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Looking for CFS/ME Docs in Central Texas (Austin or San Antonio)

Discussion in 'ME/CFS Doctors' started by chilove, Nov 30, 2013.

  1. chilove

    chilove Senior Member

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    Hi all,

    Does anyone know of any good doctors in Central Texas?

    Thanks!

    Audrey
  2. minkeygirl

    minkeygirl Senior Member

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    Left Coast
    I just remembered I heard about a doc in Houston. If I can't remember I need to contact a friend. I'll get back to you. (I don't know if he's CFS but he does interesting stuff).

    Another thing you can do, which is how I found my current doc is Google. I used all sorts of options, CFS in (my city) naturopath, integrative, functional medicine.

    Then I found her website and saw that she did methylation so I emailed her. She totally gets it.

    Mink

    Here's the doc I mentioned above.

    http://www.comp-health.com/allergy.html
    Last edited: Nov 30, 2013
  3. JohnnyD

    JohnnyD Senior Member

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    Dr. Patricia Salvato, in Houston is a long time HIV and CFS/ME M.D.
  4. perchance dreamer

    perchance dreamer Senior Member

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    In Austin, Dr. Kendal Stewart at the NeuroSensory Center. He's helped me tremendously with CFS and fibro.
  5. chilove

    chilove Senior Member

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    Thanks so much guys! I will check them out! Perchance Dreamer I would love to meet other people in the area for support if you are interested.
  6. minkeygirl

    minkeygirl Senior Member

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  7. Iamawake88

    Iamawake88

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    Klein, TX
    How do I get in to see Dr. Patricia Salvato!! I can't even seem to get Maria the new patient coordinator to call me back! If she's as good as I hear, even if her staff is not responsive to our needs, I don't care I can't take this back and forth feeling of I'm fine I don't need any hlep with this to OMG, I've just been run over by a truck. Next week my wife gets knee surgery. If I don't hear back from a doctor that knows something about ME/CFS by the following week, I am going to Dr. Salvato's practice and camp out there in the waiting room until they see me.
  8. Iamawake88

    Iamawake88

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    Klein, TX
    Recieved a call from Dr. Salvato's office this week. Wait time for first appointment: 6 weeks. I'm happy with that. Actually waited longer than that between a referal and the refusal to be seen by the neuromuscular dept at Baylor. At least I am now more organized with my health history. Thinking of starting a symptom journal with an app called Track & Share. Haven't been too good at keeping up with such stuff. Is there a thread here centered around the process by which a PWCFS can keep on-going track of symptoms and relate with correlating activity/diet/treatments? Has there been mentioned any recommended methods or tools for such? Later this weekend I may try to find where to repost this question to get more responses.
  9. Andrew

    Andrew Senior Member

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    Los Angeles, USA
  10. Iamawake88

    Iamawake88

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    Just an update here. The appointment I spoke of was supposed to be two weeks ago. I had to cancel it to go away to a funeral for a family member in upstate NY. Sitting in those cramped seats for the hours it takes to fly up there and back was torture. The doctors office returned my call last week to reschedule. Now I'm in a nine week holding pattern!! They would not consider that I had already waited 7 weeks from the first scheduling and my reason for the postponing.
  11. chilove

    chilove Senior Member

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    Bummer lamawake, I'm on a 8 month waiting list to see Dr. Stewart in Austin. Please let us know how it goes when you do get to see her
  12. Iamawake88

    Iamawake88

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    Klein, TX
    Will do; you too. Wow! Supply and demand I guess. And no wonder these specialists are no longer taking insurance (as I saw noted in another of your posts). Probably able to see more patients after cutting out the clutter and hastle.

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