From a friend through my Lyme support group: My daughter shared this with me( she is a lyme sufferer too). If you havent seen this 15 min video i recommend you watch this so you can have a true understanding of the lyme controversy. Please feel free to share this with your friends ,family, post on yourFB page, etc. I think this girl did an excellent job explaining this to the public. I will be posting on my page also. Ppl need to know the truth. While trying to heal from this disease, I feel it is my obligation to inform as many ppl as I can so that as many lives as possible can be saved. Again knowledge is power and if everyone is not aware of the truth in our country, change will not take place. It is very emotional for me because I got this disease next to Lyme Ct (my once beloved hometown), in the 70s or possibly the 60s. Now when i come back here for treatment, i have nightmares about CT and all the lies i was told as a kid regarding the Spirochetes that were showing up in my blood back then. I was told by doctors not to worry about it, many ppl have these. So as i continued to suffer and could not go on to graduate school, i tried to be very positive despite the falling apart of my body. With the Spirochetes still in my body after years, i was told it was okay to have a child. I begged for proof, they had none for me and there was no internet. I now have a 21 year old child who is a carbon copy of me. Her suffering from Lyme and Cos like me, has morphed into Diffuse Scleroderma ( the very bad form) and RA. Our real diagnoses were not made until 6 mos ago. I have not thrown in the towel yet but i wanted to spread the awareness to as many as possible. As a teacher i feel an obligation to inform. Spread the truth. Good health to all of you. https://m.youtube/watch?v=OrLJLgoNgA4
Posted on: Tue, 19 Aug 2014 21:17:46 +0000
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