• 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: How long does it usually take for Diamox to work?

NEW STUDY! Parasym Plus™ for Multiple Sclerosis › Forums › PrettyIll.com Discussion › EDS/MS/Chiari › How long does it usually take for Diamox to work? › Reply To: How long does it usually take for Diamox to work?

September 26, 2016 at 11:21 am #6020
Dr. Diana
Keymaster

Hi Bea, The first thing is always to check the CO2 — it can change quickly. Our patients have a standing order and for a while, check electrolytes at least every 2 weeks (or if they feel like Diamox is not working as well as it used to). Only then, should you try to increase the dose to see if it is not as strong as you need. Please remember the evening dose is the most important, and needing 500mg at night is not unusual at all. Everything I know about making Diamox work (and keeping it working) is in the chapter on Diamox pearls in The Driscoll Theory. More advice is in some of the videos like this one: (cut and paste into your browser): http://prettyill.com/videos/watch/lets_talk_about_diamox_updated Good luck, my friend!

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