Psoriatic Arthritis Knowledge Base
Psoriatic arthritis?i have costo,now my specialist thinks i have psoriatic arthritis as well, i was wondering what are all the symptoms does anyone know, my back hurts every day so does my neck and ive so many other symptoms to can any one offer me help on this please
Psoriatic Arthritis?I have psoriatic arthritis and some of the areas of my affected by this is my wrists and fingers. Last night I got a horrible pain in between the pointer and middle knuckle on my left hand. It is to the point where I cant turn a doorknob or lift something as light as a phone with my left hand. It is painful to pick up my 13 month old daughter, get her dressed etc. My question is, can psoriatic arthritis affect in between your knuckles, or is something completley unrelated? Thanks in advance for all your insight!!
Psoriatic Arthritis-Are liver biopsies extremely painful?Methotrexate 7.5 per week. Diagnosis-Psoriatic arthritis.
I was recently diagnosed with psoriatic arthritis after over 8 months of misdiagnoses and mystery. I just began treatment with methotrexate (3 days ago). The doctor mentioned the frquent bloodwork that has to be done and the liver biopsies to test the toxicity on my liver from prolonged use in the future. I am concerned about the liver biopsy-pain and recovery time. Anyone with personal experience?
Arthritis,psoriasis,psoriatic arthritis,some types of Asthma are linked one viruse?In my research,I think that psoriasis,Arthritis,Psoriatic Arthritis and some types of Asthmaand some types of kidney problems are linked with one particuler kind of virus cells.
Because I can giving only one Herbal treatment cures all these disease.So i can give this answer.
I am an Indian in Tamilnadu.I have been giving this treatment freely to poor and lonly peoples.This is not advertisment ,only on service motive.
I DON'T KNOW FLUENT ENGLISH.THANK YOU.
kamalisethu@yahoo.co.in
Weird psoriatic arthritis?im 16, and my doctor said i have psoriatic arthritis. i think hes wrong. the lower articulations in 2 fingers hurt, and every so often some months, it switches to 1 or 2 other fingers and it ends in those (that is from that arthritis). next, the doctor told me my nails were tipping or something like that, i forgot the name of that action, yet I dont think hes right my mom and i, and my friends and i checked the nails and we all have them exactly the same. next, i dont have anything of psoriasis. the little red things u get in your forehead/head, no symptoms at all of psoriasis. do u think my doctors wrong?
Help with psoriatic arthritis?My sister has a terrible case of psoriatic arthritis, and it appears to be taking over her body. She is terribly itchy, and her joints are beginning to creak, and she is only 18! She is very embarassed by the rash, and the physical symptoms are a bother to her, and I hate to see her going through this. Her dermatologist has recommended a shot that she has to give herself weekly, but insurance is taking months to approve this, and I have heard this can cause acute kidney failure. What can she do until this is approved? And does anyone know of better options?
I suffer with psoriasis and psoriatic arthritis. What medications do you take? I take raptiva & embrel?I've had psoriasis and psoriatic arthritis for over one year now and it's a terrible disease. I've tried external creams, shots, and Remicade infusions. I've also lost my hair and lost my finger nails and toenails. I've had to wear slippers for over a year due to the loss of my skin on the bottom of my feet. The has been devasting to my mental state of mind as well as my social activities. I hardly go out of the house because it's difficult to walk and do every day activities like I use too. When I do go out I have to use a wheelchair. My doctor currently dropped my Remicade infusions and will put me back on my Embrel injections along with Raptiva. This will require me to have 3 injections per week. Thank goodness shots don't bother me. Is their anyone out their who can identify with what I'm going through. I don't wish this physical pain on anyone. I don't know from day to day how I'm going to feel physically or mentally. It is a chronic illness that will never go away...
What is the cure for psoriatic arthritis?I know someone with psoriatic arthritis. What is the cure? Please don't waste my time with anecdotal evidence from anonymous people who drink expensive imported juice and claim to be healed.
What treatments and cures are available? What science is behind the remedies?
Can the severe symptoms of psoriatic arthritis be reduced?After several mis-diaganoses since my first visit to hospital in September 06 - they thought it was fractured metatarsals/ cuboid bones - my specialist has eventually realised that I am a long standing sufferer of Psoriasis. Psoriatic Arthritis is now suspected after a bone scan and the blood tests should confirm it.
I am due to see my specialist again on 10th January and the foot pain/ difficulty in walking has now spread to my knee causing locking, extreme pain and clicking noises.
Even more tests and delays are now anticipated, possibly a MRI scan with a 19 week waiting list and a sample of fluid from my knee. Meanwhile I am only taking un-prescribed drugs - Ibprofen and Anadin Extra - and am worried that irreversable damage may be caused due to the delay in diagnosis. Is there any light at the end of the tunnel? Will I always suffer pain and disability? Why don't doctors ask the right questions & arrange the right tests when you see them? I feel let down by our Health Service
If Psoriatic Arthritis is a "T" cell malfunction, does exercise have the same benefis as those with Osteo ?I know that strengthening and stretching are good ways to support joints and maintain an active lifestyle with Arthritis, but the cause of my condition is genetic, and not physical. Will excercise have the same effect for me as it would for someone with Osteo-Arthritis, or even Rhumatoid?
Thanks for the answer...
I am a tennis pro who teaches full time on hard courts. I am worrie that my career is going to aggrivate my condition. Am I kidding myself in thinking that I can maintain my condition AND teach tennis for a living?
Humira Injections - Psoriatic arthritis?I was just diagnosed with Fibromyalga & Psoratic arthritis.
Has anyone out there been diagnosed with the same, and taken the Humira injections?
did they help with.... pain, stiffness, skin issues?
