I am now in position to sell my used RIFE MACHINE for HALF PRICE to someone from Lyme disease community!! If you dont know what it is do some research and maybe check out Rifing Lyme, RIFE LYME or Lyme Disease rifers FACEBOOK PAGES. Many seem to swear by it.
@callednchosen i think you are a little misguided when it comes to the m obey issue. Many LLMD has to take cash instead of taking insurance due to the fact insurance companies hunt them down for treating lyme to shut them down after suing them for malpractice. the amount they charge isn't much at all comparing to any of your regular drs. they actually charge more than LLMD for a follow up appointment you have at your PCP or specialist. The only difference you never see the amount since it gets submitted directly to your insurance.
I am getting rid of a Flexi Lite worth Twenty Thousand dollars. I am in California. I'm asking for five thousand five hundred dollars. It comes with 7PSI upgrade and an industrial concentrator.
Pshew . . . 2 to 3 years of doxicycline years ago; then again for 3 months 2 1/2 years ago; weekly injections of a cocktail of Glutathione and some other stuff for the last 2 1/2 years, plus 1800 mg of Valtrex daily for the last six months; not sure how long we will keep this up. I also have had HHV6, myalgic encephalomyolitis, fibromyalgia, sjogren's, etc., etc., etc. My doctor is one of the few in the country who actually treats these "off the grid" illnesses. PATRICIA SALVATO, M.D.
@jennluvsnkotb74 Yes thank you he doing so much better he stopped limping after being on the antibiotics for like 3 days. It took the litte guy about 3 days or so longer to start jumping on the beds etc…. and after about 5 to 7 days to get his normal eating habits back. I love that little dog so much ! He is my son !
I am having good success with the Salt/C protocol, google it. it is simple. also, try samento/banderol tincture and colloidal silver. also try Teasel tincture. antibiotics are good for a start,. but i like the salt/c protocol, there is a book my mark fett on it. also a yahoo group you can go and talk to other peple who are on it. also there is the cowden protocol. there is no reason to live in 24 hour pain. salt/c will give you your life back.
Have you watched the documentary "under our skin
'? or The documentary on Plum Island? Most people do not know they are infected or think they may have it but nnot get help. I'm quite sure you are aware of that now. it's sad that you have gotten lyme. I live with it daily. I know the struggle. Bless you and I hope and pray you get relief soon.
It infects way more people and is just as pernicious in the end. I'd say that it's at least just as bad, it's just played down by insurance companies, CDC etc.. I'm fucking 31 and I can't even wax my car or mow the lawn. I'm basically bed ridden most of the time. It fucking sucks, and I can't get help. At least people with HIV can get help, and have doctors actually willing to help them.
Wrote a Lyme disease brochure with the help of 2 Lyme disease specialists. Will email to anyone interested. God bless, Elaine
I am now in position to sell my used RIFE MACHINE for HALF PRICE to someone from Lyme disease community!! If you dont know what it is do some research and maybe check out Rifing Lyme, RIFE LYME or Lyme Disease rifers FACEBOOK PAGES. Many seem to swear by it.
@callednchosen i think you are a little misguided when it comes to the m obey issue. Many LLMD has to take cash instead of taking insurance due to the fact insurance companies hunt them down for treating lyme to shut them down after suing them for malpractice. the amount they charge isn't much at all comparing to any of your regular drs. they actually charge more than LLMD for a follow up appointment you have at your PCP or specialist. The only difference you never see the amount since it gets submitted directly to your insurance.
Elaine: I am interested in the information please.
Többek között a CD57 teszt működéséről esik szó.
How Lyme Disease and Its Treatments Work
Many of us feel all alone. Please read reply below for support group.
I am getting rid of a Flexi Lite worth Twenty Thousand dollars. I am in California.
I'm asking for five thousand five hundred dollars. It comes with 7PSI upgrade and an industrial concentrator.
Message me. It's been used about 20 times.
Pshew . . . 2 to 3 years of doxicycline years ago; then again for 3 months 2 1/2 years ago; weekly injections of a cocktail of Glutathione and some other stuff for the last 2 1/2 years, plus 1800 mg of Valtrex daily for the last six months; not sure how long we will keep this up. I also have had HHV6, myalgic encephalomyolitis, fibromyalgia, sjogren's, etc., etc., etc. My doctor is one of the few in the country who actually treats these "off the grid" illnesses. PATRICIA SALVATO, M.D.
what's their plan?
@jennluvsnkotb74 Yes thank you he doing so much better he stopped limping after being on the antibiotics for like 3 days. It took the litte guy about 3 days or so longer to start jumping on the beds etc…. and after about 5 to 7 days to get his normal eating habits back. I love that little dog so much ! He is my son !
I am having good success with the Salt/C protocol, google it. it is simple. also, try samento/banderol tincture and colloidal silver. also try Teasel tincture. antibiotics are good for a start,. but i like the salt/c protocol, there is a book my mark fett on it. also a yahoo group you can go and talk to other peple who are on it. also there is the cowden protocol. there is no reason to live in 24 hour pain. salt/c will give you your life back.
Have you watched the documentary "under our skin
'? or The documentary on Plum Island? Most people do not know they are infected or think they may have it but nnot get help. I'm quite sure you are aware of that now. it's sad that you have gotten lyme. I live with it daily. I know the struggle. Bless you and I hope and pray you get relief soon.
@spartan18458 You're wrong. Lyme can be spread person to person and mother to fetus.
Hi. No.. Lyme does not cause Lupus. Presentations are fairly different. It's pretty hard to confuse both of them.
It infects way more people and is just as pernicious in the end. I'd say that it's at least just as bad, it's just played down by insurance companies, CDC etc.. I'm fucking 31 and I can't even wax my car or mow the lawn. I'm basically bed ridden most of the time. It fucking sucks, and I can't get help. At least people with HIV can get help, and have doctors actually willing to help them.