Connect with others who understand.

  • Learn from expert-reviewed resources
  • Real advice from people who’ve been there
  • People who understand what you’re going through
Sign Up Log In
Powered By
Real members of myRAteam have posted questions and answers that support our community guidelines, and should not be taken as medical advice. Looking for the latest medically reviewed content by doctors and experts? Visit our resource section.
A myRAteam Member asked a question 💭
Wichita Falls, TX

Are RA and fibromyalgia related
don't have markers in my blood work but how can u fake so much pain,
How long does it take for methotrexate start working, this is my 4th week and I'm not feeling any relief,

October 14, 2015 (edited)
 · 
Reactions
A myRAteam Member

Yes unfortunately it takes awhile for the meds to kick in. Autoimmune diseases are horrible. My blood markers look good a lot of the time however if you have a good doctors he/she will know that it can be a false positive /negative. When they look and feel the joints that is the true test. I have seronegative RA. My grandmother had RA. My mother had RA. My father had ALS. Hope you feel better soon.

October 15, 2015
A myRAteam Member

I've been told a minimum 6 weeks but that docs usually like to reassess meds 3 months after a med change.

October 15, 2015
A myRAteam Member

RA and fibro are both autoimmune , you can be seronegative and stil have RA, my rheumy told me it takes 3-6 months to see the full effect of methotrexate (6 months for full effect) such a bummer these meds take so long to work. Praying you feel better

October 14, 2015 (edited)
A myRAteam Member

Freeman, It can take up to 6 months for new meds to start working. If it's not working for you you should go back to your Dr. There are so so many medication for RA, they can change or add. It is just a matter of finding the right medication for you. Good Luck.
Bless you and yours

October 20, 2015
A myRAteam Member

I am RF negative (seronegative) as well. Was told it was fibro for years then Rheu says seronegative RA. He told me if anything the fibro was secondary. I find it hard to be told one thing for years then another thing and how to discern them. I have also been asking myself why do I need to discern them? I guess because I need to put things into their "box" to label them. This is very frustrating with not always an answer. I take MTX and I truly don't know if it's working- but he keeps me on it. You may need to add a drug. I was on sulfasalazine but then he stopped that and added plaquenil. Talk with your doctor because it seems like it's a lot of mixing to see what helps you. Good luck and best wishes.

October 19, 2015 (edited)

Related Questions

View All
A myRAteam Member asked a question 💭
Las Vegas, NV

A myRAteam Member asked a question 💭
Walnut Creek, CA

A myRAteam Member asked a question 💭
Houston, TX