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Dr. Diana, both a doctor (therapeutic optometrist), and a recovered POTS and ME/CFS patient, offers help and hope for POTS, Dysautonomia, Ehlers-Danlos syndrome, Chronic Fatigue, Chronic Lyme, vascular abnormalities, Fibromyalgia, and Multiple Sclerosis. Dr. Diana is now working full time at POTS Care.

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Reply To: Mm, could it be dysautonomia

NEW STUDY! Parasym Plus™ for Multiple Sclerosis › Forums › PrettyIll.com Discussion › POTS › Mm, could it be dysautonomia › Reply To: Mm, could it be dysautonomia

February 16, 2013 at 6:14 pm #3478
Barbara
Participant

Hi Barbara
I shall have a look at Dr Myhill’s work. It’s intriguing. You would think her work would have far reaching implications for all chronic pain syndromes. Can I ask what treatment you were given? Are we talking replacement enzymes, that sort of thing or more functional treatments? Is beyond me….

Dr Myhill’s work certainly does have far reaching implications, judge for yourself.
Here’s a link to a report of the medical research study/paper:-

http://anh-europe.org/news/chronic-fatigue-syndrome-can-no-longer-be-labelled-psychosomatic

Dr Myhill has thousands of followers, her work is very detailed and she does her best to educate people as to what’s going wrong and how best they can remedy it.

I’m currently on CoEnzyme Q10 to help muscles, Vit C every mealtime to help digest food better, I did take oral Complex B vitamins but have realised I need something more comprehensive (I was already on Vit D & Calcium – along with the ZZ & Diamox combination). Just these have still brought about changes. I’ve recently bought Multi-vitamin + mineral transdermal spray and Magnesium transdermal spray from her website, so lets see if these change anything else. There are still other things in her recommended regime that I have to take on but I’m doing it bit by bit.
Regards
Barbara
(UK)

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