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PrettyIll

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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: My girlfriend have EDS Type 3

NEW STUDY! Parasym Plus™ for Multiple Sclerosis › Forums › PrettyIll.com Discussion › EDS/MS/Chiari › My girlfriend have EDS Type 3 › Reply To: My girlfriend have EDS Type 3

April 8, 2015 at 1:17 am #5419
Chloethomas
Participant

It’s a chronic illness, which means there’s no cure, but that doesn’t mean her quality of life can’t be improved — it certainly can!
Buy the Dr.Tinkle book on EDS Hypermobility for more information.
Pain is very individual – but TENS machines, heat packs, anti-inflammatory foods, rest & relaxation, meditation for chronic pain can all be used in conjunction with stronger medication.
Don’t bother talking to psychiatrists about Ehlers Danlos. Use them for mental / emotional support with anxiety, depression, chronic pain. And find a doctor who specialises in connective tissue diseases in your area – they can refer you to support groups, and other professionals to add to her “team”

Oh also also — BEST. BOYFRIEND. EVER.

Sending you my best

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