posted
I see a known dr. in my state, but all he's had to say about supplements was to be careful.
Do most people see two drs. for the whole picture, or are there drs. who embrace both sides (abx and supplements - well, I haven't gotten down the abbr. for supplements yet!
I am seeing a naturopath,as well, but he's mostly using minerals, some adrenal support and DHEA (which makes me too hyper for some reason).
THanks again - this board, if not the abx will save my life, or at least some of my sanity!
-------------------- June Posts: 22 | From CT | Registered: Jan 2006
| IP: Logged |
mbroderick
Frequent Contributor (1K+ posts)
Member # 5220
posted
My LLMD is extremely knowledgeable about supplements. You can have blood tests done to see where you're deficient and work off of them, or research on your own if your LLMD doesn't know anything. Personally, I'd like a doctor who can treat me with more than just a traditional medicine approach - ESPECIALLY Lyme.
Posts: 2097 | From PA | Registered: Jan 2004
| IP: Logged |
Since I know who your LLMD is I will share my experiences.
He practices very evidence-based medicine and anyone who has ever seen him give a public presentation knows that every statement is supported by one or more citations. He sticks to pretty "traditional" medicine in the sense that he doesn't make diet, supplement, alternative, etc. recommendations.
I respect this. It is his niche and he is VERY good at it. I would rather have a doctor that is very good at one thing than one who dabbles in this or that. Ever hear the expression "Jack of all trades but a Master of none"?
Because I believe in alternative treatments I, on my own, see a naturopath, nutritionist, do acupuncture, herbal remedies (Dr. Dhonden), etc.
LLMD is fine with these things and feels that they "can't hurt." I get the impression that he doesn't believe in them but, unfortunately, there are not a ton of studies and money put towards these therapies. I run everything by him because I consider him to be my "Ring Leader" for treatment.
Just my two cents. You are in very good hands in terms of treating lyme and other TBD.
--Bluetick
Posts: 98 | From MA | Registered: Dec 2005
| IP: Logged |
Andie333
Frequent Contributor (1K+ posts)
Member # 7370
posted
My LLMD is also very knowledgable about supplements and other alternative treatments (suggested detox foot pads). Mostly, suggestions fall within the range of Dr. B.'s guidelines.
In addition to seeing this doctor, I also see an acupuncturist weekly and take Chinese medicines that are recommended. Plus, I consult with an herbalist about all of this and read on my own.
So far, everyone's coordinated and seems to be moving in the same direction. Since I was completely clueless about this disease, I've appreciated my LLMD's approach.
Just my 2 cents.
Andie
Posts: 2549 | From never never land | Registered: May 2005
| IP: Logged |
posted
Wow, everyone's input gives me quite a bit of food for thought.
Bluetick, I am getting more confident, too. Tahnk you for you words. I think I am just a bit overwhelmed. ( I love doing research in my own branch, but medical stuff usually makes me sick - but I guess I'll just have to do it.)
The problem seems to be that the LLMD and the ND I see, neither look over the fence, so now I am the one who has to connect all this. I will try, but I would rather trust someone like dr. H in NYS who does both, and seems very good at it.
Well, I guess there's no escaping the endless research on supp. and abx interraction. That's where my little energy will go beyond what my son gobbles up. The rest of my work will have to wait, and wait, and wait some more.
I can't tell you all how much your help and input have helped me, as a newbie here, who realizes more and more she should've known lots of this info long ago. Thank you.
Best of health to all,
-------------------- June Posts: 22 | From CT | Registered: Jan 2006
| 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/
UBBFriend: Email this page to someone!
![[Smile]](smile.gif)
Printer-friendly view of this topic