posted
I am trying to discern if I have Bart or Babs or both.
My LLMD put me on Enula and then when I recently saw him, he wanted me to try Clinical Response Formulas BLT for what he thinks is Bart. It's his own concoction . BLT is red root, boneset, teasel, black walnut hulls, sarsaparilla and other herbs.
Anyone taken these and herxed?
I have been on the BLT for 4 days no and no real herx, maybe some chills and minor headache the first few times but hard to tell.
I just took the Enula and it made me feel instantly a little better.
Anyone know if they can be combined?
Who has done well on these or herxed?
Thanks!
Posts: 770 | From USA | Registered: Jul 2006
| IP: Logged |
posted
Myco, I'm curious what your BLT dose is. Mine is 2 dropperfulls twice a day, which seems pretty high.
Posts: 311 | From CA | Registered: Jul 2008
| IP: Logged |
posted
What abx are you using to treat your Bart Janice?
Posts: 770 | From USA | Registered: Jul 2006
| IP: Logged |
CD57
Frequent Contributor (1K+ posts)
Member # 11749
posted
Hi Myco -- we have the same LLMD. I took BLT also for awhile but quit because I didn't notice much. I may start it up again. Janice, the LLMD works with the Dr T so they did their own tincture together.
Posts: 3528 | From US | Registered: Apr 2007
| IP: Logged |
posted
I'm taking Omnicef, plaquenil, and zithromax. I don't know if they treat Bart at all. I don't even think I have Bart. I'm about to start Rifampin, which I think is for Bart. I wish I had time to ask my LLMD why he thinks I have Bart, but the appointment was so rushed.
Posts: 311 | From CA | Registered: Jul 2008
| IP: Logged |
My husband has been taking BLT drops for a couple of months. He has a clinical diagnosis of bart. He treated for babs in the past (lots of Malarone); fingers crossed, I think it may be gone.
Anyway, he felt a very definite herx when he started a very low dose of BLT drops. He slowly worked his way up to 50 drops a day, and for most of that time, had a reaction each time he increased. More recently, he hasn't noticed a big reaction.
He has not taken Enula, so can't speak to that.
Hope this helps. I hope you'll continue sharing feedback on your response to both the Enula and BLT.
Viva
Posts: 532 | From southeast US | Registered: Oct 2005
| 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/