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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: re your 'head circumference' study and…

NEW STUDY! Parasym Plus™ for Multiple Sclerosis › Forums › PrettyIll.com Discussion › The Latest Research › re your 'head circumference' study and… › Reply To: re your 'head circumference' study and…

June 25, 2011 at 9:11 am #1260
momcat7
Participant

Bearcat..I will take a look for the study. Thanks for understanding why I feel the need to post those statements about being cautious about using meds. I always worry about someone being desperate and sick of Drs. and reading something like my post and making themselves worse. It’s the “middle school teacher’ in me.lol

I have lived the progesterone/estrogen conundrum. At this point I’ve had a hysterectomy and find I am better off with no hormonal support. It’s always a trade off. My androgens are high due to Polycystic Ovary Syndrome POS, but those symptoms are preferable to me than others. For younger women in the throws of PMS issues getting good support from an EDS knowlegible doc is crucial.

I too suspect that “my brain” is always a little waterlogged lol and so a little onslaught becomes a big cascade.

FYI I am meeting with a group of EDSers today in Mid Michigan.We are starting a group. I will direct people to this site.

I am having the worst time spelling and typing this week..and I can’t get spell check to work in my posts..so sorry!!!!

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