For all those interested in the Ky. doc, someone called him and learned he had been hospitalized. The message on his answering machine advised people to get their charts and seek other doctors. Sue G.
Posted by livinlyme (Member # 3773) on :
Bump up for help!
My2, that is horrible news.. someone help My2 get another contact for an LLMD!
Posted by Lymetoo (Member # 743) on :
Does the dr have Lyme disease too? Whatever it is, he must be really sick.
There's always Dr C in Missouri.
Posted by my2haveit (Member # 7712) on :
Livinlyme, that is so caring of you. Thank you for such concern.
This is how things are, though. My daughter and her family in Ky. have chronic lyme.
When I got the docs' contact info, I encouraged them to see him.
They had valid major obstacles to being able to see him , or any other distantly located Lyme friendly doc.
So I researched the salt/vit C protocol as the one most available to them for now, and pushed them to try it.
They should be starting on it about now.
When a poster asked about treatment in Ky., I offered this doc's contact info.
He, plus several more from this forum, e-mailed me for the doc's info.
That's how I learned about the doc's hospitalization.
We have no access to an experienced LLMD where we live in Florida, and my spouse got badly ill from the antibiotic treatment for Lyme.
So we are using rife, and it's making a huge difference in the past 3 months of treatment.
I empathize with your Lake City location and its isolation from effective Lyme help.
It's still good to learn of all the LLMDs available.
I would still be glad to know about any Lyme friendly docs near my daughter in case they're ever able to see one.
But for now, we aren't the ones seriously needing a Ky doc. The ones who e-mailed me really need one, though.
[ 04. October 2005, 03:28 PM: Message edited by: my2haveit ]
Posted by livinlyme (Member # 3773) on :
Hey,, if you or anyone else are ever done with their rife machine and want to donate it to a worthy cause! PLEASE LET ME KNOW!!! there is a whole family here that will beenfit from it and I have a big mouth.. so it would be good publicity!!
I am desperately trying to hang in there, but I am not sure I can much longer...even if I get a job I might not hold it long.. and ruin everything I have establish for a disability case..
Posted by my2haveit (Member # 7712) on :
Lymetoo, that doc told me many months ago that he had Lyme for about 16 months, and he had used Samento for a few months and still couldn't increase his dose past 1 drop.
He is an older person and he may have other health problems that are age-related.
I was still sad to hear it. Every Lyme friendly doc is so precious.
Posted by my2haveit (Member # 7712) on :
LivinLyme,
I can't imagine giving up our machine. If you lived nearby, we'd love to share it with you.
Of course, it can be risky. A science writer and researcher had posted on here along time ago about an adverse effect she experienced with her heart after rifing.
She has since referred to it on other forums, indicating that she still has trouble from it.
Another poster generously shared, with this forum, her log of her use with her machine, which is similar to ours. That may have been last year.
She got seriously ill and was hospitalized. Her dr. took out her gall bladder, but it didn't help.
She still hasn't fully recovered and said she didn't know if rife was to blame or not.
From her log, it seemed to us that she got into trouble when she rifed for parasites, which we learned can be tricky and even harmful, if not done just right.
Since there isn't enough publicly shared information about rifing, it's hard to know how to rife for parasites "just right".
![[Frown]](frown.gif)