What did you feel where the drawbacks ??
Are you still taking the injections?
thanks !
Does my boyfriend really have Psoriatic arthritis?after reading up on this arthritis i really dont think this is what he has. his toes and fingers are curving real bad and he is in pain all the time. His fingernails are fine, his skin is fine except on his shin's and scalp. i want to help him feel better. a doctor treated him for over a year saying he didnt have arthritis, he is adopted so no family history. his back and neck are fine. he doesnt feel hot feelings in joints.
Do any one have psoriasis, arthritis or psoriatic arthritis or asthma?kamalisethu@yahoo.co.in
We discovered one miracle herb.It cures all types of psoriasis,arthritis,some types of asthma and some types of kidney,nervs problems.In my research these are linked by one virus.Our herb kills these virusus.So these diseases are totaly and very quickly cured.Around the world these are only controlable disease.But in my research these are very simply cured.I don't know fluent English.I am INDIAN in Tamilnadu
Has Any one taken the Disease Modifying Drug (DMARDs) for their Psoriatic Arthritis?As a Arthropathic Psoriasis sufferer i have taken my Triamcinolone (trade names Kenalog, Aristocort, Nasacort, Tri-Nasal, Triderm, Azmacort, Fougera) injection, but it seems to have made it worse...
So i my next course of treatment is the Disease Modifying Drug (DMARDs)... i have been told that i will be taking this for about 1 year.
My Question here is... Are any of you Psoriatic arthropathy sufferers taking this drug? If yes did you see any improvments and did you have any short/long term side effects while taking this drug?
Please only answer if you have had personal experience with the Disease Modifying Drug (DMARDs).
I am 31, in the prime of my life, and have had Psoriatic Arthritis for 5 years.?I am also a a tennis pro, but the arthritis is getting to the point that even teaching is becoming difficult with swollen joints in my elbow in my playing arm, my ankle and in all of my metatarsals in my feet. I can no longer play tennis anything like I used to and lose matches to people I should easily beat.
I've tried Glucosamine, Omega 3, I exercise regularly and commute on my bicycle every day, but I am still in pain despite taking 12-16 hundred milligrams of ibuprophen every day.
AM I kidding myself in thinking that things will get better and I can persue my career path, or should I cut my losses and move on?
Arthritis pain. On strong drugs + painkillers...?Hi all,
First of all I have Psoriatic Arthritis, which is very similar to Rheumatoid but Psoriatic is more aggressive. I'm 26 and have arthritis all over my body. I'm under hospital treatment and take an ex-cancer drug (Methotrexate) but have been switched to Enbrel now.
I'm having problems with pain management. I take a higher dose Cocodamol at the moment with the highest dose of Diclofenac but it's not working. I'm in a lot of pain. They are tying to put me up to a different painkiller but I have problems with my liver acting up when they made my painkillers stronger last time.
I don't know what to do as it's so hard coping in pain all the time, but then having liver problems when they make them stronger. How do you cope? Have you found a certain painkiller to be wonderful? If so, please could you tell me the name of it and what dose you are on. Thank you.
spyrogirlkim - I'm sorry to hear of your illness. Best of luck hun.
Rev TL - I'm not being a walking experiment, I'm just doing what my Rhumotologist says, after all it is the NHS I have no options.
dbiebel@sbcglobal.net - Thanks but I eat very healthily now as it is.
gillianprowe - My skin condition is fine, the MTX is controlling that, if I stop it, it comes back. When I say arthritis all over body I mean I have it almost everywhere. Back, neck, elbows, fingers, wrists, knees, hips, toes. I'm pretty close to having a wheelchair too, I'm in a disability changed home. I know what Psoriatic arthritis is, just not enough characters to describe everything. I was diagnosed at 13 but everything went downhill after having my children. I went from a horseriding person to stuck in chair 90% of the time and very fast too! The doctor at the hosp says they not inflammed but damage has been left and they still hurt a lot. As for the diclo I take max dose (150mg) I said max dose in orig post.
Was recently diagnosed w/Rheumatoid Arthritis.Have had a cold for 3 wks.Is my immune system worse as a result?I am an otherwise healthy 40 year old male. Have few effects except for strong bilateral pain in elbows and sometimes minimal wrist/finger pain. Scored a "4" on rheumatoid factor test (very small amount but nonetheless it's there. Doctor put me on ibuprofin and Plaquenil. She thinks I'm in early stages of R.A. or possibly psoriatic arthritis. I'm curious to know if this sounds like the correct diagnosis to others PLUS I'd REALLY like to know if I DO have the disease, is my immune system compromised now? It seems ridiculous to have a cold for this long (3 weeks). Also I came down with conjunctivitis for a week in July. Dont know how, but Internet says this could be another clue that I have it. Maybe I'm just in the denial stages, who knows. This is all very new to me. I'm worried that if I do have R.A. that I'll constantly have to be worried about getting sick from the common cold, etc. Would appreciate any personal takes on this. I have of plenty basic info from Internet websites, thx!
Do you take Methotrexate for arthritis?How long did the sickness last for, does it ever go away, I am really ill the 24 hours after I take it and had to discontinue it as it had too much of an impact on my life (missed days at work etc).
Is there any method I can use to be less sick?
I am taking Mtx for Psoriasis and psoriatic arthritis.
Whats the best arthritis treatment?I have rheumatiod, osteo and psoriatic arthritis and am currently taking 6 Sulphsalazine tablets daily. It's the second time of trying them as I reacted badly the first time I took them. I am wondering if there are any other tablets I could take.
I'm going to the dr's on Friday to enquire about this, and could anyone on here give me any clues as to what to ask for.
I am seeing a rheumatologist.
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