how do i search for a provider and fibromyalgia | MyFibroTeam

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Top 10 Search Results for "how do i search for a provider"

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Do People With Fibromyalgia Get Pain In Middle Of Chest With Radiating Pain In Left And Right Arm
A MyFibroTeam Member asked a question 💭
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A MyFibroTeam Member

Yes, for me I had first costochondritis and thought it was a heart attack, then my doctor mentioned that since it’s constant (every single day for 4 years now), it’s Tsieze Syndrome
Fibro triggers… read more

Chest And Armpit Pain
A MyFibroTeam Member asked a question 💭

does anyone else get chest pain or feel like the centre of their chest is bruised when they press on it?? also have like achey muscles around my armpits and had sharp pain in my armpits a few weeks ago!! i've been to the doctors so many times with so many different symptoms over the past 8 months that they just brush me off and tell me there's nothing wrong. had blood tests, paid for a private brain MRI as they wouldn't give me one, all normal. they won't diagnose me but i have all the symptoms… read more

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A MyFibroTeam Member

Part of my fibro pain are the lumps called myofascial pain. I have them everywhere. Doctors don’t talk about them. I did finally find a doctor that told me what it is. It very painful when touched on… read more

I Need Advice On The Severe Leg Pain That I Experiencing. Injections In The Back For Leg Pain? Tramadol & Hydrocodone Together?
A MyFibroTeam Member asked a question 💭

I recently consulted with a different rheumatologist who sent me to a neurologist and a pain specialist. The neurologist wants to do a sleep study. My problem though is the pain in my legs. I also have pain at times in my shoulders and neck, and I have arthritis in my right foot at the base of my big toe which is hurting a lot lately. In the past I have taken hydrocodone, but my former rheumatologist switched me to Tramadol. I was taking 300 mg per day. The pain specialist allowed me to… read more

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A MyFibroTeam Member

I asked for a higher dose of tramadol until my surgery & after if they don’t send me home with any.
I was diagnosed with fibro in 2004 & neck issues got worse about 2007.

Tips For Navigating This Site
A MyFibroTeam Member asked a question 💭

In conversations on this site I've seen some great navigation tips. Could we add the things we've discovered here so everyone can learn from each other?

For example search for the Q&A titled "Questions& Answer Links Tip" (which is a did-you-know about clicking the Q&A tab on the menu vs. the Q&A tab under your profile.)

My ex: when you have a question to ask, it seems you'll get many more answers by posting it on the Q&A board than by just posting it on your profile page.

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A MyFibroTeam Member

Ohhh, Janet, that is a great tip! LOL 😆😆😂😂

Name A Provider?
A MyFibroTeam Member asked a question 💭

Lately, a lot of us Fibromites have been thru so much negative, so I thought if we named just 1 provider, collectively we could reach 100,000 names. If we put a name here and under our providers list, we could watch it grow?? Anyone not in it we proceed with caution.

A MyFibroTeam Member

oh, you're very welcome!!!! Have a great day!

Has Anyone Tried Accupuncture? Anyone In My Area Know Of A Good Provider? How Do I Choose A Provider?
A MyFibroTeam Member asked a question 💭

I am wondering if anyone has tried acupuncture for just general pain or only for specific area pain. Any recommendations for a provider in my area? How do you select a provider? Once you start do you have to continue to return for more treatments? Thanks for all your help!

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A MyFibroTeam Member

I have had acupuncture with the lowest electrical pulses in my hand because it became " stuck" . Was very difficult to move. The treatment was amazing . It lasted for 8 months. I have to go back. I… read more

Attention Ladies 😊
A MyFibroTeam Member asked a question 💭
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A MyFibroTeam Member

To cute !

What Natural Supplements/remedies Do Any Of You Take In Support Of/or Instead Of Prescribrd Medicines?
A MyFibroTeam Member asked a question 💭

Can I please call on your wealth of experience and knowledge when I ask you what natural supplements do you take? I already take magnesium, vit B & evening primrose but I am thinking more about exploring and trying others. I don't know if this is the best approach to take, but I reckon if anyone can/will give me honesty in their answers, it's all of you. Right now I am open to all suggestions about supplements (I shall be exploring therapies another time, fairy steps). Thank you x

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A MyFibroTeam Member

Taking Fibroprin Biotene, Magnesium & Tumeric, Vitamin D 5000 iu, Centrum Silver Vitamin

Is There A Way To Search For Discussions About A Certain Topic?
A MyFibroTeam Member asked a question 💭

I’ve been a member here for a long time but mostly just read articles. I feel like questions I might have have already been discussed. How do I find those discussions?

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A MyFibroTeam Member

Im on my phone and i see across there's 2 rows the second row shows Resources Q&A Meet Others above there's a search button 😉

Do Anyone Know How Do You Go About Getting A Therapy Dog.
A MyFibroTeam Member asked a question 💭
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A MyFibroTeam Member

@A MyFibroTeam Member there's websites that teach you how to do your own service training. It is very important to learn how to identify the qualities of a dog that is likely to be able to handle it… read more