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Real members of MyFibroTeam 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.

Top 10 Search Results for "Pamelor"

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My Own Team

My Own Team

Is there a shortcut to get to my own team?

A MyFibroTeam Member

Just add them 2 ur team that's how I've done it at least

Does Anybody Knows Or Taken LDN Lower Dose Naltrexone? How Is It Does It Work??

Does Anybody Knows Or Taken LDN Lower Dose Naltrexone? How Is It Does It Work??

A MyFibroTeam Member

www.lowdosenaltrexone.org has an impressive amount of material if you are interested in looking deeper into the dosage, studies, and providers. They also have a printable info sheet to give to your… read more

Could Someone Explain The Spoon Theory To Me Please?

Could Someone Explain The Spoon Theory To Me Please?

A MyFibroTeam Member

I learned another tip that we could use to explain to people is use pennies as a way to explain each step of the day.

"Pain"

"Pain"

I was diagnosed with Fibro in Sept and I guess I'm still trying to make sure that's really what this is!!

When my doc talks about "pain" I'm not sure if it's the same pain I'm feeling. I think of pain as in a broken bone, child birth, etc. My pain is waking up with achiness all over, stiff/throbbing hands, feet, knees... Feels like the flu. Then during the day my neck gets very stiff and it is painful to touch my chin to my chest.

Is this what others experience as well with Fibro or does it… read more

A MyFibroTeam Member

Some days I ache all over feels like I've just ran a marathon

Pamelor

Pamelor

Is Pamelor as strong as elivil? Does it add to weight gain?

A MyFibroTeam Member

I have taken these for 6 years
Work great for me
I do know they don’t suit everyone some people find it hard to have a clear head in the mornings .

Cymbalta

Cymbalta

I'd say it's the fibromyalgia as I suffer with extreme hot sweats waking up freezing cold as I am that wet head to foot, my hair will be drenched wet through and this has been going on for few years before being diagnosed with anything and before taking any medication ,
I have only been taking duloxotine For several weeks and I was the same before these x

A MyFibroTeam Member

Cymbalta was horrible for me- hot sweatie- I forgot what else it has been so long. coming off of it was horrid

Lyrica & Cymbalta Long Term Damage

Lyrica & Cymbalta Long Term Damage

I’m taking Lyrica & Cymbalta to treat my fibromyalgia. I’ve heard that these drugs are very difficult to get off because of the intense withdrawal symptoms and that they can cause brain damage, Alzheimer’s, etc

My dr did not explain this to me before prescribing and now I’m a little concerned that i may be limiting my pain whilst damaging my brain.

Please advise if these risks are real and please share your experiences.

A MyFibroTeam Member

I was prescribed pregabalin by my doctor, but I haven't taken them yet...got them in June
I just recently have started losing weight! I really don't want to gain it back. I was afraid weight gain may… read more

Pamelor

Pamelor

I was just prescribed this my Dr, and was wondering if it has helped anyone with their fibromyalgia systems?

A MyFibroTeam Member

Thank you!

I Was Diagnosed Two Weeks Ago, Trying To Learn More About This Disease. Are My Symptoms Common?

I Was Diagnosed Two Weeks Ago, Trying To Learn More About This Disease. Are My Symptoms Common?

Hi! This is my second time posting, I am new to being diagnosed and this website! This post is long and I would be so appreciative if you took the time to read it (or skip to the bottom to read my questions.)

I was diagnosed two weeks ago and I am having a lot of “do I really have fibromyalgia?” thoughts because my symptoms come and go. I know that is the nature of fibromyalgia, but since I was recently diagnosed and I am only 20, I just have so many questions.

When I was diagnosed, I think… read more

A MyFibroTeam Member

Mine started like that but has gotten worse over time and if I do to much I usually pay dearly with flare ups for the next few days. It is a crazy diagnosis to figure out as it can change daily on… read more

Traveling And Flares

Traveling And Flares

I seem to flare the day of/day after traveling. Day of traveling with mostly with car travel, day after with flying. I love to travel but seems I always pay the price for it. Does anyone else experience this?

A MyFibroTeam Member

i am in pain 24/7, but i do feel it more when traveling... even the shortest drive can bring the pain 10 fold...