Connect with others who understand.

sign up log in
About MyFibroTeam

Connect with others who understand.

sign up log in
About MyFibroTeam
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.

MS

MS

I’m beginning to wonder if I have MS as well, or maybe instead of fibromyalgia. My doctor doesn’t take me seriously. I’ve been having a lot of internal tremors and external. The only way to find out is by getting an MRI. Has anyone else felt this?

posted 5 months ago
A MyFibroTeam Member said:

Look for a doctor that knows how to diagnose tremors. Agree with other peoples comments, don’t stop until you are satisfied with the answers your given.

I have a small problem with tremors that I've had long before I got Fibro. They only happen when I am under extreme stress, and that rarely happens.

But since you're concerned about your tremors and since there are different types of tremors, it is my understanding the earlier you treat your tremors the better.

Please make a journal concerning every specific detail you can make about your tremors and then take your notes with you to your doctor appointment. Being extremely specific will be helpful to a good doctor.

“ It is generally accepted that there are six main types of tremors.
* Resting tremor
* Action tremor
* Postural tremor
* Kinetic tremor
* Intention tremor
* Task-specific tremors”

https://essentialtremortreatment.com/six-types-...

edited, originally posted 5 months ago
A MyFibroTeam Member said:

Don’t let anybody blow you off! Keep going till you are satisfied. It’s your body and your health..🙏🏻❤️🌸🦋

posted 5 months ago
A MyFibroTeam Member said:

He won’t order an MRI, but I’m gonna try to get in with a neurologist and see what they think.

posted 5 months ago
A MyFibroTeam Member said:

I haven't felt that way but I would listen to my gut...mine has never steered me wrong. Find a better doctor if you can. Will this doctor order an MRI or do you have to go somewhere else?

posted 5 months ago
A MyFibroTeam Member said:

In 2011 when I had my first flare up which was MASSIVE ! and had to give up work, I believed I had ms, even to this day I think so, but I now have metastatic lung cancer so means I have regular brain and spine MRIs and no ms shows up.

posted 5 months ago
Already a Member? Log in