methotrexate for crohns
Posted , 4 users are following.
I've had crohns for 15 years and recent MRI has shown stricture and fistula. I'm now on methotrexate injections and wondered if anyone else has been on this treatment? Nausea is tough going and dread having the injection as it makes me feel so ill. Anyone else have experience of methotrexate?
1 like, 11 replies
Jokuar tracey36633
Posted
I'm sorry you're getting those side effects.
Have you tried Aza or 6MP before you got put on Methotrexate?
I am on 6MP having had bad reaction to Aza and have been told Methotrexate is my next option if 6MP does no good.
Is Methotrexate only administered by injection?
Wish you luck
Regards
Pete W
tracey36633 Jokuar
Posted
kim46236 Jokuar
Posted
Dulcie1925 tracey36633
Posted
I was on methotrexate and unfortunately it made me feel so ill I had to stop taking the injections.
I am on azathioprine at present, but I am starting vedolizumab this week.
This is by infusion. I found the methotrexate didn't help my crohns either.
Speak to your medic who prescribed this, it can be harsh on the stomach.
hope things get better.
tracey36633 Dulcie1925
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kim46236 tracey36633
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He wanted to put me on tablet form which i take 6 x 2.5 grms a week, i saw the doctor and she told me to take folic acid every day apart from my metotraxate day, which has helped with the sickness, i still get tiired on the days after, and usually suffer from aching joints, and sore mouth with a tongue that feels although it has glass in it, but apart from that im ok, try too persevere with it, as i think it does get easier , hope you feel better soon
Bong1968 tracey36633
Posted
Has your doctor prescribed this for you?
I only had 10 injections before stopping but felt queasy with the treatment.
I did develop a liking of ginger biscuits during this time. They helped a lot to quell the nausea!
Hope things improve for you soon!
tracey36633 Bong1968
Posted
Bong1968 tracey36633
Posted
I stopped the Methotrexate because I hadn't seen any improvement.
I work in an environment where people don't think twice about coming into work with infections, colds, 'flu etc. and I was constantly on edge that I would pick something up that my body wouldn't be able to shake off.
To be honest it had got to the stage with my Crohns that the only option was surgery - which I had in April.
The diseased part of my terminal ileum had calcified and I had a fistula from that to my sigmoid colon.
I now have a temporary (I hope!) loop Ileostomy which will hopefully be reversed in the new year.
It's nasty to feel nauseous all the time and I hope tha
t you can find something to ease the symptoms soon.
Stayk838 tracey36633
Posted
tracey36633 Stayk838
Posted