One thought on “Buddy System for the US Lyme Patients”

  1. I am a member of lyme buddies usa, but am unable to use the internet due to emf challenges ( no pc/ Ethernet). I there a way I can have some one to share our lyme challenges with via phone? I can receive msgs via email, but prefer talking & listening via land lines if possible, I can only make local calls, but can receive calls feom anywhere. I am very isolated due to unbelievable Immune weakness amogst the many symptoms of lyme. Thank you for creating this group & providing hope. My email is heatchap@hotmail.com. Please feel free to contact w/ any thoughts on how to connect with out having to do so via Facebook or internet if possible. Thank again for being a vessel of hope!

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