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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: Geographic tongue and EDS

NEW STUDY! Parasym Plus™ for Multiple Sclerosis › Forums › PrettyIll.com Discussion › The Latest Research › Geographic tongue and EDS › Reply To: Geographic tongue and EDS

August 19, 2013 at 4:14 pm #4139
Jrl_3327
Participant

Hi I have had life long symptoms that were all over looked until 2011. I myself don’t have a geographical tongue but my 11&1/2yr old son has it and I noticed it before age 2. Well my sister whose a dental hygentist told me what it was when I showed her the weird design on his tongue. All 3 of my children have really bad allergy problems. I have some but not as bad as my kids. My oldest daughter now 17 says nothing helps her all she uses is eye drops also Me and my other 2 take zyrtec which seems to help well for me more so. My son’s tongue now gets sores that are painful we have fig out surgar is one thing that triggers the sores. Does your tongue hurt by chance bc my son’s just started in the last 3 months or so?

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