Hi - Just wanted to put this out there as an option for people in the SE PA area:
I recently started with a new LLMD in PA to treat Bartonella and I already have more confidence in him than my last LLMD. He seems very knowledgeable, understanding, and compassionate. The office staff are friendly, professional, and helpful.
Something surprising was that while he offered to order tests, he acknowledged their inaccuracies and said it might just waste money - that it was clear Bartonella was the culprit based on my symptoms/issues. This was a relief as I was dreading having to spend $1,000+ on Galaxy Lab tests.
Office visits are $180 - so not too expensive, relatively speaking. He often treats the Amish & Mennonite since his office is out in the area of Lancaster/Lebanon counties. I believe this is why his rate is so reasonable as it's hard to get significant dollars from people who live on a pittance.
It's an hour and a half drive for me but will be worth it. My visits will occur every two months, along with monthly blood test checks. Plus, I intend try to recoup some of the "out-of-network" cost from my insurance, if able.
PM me if you would like his name/number.
Posted by Bartenderbonnie (Member # 49177) on :
Good morning xoxoxox
Yes, I would like the name of this wonderful LLMD to add to my lists.
So happy you found a more adorable option, most LLMD's are so expensive it causes many Lyme patients to go without treatment. I still can't believe we do not have insurance coverage for LLMD's. MAKES NO SENSE!
Also a favor to ask. . There is a new poster who is looking for LLMD near Philadelphia for her 15 year old son who is struggling. Mainstream medical doctors are offering no help for this family. Could you please pm the name of the LLMD too?
Thank you so much. We are all in this together.
Posted by Lymetoo (Member # 743) on :
XO ... Someone also PM'd me for the name of a good doctor in Central PA.
Posted by xoxoxox (Member # 18778) on :
PMs sent to you both Posted by xoxoxox (Member # 18778) on :
Also, to note - this office does accept some insurances, just not mine (Aetna) so do ask about that!
Posted by Bartenderbonnie (Member # 49177) on :
Thank you Danni So very nice of you!
Posted by InUsITrust (Member # 52163) on :
Any referrals for a Lyme literate MD in SW PA? Pittsburgh or surrounding area?
New to this, but reading A LOT and already seems like I need to find a LLDR to cut to the chase. Any help appreciated, sorry to use this post but it already focuses close to where I'm looking. Thank you, Brian
Posted by Bartenderbonnie (Member # 49177) on :
I will send you a private message. Be sure to research each LLMD. Search for patient reviews. Connect with your local Lyme support groups. Lyme sufferers in your area will provide their first-hand experiences and offer valuable information to help you navigate the best way foward.
Also ulitize lymenet's 'search' function located in the middle of the page for all things Lyme. It is another tool in your arsenal box . Feel free to post any questions you may have and a Lymenet member will respond with their experiences.
Healing wishes.
Posted by hopingandpraying (Member # 9256) on :
InUsITrust - Welcome to Lymenet!
You need to be evaluated and treated by a Lyme-literate doctor (LLMD). Non LLMDs have no clue about this horrible disease or its complex treatment!
A LLMD is one who has treated Lyme disease and the co-infections which come with it for many years and has gotten patients well. A good one will follow Dr. B's Guidelines, the "gold standard" for Lyme treatment.
Unfortunately, LLMDs are far and few between. You need to go where they are.
Also most LLMDs do not accept insurance due to the politics surrounding this horrible disease. Read poster TF's explanation, "Why Lyme Doctors Don't Take Insurance":
When calling for an appointment, ask if they have any cancellations or a waiting list. Patients have been able to get in sooner by doing this.
I don't have any names of LLMDs for you in SW PA. Contact the Pennsylvania state Lyme Support groups. They would know better about PA and might be able to help you.
Read the books written by the top LLMD, Dr.H titled, "Why Can't I Get Better?" and "How Can I Get Better?". They are an excellent source of information.
Also "Cure Unknown" by Pamela Weintraub. Check your local library or buy them used online.
[ 07-27-2020, 11:27 AM: Message edited by: hopingandpraying ]
Posted by LisaK (Member # 41384) on :
Bonnie, that list (I find) on ILADS is not really up to date, unfortunately. and although there are many drs listed , some are NOT lyme friendly, meaning they seem to be into it for money or are not very qualified as others might be, etc.
I thought ILADS would have the best of the best on there. so I was disapointed - more than once.
Posted by Bartenderbonnie (Member # 49177) on :
Sorry LisaK
Did you fill out the e-mail to ILADS at the link above? I haven't heard it was out-of-date, I will look into it.
Anyone who is reading. . . . You must research all LLMD's referrals sent to you. To do this, Google for patient reviews or connect with your local Lyme support groups. A good LLMD is one who devotes a majority of his/her medical practice to Tick Borne Infections and has treated for atleast 10 years. This iwill give you the best chance for sucess.
Posted by marie (Member # 3980) on :
TF had a lot of information on the llmds with patients experiences. Wish she would return to site.
![[group hug]](graemlins/grouphug.gif)
Mainstream medical doctors are offering no help for this family. Could you please pm the name of the LLMD too?![[Smile]](smile.gif)