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Comments (2,271)

I found Fosamax difficult to take, and was switched to Risendronate … no problems with that...

https://connect.mayoclinic.org/comment/1037472/

On 10 mg of Prednisone and Methotrexate

Discussion: PMR, Osteoporosis and Fosamax?

Support Group: Polymyalgia Rheumatica (PMR)

Posted: Mar 21, 2024

I have never heard or read about Entyvio being used to treat collagenous colitis. More common...

https://connect.mayoclinic.org/comment/655548/

include steroids such as Budesonide, methotrexate

Discussion: Microscopic Colitis: How to you keep it under control?

Support Group: Digestive Health

Posted: Nov 19, 2021

Actually it doesn’t have nasty side effects. An increased openness to infections. But nothing else. Methotrexate...

https://connect.mayoclinic.org/comment/993553/

Methotrexate has more, at least for

Discussion: PMR Taper and pain

Support Group: Polymyalgia Rheumatica (PMR)

Posted: Jan 8, 2024

When my hair started falling out while taking Methotrexate my doctor doubled my dose of folic...

https://connect.mayoclinic.org/comment/918006/

hair started falling out while taking Methotrexate

Discussion: Hair Loss wig ordered

Support Group: Polymyalgia Rheumatica (PMR)

Posted: Aug 24, 2023

Judy here- I've been taking monthly actemra infusions for 6 months. Much improved symptoms and able...

https://connect.mayoclinic.org/comment/776217/

taper to 4 of prednisone and 4 tabs of methotrexate

Discussion: Anyone tried Actemra (Tocilizumab) to treat PMR? FDA approved for GCA

Support Group: Polymyalgia Rheumatica (PMR)

Posted: Nov 22, 2022

I have been taking methotrexate for about 3 months as I try to wean off methylprednisolone...

https://connect.mayoclinic.org/comment/1217963/

I have been taking methotrexate for

Discussion: Using methotrexate with PMR

Support Group: Polymyalgia Rheumatica (PMR)

Posted: Jan 21 8:11am

It’s not so much that folate is recommended because someone has a diagnosis of RA, it’s...

https://connect.mayoclinic.org/comment/1365677/

it’s a requirement for patients on Methotrexate

Discussion: Rheumatoid arthritis.

Support Group: Autoimmune Diseases

Posted: Aug 7 11:15am

I didn't feel the dizziness with methotrexate but after a year and a half of being...

https://connect.mayoclinic.org/comment/1334249/

didn't feel the dizziness with methotrexate

Discussion: Mental fog and slight dizziness on Actemra

Support Group: Polymyalgia Rheumatica (PMR)

Posted: Jun 24 12:41pm

Thank you for your comments. I appreciate any input I can get. Maybe I’m just not...

https://connect.mayoclinic.org/comment/1109576/

Maybe I’m just not giving methotrexate

Discussion: MOVING AND EXERCISE WITH PMR

Support Group: Polymyalgia Rheumatica (PMR)

Posted: Jul 21, 2024

Thanks. For me, at this time, the non-movenent pain is more of a stiffness and discomfort....

https://connect.mayoclinic.org/comment/953704/

the continual fatigue while on the methotrexate

Discussion: PMR: Hydroxychloroquine or low dose naltrexone

Support Group: Polymyalgia Rheumatica (PMR)

Posted: Oct 25, 2023

@sabrina95123 I had ground glass opacities last year. It turned out that the medicine I was...

https://connect.mayoclinic.org/comment/870171/

out that the medicine I was taking, methotrexate

Discussion: Groundglass opacities within the lungs what does it mean?

Support Group: Lung Health

Posted: Jun 1, 2023

@becsbuddy - yes, I do have OLP too. It had cleared up completely when I was...

https://connect.mayoclinic.org/comment/680273/

completely when I was on the full dose of Methotrexate ... As soon as I got off Methotrexate my ... haven’t been quite as effective as the Methotrexate

Discussion: Tongue-biting with oral lichen planus

Support Group: Autoimmune Diseases

Posted: Feb 12, 2022

Thanks. There is a question about the cause of my lung situation. One doctor thinks it...

https://connect.mayoclinic.org/comment/687668/

One doctor thinks it could be Methotrexate

Discussion: My Journey with Polyarteritis Nodosa (PAN)

Support Group: Autoimmune Diseases

Posted: Mar 8, 2022

I'm afraid I'm not getting much relief yet but my Dr said it would probably take...

https://connect.mayoclinic.org/comment/652705/

At least methotrexate isn't very

Discussion: Rheumatoid Arthritis (RA) - Introduce yourself and meet others

Support Group: Autoimmune Diseases

Posted: Nov 9, 2021

Yes my rheumatologist wanted to switch me to a monthly infusion or injectable but the methotrexate...

https://connect.mayoclinic.org/comment/1310187/

monthly infusion or injectable but the methotrexate

Discussion: PMR and the taper

Support Group: Polymyalgia Rheumatica (PMR)

Posted: May 22 9:39am

@mia447 I do not (have fibro) and I do manage my RA with minimal meds...10 mgs...

https://connect.mayoclinic.org/comment/145360/

my RA with minimal meds...10 mgs of methotrexate

Discussion: Rheumatoid Arthritis (RA) - Introduce yourself and meet others

Support Group: Autoimmune Diseases

Posted: Mar 17, 2019

You likely wont be able to take Prednisone for the long term. Believe me, many of...

https://connect.mayoclinic.org/comment/1275545/

pain and inflammation returns, maybe Methotrexate ... acid to mitigate some side effects of Methotrexate ... After methotrexate for about a year, ... That worked a couple of years but the methotrexate

Discussion: Ra meds

Support Group: Autoimmune Diseases

Posted: Apr 6 11:05am

I have been on Rinvoq, Simponi Aria, Humira, Remicade and Avsola. It seems that some meds...

https://connect.mayoclinic.org/comment/1207674/

I have also taken methotrexate and hydroxychloroquine

Discussion: Biologics side affects

Support Group: Autoimmune Diseases

Posted: Jan 9 12:43pm

My PCP has just prescribed Cymbalta to try to deal with the depression and pain of...

https://connect.mayoclinic.org/comment/894082/

I have been on methotrexate for 3 months