Looking for a LLMD in NYC

Hi Yanique! I am so glad you finally convinced someone to test you, and you are one of the lucky ones to actually get a positive test, because Lyme bacteria are so evasive and testing methods in the labs aren't the best.

First, you need to go to your profile and enable members to see your email address. We can't/don't mention names on here on the forum, as it's public and our LLMD's get harassed.
There is a drop down option on your profile where you can ok the viewing option.
Someone with names can then email them to you.

Second, we encourage all new members to read over our "New To Lyme?.......start here" intro thread.
It's filled with a lot of valuable information to help you through your journey of healing.

LOL. I see you have just enabled your email. That was fast! Or I am too slow!

Here is a list of names. I have absolutely no knowledge about any of them. So you might want to call and ask all the particulars, price, treatment, etc.

/sites.google.com/site/lymedoctors/new-york

This might take them awhile to reply, but it is another option for finding a LLMD.

/globallymealliance.org/

If you use the global lyme alliance, could you let me know how it works out. I just saw this because of another member was using this as their donation site for Smiles.Amazon. I thought it was cool that they will refer a doctor.

Very interested in how fast they respond and if they suggest a lot of doctors or just one. Thanks. \

Good luck