Recent appt w/ Dr Jemsek from "Under our Skin"

[ewford]

I recently had an appt w/ Dr Jemsek and got the low down.   Jackie, I explained everything I was aware of that you have heard me talk about here.  He said I was spot on, including hysterectomies.  He basically said if the IDSA and the CDC do not get their collective heads out of their keyster, we are gonna be in a world of hurt at the rate this is spreading.  There has been some recent talk about Tindamax as a VERY viable alternative to Zithro as Tindamax can eliminate the cystic as well as the spirochetal forms.  This is from Dr Eva Sapa's research.

  I have available a list of suggested nutracells for anyone interested, recomended by him.  PM me and I will send you a list.

[sufferininga777]

I hope all the doctors with their heads up their keyster get this and go to all their illerate doctor friends who let them suffer. I hope they all suffer because the figures I have say 420,000 reported cases I say again REPORTED  cases a year, is at pandemic levels.I wonder what the figures are for unreported cases . Probably more because their heads are up their butts and up the pharmaceutical companies and insurances butt.

[nutrinut_bob]

Just read an interesting study.  They were checking to see if wild turkeys in S. California could be carriers of Lyme.  Now if the governmental agencies can do this, meaning they recognize Lyme, why can't it be medically recognized?  By the way, the final decision was wild turkeys didn't make for good carriers as their complement system killed the spriochetes.  Only one tested had Lyme, and it also had a brown dog tick on it, but the brown dog tick didn't have Lyme.  So why aren't our complement systems capable of killing the spiros?  Dietary factors, genetic factors.  Want to bet that there are few cases among the tribes in the Amazon forest, except for those who eat the foods of our "more advanced" society?

[ewford]

I still get pissed at hearing Somataform or Munchausens.  Now I know how they feel and completely understand them.  

[nutrinut_bob]

All I can suggest is that we point as many people from the other forums, such as AI, that might be victims of Lyme to this forum.  At least let them consider the possibility and seek help in a better direction than what their present physician(s) have them pointed. I've been packing this stuff longer than about anybody here, since at least 1968 and possibly before. I know the symptoms, have them in mind and know at about what age they came on. Still haven't figured out if it came from that immunization, or the dog ticks I had on me when I was young, though they're not supposed to be carriers.  But I can say that
I can't begin to express the physical changes I'm going through, being able to feed me instead of these parasites. It's pretty wild to be 53 and growing!  I'm gaining muscle where I never had muscle, joints that used to snap and pop no longer do. I tan rather than blister and peel, without a layer vermin under my skin.  But I'm not finished yet, still getting drainage out of my ears (under the skin), still see floaters in one eye, and still have tinnitus, though the volume is greatly diminished.  Do you all realize they used to put people in the nut house for saying they hear bells, or saw something that wasn't there?  Wasn't that long ago either, and some tried to eat odd herbage, self medicating in some cases, and that made them appear even nuttier in the eyes of the system.

[ewford]

http://www(dot)ncbi(dot)nlm.nih.gov/pubmed/21753890

here ya go Jackie, just for you.

[ewford]

Sorry, posted wrong page.  This is a blog that the dr used Tindamax from Dr Sapi's work.  Now I have to find the URL in my favorites.  my bad.

[JackieCalifornia]

Just to be clear, this is not a research paper, but is a blog by an MD on the East Coast who specializes in Lyme.  The post talks about Tindamax, but is not written by Dr Sapi.

I have read this doc's blog for a few years (except when he stopped posting for about a year recently) and it's interesting but rather disjointed.  fwiw.

[ewford]

http://lymemd.blogspot.com/2011/07/everything-you-thought-you-knew-about.html

[ree427]

Where can I find Dr. Sapi's research on Tindamax? I was on her website and saw peer reviewed articles on cancer, but no Lyme. I was on Tindamax years ago for a so-called parasite before I knew I had Lyme and herxed very badly. I thought I would die and at the time had no idea why I was having such a reaction. The doctor prescribed it to me instead of Flagyl because I could not tolerate the Flagyl at all. I would be very interested to read the research and take it to my doctor.
Thanks

[ewford]

I was never a "woe is me".  I'm about as proactive as possible going to Autoimmune boards, sexual health boards and so does Bob and Just not Sure and others.  They are telling people to repost here to get more info (and I have stated to some that info might come from you).  I just restored my neices 65 Mustang, and was having it appraised.  I met a tow truck driver and we started talking, got on the subject of Lymes, and turns out his fiance has every single symptom, and been to numerous doctors all without diagnosis.  I told him about proper testing, and all the info you commonly report here.  
  Now if that's not being proactive, I don't know what is.  I get the word out on a daily basis and am astounded at the number people sick with Autoimmune like illness.
  As far as what do you think should be done?  EDUCATION through discussion. I know you like the touchy feely approach for obvious reasons.  My approach is to openly discuss and help people find their way.  Is that not good enough for you?  What do YOU propose I do instead?  Myco's are DEFINATELY a part of this illness, there is no denial.  Should I not discuss them just to make you happy?
  My PROACTIVE  approach is to get people to realize they are not alone in this illness.

[JackieCalifornia]

ewford and nutrinut, what do you think people should do?  

I certainly understand your displeasure with the medical world on this topic, but what are your thoughts on how to get through it?

"All is lost, woe is me" leaves one with a hopeless feeling, and proactive approaches are needed.  What are your ideas?

[nutrinut_bob]

I agree ewford, but the docs aren't going to let go of any of their income sources.  Another thing to consider is, just how many of those doctors are walking around with it unknowingly.

[ewford]

Hiya  JNS 123.  i have to play nice.  You have done a great job helping spread the information on mycos.  I told you...all these AI illnesses have too many similarities.

[justnotsure123]

good to see you back bro!!