Rheumatoid Arthritis Support Group
Rheumatoid arthritis is a chronic, inflammatory, multisystem, autoimmune disorder. It is a disabling and painful condition which can lead to substantial loss of mobility due to pain and joint destruction. The disease is also systemic in that it often also affects many extra-articular tissues throughout the body including the skin, blood vessels, heart, lungs, and...
I can sympathize with you. I try to put off doctor appointments unless I have to go. I still feel like I get the "oh, you again, what is it this time" from the docs.
You just want to tell them, listen, I really wouldn't be here if it wasn't something that I really just can't ignore any longer.
Know that you are not alone in this fight, we are all here for you if you need us.
Kim
Know that you have plenty of company & understanding.
You do what you have to do.
It's not worth suffering if something can help.
Think it's safe to say we all feel the same as you at one time or another.
Your worth it & do what it takes to feel better.
Hugs
Sammy
Well, I can certainly guarantee that you are not alone. I am right there with you. Miserable, and with horrible foot pain. I recently went to a podiatrist who had custom orthotics made for me, but I am still having awful foot pain. I had to pay $350 for them, haven't even paid for them yet, and don't want to go back and pay any more for something else that won't work. I was just looking online for a foot massager. Seems there are some out there that vibrate that may not hurt. My RA doc doesn't think my foot pain is from RA. Strange, because when I was in remission, my feet did not hurt at all. I think the only thing we can do is continue to try new things until something helps.
It is common sense to take a method and try it. If it fails, admit it frankly and try another. But above all, try something.
Franklin D. Roosevelt, Looking Forward
So far Trooper45 yrs the only relief I get for foot pain are my ice packs. I literally sleep with them cocooning my feet.
I know exactly how you feel! I also have a loving husband who supports me but he doesn't really have any idea what it's like for me. He has his own issues related to diabetes so he does understand the chronic disease part, but he's not in pain every day, all day.
I feel like the only ones who can truly understand are the fellow RA Fighters who are going through the same things we are.
just think of how shallow you would be if you had perfect health, still and understood no one and anything but your goddess body/health and the physical pursuit of every goal you ever wanted to mow down - i know a couple folks like that....and they suck at getting the frailty of life
this crap disease invades your every point in your body that is why you feel like a hypochondriac because you have to keep a separate calendar just to remember meds, infusions, prescription renewals, authorizations, appeals, referrals, physical therapy appointments, orthotics, injections, pulmonologists, the liver doctor who drones on and on, the orthopedic who always wants to operate, the neurosurgeon who will not believe you can't swallow right, the ENT who wants to give you acid meds just to cover it up, the primary care who is tired as crap of you, and the NP who sees you when you get something ridiculously wonderfully routine like a freakin' strep throat.
otherwise, you do feel like a goddess.
we get it
you feeling better tonight?
Depot
I've had an unbelievably frustrating stretch on the medical front, and everyone's words ring sooooooooo true.
What I wanted to say is yes I am so tired of try this drug no you cant take that drug because you get infections so go off this drug take this antibiotic and when your done with that start this new shot. Ughhhhh this is my fight now and I do it alone with no husband for the last 14 years...sorry guys just venting......whew.... take care all of u