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» LymeNet Flash » Questions and Discussion » Seeking a Doctor » Doctors in CT, NY and MA

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Author Topic: Doctors in CT, NY and MA
Janesir
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Member # 27499

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Hello,

12 years ago I started Lyme treatment. I am feeling very badly now. Have been to top Lyme doctors already.

Looking forward to your suggestions.

Posts: 11 | From Goshen, CT | Registered: Aug 2010  |  IP: Logged | Report this post to a Moderator
TF
Frequent Contributor (5K+ posts)
Member # 14183

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The number 2 lyme doctor in the eastern U.S. is in Washington, D.C. and is currently taking new patients.

This is a great opportunity for you. This doc has been closed to new patients for the last 2 1/2 years.

You would only have to appear in person once every 6 months, so that is not much traveling at all. Let me know if you want the name. If I were you, I would go to her if at all possible.

There is a great lyme doc in Connecticut, but the wait to get in is 1 year. The D.C. doc should be able to see you in about 2 months.

I checked your previous posts and I see the docs you saw in the past. Some aren't so good in my opinion.

Posts: 9931 | From Maryland | Registered: Dec 2007  |  IP: Logged | Report this post to a Moderator
hopingandpraying
Frequent Contributor (5K+ posts)
Member # 9256

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Welcome back to Lymenet! PM sent for CT & MD.

So sorry you are still having health problems.

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.

Here is a link for them:

http://www.lymenet.org/BurrGuide200810.pdf

LLMDs are far and few between, unfortunately. You need to go where they are. At least half of all Lyme patients travel out-of-state to get proper care.

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":
http://flash.lymenet.org/scripts/ultimatebb.cgi?ubb=get_topic;f=2;t=025539;p=0

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.

Check the online state Lyme groups at:
https://groups.yahoo.com/neo/groups/ConnecticutLyme/info

Maybe they can help.

Some more resources for you (including Support Groups info):
http://whatislyme.com/websites-and-support-groups-by-state/

http://www.lymenet.org/SupportGroups/UnitedStates/Connecticut/

Read the books written by the top LLMD, Dr. H, titled, "Why Can't I Get Better?" and his new one, "How Can I Get Better?". They are an excellent source of information.

Read "Cure Unknown" by Pamela Weintraub. Get it at your local library or buy it used on Amazon.

View "Under Our Skin" for free on http://www.veoh.com/m/watch.php?v=v21055812yWtmpgB8

Posts: 8981 | From Illinois | Registered: May 2006  |  IP: Logged | Report this post to a Moderator
Tincup
Honored Contributor (10K+ posts)
Member # 5829

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Janesir,

So sorry to hear about your situation. Offering my opinion here, want you to know the following is not true.

Quote- "The number 2 lyme doctor in the eastern U.S. is in Washington, D.C. and is currently taking new patients."

With all due respect, please remember everyone has an opinion, and the one above isn't shared by me or anyone I know.

That said...

I am sharing below a large list of Lyme treating health care professionals names and contact info for you to consider. Narrowing down your choices by contacting their offices and reading their websites in advance may help pick someone more in line with your needs.

If you go to www.MarylandLyme.org and look at the menu to your left you will see "DOCTOR REFERRALS".

Click there to find the names and contact information for health care professionals treating Lyme & TBD's in your state (or any state). You may want to review options in states near-by also.

There is also a page with support group information, one for alternative medical professionals, educational conferences across the country, labs and their contact information, one for mental health providers, MTHFR and Morgellons providers.

There is also a list of TBD with how to diagnose (testing), a list of symptoms for each disease and treatment info with links to the treatment guidelines.

Hope that helps in your search!

Good luck and feel better soon!

--------------------
www.TreatTheBite.com
www.DrJonesKids.org
www.MarylandLyme.org
www.LymeDoc.org

Posts: 20353 | From The Moon | Registered: Jun 2004  |  IP: Logged | Report this post to a Moderator
   

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