’ve had both herniated and bulging disks…. CFS, remissive hep c (I had the treatment and it was “cleared” after 11 years of being positive) but I will always have to deal with the fact that I had it causing damage to my body for all those years. I’m a carrier for the Epstein-Barre Virus and Cytomegalovirus both of which can cause mono and are possibly what triggered the fibromyalgia.
most of these things have been passed on to me by my mother and her mother. I am/was a Nurse and I am 100% DISABLED. I have lost my identity and everything else I loved about life because of PAIN. IT SUCKS!!!
Jen
I 1000% agree. I just turned 43 last month and I feel like I am 80. I live in a Queen sized island 95% of my life because of the pain. I have fibromyalgia and arthritis (arguments that it’s RA vs. OA – Doctors are assholes) and I am a Cancer Survivor with massive nerve damage from the surgery and radiation treatments. Degenerative disks in my spine, I’ve had both herniated and bulging disks…. CFS, remissive hep c (I had the treatment and it was “cleared” after 11 years of being positive) but I will always have to deal with the fact that I had it causing damage to my body for all those years. I’m a carrier for the Epstein-Barre Virus and Cytomegalovirus both of which can cause mono and are possibly what triggered the fibromyalgia.
most of these things have been passed on to me by my mother and her mother. I am/was a Nurse and I am 100% DISABLED. I have lost my identity and everything else I loved about life because of PAIN. IT SUCKS!!!