Hi everyone my name is Robin I live in beautiful SW Florida 46 years old female who was diagnosed with RA PSA MS Fibromyalgia high blood pressure neuropathy and a list a mile long if other related symptoms. Feeling very frustrated having allot of side effects from all the meds I'm in. Recently I got switched back from injectable Methotrexate to oral I have now been developing mouth sites in the roof of my mouth swollen and very sore right glands and extreme exhaustion . I was wondering if anyone who takes Methotrexate has experienced these symptoms . Frustrated don't know if it's that drug doing it or another drug or if I'm just getting sick ugh!!! Any feedback would be greatly appreciated. Thank you.
Feeling frustrated: Hi everyone my name is Robin I live... - NRAS
Feeling frustrated
Welcome to the site Robin. How much folic acid do you take?
Thank you so much. I take a small dose everyday except the day I don't take methotrexate. I forgot the mg .
I believe mine is 5 mg. Yes I will be calling him first thing the morning. I also just got a flu and phuenmonia shot two weeks ago
How come you switched from injecting mtx to oral?
New Rheumatologist take I sections 3 times a week for my MS. Started getting allot of pits and muscle atrophy from so may injections per week even though I was rotating different areas
MS is awful. I had ms from 1990 to 1997 before the meds were invented. I was lucky that it "just went away" . What type do you have? How long have you had MS?
Was diagnosed in 2014 I now have secondary progressive . My father had it also
I'm glad there are meds available for MS now.
I was 23 when MS reared it's ugly head. I still fear it, as it can come back eventhough it's been almost 20 years since it went away.
I was diagnosed with RA in 2014. I was stuned, but kind of thankful because my kids were grown.
Yes I'm glad there are a lot more meds out there for MS. Tbwy definitely have come along way. Unfortunately my body seems to reject allot of them . This is the 5th one I am trying
It's 11 pm here, so it must be about 2 am where you live. I guessing you have insomnia? This is a UK site, so the majority of the good people of this group are still sleeping. You shall have a lot more responses in a couple of hours. We are so lucky that the Brits welcome us North Americans
Oh wow! Had no idea yes it's 2:17 in Florida. Yes I insomnia is a huge problem with me .
How is the weather there?
We're just getting up...7am in UK and I'm in France so 8.00am
Good morning Helix. I'm off to bed soon, though I am hearing water pouring down my chimney....going to have to wakeup my hubby to investagate this water.....
Oh no hope it's nothing to serious!
Front page of newspaper this morning is about bad storms in Ontario....
Oh no that's never good.
Everything is OK, thank God. Crazy freak storm here. Hubby says he needs to change the flashings tomorrow on the roof.
Yes, Ontario in the winter is crazy cold. British Columbia's lowermainland has mild weather, excluding today... lol.,. we get the snow every 5 years or so. BC is about 4000 miles from Ontario. I think you live closer to Ontario than me
😀😀
Wow! That is very interesting facts I did not know. Thanks for sharing that. And yes I think I am closet lol 😊
I got bad mouth ulcers from oral methotrexate, which completely stopped when I switched to injections. And it's such a small needle that's only sub-cutaneous seems remarkable that it's causimg muscle atrophy - can you ask your rheumy if there are other options. Mouth ulcers are a pain!
Well I also take 3 other injections per week for my MS so maybe the combination of all the injections caused it. Yes I will def be calling my Rhuemotoligist tomorrow to discuss. My mouth and glands are so painful right now can barely eat or swallow
Welcome to our friendly corner of the internet, Robin. Firstly, you are one brave lady for facing all the health problems that you do. Secondly, you have such a pretty eye colour. Thirdly, I'm very jealous of you living in the sunshine state while I live in England which is mostly grey and cloudy.
I get a very swollen roof of mouth and my dentist told me that it could be a sinus infection or allergies. She also suggested various medications. My doctor wasn't much use, so I would recommend that you see a dentist if you can. I don't know if you can get these in the US but I used to have steroid meltlets which you pressed against each ulcer and they were really good. Please do get checked out by a doctor for the swollen glands. If you're on lots of meds that suppress the immune system, you may have an infection.
Take care.
Good morning too you . Thank you so much for your kind words and compliments. I also am sorry that you are dealing with this too it really sucks. I am in steroids for my psoriatic arthritis but having issues with them now too and I woke up from maybe 2 hours of sleep in so much pain I can barely swallow.and my mouth is so sore. I left a message with my primary and Rhumetolofist this morning. I never thought about seeing a dentist for the ulcers in my mouth and those tablets hmmm might have to check them out. Thank you for that great piece of advice. Oh by the way I'm jealous of where you live lol I have always wanted to take a trip over there maybe someday I will😊 Have a blessed and pain free day 😊
Hi Robin and welcome, sorry that your not feeling the best right now but keep chin up as things will get better , I'm suffering quite a lot off fatigue right now and have had a heavy cold for 2 weeks which won't shift , I have RA,OA and Angina I'm on mtx injections and Benepali inj (Bisomar) plus other meds, I get ulcers from time to time and they are a pain, hope you feel better soon xxx