This is topic ISO ASAP-Lyme Dr & Neurologist-IL, IN, KY, MO, OH, TN-Prefer takes Medicare/Payments in forum Seeking a Doctor at LymeNet Flash.


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Posted by jjeennnniiee (Member # 7964) on :
 
Both myself and my mother reside in S.W. Kentucky. We both need a Lyme Literate Medical Doctor. I especially need a Lyme Literate Neurologist as well. Both ASAP!!!

Our Preferred States (in no particular order) are listed below. We can travel farther though, to other states, with the help of Angel Flight Ministries, if needed...

Illinois
Indiana
Kentucky
Missouri
Ohio
Tennessee

Unfortunately, myself and my mother are both low income. Myself, more so than my mother, but my mother can help me out some.

So, we would prefer that the doctors take Medicare or perhaps have a payment plan. It's not necessarily a requirement though. Just a preference, as far as being our best option, considering our poor financial situations.

If we can possibly find some doctors that do one or both, in any of the states listed above, that would be great. If not, then we're willing to consider what our other options are.

We just need a really great list, in order to get a really firm idea, of what all of our available options truly are, so we can make a solid decision.

Thank you very much. We really appreciate your help.
 
Posted by hopingandpraying (Member # 9256) on :
 
I don't know of LLMDs who take Medicare or offer payment plans. You would have to call their offices to find out.

I only know of one LL Neurologist and he is in CT. Does not take insurance and only treats neurological problems resulting from Lyme, not Lyme itself.

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

Maybe they can help.

Some more resources for you (including Support Groups info):

www.kentuckyindianalymesupport.org

http://whatislyme.com/websites-and-support-groups-by-state/

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

Here is a link found on Lymenet for "Financial Help and Other Information":

http://flash.lymenet.org/scripts/ultimatebb.cgi?ubb=get_topic;f=3;t=023463;p=0

The Lyme Disease United Coalition has good information for financial resources on their website:

http://www.lduc.org/lyme-disease-resources

Scroll down for financial help, etc., available from several sources.

The Lyme Test Access Program (Lyme-TAP) is a nationwide patient assistance program to provide assistance for initial Lyme-related lab tests to patients who demonstrate true financial need. I think coverage is up to 75%.
View on www.lymetap.com

"Help For You" link here...

https://sites.google.com/site/marylandlyme/help-for-you
 


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