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» LymeNet Flash » Questions and Discussion » Medical Questions » update on Ky doc

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Author Topic: update on Ky doc
my2haveit
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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.

Posts: 61 | From Florida, USA | Registered: Aug 2005  |  IP: Logged | Report this post to a Moderator
livinlyme
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Bump up for help!

My2,
that is horrible news.. someone help My2 get another contact for an LLMD!

--------------------
"Hatred paralyzes life; love releases it. Hatred confuses life; love harmonizes it. Hatred darkens life; love illuminates it."

Posts: 1389 | From who knows, who cares, but somewhere over the rainbow | Registered: Mar 2003  |  IP: Logged | Report this post to a Moderator
Lymetoo
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Does the dr have Lyme disease too? Whatever it is, he must be really sick.

There's always Dr C in Missouri.

--------------------
--Lymetutu--
Opinions, not medical advice!

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my2haveit
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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 ]

Posts: 61 | From Florida, USA | Registered: Aug 2005  |  IP: Logged | Report this post to a Moderator
livinlyme
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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..

[Frown]

--------------------
"Hatred paralyzes life; love releases it. Hatred confuses life; love harmonizes it. Hatred darkens life; love illuminates it."

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my2haveit
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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.

Posts: 61 | From Florida, USA | Registered: Aug 2005  |  IP: Logged | Report this post to a Moderator
my2haveit
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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".

Have you checked out the salt/vit C forum, http://health.groups.yahoo.com/group/lymestrategies/ ?

Several posters are starting to go back to work due to their health improvements from being on that protocol.

I've been on it a while, though I don't have an active Lyme infection. I wanted to experience it before pushing it on my daughter and her family.

It's being used with animals, kids and babies, who are showing improvements.

There's a lot of active support on that forum -
a lot of methods for dealing with specific problems while trying to stick with it.

The protocol is in active research mode and users are asked to fill out a survey before using it.

Many users post progress reports, for good or bad, to share with the rest.

Some users are doing it under the supervision of doctors, and doctors are invited to participate.

The forum is free for lurkers and posters, $29.95 to access the files.

The protocol is cheap, easy, and readily accessible.

It's experimental, like rife, MP, etc.

I believe all treatments can be risky, and I believe no treatment for Lyme at all is riskiest.

Just a idea.

Good luck,

Sue G.

Posts: 61 | From Florida, USA | Registered: Aug 2005  |  IP: Logged | Report this post to a Moderator
   

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