posted
Well, my dad said to never let money decide treatment, that he would fill in the gaps .... so, that being said, I still see an ILADS LLMD and am on abx plus herbs. Haven't had to tap into Dad's money stash yet.
I'm looking into the Bionic 880 (owe you a PM) .... waiting impatiently till GiGi and others get back from Germany. Thinking of going to Germany for treatment and coming home with one like GiGi is. (Of course, I would share if I did this. )
-------------------- sixgoofykids.blogspot.com Posts: 13449 | From Ohio | Registered: Feb 2007
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posted
I would go for IV with a nurse at home. If I had that kind of money. ------- The Bionic 880, I think it is soooo strange, I hope it works, but you know I have actually lived In Prorzheim in Germany one year, just a block from where this alternative doctor works, and I have met many hundred germans on Lyme treatment in my LLMDs office and NONE of them has said anything about Bionic.....
so strange.....
Posts: 347 | From sweden | Registered: Feb 2008
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tailz
Unregistered
posted
I would use it to buy a home in an EMF/RF-free area, purchase miles of land around it (to avoid the installation of cell phone towers), and refuse to sell the land to anyone. The home would be solar-powered or wind-powered or whatever technology would bring the least EMFs/RFs into the environment.
I'd buy myself a dog or two, a few more cats, some horses, put up a few bat houses to control the mosquitos, and live alone in the wilderness, taking in strays, feeding tick-infested deer from high-EMF areas, waiting for nature's inevitable retaliation against wireless technology. My Lyme would be in remission without the exposure to EMF/RF anyway.
I may even begin collecting seeds for the upcoming food shortages the Bible foretells.
Maybe I'd even begin to build an ark...
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Tincup
Honored Contributor (10K+ posts)
Member # 5829
posted
If I had 200 million dollars?
I would open a treatment center with little apartments where folks could stay.... and the best of the best of everything... so everyone could get treated using any and all options available.
posted
If I had 200 million dollars I'd run for office and change things so Lyme can get properly diagnosed and everyone can get the right treatment they deserve.
With that kind of money I could run independently and not worry about special interest groups or being "loyal" to party politics.
-------------------- C.D.C = "Country Doesn't Care" Ticks are like Snipers, you don't know they're there, until you see the bullseye. Posts: 86 | From Upstate New York | Registered: Jun 2007
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posted
I think steel is asking what treatments we would do. Since I'm pretty much "well" I would get weekly glutathione and other good supportive things like that.
Maybe even buy a good quality Transfer Factor.
But what I'd REALLY like to do with that much money would be set up a foundation so that Lyme patients could obtain the treatment that so many cannot afford.
You would have to qualify, but the qualifications would not be that hard. If Tincup and I got together, no one would have to go homeless because of this %$#& disease!
PS to tailz... The ark would do no good. God said he would never again flood the earth.
(tell that to those in the Midwest right now!! )
-------------------- --Lymetutu-- Opinions, not medical advice! Posts: 96222 | From Texas | Registered: Feb 2001
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Taliz is not totally alone. One of the things I would do would be move to a house in the country where I could plant a garden and grow organic food and have an herb garden. Of course it would be even better if I could hire a cook as well.
Actually maybe I should just move in with my parents. Have seriously considered this as they live on a 1000 acre farm in central West Virginia. I think some pets and less stress would be very helpful for hubby.
I like Tincup's answer as well -- one of the things I have dreamed about is taking hubby to 3 or 5 different LLMD's and getting their treatment suggestions. As they say, two heads are better than one. And just imagine if all the docs were in the same place how simple that would be.
If you have ever tried to find a neurologist and a gastroenterologist who specialize in Lyme and tick-borne diseases you have to travel hundreds of miles as they aren't in the same place. And forget it if you also need a pulmonologist, a cardiologist, a psychologist etc etc.
Some of the treatments we have had to forgo for financial reasons include weekly massages. I always come up short on money for supplements. And testing. I would do additional tests for viruses, immune system function, possibly genetic testing, follow-up hormone testing and various nutritional tests.
The one treatment I would like to try again is UVB -- ultraviolet blood irradiation. Don't know if it was working on viral issues or something tick-borne, but it definitely did something the 3 treatments hubby had.
Or another option would be to hire a doc to call and consult other docs for suggestions.
I would definitely have many more bloodslides looked at -- by Fry lab and anyone else I could find who knows what they are looking at.
Most of all I would love to find a curious neurologist. It would be so nice to see some journal articles that mention tremors, muscle spasms and myoclonus as possible symptoms of Lyme and tick-borne illnesses. It would be vindication of a sort to be able to show all the neuros that anxiety and depression are not the only thing that causes tremors.
Actually I have been making my list for awhile. Hubby recently enrolled in a catastrophic health insurance plan. It has a waiting period of 2 years. If he is not well by then, then I plan on utilizing this policy to get additional testing and treatment.
Bea Seibert
Posts: 7306 | From Martinsville,VA,USA | Registered: Oct 2004
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