Jump to content
  • Welcome to Celiac.com!

    You have found your celiac tribe! Join us and ask questions in our forum, share your story, and connect with others.




  • Celiac.com Sponsor (A1):



    Celiac.com Sponsor (A1-M):


  • Get Celiac.com Updates:
    Support Our Content
    eNewsletter
    Donate

Seeking Primary Care Dr In San Antonio (celiac Knowledgeable)


Lady Buchanan

Recommended Posts

Lady Buchanan Newbie

Howdy.

I'm a bit new around here. This is my first posting so if I muff it, please be patient. :rolleyes:

I live in the San Francisco Bay Area and am living quite successfully with gluten sensitivity. I have a wonderful Doc who started life as a Clinical Nutritionist and went on to add D.C. to the list of initials after his name. He's been the BEST in helping figure out why I was sick.

Now that I'm educated, I can see the advanced symptoms on my Mother who lives in San Antonio, Tx. I've spent the last few weeks trying to find a Primary Care Physician there that she can start with. While I have found some well-recommended names, they are not Primary Care docs---and they don't take insurance, rather a problem.

Does anyone out there know of a good Primary Care Doc in San Antonio?

Many Many Many thanks! :D


Celiac.com Sponsor (A8):
Celiac.com Sponsor (A8):



Celiac.com Sponsor (A8-M):



penguin Community Regular

I'd try poking around www.alamoceliac.org , it's the website for the GIG in Austin, San Antonio, and Corpus Christie. I don't know if there's dr. info on there or not, but you could always call the San Antonio contact and see if they know anyone.

floridanative Community Regular

Go to www.chickenparadise.com. The woman who owns/runs this B&B in San Antonio runs the Celiac support group there. Her name is Ann and you can e-mail her from her site. She's an angel and will be glad to help you. Good luck to your Mother. I had a heck of time gettng my own Mother dx'd in FL but I finally got it done.

Lady Buchanan Newbie

Gosh, you guys are great. Thank you! Interestingly, I've already chased down the avenue of talking with Ann, the support group leader there. She was an angel! And she did indeed have some names, but they were not primary care docs, unfortunately. I called the people she recommended and tried to network with them to see if they knew any primary care docs, but I came up blank. So I was hoping a general query out here would turn up someone.

And the alamoceliac.org site didn't have an area for the names of docs. I think the gluten thing is still so new to the western medicine world here in America that the docs who do know about it aren't aware that they should advertise themselves.

Best, Cindy!

Archived

This topic is now archived and is closed to further replies.


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,038
    • Most Online (within 30 mins)
      7,748

    Briannas01
    Newest Member
    Briannas01
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Scott Adams
      This is an older article, but may be helpful.  
    • gfmom06
      I have had orthodontic work done. The 3M invisalign material was no problem. BUT my retainers are another matter. They seemed okay for a few months. Now, however, they cause a burning sensation on my tongue, gums and insides of my lips. The burning sensation is now spreading to my throat. I notice it when I breathe. This is annoying and interferes with my enjoyment of eating. I am visiting with my provider tomorrow. We'll see where this goes from here.
    • Beverage
      Exactly which blood tests were done? There are a few different ones and some docs don't do them all. Also, your results and reference ranges for each?
    • Jmartes71
      Thankyou so much for your words.Its a hard battle when a supposed well known hospital whose celiac " specialist " has down played me because my colon looks fine and put it in my medical and so pcp doesn't take seriously. In their eyes we all carry that gene.Im having alot of bad days trying to be positive because of it.
    • Scott Adams
      Your experience is both shocking and critically important for the community to hear, underscoring the terrifying reality that cross-contamination can extend into the most unexpected and invasive medical devices. It is absolutely devastating that you had to endure six months of sickness and ultimately sustain permanent vision loss because a doctor dismissed your legitimate, life-altering condition. Your relentless research and advocacy, from discovering the gluten in MMA acrylic to finding a compassionate prosthodontist, is a testament to your strength in a system that often fails celiac patients. While the scientific and medical consensus is that gluten cannot be absorbed through the skin or eyes (as the molecules are too large to pass through these barriers), your story highlights a terrifying gray area: what about a substance *permanently implanted inside the body*, where it could potentially shed microparticles or cause a localized immune reaction? Your powerful warning about acrylic lenses and the drastic difference with the silicone alternative is invaluable information. Thank you for sharing your harrowing journey and the specific, severe neurological symptoms you endure; it is a stark reminder that celiac is a systemic disease, and your advocacy is undoubtedly saving others from similar trauma.
×
×
  • Create New...

Important Information

NOTICE: This site places This site places cookies on your device (Cookie settings). on your device. Continued use is acceptance of our Terms of Use, and Privacy Policy.