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Methotrexate and the Coronavirus?
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Lesfez
Lesfez
Last activity on 13/10/2017 at 07:58
Joined in 2017
1 comment posted | 1 in the Psoriatic arthritis Forum
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Also concerned take it and a biological x not taking it isn’t an option as I flare within a few hours of missing it ... self isolation is the best defence .. hard when you have family around you xx stay safe
andreag
andreag
Last activity on 20/10/2020 at 13:11
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2 comments posted | 2 in the Psoriatic arthritis Forum
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I'm taking a biological therapy adalimumab does that mean I have to self isolate for 12 weeks as no one is telling me anything and my hospital is to busy
dadofalad78
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dadofalad78
Last activity on 07/08/2020 at 15:38
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10 comments posted | 8 in the Psoriatic arthritis Forum
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@psorinotsorry My son's rheumatologist advised him to continue taking his methotrexate as it's generally not immunosuppressing at the dose he's taking. @andreag I'm not a GP, but I believe biolgics, like steroids, are immunosuppressors. There's an abundance of information on the NHS coronavirus site, maybe try to sift through there to find some advice? I believe they've set up a online help line.
andreag
andreag
Last activity on 20/10/2020 at 13:11
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2 comments posted | 2 in the Psoriatic arthritis Forum
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Hi I don't take methatrexat I just take adalimumbab through injection it says plenty about other things but it's all very confusing thank you anyway stay safe and well xx
Traceyb69
Traceyb69
Last activity on 08/05/2024 at 20:43
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1 comment posted | 1 in the Psoriatic arthritis Forum
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Hi,
I am on Methotrexate and have been advised by our IBD team at the local hospital to continue taking it. The danger is if you stop taking it, have a flare-up and catch the coronavirus, then that is more dangerous because of course your underlying condition has flared.
Courtney_J
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Courtney_J
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Last activity on 13/10/2022 at 16:47
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1,280 comments posted | 14 in the Psoriatic arthritis Forum
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Thank you everyone for sharing your thoughts and advice.
If you haven't seen it already in your notifications, we're currently running a survey on the impact of the coronavirus on patients with chronic conditions. We're hoping to better understand how your daily life and the management of your disease has been affected. If you haven't yet had the change to take it, I'll link it here:
Carenity survey: Impact of COVID-19 on patients living with a chronic disease
Take care,
Courtney
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Courtney_J, Community Manager, Carenity UK
Starke
Starke
Last activity on 07/08/2020 at 15:26
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6 comments posted | 6 in the Psoriatic arthritis Forum
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I'm on 10 milligrams of methotrexate, I haven't stopped it at all. I continue to take it because at one point I had a bad blood test for liver enzymes, so I stopped it for a month and after that the pain got worse...it takes about 6 to 8 weeks for it to get better. My rheumatologist monitors me very well, she's not easy to get on the phone since she sees so many people. But she rings me back and listens and answers my questions.
We're definitely more vulnerable to infections. You have to be very careful. Especially right now, washing your hands thoroughly, using hand sanitiser gel if you can't wash your hands, disinfecting the shopping, all that. Avoid all contact with others where necessary. My rheumatologist told me not to go to work because I'm a supermarket manager and it wouldn't be good to be in contact with everyone. I'm lucky and got a letter to let me stay home.
Everybody take care of yourselves!
Happychick46
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Happychick46
Last activity on 13/04/2021 at 22:46
Joined in 2020
5 comments posted | 2 in the Psoriatic arthritis Forum
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Morning.
I'm on methotrexate. And I been talking mine all the time. I been advised to stay in, I just follow all government guildlines. So I'm not too concerned about carry on. And I been pretty good. I know I'm high risk, had a letter to confirm this. So far all good.
Happychick46
cwissy
cwissy
Last activity on 18/05/2020 at 17:17
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2 comments posted | 2 in the Psoriatic arthritis Forum
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Hi Everyone, I am taking sulfasalazine as I have two types of arthritis. Do you have any advice re self isolating. I cant find any information
Trailie
Trailie
Last activity on 05/04/2020 at 18:33
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1 comment posted | 1 in the Psoriatic arthritis Forum
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Hi all, if you have not received a letter saying about shielding for 12 weeks you can get more information on the Government website.
Take care and stay safe x
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reikiboo64
@Courtney_J
Hi
Well where do I start!
I get frustrated by the constant exhaustion in my muscles. The slightest action feels like I have just done a work out to that part of my body whether it be an arm or a my legs for example.
I am aware that my disease isn't managed at all yet even though I have been diagnosed 18 months or so. It just feels like Russian Roulette with my medication as to whether I will be allowed to continue it from one blood test to the next as my liver rebells.
Everyday a new part of my body starts to creak and feel stiff and painful. To be honest it's scaring me just how quickly things are progressing. It is really getting me down. I can't walk far, self care is difficult . I'm determined to be independent so I'll struggle to succeed in the task.
I want to have the energy to get through my day as I work full time running a women's refuge which is mentally very demanding but fortunately not too physically. I'm so tired at the end of each day. It's an uncomfortable exhaustion. I also suffer from Narcolepsy diagnosed at a similar time to the arthritis, and this also gives me fatigue- I have a double whammy of fatigue.!
I am shielding at the moment so I have had a chance to rest. The first week off work I slept solidly and now I feel more rested. I confess I am anxious about becoming so exhausted again but I am determined this illness won't stop me from doing what I love.
Overall I feel distressed with it all and just want it to go away, My healing has gone to pot. I have put weight on as I can't exercise, I dread going upstairs and at times I just don't know how to deal with it.
Sorry to sound so down hearted, I just don't feel I can bring any positivity to this discussion.
x..
See the best comment
Living with psoriatic arthritis
What is your biggest daily challenge whilst living with psoriatic arthritis?
reikiboo64
@Courtney_J
Hi
Well where do I start!
I get frustrated by the constant exhaustion in my muscles. The slightest action feels like I have just done a work out to that part of my body whether it be an arm or a my legs for example.
I am aware that my disease isn't managed at all yet even though I have been diagnosed 18 months or so. It just feels like Russian Roulette with my medication as to whether I will be allowed to continue it from one blood test to the next as my liver rebells.
Everyday a new part of my body starts to creak and feel stiff and painful. To be honest it's scaring me just how quickly things are progressing. It is really getting me down. I can't walk far, self care is difficult . I'm determined to be independent so I'll struggle to succeed in the task.
I want to have the energy to get through my day as I work full time running a women's refuge which is mentally very demanding but fortunately not too physically. I'm so tired at the end of each day. It's an uncomfortable exhaustion. I also suffer from Narcolepsy diagnosed at a similar time to the arthritis, and this also gives me fatigue- I have a double whammy of fatigue.!
I am shielding at the moment so I have had a chance to rest. The first week off work I slept solidly and now I feel more rested. I confess I am anxious about becoming so exhausted again but I am determined this illness won't stop me from doing what I love.
Overall I feel distressed with it all and just want it to go away, My healing has gone to pot. I have put weight on as I can't exercise, I dread going upstairs and at times I just don't know how to deal with it.
Sorry to sound so down hearted, I just don't feel I can bring any positivity to this discussion.
x..
See the best comment
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psorinotsorry
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psorinotsorry
Last activity on 02/07/2020 at 14:46
Joined in 2019
6 comments posted | 4 in the Psoriatic arthritis Forum
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Good morning everyone,
For those like me who take Methotrexate what do you think about the risk of coronavirus? Methotrexate weakens our defenses and also brings a certain risk to the lungs. Shouldn't my treatment be interrupted until this all passes or at least until the risks become better known?