New era for ME/CFS research as top cytokine study attracts media headlines
The immune systems of patients who have recently developed ME/CFS look markedly different from those who have been ill for much longer, according to a major new study from Drs. Ian Lipkin and Mady Hornig at Columbia University. This shift in immune function hadn’t been seen before.
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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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    :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

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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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