ankylosing spondylitis Information
Which unprescripted medicine do you find most effective for ankylosing spondylitis?
I have tried several Nsaid's and none of them i find helpful for the pain and stiffness. I dont wanna do harm to my body if it is not going to take away my disturbing symptoms. I just need your opinion on which drug worked for you best?
How to reduce pain in ankylosing spondylitis and increase mobility,pls suggest drugs with minimal side effects?
Can a lady suffering from ankylosing spondylitis have a baby with out any danger of child suffering from same?
a young married woman is diagnoised for antylosig spondilitis. will this disease be passed on to a child born in future, since this disease is genatic and may be passed on to next generation
I have a severe case of ankylosing spondylitis, what should i do for a living ?
Is there anyone out there with ankylosing spondylitis that has taken prednisone?
i am on ssi and was taking high amounts of prednisone and couldnt sleep and had to do something with all that energy,could someone explain to our ignorant government the hell this disability does for someone.pain killers and injections every week help, and now i lowered my prednisine a lot.someone explain to them that there are days you feel ok not great but enough where you have a little self esteem.i will always do electronic tinkering when feeling good till i lose my arm ability.i am not just going to sit in a corner and die.this disability was with me since i was 3 years old.i got pnuemonia 3 times when 3 years old and have had it 7 more time since.this is a autoimmune desease and much still has to be learned about it.symtoms are dragging, pain in joints, frozen neck and other malidies.if you have this disability please answer.
Getting disability for ankylosing spondylitis?
I did a bit of research being diagnoses with this recently I can barely walk most days it's effecting my hips horribly but I have no fusion of the spine yet. I'm 26 and I have not worked very much so idk if I'm able to receive disability for my condition but I'm on Humira and I'm honestly barely making it out of bed it just seem silly I have to have fusion to get disability when it's blatantly obvious I'm in nowhere near shape to work. I want to finish school online since this disease killed the career I was going into, the disability would be nice to finish my degree as well as just in general since I'm physically unable to do much of anything.
Is there any way to put ankylosing spondylitis into remission?
My family carrys a rare disease called ankylosing spondylitis and I wanna know is there anyway to put this thing back to sleep I've heard of many people putting it into remission but I wanna hear how you did it or maybe any ideas on how it could be done.
Any chance for someone diagnosed with ankylosing spondylitis doing weight training?
There's a high chance of me contracting a disease called ankylosing spondylitis AS , it's an autoimmune, lifelong conditions which cause joint pains and fused vertebrae. I started to work out weight training, cardio, etc for 6 months before this diagnosis, I do this with passion and commitment. I'm by no means an expert by I learn everyday. I'm devastated and is now wondering if there's anyone out there with similar conditions who is still working out? if yes, could you inform me on the kind of exercises to do avoid? I know this is a long shot but I really love having a good body, it's one of the very few accomplishments that I might be proud of one day i'm a talentless, depressed, physically unattractive guy and I just can't believe this will be taken away from me.
How to sleep with ankylosing spondylitis ?
Any trick will do the job
If I have Hla-b27 gene and sacroilitis will I develope ankylosing spondylitis?
And if it is not defent what is the likely hood I will, or precentage of people that do. And what are the questions i should ask my rhematologist. Oh and I'm 16, and how can i destinguish between sacroilitis and ankylosing spondylitis.
How can i tell if i have ankylosing spondylitis?
i have scoliosis, but I've also looked up the symptoms of ankylosing spondylitis, and all he symptoms fit.... I'm really sore in the morning, lost a lot of rotation, really hurts when i sand for a long time... help plzzzz thanks
Ankylosing Spondylitis anyone?
So I have ankylosing spondylitis on my sacroiliac joint but I don't know anyone who has this. Besides, I made new exams and my doctor told me that it seems that I no longer have this, but I keep having a lot of pain. Is this normal? I'm also taking some vitamins for my bones since the pain can be caused by arthritis.
Ankylosing spondylitis: Why does stretching in one direction cause agitation and the other doesn't?
I have ankylosing spondylitis.I noticed that whenever I bend my back backwards, back of head backwards it inflames my back and I find it quite painful for quite a while afterwards and stiff. If I bend the opposite way forwards , it relieves this inflamation and stiffness, and never inflames. Why is this?
I was just diagnosed with ankylosing spondylitis. I havent done a ton of research but ever since I can remember, I can crack almost every joint in my body neck, shoulders, elbows, wrists, fingers, my whole back, pelvis, knees, ankles, and toes. Does this have something to do with each other? Also, any suggestions on back pain relief would be great. The nights are terrible and the mornings are just as bad.And I always get these intense headaches in my temple areas and they only last about 30 seconds and go away...it only happens once in a while, but could that have something to do with AS too?