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Methotrexate and Humira

Posted , 4 users are following.

regina50099
regina50099

A month ago I posted I was starting Methotrexate. Pain and swelling was unbearable. My RH factor was very high so I was put on Humira. Just had my second injection yesterday.  I can finally say my pain is tolerable! So thankful. Swelling in hands have not gone down though. I also have scleroderma so that is most likely the reason for that. I hopeful that my improvement will continue. I’m thankful that this treatment worked for me.  I know for others it’s not the right combination. 

Good luck to all. This forum has really helped me. So glad I found you all 

1 like, 4 replies

4 Replies

  • blair97497
    blair97497 regina50099

    Posted

    Thanks for keeping us in the loop Regina. That sounds like a really fast improvement and I hope your positive response continues and things keep getting better for you. It took me many months of methotrexate and Hydroxychloroquine to gradually get results, so I am impressed. 
  • gaz1234
    gaz1234 regina50099

    Posted

    Snap

    I'm on the same as you and have been for years. It works for me regarding all my levels and blood test results. Still get a lot of pain but p/killers help. Going to rheumy again in August they'l probably put my mtx intake up. Currently on 15 mgs weekly as well as humira injection which i give myself once fortnightly. I still have swollen joints, have done for yrs, just gotta crack on eh. Anyways take care and i wish you well.

    Regards Gaz

    • regina50099
      regina50099 gaz1234

      Posted

      Well I thought I was doing good. Dr took me off Methotrexate and Humira. Put me on Cellcept. 500mg twice a day and 5mg prednisone.  The swelling and stiffness in my hands is due to the scleroderma. Never heard of this med. anyone else?  So frustrating 
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