humira and ankylosing spondylitis

I changed to Humira recently and was wondering if anybody has had success with humira who has ankylosing spondylitis. Any feedback would be appreciated.

I have ankylosing spondylitis currently take Humira and antiflamitories. I avoid sugar and certain meats like chicken and pork to avoid attacks. However one thing I can't avoid is weather changes such as spring and fall. This last year has been a real rough the attacks have been really bad. Any suggestion?

I have ankylosing spondylitis and just had my first Humira shot 2 days ago. Today I woke up feeling very achy, my nose is stuffy and my throat is scratchy. I don't know if it's allergies, an infection, or a side effect from the Humira. Has anyone else had this happen shortly after starting this drug? I am planning to call my doctor on Monday but just trying to figure out what's going on.

ok so i have Ankylosing Spondylitis and my hubby is in med school, he just learned of a procedure (surgery) that puts like a fake cartialge between the spinal bones. and that prevents the bones from fusing together. now i have never heard of it and it sounds scary, like do they cut my whole back open or just little incisions? its supposed to take 2 months to recover and 6 months to be fully back to normal.

I have ankylosing spondylitis and irritable bowel syndrome. I think they are most definitely related. I've been following a low starch diet (Carol Sinclair's IBS Low Starch Diet) and it has really helped. I've also recently started seeing a nutritionist and had food intolerance tests done, am taking Schussler Tissue Salts and incorporated the Anti-Inflammation Diet Plan into my menu planning. All this is detailed on my blog www.bonappetitreview.blogspot.

My cardiologist suggested their maybe a correlation with Cardiomyopathy and my AS, last year I was diagnosed with AS (Ankylosing Spondylitis). From what he told me that this is a progressive disease and he will monitor my condition and treat with medications for now. I will see him in 2 months, but wondered if this enough? I have almost all the symptoms of Dialated Cardiomyopathy, except swelling. Should I be really concerned? What is the likely prognosis of someone with this condition.

I am a Vietnam Vet and I have been diagnosed with ankylosing spondylitis and I am wondering if there is a link between ankylosing spondylitis and agent orange?

I am currently diagnosed with Ankylosing spondylitis and Fibromylgia. Been on treatment since 2015. Humira and methotraxate for AS and valdoxane for FM. However my Rhumy cannot give me an explanation whats causing my weakness or numb feeling. I have also had a skin biopsy done for a rash I have developed. Result was vasculitis. Now that I am having another episode of weakness on the left side my Rhumy has requested for another Brain and neck scan.

I am a 44 year old female and have Ankylosing Spondylitis. In the past 2 months I have injured my ankle, my achilles tendon, had plantar's fasciatis (forgive my spelling please!) and now I have pain by the knuckle in the top of my hand and a popping feeling. So I assume I have injured some sort of tendon/ligament there. This is an awful lot in a short time.

Yesterday my rheumatologist has finally decided to give me something other than anti-inflammatories and anti-depressants for my list of symptoms which he has decided are due to either Ankylosing Spondylitis, Psoriatic Arthritis (Palindromic Rheumatism was mentioned too) or possibly all of the above, with a side order of Fibromyalgia. Just wondering if anyone here has taken Humira (Adalimumab) as I've read about it and am freaking out a bit!

This also depends on the geographical area, the incidence of ankylosing spondylitis in your area and other environmental and genetic factors. Please discuss with a specialist in your area. Take care! The medical advice given should not be considered a substitute for medical care provided by a doctor who can examine you. The advice may not be completely correct for you as the doctor cannot examine you and does not know your complete medical history.

I have had ankylosing spondylitis for 6+ years. I take methotrexate and Enbrel (alternative to Humira and Remicade). I live a virtually pain free life except for an occasional flare. These 2 drugs gave me back my quality of life and hope. Hang in there. I believe quality of life is important and there are drugs out there to give that to us. Don't be afraid to try the medication. Be aware that you need to be more careful about getting sick.

regulators have approved the drug for rheumatoid arthritis, psoriatic arthritis and ankylosing spondylitis, a painful, progressive form of spinal arthritis. All three forms of arthritis are chronic disorders in which the immune system attacks joints, causing stiffness, pain and restricted motion. The drug is injected under the skin once a month. It is made to be used alongside drugs that suppress the immune system.

Sister has the ulcerative colitis, and ankylosing spondylitis. I have HLAB27 but other stuff going on with muscles sore, rash, fever, swelling of them various places. Bone aches No Sjrogens, no lupus, no lyme.

Cancer has not returned. However he is diabetic and last year was diagnosed with ankylosing spondylitis. He was taking remicade by infusion but had to stop that due to his chronic anemia. The rheumatology doctor told him that the ankylosing spondylitis can cause ulcerative colitis and crohn's. He is now 74 has had 32 blood transfusions over about 16 months and has also been diagnosed with crohn's disease. They believe he is bleeding internally.

Ask around, Google Local "Rheumatolagsts" and "Ankylosing Spondylitis". The tests are painless and easy to get: X Ray of pelvis and blood test for AK gene, and Sedimentation Rate. I was originally diagnosed with Rheumatoid Arthritis fo 40 years. Treatments are quite different, though both are immuno insufficient, and probable inherited. My father always complained he that he couldn't reach his feet. Ask your doctor for copies of your blood tests.

Ankylosing spondylitis is most likely a multifactorial condition, which means that it involves a combination of genetic, lifestyle and environmental factors. Having one copy of the HLA-B27 variant (of the HLA-B gene) causes an increased risk to develop ankylosing spondylitis; however, most people with this variant do not develop any symptoms of ankylosing spondylitis even when inherited from an affected parent. We all have two copies of the HLA-B gene - we inherit one copy from each parent.

I was diagnosed with reactive arthritis with I was maybe eight years old but once I was 19yrs old it became clear that it was something more. I was finally correctly diagnosed with Ankylosing Spondylitis at the age of 20. I was in the middle of college and struggling to succeed in my course work because of the pain. But I haven't let pain stop my life yet.

Hi, about 2 years back when i had uveitis second time i got diagnosed with Ankylosing Spondylitis as i was having some backpain also (which i was thinking is due to my posture) and also hla-b27 is found positive. i had uveitis again 3rd time last year and after that i have deloped some floaters also in the eye.

s Disease, enthesitis, peripheral arthritis and osteo arthritis ( both left and right body), Benign Prostatic Hyperplasia and Prostatitis with Erectile Dysfunction, Haemorrhagic Pineal Gland Cyst, Hiatus Hernia and Diverticulums, SSS Sick Sinus Syndrome, peripheral oedema, On DDD pace maker, Inappropriate Sinus Tachycardia with plenty of unexplained and abnormal ECG's , Lung Fibrosis secondary to AS ( breathing problems) on oxygen, multiple PVC episodes, Dysautonomia, Hypovolaemia and late

I was told in February of this year that I have arthritis in my lumbar spine. This was a year after I started having severe lower back pain. I also have a herniated disk, early DDD and stenosis. I was sent to a neurosurgeon who said I was not a surgical candidate due to my age (26). My doctor then sent me to pain management because he had nothing else to offer me. I never had blood work done. Only an XRAY and MRI.

Most of the members here are people just like you, looking for support, share ideas and experiences and resources for suggestions for improvement or solutions to our issues. Some Doctors do participate here occasionally, contributing their expect opinion, with the understanding that this is just a medical opinion and NOT a diagnosis or a treatment prescription.

Does anyone have Ankylosing Spondylitis? I have suffered with the disease and related symptoms for over 30 years. My daughter who was 30 died of the comlications of this diesease three years ago.

Humira and ankylosing spondylitis

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