posted
Once again, I've had to stop my abx because of a rash. We don't believe it is Lyme die-off, but more of a reaction to the abx building up in my system.
This is the 3rd time I've had to stop them in the year and a half of treatment.
How can I ever get will if I have to keep going back to square one? I have to start each one slowly, and one at a time. I'm on biaxin, plaquenil and doxy.
-------------------- "Few of us can do great things, but all of us can do small things with great love". Mother Theresa
posted
I do take olive leaf and chlorella daily. We don't think it's really an allergy because it takes months to build up. I AM allergic to plain penicillin, so those are out.
I am just getting so discouraged wondering if I'll ever feel better.
I do get relief from PT and going to a therapy pool, but all the aches, pains, cognitive stuff....are coming back full force.
-------------------- "Few of us can do great things, but all of us can do small things with great love". Mother Theresa
lymie tony z
Frequent Contributor (1K+ posts)
Member # 5130
posted
hurting gramma,
Don't be too too dicouraged.
All of my abx protocols have been interupted as well and I have never been on an IV longer than three months(once).
And I have had repeated improvements...seems like almost every different abx I have tried killed a strain or two and I lost a symptom here and there.
Just wish I could find the fatigue strain or the one that gives me pain and weakness whenever I try to do physical stuff....
Almost ALL my cognitive problems are gone....although some around here have accused me otherwise...LOL
So hang in there....you'll get better...it just may take you a little longer....
Orals never seemed to be as effecacious as IV's in my case.
May...yeah I tried all three of the ones you mentioned and astragalas(among other things) as well early on in my alternative self help treatments.
Although I think I got a herx from the grapfruit seed extract I used about four times the dose(I ramped it up)...so who knows....
But abx worked best for me.
zman
-------------------- I am not a doctor...opinions expressed are from personal experiences only and should never be viewed as coming from a healthcare provider. zman Posts: 2527 | From safety harbor florida(origin Cleve., Ohio | Registered: Jan 2004
| IP: Logged |
The Lyme Disease Network is a non-profit organization funded by individual donations. If you would like to support the Network and the LymeNet system of Web services, please send your donations to:
The
Lyme Disease Network of New Jersey 907 Pebble Creek Court,
Pennington,
NJ08534USA http://www.lymenet.org/