I’m new: Hello everyone, my name is Bryan and i have... - NRAS

NRAS

36,577 members45,185 posts

I’m new

bcole5581 profile image
18 Replies

Hello everyone, my name is Bryan and i have the RA!! I was diagnosed in June of last year.. currently taking Metotrexare once a week ( does anyone else feel like garbage while taking it?). Still sore in the mornings.. better by lunchtime..

Written by
bcole5581 profile image
bcole5581
To view profiles and participate in discussions please or .
18 Replies
rab1874 profile image
rab1874

Welcome Brian, sometimes it can take up to 12 weeks to work properly, I take mine before I go to bed then I’m not too bad the next day and drink loads off water as that helps with the sicky feeling but I’m still tired sometimes the next day

bcole5581 profile image
bcole5581 in reply to rab1874

Thank you!

PinkLamb profile image
PinkLamb

Hi Brian, and welcome, I have had RA for about 15 years now, I used to take the tablet form of methotrexate, and I used to feel lousy, it got to the point, I really didn't want to take it because of the sickly horrible effect it had on me, so I informed my consultant, and I was able to change for the injection, which is much better for me,

Maybe you could speak with your health team, how it's making you feel

Good luck

X

bcole5581 profile image
bcole5581 in reply to PinkLamb

Thank you!

Thingybob profile image
Thingybob

I have exactly the same symptoms. I have been to the OT today and he suggested compression gloves at night for the stiffness plus continuing with daily exercises with theraputty. The exercises deff help. I also saw the rheumy re feeling rubbish after the methotrexate. I am on injections which helps plus daily folic but she also suggested i creasing the other drug -sulpha- ?

heyitsmee profile image
heyitsmee in reply to Thingybob

I wear compression gloves during the day to keep my hands warm when typing and when they are feeling a bit swollen. Definitely helps!

bcole5581 profile image
bcole5581

Thanks!! I’ve been trying to get the gym at least 3 times a week for some light training.. it hasn’t been going to well.. lol.

I lm also taking folic acid daily and i pop a leucovorin 12 hrs after the dose of metho..

Mmrr profile image
Mmrr

MTX injections help reduce the side effects. I took plenty water, around a pint before and then again after injecting, and lots more during the day. I found eating carbs helped with nausea too. If you can plan for a quieter day the day after injecting, and accept that you may not be so good that day, it helps the stress levels.

The tiredness for me, did improve over time, but even now I feel better in the afternoon than the morning. I think it is the way it is for some folks with RD. Good luck.

bcole5581 profile image
bcole5581

Thanks for the feedback!

sylvi profile image
sylvi

I haven't had any side effects with MTX so am unable to comment. Welcome from me.xxx

heyitsmee profile image
heyitsmee

Welcome Bryan!

Sarah_89 profile image
Sarah_89

Hi Bryan, welcome!

I think Methotrexate is the drug most people start on as it is one of best for slowing down the disease while not having the side effects of biological drugs. When I was first diagnosed I found methotrexate to be great, it pretty much put me into remission once I'd been taking it for a few months.

Unfortunately after about 4-5 years I had to switch to a different drug due to side effects, but while I was on it the methotrexate worked great!

I hope that your symptoms soon start improve!

bcole5581 profile image
bcole5581 in reply to Sarah_89

The side effects are what I'm worried about...

Sarah_89 profile image
Sarah_89 in reply to bcole5581

I think that everyone responds differently and you may not get any of the side effects. With the methotrexate the only side effect I had was nausea, but this can be fixed by taking it as an injection so it bypasses the stomach altogether :)

If you do get side effects though it's best to speak to your doctor right away. I persevered and ended up making such a strong association between the medication and the nausea that even when I injected I found the nausea to be intolerable. Ridiculous I know but it's difficult to break such a strong association.

Anyway it seems a lot of people get very good results with methotrexate so it's definitely worth persevering with! :)

Clare-NRAS profile image
Clare-NRASPartnerNRAS

Hello Bryan

Take look at the information video on the NRAS website that you may find helpful. Switching to injectable rather than tablet form of MTX does seem to help alot of people deal with the nausea as of course it is bypassing the gut.

nras.org.uk/methotrexate

bcole5581 profile image
bcole5581 in reply to Clare-NRAS

Ill take a look.

RADOONE profile image
RADOONE

It works it really does I went through hell for the first 4 months but now I have my mobility back and realativly pain free still very fatigued but I can handle that sickness had now stopped it dies take time to work but I am glad I stuck with it 😊

bcole5581 profile image
bcole5581 in reply to RADOONE

thanks!

You may also like...

Hello - I’m new here!

Hi I’m Jules - I have RA and atrial fibrillation (had cardiac ablation but AF returned infrequently)

Just joined - I’m new

everything and some I feel depressed. I glad that I have found a group of ‘like minded’ people...

I’m new to this forum

effects and have managed with NSAIDs until last year. Was admitted to hospital last June and was...

I’m new here

Morning everyone, I was recently diagnosed with Seropositive RA, i was given a short course of...

I’m New Here

hydroxychloroquine might take up to 7 weeks to take effect and I was wondering has anyone else had...