cottonbrain
Frequent Contributor (1K+ posts)
Member # 13769
posted
Hi everyone. I have an appt with Dr F and wonder if anyone is familiar with him?
Do you know what type of protocols he typically uses?
I am in Charlotte, NC. I saw Dr J in SC a couple times but need a new LLMD--he is way out of my price league.
thanks in advance!
------------- Diagnosis of CFs/ FM for fifteen year.
Recent dx of neuroborreleosis.
I am mostly housebound due to probs with photosensitivity and migraines. Also the usual Lyme stuff like fatigue, mcs, cognitive problems, memory, word recall, weakness, malaise --
Posts: 1173 | From USA | Registered: Nov 2007
| IP: Logged |
mbroderick
Frequent Contributor (1K+ posts)
Member # 5220
posted
I've heard excellent things about him. He's also in practice with a LL Rheumatologist. Dr. F's fees seem 'hefty', as well, and he doesn't participate with insurance. It might be best to clarify the costs ahead of time. I know that the first visit is quite expensive.
Send me a private message if you need additional LLMD names, although Dr. F. really does sound extremely knowledgeable and has fabulous credentials. It's always a good idea to try to get the absolute best doc possible.
Hope your appointment goes well.
Posts: 2097 | From PA | Registered: Jan 2004
| IP: Logged |
posted
the complimentary pens in the office do say "GO WITH THE BEST!"
Posts: 35 | From Washington, dc | Registered: Jul 2007
| IP: Logged |
cottonbrain
Frequent Contributor (1K+ posts)
Member # 13769
posted
thanks to you both for the replies.
Do you know what kind of protocols i can expect with Dr F?
The reason I ask is because someone on the board went to his office (not to him though) and was treated with only one antibiotic at a time -- apparently the treatment was not very aggressive.
Sincce i have been ill so long, 15 years, and have a dx of neuroborreliosis, I want to make sure i get the right treatment.
Thanks again for responding!
Posts: 1173 | From USA | Registered: Nov 2007
| IP: Logged |
posted
i see dr. m and i feel very confident in his knowledge of treating lyme and coinfections, but i've only been on the medical merry-go-round since May 2007.
i am currently on 5 different medications so at least in my case, the treatment has not lacked aggression.
the first meeting with him we met for the full time alotted (over an hour). he even looked up directions for me to get home, which i thought very friendly and appreciated his time.
Dr. F has been on a lot of the Lyme news coverage around Washington/Virginia/Maryland. Links can be found somewhere on Lymenet although i'm not sure where. but if you want a preview you can find it.
Posts: 35 | From Washington, dc | Registered: Jul 2007
| IP: Logged |
for my insurance company, the "usual customary rate," or whatever it's called, for the first visit with dr. m was around $290.
i think the office charges $375 for the initial visit, but after that it's between $110 and $150.
i'm not sure if this is inappropriate information to share on the forum. if it is please let me know and i'll take it down.
Posts: 35 | From Washington, dc | Registered: Jul 2007
| IP: Logged |
cottonbrain
Frequent Contributor (1K+ posts)
Member # 13769
posted
cidanu, thank you so much for the replies! You have set my mind at ease.
I'v seen lots of people post what their docs charge, so i don't think that will be a problem-- and I appreciate the information.
Thanks, everyone!
Posts: 1173 | From USA | Registered: Nov 2007
| IP: Logged |
I have been seeing Dr. F. since May 2006. He is the only Dr. that has helped me get my life back!! All the other Dr.'s were telling me I was just depressed. When in reality I was pretty sick. I have nothing but great things to say about Dr. F and his office. I have seen slow but steady improvement. He and his staff are very lyme literate. I travel from Delaware to see him. Best of Health to you.
Posts: 33 | From Delaware | Registered: Nov 2006
| IP: Logged |
cottonbrain
Frequent Contributor (1K+ posts)
Member # 13769
posted
thanks, cancuncmom! I really appreciate your input.
I'll be seeing Dr F in about a month -- can't wait to finally get some real treatment!
Posts: 1173 | From USA | Registered: Nov 2007
| 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/