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I've been trying to get it together enough to start a blog... I really want to author a blog, but FB was so much easier to set up. I want to tell my story with no censors,I feel it would be easier to let it all hang out on a blog... I want to build a strong support community page for lyme on fb and blog to tell my story. I'm new to this and just throwing ideas around What do ya'all think? trying to get the hang of it all I haven't created the blog yet, but I have started a community page to share my experience strength and hope. Feel free to visit me there and let me know if you guys have any websites ect, that you like to visit for lyme support including your own pages Love and thanks facebook.com/lymelight
-------------------- Hoping for Hope Lyme, Cfids, Hormone imbalance, hypo-thyroid, immune deficiency Posts: 44 | From North Hollywood | Registered: Jan 2014
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Naomi I would love to join your page…so its just Facebook.com/lymelight? Yes do share your experience, strength ,hope,…..but also share what treatments helped. I find too many folks on these blogs, pages, forums, message boards for lyme &Co don't realize how many people out here are very sick with this and for a variety of reasons have to access to a LLMD We are either self treating and searching the forums for ideas or we have a doc who is not a LLMD doc and is open to the information we learn about from other and take to them. Too often when questions are posted an answer comes back….get a LLMD. If I had one of those I would to have to spend my life on forums. I am really interested in your experience as I believe you had Babesia which is what I am struggling with now.
Posts: 51 | From Albuquerque | Registered: Feb 2014
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Love and thanks facebook.com/lymelight
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