• 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

Susanhurts

  • Profile
  • Topics Started
  • Replies Created
  • Engagements
  • Favorites

Forum Replies Created

Viewing 3 posts - 1 through 3 (of 3 total)
  • Author
    Posts
  • September 11, 2015 at 10:42 pm in reply to: Sodium Bicarbonate tablets …with other meds…Newbie. #5656
    Susanhurts
    Participant

    Dear Dr. Diana,
    Firstly let me say that I am so thrilled to be coming to your PotsCare facility next week. I know it will help me tremendously. My doctor is pleased, also. I am doing better on the Diamox. I have not been tested for anything to do with kidney stones, though. I will bring this up when I am at PotsCare. I must say that NOTHING has made since for the last thirty, yes thirty years, of my suffering until I tried the H1 H2 blockers and the Diamox. Unbelievable. That is why I am traveling such a long way because I know that there is more help to be had.
    Thank you,
    Susan

    August 30, 2015 at 3:45 pm in reply to: My nose runs when I drink the "eight glasses" of water after concussion that has thrown my C1 C2 out…HELP! #5648
    Susanhurts
    Participant

    Thank you both. Yes, Dr. Diana…I am now on Diamox. Big help. It seems that I may need more than the 125, 125, and 250. Does it stop working as well? I am using the drops I purchased from your site and staying alkaline. I wish I could be more so. Do you know people who take more Diamox? My doctor has basically given me free rein. He watched all of your videoes. The H1 and H2 helped much but gave me real gut issues. My stools became clay colored. I was on Pepcid 20 twice a day, zyrtec twice a day, ketotifen 1 pill 4 times a day…Help.

    August 14, 2015 at 11:11 pm in reply to: I feel so lost….EDS, POTS, MCAD, and lyme #5601
    Susanhurts
    Participant

    Dear Dr. Diana,
    I have the Driscoll theory. I cannot find the free brochure on POTs.com. I did find the website, though. Very exciting. I am taking the antihistamines and they are helping. I bet you are quite correct that it is not the BOTTOM LINE. I do know that they help. I had a concussion and it brought out all kinds of symptoms. Firstly clear fluid ran from my nose. Now, when I drink quite a bit of water my nose runs. Go figure that out…My lyme would be late stage but my blood work is inconclusive. I have, as you know, POTS, EDS, and MACD…genetic variety. Heck, I even had a surgery done to enlarge my urethra at the age of 2 because I was having so many cystitis infections. Now I know that my C1 C2 are out of place. The night of the concussion, when I lay down seven hours later, I got the most FEROCIOUS HEADACHE! This sounds like too much pressure to me. I cannot get alkaline! My BUN levels have always been slightly elevated or high. My lyme doctor has given me the Diamox. I took it…it tried to work. I would love to see any information from POTS.com. I went to the website and it just talked about who you will treat. People like me! I am not in great shape to travel…I am in CA with an integrative lyme specialist. We have not started treating the lyme. I am so sensitive.
    I am a “Valley Girl” from South Texas. It would be great to be treated closer to home. Ranching family. My
    grandfather was Lloyd Bentsen and my mother is Betty Bentsen Winn.
    Thank you,
    Susan

  • Author
    Posts
Viewing 3 posts - 1 through 3 (of 3 total)

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