has anyone had any experience with cold laser treatment and fibromyalgia | MyFibroTeam

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Top 10 Search Results for "has anyone had any experience with cold laser treatment"

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Fibromyalgia /PIP/ Disability Classification UK
A MyFibroTeam Member asked a question 💭

Hi, Technically this is 2 questions but they are interlinked so I thought I'd ask them together x

I am already on P.I.P because of my Disc Degeneration, but now I've been diagnosed with FM as well, should I try to get my award updated or leave it till my review next year. (I don't want to end up losing what I already have)

Part 2 Has FM been classified yet in the UK as a long term disability? I know it has in America and Northern Ireland but not sure about here.

Thanks for your advice x

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A MyFibroTeam Member

ADP is for people living in Scotland, if you're already claiming PIP in Scotland then you'll be transferred over. PIP is about how your health conditions affect your ability to carry out various… read more

Homeschooling
A MyFibroTeam Member asked a question 💭

Does anyone here homeschool.. How does it go, do you use an online program or books.

Have you ever heard of "Life of Fred" or LOF.

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A MyFibroTeam Member

There could be multiple reasons that in school learning does not work for some and only communicates with some, which teachers having pets in their classroom. Also there is so much bullying from other… read more

Duloxetine
A MyFibroTeam Member asked a question 💭

I would like to come off Duloxetine what side effects have any members had and how long did it take

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A MyFibroTeam Member

I had no side effects

Feel Like I'm Losing My Mind
A MyFibroTeam Member asked a question 💭

I have trouble with words my brain will think one thing and my mouth will say another but I won't even realise until someone points it out and the other day I was helping my 4 year old learn to write but everything I wrote down the letters got jumbled up no matter how hard I tried to concentrate (I know how to spell the words) is this a fibro thing or am I genuinely starting to lose my mind now 😕

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A MyFibroTeam Member

Same thing here. I have both fibro fog and chemo fog. I don't know what might come out of my mouth.

Can Anyone Share Their Pain Clinic Experience In The UK?
A MyFibroTeam Member asked a question 💭

Hi All, just wondering if anyone has come across a Pain Clinic or Support group for Fibromyalgia in the UK or in particular Leeds? I am just fitting the piece of the puzzle now, I have been living with FMS for a very long time. I am getting so frustrated with the lack of support from medical professionals and people who claim to be a support group but I am still waiting for their call, having started inquiry 6 months ago. I have been now discharged from Rheumatology, and I don't think that was… read more

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A MyFibroTeam Member

Stretches help me alot.

A Question For The Christian Warriors
A MyFibroTeam Member asked a question 💭

For those of you who are Christian, how has your spouse or SO handled your DX or even your bad days. I thought everything was going better but after the "new Dr " check up (he made me an appointment with his Dr) the SO asked me if I was tired of Dealing with it all. Then told me I can get healed and prayed over. I let him know I've done that, so now I am not sure if He is questioning my faith, since I have not gotten better. How have you and yours handled all of this?

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A MyFibroTeam Member

I've heard so many people say that their spouse left them because of it. Karma will come his way. I believe in God and I think God should be the first priority. I pray, alot. Prednisone has been… read more

I Have A Migraine Here At Work. Pain Center Recommends ER. Can't Afford It. Any Suggestions As To What I Should Do To Reduce The Pain?
A MyFibroTeam Member asked a question 💭
A MyFibroTeam Member

While at work, put something dark on your eyes and lay down on break. Sometimes caffeine helps me. Quad Venti iced white mocha

Have You Noticed A Connection With Food And Flares?
A MyFibroTeam Member asked a question 💭

I’m sure a lot of you have tried dietary changes in attempts to alleviate your suffering. What connections have you been able to make between your food and fibro symptoms? Or perhaps certain supplements help or hurt? Please share.

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A MyFibroTeam Member

Yes, I react badly to gluten, dairy and soy aswell as get migraines from bananas and avocados. Ifind my anxiety spikes, pain increases and I become very thirsty.

Doe You Think You Had Fibromyalgia Since Childhood?
A MyFibroTeam Member asked a question 💭

I remember when I was growing up..I had all the symptoms..of Fibro..when I would get cold..I would hurt so bad..sometimes I would cry..( was called a drama queen)..also I would forget everything ( was called a space case )..sometimes I couldn't go to sleep all night and would wonder why people had to sleep?...also was called ( a bull in a china shop) ( because I would drop things or walk into things...my question is does anyone remember having all these symptoms growing up?

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A MyFibroTeam Member

@A MyFibroTeam Member that does seem to be the common theme in most of our answers.....interesting I will bring that up to my dr when I gin on the 10th.

Aromatherapy Oils
A MyFibroTeam Member asked a question 💭

What aromatherapy oils work for fibromyalgia or for general health? Suggestions please...

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A MyFibroTeam Member

Depends on the oil and how much, how it's used