posted
I can't saw anything specific, but frequent myers cocktails were major part of my son's treatment.
He got well. Our insurance paid for it.
-------------------- Son, 26, Dx Lyme 4/10, Babs 8/10 Had serious arthritis, all gone. Currently on Valtrex Daughter, 26,bullseye 7/11 arthritis in knees, cured and off all meds. . Self:Lyme, bart, sxs gone, no longer treating. Posts: 496 | From Washington, DC | Registered: Jul 2010
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posted
It can really help you feel better. It doesn't work for everyone but you should give it a try.
It takes several weeks sometimes to realize the benefits of the treatment. It helped me.
Your doctor is expensive, myers cocktail cost me $35 for each treatment. It is an IV push.
-------------------- Faithful
Just sharing my experience, I am not a doctor. Posts: 2682 | From Colorado | Registered: Oct 2009
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Judie
Frequent Contributor (1K+ posts)
Member # 38323
posted
"Our insurance paid for it."
Wow, I wonder what the insurance code is.
If anyone knows more about this, please PM me. I can certainly use some financial help if my insurance will pay.
Posts: 2839 | From California | Registered: Jul 2012
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beaches
Frequent Contributor (1K+ posts)
Member # 38251
posted
Yeah Judie, you and me both.
A one-time treatment didn't help DD at all. Then again, it wasn't realistic for us to travel a great distance to have it done on a weekly basis, not that the LLMD recommended that.
Wondering if some LLMDs would prescribe it for patients with piccs/ports so it could be infused at home on a weekly basis?
Posts: 1885 | From here | Registered: Jul 2012
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Judie
Frequent Contributor (1K+ posts)
Member # 38323
posted
"Your doctor is expensive, myers cocktail cost me $35 for each treatment."
Thanks, that's what I was thinking. I wonder why the price is so high...
Posts: 2839 | From California | Registered: Jul 2012
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MannaMe
Frequent Contributor (1K+ posts)
Member # 33330
posted
My husband had Myer's cocktail once every 6 weeks while on ABX. his was an IV drip - took about an hour or longer to get it.
He also got a bag of glutathione after the cocktail was done.
Friends of our get the myers cocktail - they said it really helped them to feel better, though sometimes it took time till they noticed a difference.
Posts: 2249 | From USA | Registered: Aug 2011
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posted
faithful, where did you get your myers cocktail? I would like to start really hitting my immune system to see if I can't get my stubborn symptoms to wane.
Just out of curiosity, did your current LLMD prescribe it and why did you take it?
Posts: 538 | From kentucky | Registered: Nov 2011
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posted
I had an integrative doctor who's office did them. I had to go to the office once a week. I did this before I knew I had Lyme.
After I was diagnosed, my LLMD prescribed this from Infuserve but they do an IV bag that had different components and it did nothing for me.
Every doctor has their own measurements of the ingredients that go into a myers cocktail. I got the prescription from my integrative doctor and tried to get Infuserve to make it, but they couldn't get one of the ingredients and still wanted to do a bag at $60 each.
My integrative doctor only charged $35 and my insurance paid for part of that. So I just stopped them. Now I inject 10 mg methylcobalamin daily and make sure I take adequate magnesium.
With Lyme you are deficient in a lot of nutrients and this does help things along. The cocktail does jump start everything if you can do them.
-------------------- Faithful
Just sharing my experience, I am not a doctor. Posts: 2682 | From Colorado | Registered: Oct 2009
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Judie
Frequent Contributor (1K+ posts)
Member # 38323
posted
Thanks everyone. I think I'll try it once and see what happens (but expect that it might take more than one treatment to feel anything).
I definitely feel deficient.
One of the times I felt great was when I was in the hospital after having such bad dizzy spells.
They said I was low on potassium and put me on an IV (prior to the potassium results coming in). I have no idea what was in there, but I felt great after 5 minutes.
Insurance paid for it at the time though....
Posts: 2839 | From California | Registered: Jul 2012
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