Guest guest Posted November 7, 2005 Report Share Posted November 7, 2005 Well i have no insurance and can't get SS so...that makes no difference really.But it would help to know what in the heck it is so we might know if it's treatable or not . Re: [sPAM] Re: [low dose naltrexone] Re: PCP wants to treat with LDNwithout neu... In a message dated 11/6/2005 2:31:06 PM Central Standard Time, oothappam@... writes: My neuro doesnt think i am too old to have MS (I am 49) but its the fact that lumbar puncture and MRIs show NOTHING that makes it hard to give a dx of MS officially.BUt I hae all the signs and symptoms, except that l'hermittes thing. I am so glad he was willing to let me try this LDN anyway. Nola +++++++++++++++++++++++++++++++++++++++++++++++++++++++++++++ There are many demylinating conditions that don't have a name. I guess for insurance and SS reasons a diagnosis could be helpful. Still, LDN seems to me to be the best bet! Marcie Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 7, 2005 Report Share Posted November 7, 2005 In a message dated 11/6/2005 11:42:29 PM Central Standard Time, oothappam@... writes: Well i have no insurance and can't get SS so...that makes no difference really.But it would help to know what in the heck it is so we might know if it's treatable or not . +++++++++++++++++++++++++++++++++++++++++++++++++++++++++++++ I think, at times, traditional medical professionals have a hard time admitting that they really don't know what something is, so they will call it this or that. Personally, there is no effective treatment for many conditions (MS being one of them) so a dx doesn't mean too much. JMHO. Marcie Quote Link to comment Share on other sites More sharing options...
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