I'm flying next week and a little nervous about having to take my Kiniret with me. Anyone have advise for travel with a biologic that is in a syringe and has to stay cold?
I was taking methotrexate but was unable to continue do to severe nausea . I have been given Humeria but have been hesitant to start . Has anyone used this and had good results?
Diagnosed in January 2015 with RA.. When she came on it was very fast and and progressive, I am on Methotrexate, Plaquenil, and prednisone... That didn't help much at all.. So then she started me on humira... worked amazing... I was into my 3 rd shot and had an allergic reaction. So now She is taking me off of it.. ok, but why can't I go on another biologic?
Has anybody experience a Burning Skin sensation on Enbrel...My rear upper thigh is burning this past week...any ideas or suggestions..
Today I stumbled across a scientific article from the American College of Rheumatology (https://www.sciencedaily.com/releases/2014/11/1...) linking the use of IUDs and the risk to develop RA. I personally find this troubling due to the fact that I had my Mirena IUD inserted in Feb 2017, started feeling my first symptoms of joint pain 2 months later in April, and got my RA diagnosis in November of 2017. Just curious if any other women out there explored this as a potential factor.
Hi everyone, serious question here.
Why would my rheumatologist prescribe Plaquenil with a low ANA and no definitive diagnosis yet? Thanks for reading!
I just feel as if family/friends/significant others don't understand when you say you aren't feeling good. I don't want to even admit out loud that I am in pain because I feel like they think I'm trying to get out of something or making excuses. Does anyone else ever feel this way?