Is there anyone out there with both PsA & Fibromyalgia? I would love to hear from you to share experiences.
Has anyone experienced bad side effects from taking Methotrexate tablets? When I took them I suffered from really sore and big mouth ulcers so I stopped taking them after one week as the medical leaflet that came with the tablets stated to stop if mouth ulcers and sickness occurred. My rheumatologist suggested I tried taking them again. I questioned this because of the unpleasant side effects from taking them before but he insisted I did. I took them again and as I expected the same side effects occurred. On my return to rheumatology it was advised that I should take Methotrexate injections and was told that this would bi pass the oral stage so would have the more desired outcome. I have yet to try the injections as I have yet to have the education I have to have before I can start taking the injections ( the hospital has to show me in person how to do the injections myself )
Has anyone had a similar experience as I did with the Methotrexate tablets and then went on to take the injections? I would love to hear from you.