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CSUN Researchers: HOPE for TTT, ANS, POTS, ME,dysautonomia

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Uploaded by on Feb 10, 2010

This is my first visit to the CSUN laboratory where two Ph.D.s, Dr Paula Thompson and Dr."Vickie' Jaque are redefining testing capabilities for dysautonomia. This research offers great hope for all of us! TTT = Tilt Table Test; ANS = Autonomic Nervous System; POTS = Postural Orthostatic Tachycardic Syndrome; ME = mialgic encephalopathy; ANS = 2 Categories: Parasympathetic + Sympathetic Nervous Systems. ttt

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Uploader Comments (DysautonomiaMD)

  • Just touchiing bases to wish you all the hopes and inspiration that the great year ahead, 2011, awaits! LoLv to all those who have helped in this cause...

  • Visiting the lab again next week....

    and will work out a system so that others may be researched here at CSUN, also.

  • OMG! this is so exciting!!! if you guys need any more test subjects please contact me!! the TTT is torture.....

  • @stillpressinon : California State University, Northridge is in the burbs of Los Angeles....where are you in this life? Are you able to travel? LoLv, and

    THAT's the Spirit!!!!!!!! Highest Personal Regards, Dr Margaret

  • I am sooo excited to see this happening...I was diagnosed with MVP/Dysautonomia Syndrome in 1991 in Birmingham Al and had a horrible experience in 2004...since then I have really been working on doing the right things to prevent a "big" episode...I am 49 and back in college to become a nurse and want to help others who have dysautonomia...am relieved to see it being recognized...

  • @sherryh2009 : I love your plans, and how God has shown you this 'circle' of life you are to take. Am sure that you will help us along the way, as the timing is right. Best wiishes in all your endeavors and you keep on with your goals....God will see you through, and with His Blessing, it will happen. Highest Personal Regards, Dr Margaret

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  • This is awesome!

  • wow! this is cool

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  • Thank you so much for sending me the literature manuscript of this research; I have forwarded it to Dr. Jaque at CSUN and we are all excited about future prospects that will put not only dysautonomia on the 'map', but will also put symptom relief, earlier detection, better remedies, and one day, a CURE!

    LoLv and Appreciation for your unhesitating willingness to contribute to this cause.

    Margaret

  • I actually had a migraine during this vid, and it escalated over the next days such that I needed an ER visit for all the pain and vomiting.....

    ...but it was worth it, and God is able to work even in the worst of circumstances.

    Please visit my blog for a SURPRISE!

    I'm applying to CSUN Graduate School, to work in this lab. Application is submitted, and I got my first letter of recommendation from a previous teacher (who still remembers me)....we will post it there so you all can see HOPE. LoLv

  • ...and ground-breaking research for dysautonomia and ME, also perhaps for CFS and fibromyalgia.

    ....I have a surprise in the works....please keep praying that God opens all the right Doors ahead of us!

    ...and no matter what, I will keep you all informed on YT, each step of the way....if you see I am silent for a few days, expect a new vid, OK? I will never leave YT....you are my hope and my cause. LOLV, Margaret

  • As you will see, this is a great venture and God is leading the way.....what are the chances that I ever would have met these researchers? It was through a friend. Coincidence or God?

    It is an answer to our prayers...and more excitement awaits!

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