Why do I blog about my experiences with Lyme Disease?
Why do I tell others about my life?
Why do I share so openly and honestly about my feelings about the doctors that don't treat Lyme appropriately?
I got the answer today.
Not one, but TWO friends emailed me today. I have often thought that if the pain I had for 12 years prior to my diagnosis could help one person it was worth every moment.
Now I have the opportunity to possibly help impact the lives of my friend's family members.
You don't *get* Lyme until you GET Lyme. No two Lyme patients are the same either. I have had a pretty rocky journey, others have it worse than me and I know others that were treated with two weeks of Doxy and are fine.
I hope that those that my friends know will be in the two weeks of Doxy and they are fine. In my experience, that is rarely the case.
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