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Top 10 Search Results for "what to engrave on a fibromyalgia medical id"

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As Any One Tried Versatis Medicated Plasters That As Lidocaine In For Pain .
A MyFibroTeam Member asked a question 💭

A friend as versatis medicated plasters for pain and said they helped with her fibro pain she puts them on morning or night and leaves them on for 12 hours then take off for 12 hours. Wondered if any body tried them and got some relief.

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A MyFibroTeam Member

Yes I have tried and use the Versatis medicated pads on both my hips which are very sore. They do work but should only be used 12hours on and 12 hours off
I hope that information helps, the other… read more

Should I Get A Medical Id Bracelet For Fibromyalgia?
A MyFibroTeam Member asked a question 💭

Do u have to have an illness worse than fibromyalgia to get a medical id bracelet? Or, can it be for something like this illness plus others.

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A MyFibroTeam Member

I have a medical alert bracelet saying about me having fibromyalgia and allergic to surgical tapes.

How Do I Get This Id?
A MyFibroTeam Member asked a question 💭
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What To Engrave on a Fibromyalgia Medical ID: 5 Essentials and Other Ideas Read Article...
A MyFibroTeam Member

Does anyone know where I can get a free medical bracelet for fibromyalgia I'm not working applied for my disability I need help getting one

Do You Use A Medical Journal Or Planner?
A MyFibroTeam Member asked a question 💭

I need to get more organized with my symptoms, medications, and anything medical related to my fibromyalgia. Do you use a medical journal or planner? Not just a blank journal that you write in, but one that is pre-printed with what you should write down. I found one on Amazon by CleverFox but it's a bit expensive right now and I wanted to see if there are any other alternatives.

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A MyFibroTeam Member

Keep at it 🙂

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.

Were You Given Tests Prior To Diagnosis?
A MyFibroTeam Member asked a question 💭

I was told 2 days ago that I have Fibro by a rhumatologist. My issue is that they looked a questionaire I filled in and went off of that. I walked into the room and was told "ypu fit the classic profile of someome with fibromyalgia, we're not going to do any bloods/scans/xrays because they would just come back normal." My issue with this is, what if its one of the many other conditions that have similar symptoms? I've had no tests done by my GP prior to this either. Has anyone else had this… read more

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A MyFibroTeam Member

That's the way it was for me. The rheumatologist literally looked at all the tests that 4 or 5 specialists had all done, announced that I had fibromyalgia and then informed me that he doesn't treat… read more

Navigating This Site.
A MyFibroTeam Member asked a question 💭

Does anyone else get a little confused when getting around this site? I have problems with it. Maybe because I have to use my phone. It's it easier on a PC?

I ask this question because I can't help but notice people do not send to stay active. My self included. I feel more people would join and stay active if it had the simplicity of a Facebook group. It's so much easier to share things and be involved.

Is this a possibility? Or is there something that can be done to make this page more… read more

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A MyFibroTeam Member

I go through stages. I haven't been on this site for a long time but before that was addicted to it. I think my pain levels dictate to me whether I'm going to use it or not. If I'm in a lot of pain I… read more

Would Someone Please Explain This, Is Fibro Autoimmune Or Not?
A MyFibroTeam Member asked a question 💭

I found a question and answer on Google that just doesn't make sense to me. First I read that it may be different in different people,, meaning (?} that it could be autoimmune. Then it says Fibro is not autoimmune, which I thought it is. So, here's Google's answer.

Is fibromyalgia autoimmune or neurological?

They may be different in different people. Current research suggests involvement of the nervous system, particularly the central nervous system (brain and spinal cord). Fibromyalgia is… read more

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A MyFibroTeam Member

From what I understand it is not autoimmune. It is neurological and muscular. But, I am no expert.

Do You Wear A Medical Id Bracelet?
A MyFibroTeam Member asked a question 💭

I came across a website that said that those with fibromyalgia should wear a medical id bracelet in case you are injured so doctors know your pain could be from fibromyalgia and so that they don't run needless tests. While this does make sense I can also see how this could be a problem. If I was in a position where I was injured, like in a car accident, I would want all tests run. Just because a certain part of my body has frequent fibromyalgia pain that doesn't mean there couldn't be some other… read more

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A MyFibroTeam Member

Websites say al sorts of things. This maybe just ignorantly tries to promote wider use of medical bracelets. Wrong reasoning. In case of medical emergencies the worst thing you can do to default to… read more

Has Anyone Tried Dronabinol Or Medical Marijuana For Pain Relief?
A MyFibroTeam Member asked a question 💭

After years I asked my Doctor what she thought about medical Marijuana? Surprisingly she thought that it was a good idea. It’s the only thing that gives me a few hours of escape from my pain, depression and all of my Fibromyalgia companions that don’t allow me to live any resemblance to a life with quality.

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A MyFibroTeam Member

I did that for about three years bit then I started to feel paranoid and had to stop.