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Rheumatoid Arthritis

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Real members of myRAteam have posted questions and answers that support our community guidelines, and should not be taken as medical advice. Looking for the latest medically reviewed content by doctors and experts? Visit our resource section.
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Does Anyone Else Feel Like A Whimp When They Have To Admit That They Are Just Not Having A Good RA Day?

Does Anyone Else Feel Like A Whimp When They Have To Admit That They Are Just Not Having A Good RA Day?

I just feel as if family/friends/significant others don't understand when you say you aren't feeling good. I don't want to even admit out loud that I am in pain because I feel like they think I'm trying to get out of something or making excuses. Does anyone else ever feel this way?

A myRAteam Member said:

Ditto Niama! Currently icing my hands on the way to work and at my desk, incognito, concealing the ice pack in my quilted lunch bag, while its… read more

posted 2 months ago

Anxiety And Insomnia

Anxiety And Insomnia

I have had insomnia for a few months and recently had shortness of breath with little exertion. I had a bad episode of aniexty last week and am now being treated for that along with my RA. Has anyone else suffered from these?

A myRAteam Member said:

I noticed if I take calcium zinc and magnesium combo I sleep better. Not sure why. I noticed it also helps with migraines

posted about 2 months ago

Is There Any Medication To Help With Fatigue?

Is There Any Medication To Help With Fatigue?

I need help with this constant fatigue. I can't get enough sleep no matter how many hours I rest. I sleep at work and have fallen asleep driving several times. Is there anything that would help? I exercise and drink water and all that jazz.

A myRAteam Member said:

i make proteins drinks ..with berries...spinich..
celery...other greens...pomogranite juice....apple juice..water...etc...and try and drink a full glass… read more

posted 3 months ago

How Do You Describe A Flare To Someone Who Doesn't Have RA?

How Do You Describe A Flare To Someone Who Doesn't Have RA?

My flares aren't always exactly the same but yesterday I flared badly. I can describe it to my daughter, sorry guys most women will get this, as the overwhelming body aches and exhaustion on PMS. My entire body feels swollen and it throbs and joints ache like a fever. For my hubby and son I can only describe it as throbbing and aching in my entire body. and exhausted like I've run a marathon and haven't slept for days. And even with all that, it doesn't… read more

A myRAteam Member said:

It is always interesting to hear other people's description of RA pain. Untreated, I like to say that someone has jabed an ice pick into all the joints… read more

posted 21 days ago

Does Anyone Find Methotrexate To Work Really Well?

Does Anyone Find Methotrexate To Work Really Well?

I keep hearing people talk about how intolerable @methotrexate is. I am curious to hear from people who find it to be helping. I started it 3 weeks ago and I can't believe how amazing I feel. Its like someone oiled my joints and told my muscles to behave! I wonder if it's something specific to my condition. I'm sero negative poly inflammatory arthritis. Essentially that just means I have Ankylosing spondylitis symptoms and RA. Virtually every joint is involved… read more

A myRAteam Member said:

I've been on Methotrexate since 1992, combined with Enbrel, I do just fine. I do injections of both.

posted 4 months ago

Outside Shoulder Pain And Trying To Sleep When You Sleep On Your Side.

Outside Shoulder Pain And Trying To Sleep When You Sleep On Your Side.

Hi Family,
I have added a new pain area and it's driving me nuts. For the last week the outside of the bone on the top of my shoulders are painful. I don't sleep well anyway and this is not helping. I sleep on my side and I can't sleep on my back or stomach. Once I lay down the pressure on the bone in my arms starts pounding. I got about 2 hours of sleep last night and that was only in the recliner, but when I tried to move, my arm I way… read more

A myRAteam Member said:

The problem with cortisone shots is that it’s a hit and miss as to the best place to put the cortisone in the arm. I had them in both my arms and it… read more

posted about 1 year ago

Does Anyone Have Wheezing Either As A RX Side Effect Or Along With RA Symptoms.

Does Anyone Have Wheezing Either As A RX Side Effect Or Along With RA Symptoms.

I had asthma as a child and have had problems only when sick with bronchitis/pneumonia. But since my RA diagnosis (or starting Methotrexate) I wheeze frequently. I find I am extremely sensitive to allergens and will wheeze with very little stimuli. I go to the allergy/asthma specialist next week, but I feel like this is not Asthma. My instinct is that it related to the RA or a medication side effect.

Thanks in advance for your… read more

A myRAteam Member said:

I took two shots of methotrexate and got instant pneumonia both times. I have been on biologics, Enbrel and now Humira , without methotrexate for 5… read more

posted over 1 year ago

Just Curious Do You Suffer From Insomnia More Since Being Diagnosed With RA?

Just Curious Do You Suffer From Insomnia More Since Being Diagnosed With RA?

A myRAteam Member said:

I get up several (3 or 4) times per night. Although I sleep with a Salivix gel in my mouth, it still goes dry. That wakes me up. I need to keep changing… read more

posted 8 months ago

1at Winter With RA. Eeeek! Any Tips?

1at Winter With RA. Eeeek! Any Tips?

Hi RA fam! So this will be my 1st fall & winter having RA. I live in Chicago and our winters are BRUTAL. It's only end of summer & already we have fall whether (which is killing me by the way). In the summer if the AC was too high I would stiffen up. I am so scared, absolutely PETRIFIED thinking of how it's going to feel in the winter. Anything I should know that will help me prepare? Any tips or things I should or should not do? Anything you have bought to ease the… read more

A myRAteam Member said:

Layer, layer, layer, Double socks in boots. Lets hope its not a bad as last year...

posted about 1 year ago

Plaquenil

Plaquenil

I've been taking Plaquenil along with Humira and since the COVID19 outbreak the plaquenil prescription I am taking is from a different manufacture. Now I am itching, get hot more and get rashes on and off and my stomach as been upset on and off. I am wondering if anyone else has had this problem? I may have to call my RA doctor to see if anyone else has had this issue. Thank for listening. Hugs.

A myRAteam Member said:

When I started plaquenil I was severely nauseated, constipated, barely able to eat for a year. Then I guess my body adapted and I am rarely nauseous and… read more

posted 3 months ago
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