NeuroTalk Support Groups - Type II Trigeminal Neuralgia

NeuroTalk Support Groups (https://www.neurotalk.org/)

- New Member Introductions (https://www.neurotalk.org/new-member-introductions/)

- - Type II Trigeminal Neuralgia (https://www.neurotalk.org/new-member-introductions/200430-type-ii-trigeminal-neuralgia.html)

thekitchenwench

01-31-2014 12:54 AM

Type II Trigeminal Neuralgia

Hi everyone :) In 2010, I was diagnosed with Type II Trigeminal Neuralgia. In 2003, our home had toxic mold in it that caused illnesses in my family of 6. Add an unhealthy diet, dental work and demylenization of some of my nerves from the toxic mold and I developed many neurological symptoms. I am currently on lyrica again because I have not been juicing and eating organic vegan.

I am here for support and information to see what is new in treatments and what works for others like me. Hope you all have a good day, or night!

Darlene

02-01-2014 12:29 AM

Nice to meet you!!

http://dl10.glitter-graphics.net/pub...zeokl4w2ff.gif

thekitchenwench,

:Wave-Hello: It is great to have you come and be with us. You will fine a great number of dear friends to listen when you are in need of ears. Please, just let us know how we can help you out. You will find out we are supportive and relaxing place.

Looks like are having a good time all around in the different forums.

Please keep us up to date on your situation. Again welcome, looking forward to seeing you around. My thoughts and prayers are with you. :smileypray:

Darlene :hug:

thekitchenwench

02-01-2014 08:24 AM

Thank-you Darlene for the warm welcome!
Anna

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