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» LymeNet Flash » Questions and Discussion » Seeking a Doctor » looking for a llmd that takes medicare NJ

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Author Topic: looking for a llmd that takes medicare NJ
col951967
Junior Member
Member # 45637

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I am aware this may be impossible but I am looking for a llmd that takes medicare. I live in NJ. I am desperate. I absolutely Can not pay out of pocket for my treatment. I really wish I could, but I,am a single Mom has already lost her home and is now living with family, so finances are beyond tight. Right now I am not being treated at all.
Posts: 3 | From mount laurel, nj | Registered: Apr 2015  |  IP: Logged | Report this post to a Moderator
TF
Frequent Contributor (5K+ posts)
Member # 14183

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I suggest you contact the support groups in your state and surrounding states. They may know of someone.

Just click on Support Groups on the left side of the page.

Sometimes there is a doctor who is not exactly a lyme specialist but they are "lyme friendly" meaning that they believe in chronic lyme and are willing to give antibiotics to folks long-term.

These are generally regular doctors who see all kinds of patients. They take Medicare.

Hopefully, someone in one of the support groups you contact will know of such a doctor.

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

They are far and few between, unfortunately. 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":

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 to see a LLMD by doing this.

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

Maybe they can help.

Some more resources for you (including Support Groups info):
www.lyme-aware.org/new-jersey.html

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

Call the Lyme Disease United Coalition at (800) 311-7518. They are very knowledgeable and might know of someone.

The top LLMD, Dr. H, has written a new book entitled, "Why Can't I Get Better?". It is 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 www.hulu.com

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col951967
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Thank you! I have read the book and have seen the movie. I have been diagnosed and have been treated over a year ago, but with only 60 days of oral cephin. I have serious neurological issues and all joint and muscle issues have returned.
Posts: 3 | From mount laurel, nj | Registered: Apr 2015  |  IP: Logged | Report this post to a Moderator
col951967
Junior Member
Member # 45637

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Thank you! I have read the book and have seen the movie. I have been diagnosed and have been treated over a year ago, but with only 60 days of oral cephin. I have serious neurological issues and all joint and muscle issues have returned.
Posts: 3 | From mount laurel, nj | Registered: Apr 2015  |  IP: Logged | Report this post to a Moderator
   

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