1. Patients launch a $1.27 million crowdfunding campaign for ME/CFS gut microbiome study.
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The Chronic Fatigue Initiative and Interview with Mady Hornig
In a follow-up article to the recent IACFS/ME conference presentation in San Francisco, and after speaking at length with Dr. Mady Hornig, 'searcher' delves deeper into the impressive work being completed by the Chronic Fatigue Initiative, and focuses in on those cytokine results ...
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More improvement!

Discussion in 'Problems Standing: Orthostatic Intolerance; POTS' started by Sallysblooms, Feb 20, 2012.

  1. Sallysblooms

    Sallysblooms P.O.T.S. now SO MUCH BETTER!

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    Southern USA
    :thumbsup: :) Still feeling better!!!!!!!!!!!!!!!!:):thumbsup:
  2. richvank

    richvank Senior Member

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    How can this be, Sally? You will soon be Wonder Woman!!! :thumbsup:

    Keep it up!

    Best regards,

    Rich
  3. Sallysblooms

    Sallysblooms P.O.T.S. now SO MUCH BETTER!

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    Southern USA
    :D Thank you Rich! Healing the nerves themselves has been wonderful, my POTS is so much better. We just got home from another trip (we are building a home in another city) and not long ago, this would have been SO hard and I would be so ill. I usually stay with my parents for things like this and hubby does it all. I can do much more now. My CFS is not much of a problem at all, just my POTS to deal with. We are so thankful for my supplements.
  4. taniaaust1

    taniaaust1 Senior Member

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    Sth Australia
    great to hear Sally :)

    I think Im doing better POTS wise too Sally, I still thou need to improve a lot more.. POTS meds, its like a crime doctors didnt try to treat the POTS side of the ME years ago. Im thinking about going out and spending 15-20mins in the garden today :)
  5. Sallysblooms

    Sallysblooms P.O.T.S. now SO MUCH BETTER!

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    Southern USA
    Wonderful Tania! Walking and standing is a wonderful thing.:balloons:

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