posted
I was reading Dr. B.s guidelines, and I feel a little discouraged. He says that the Azithromycin class of drugs have a poor success rate when administered orally. Am I taking Zithromax for nothing? If it has poor success rates, why would my LLMD give it to me?
Posts: 64 | From PA | Registered: Mar 2007
| IP: Logged |
savebabe
Frequent Contributor (1K+ posts)
Member # 9847
posted
I guess different docs have different treatment approaches. I know from personal experiences with Dr. B that he does not give zith to fight lyme. Maybe you could contact your llmd and suggest mino or doxy. This is a very complicated disease, and it takes a lot of medication adjustments to find a treatment plan that works for you.
Posts: 1603 | From ny | Registered: Aug 2006
| IP: Logged |
posted
I didn't want to take any of the Doxy, Mino, etc., because I know I'm going to be outside a lot this summer and that's something I just can't avoid.
I'm taking 2 Zithromax, 2 Cat's Claw, 2 AG-Immune, and 2 Probiotics per day. I asked about adding Artemesin, but she said not yet.
I don't see her for another 3 weeks. Is there something else I should suggest?
Posts: 64 | From PA | Registered: Mar 2007
| IP: Logged |
posted
Try not to stress out about what this doctor said or about others medications.
Your doc might be starting you on one abx slowly and then adding another with it. My LLMD starts me off slow and then increases as I adjust to them.
Base your treatment on how you feel and what you think your progress is. If you go over and over in your head what everyone has said about multiple meds you will drive yourself insane.
For example...many people don't do well on Zithro. For me combining it with Flagyll has been a life safer for me. I have taken different abx...some of them other Lyme people have raved about..and they did nothing for me.
I think it all depends on co-infections, how long you have been infected, your immune response, etc.
I use to drive myself crazy thinking I should be doing this or that but now I try to go with the flow.
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/