Guest guest Posted May 17, 2009 Report Share Posted May 17, 2009 Oh, this is very interesting. I have an apt to see Dr. Engstrom at UCSF ! I wonder if this is your doc? Can you kindly tell me if you think UCSF has been helpful at all because I intend to fly all the way out from Colorado for tests etc as doctors here have done nothing - and I mean nothing for my PN. Would be very grateful to learn your thoughts about UCSF neurology.. BTW, what his Avonex? and how is this supposed to help PN? Thanks, Colorado [low dose naltrexone] Re: Dr Kita Seattle My husband`s neuro at UCSF is the same! Even though has been stable with no progression for four years, when I ask the neuro how his other (very few I think) patients are doing, he doesnt or wont say. Like he wont give it any weight at all - really annoying. If stumbles or isnt quite so fast of one the cognative tests he says "we might have to start him on Avonex"!! We just laugh and tell him we`ll see him in a year.- In low dose naltrexone , "anotherwildflower" <anotherwildflower@...> wrote:>> Hi!> > Just wondering about others with MS who see Dr Kita in Seattle and who are on LDN. I was trying to get her impression on how others were doing and she was very vague. Just curious how things are turning out for you.>------------------------------------ Quote Link to comment Share on other sites More sharing options...
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