Comparing Humira vs Remicade

For Rheumatoid Arthritis I'm a 69 yr old woman with seronegative RA - hence it took a long time for a diagnosis. Many rheumatologists do not understand that you can be seronegative & have RA. Sad. After several years of anti inflammatory drugs & cortisone I was prescribed Humira. Took about 2 months & wow! Not so much pain relief but having so much less fatigue. As I live in Australia my experience with obtaining the drug is different to the US. My rheumatologist makes application through the federal government after other drugs have failed & they heavily subsidise. Thus far no obvious side effects. However, reading other's comments I wonder about the flushes at night - never had them as a menopausal symptom...... Wish you all the best in managing RA

For Rheumatoid Arthritis I think the shots are very painful, they sting, no matter how you inject it. Let it sit out for 20 minutes first, etc. Also- I liked the injectable pen better when I was using Enbrel. This needle is a real needle, no injectable pen. I feel it's harder to use on yourself that way.

For Crohn's Disease, Maintenance I'M 32 AND I'VE HAD CROHNS NOW FOR 14 YEARS. REMICADE WAS A GOD SEND BUT ONLY FOR A LIMITED TIME. I STARTED OFF LIKE EVERYONE ELSE WITH I.V EVERY 8 WEEKS. THEN AFTER A COUPLE OF YEARS IT WAS WEARING OFF FASTER SO THEN EVERY 6 WEEKS. THEN EVERY 4 WEEKS THEN IT WAS BACK ON THE STEROIDS ALONG WITH THE 4 WEEK TREATMENT. WELL AFTER 6-7 YEARS ON REMICADE IT WASN'T WORKING ANYMORE. I DO RECOMMEND IT BECAUSE I WOULD GIVE ANYTHING RIGHT NOW TO GET THOSE 6 YEARS BACK BECAUSE EVEN THOUGH I WAS BECAME IMMUNE TO IT I FELT 20 TIMES BETTER THEN COMPARED TO NOW. SINCE THE REMICADE NOTHING HAS WORKED FOR ME SINCE.

For Crohn's Disease, Maintenance I am 24 and I was diagnosed with Crohn's disease a year and a half ago now. I've been receiving this infusion for the past 12 months. The relief was brilliant bar constantly catching coughs, colds and flu's but it was worth it as I could lead a normal life again. My infusions were every 8 weeks and could take anything up to 4 hours but my remission time between infusions began to steadily decrease. I have now had my 9th infusion and receive them every 5 weeks. My body has grown an immunity to the drug and my doctor is changing me onto Humira as a last resort to avoid surgery. Hope this helps somebody.