• Skip to main content
  • Skip to secondary menu
  • Skip to primary sidebar
  • Skip to footer

PrettyIll

Header Right

Dr. Diana, both a doctor (therapeutic optometrist), and a recovered POTS and ME/CFS patient, offers help and hope for POTS, Dysautonomia, Ehlers-Danlos syndrome, Chronic Fatigue, Chronic Lyme, vascular abnormalities, Fibromyalgia, and Multiple Sclerosis. Dr. Diana is now working full time at POTS Care.

  • Home
  • The Driscoll Theory®
  • Videos
  • Meet Dr. Diana
  • Forum
  • Store

Reply To: MUSCLE TWITCHES, ANYONE?

NEW STUDY! Parasym Plus™ for Multiple Sclerosis › Forums › PrettyIll.com Discussion › EDS/MS/Chiari › MUSCLE TWITCHES, ANYONE? › Reply To: MUSCLE TWITCHES, ANYONE?

March 8, 2015 at 4:07 pm #5351
MJ
Participant

Hi Barbara.

Very interesting… I read the other posts that you mentioned. I believe I have small fiber neuropathy and I am in the middle of trying to get diagnosed. And that feeling of wondering if you’re going to wake up in the morning – been there too. I also have erythromelalgia but I do not have a solid diagnosis yet.

I also had a severe case of whiplash 26 years ago. I believe the whiplash was the trigger to the starting point of my decline – I was highly active and extremely athletic prior to this. Snowboarding, volleyball, golf, rollerblading etc. And now I can barely function. I’m sure everyone here can relate.

Do you think that what is happening to us – do you think anyone will figure it out in our lifetime? I often wonder if treatment will only be in time for the next generation…

MJ

Footer

PrettyIll.com

This website was created to inform, educate and brainstorm with fellow patients and doctors. The content should not be used as a substitute for professional medical advice, diagnosis or treatment. Readers are encouraged to confirm all information with other sources and their physicians. The creator of this site will not be liable for any direct, indirect, consequential, special, exemplary, or other damages arising from the use of this website.

Twitter: @prettyill

What others say

“Dr. Diana will always hold a very special place in my heart for her selfless devotion to helping everyone, not just the Ehlers-Danlos community. I hate to think what my life would be without her insight and guidance.”

-- Chris Gross

Listings by topic

  • Chronic Fatigue
  • Consult
  • Contact
  • Coping
  • Ehlers-Danlos
  • Fibromyalgia
  • Hydrocephalus
  • Mast Cell Disease
  • Multiple Sclerosis
  • Orthopedic Issues
  • Pain Control
  • POTS
  • Speaking Engagements
  • Store
  • Uncategorized
  • Vascular abnormalities

This work may not be reproduced, copied or used in anyway without the express permission of the author -- that's me © Dr. Diana Driscoll 2020