Peter Rowe - Orthostatic Intolerance in EDS/HSD

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  • เผยแพร่เมื่อ 23 ธ.ค. 2024

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  • @SpectrumOfChange
    @SpectrumOfChange ปีที่แล้ว

    Dr Rowe is the best

  • @CLove-mo7cc
    @CLove-mo7cc ปีที่แล้ว

    This has explained my condition completely

  • @marina_m11
    @marina_m11 6 ปีที่แล้ว +3

    Wonderful webinar, I learned so much! Thank you to Dr. Rowe & The Ehlers-Danlos Society for this important information. I will be on the lookout for the print out as well

  • @drnicolemeastmand.o.2974
    @drnicolemeastmand.o.2974 5 ปีที่แล้ว +1

    Thank you for this. I have Ehlers Danlos and Hypermobility, dysautonomia (positive tilt table test), etc., and a trigger event of getting hit by a semi-truck at 65 mph on 12/15/2010. All of the pieces are finally fitting together after seeking answers since childhood.

  • @lAcedUpLiss
    @lAcedUpLiss 5 ปีที่แล้ว +1

    Thank you so much for sharing this informative webinar. As someone diagnosed with EDS, POTS and MCAS I have found this information extremely helpful and look forward to sharing it with my GP and trying to implement the non-pharmacological solutions.

  • @dustyfeller
    @dustyfeller 3 ปีที่แล้ว

    13:40 No HR or BP changes but do have reduced cerebral blood flow. Therefore should respond to therapy. Dutch study.

  • @Advocate.bettie
    @Advocate.bettie 5 ปีที่แล้ว +1

    Has dr. Francis Visser publish the low orthostatic tolerance research yet?

  • @perttiylenius
    @perttiylenius 6 ปีที่แล้ว +1

    Good webinar. Thank you very much. Many things confirmed the belief that we are on the right line with medication.

    • @kengray1291
      @kengray1291 3 ปีที่แล้ว

      How do we get a print out of this presentation, if one is available. Thank you Dr. Rowe & EDS Society!

  • @divacassandra1
    @divacassandra1 8 หลายเดือนก่อน

    slide at 36:56

  • @HeidiCullinan_Author
    @HeidiCullinan_Author 5 ปีที่แล้ว +1

    This just radically changed my daughter's life and my own. We both have hEDS and have orthostatic intolerance which presents in different ways. Thank you so much!

  • @meri_soturi
    @meri_soturi 3 ปีที่แล้ว

    Great explanations and succinct information

  • @ArayaLight
    @ArayaLight 5 ปีที่แล้ว +1

    This was amazing! I hope to get my pcp/ np to listen. They are clueless on how to help me.

  • @wandaryan4250
    @wandaryan4250 2 ปีที่แล้ว

    Need a support group, we live in Surprise, Arizona

  • @slavkoputnik227
    @slavkoputnik227 5 ปีที่แล้ว

    This is extremely useful. Thank you.

  • @LaniBanani
    @LaniBanani 5 ปีที่แล้ว

    Okay trying dairy free and body shapers first. Thankyou!

  • @strengthinstripes5849
    @strengthinstripes5849 5 ปีที่แล้ว +1

    What is it called when the HR and the BP spike severely when standing?

  • @misscazb85
    @misscazb85 5 ปีที่แล้ว

    I been directed to this video from the Ehlers Danlos Syndrome Page on Facebook, really informative, would to love know how medication such as amatriplyn would affect with suspected POTs I have also got hEDS and Fibromyalgia

  • @ambertyler5844
    @ambertyler5844 6 ปีที่แล้ว +1

    How do I get a print out?

  • @lindajohnson668
    @lindajohnson668 6 ปีที่แล้ว +1

    As a certified holistic health coach who loves learning about medical conditions and investigating natural wellness solutions for them, how would I be invited to attend these webinars live?

    • @TheEhlersDanlosSociety
      @TheEhlersDanlosSociety  6 ปีที่แล้ว +1

      They're webinars - all you have to do is sign up beforehand. They're announced in our newsletter, sign up through ehlersdanlossociety.dm.networkforgood.com/forms/connect-newsletter-sign-up, at our web site www.ehlers-danlos.com/webinar-schedule/, on our Facebook page, facebook.com/ehlers.danlos/, on Instagram @ehlers.danlos, and on twitter.com/TheEDSociety - the next is scheduled on January 30, more information soon.