Guest guest Posted August 16, 2010 Report Share Posted August 16, 2010 Jo Is it truly that bad?? That we need to protect them?? I just had a conference call w Aetna & my LLMD's office mgr My LLMD wants to order some 'experimental' (as Aetna called it) labs from PharmaSan labs Will let you know how it goes My LLMD thinks normal tests will not show much since my CD57 shows I have NO immune system & the C4A implies I've been infected a VERY long time Randy On Aug 16, 2010, at 10:34 AM, " judyjo27 " <judyjo44@...> wrote: > In order to protect our sympathetic doctors from possible harrassment by people/agencies that don't believe in chronic lyme, may I suggest that doctor names be sent backchannel, directly to the person requesting the information rather than posting on this forum. Just a suggestion since we need all the good lyme practitioners we can get. jo > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 17, 2010 Report Share Posted August 17, 2010 It certainly has been in the past. I don't know if this problem is easing as I don't keep up on the political side of this. (I think the political side is very important; I just don't have the energy to keep up with it; I'm so grateful some people do). I have seen posts in the past suggesting giving provider names backchannel rather than posting them. I'm open to hearing your experience. jo > > Jo > > Is it truly that bad?? > That we need to protect them?? > Quote Link to comment Share on other sites More sharing options...
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