This is topic Seeking LLMD In TX in forum Seeking a Doctor at LymeNet Flash.


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Posted by Sbright16 (Member # 49902) on :
 
Moving to state of Texas in 1 month looking for Llmd or integrative doc preferably that will accept insurance or Medicare. Not sure where to exactly in TX but I know I need to be in an area with majority of congregated doctors that can really help my Ill daughter if one decides to not help. I know TX is huge but am looking into dallas/Houston/San Antonio/austin area all the way to El Paso EVEN New Mexico if any are there. Ty
 
Posted by hopingandpraying (Member # 9256) on :
 
Welcome to Lymenet! PM sent for TX.

Your daughter needs 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. She needs 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 you call for an appointment, ask if there are 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/TexasLyme/info

Maybe they can help.

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

www.txlda.org

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

The top LLMD, Dr. H, has written a 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 http://www.veoh.com/m/watch.php?v=v21055812yWtmpgB8

Btw - I know you are new to Lyme, but please break up your posts into 2-3 sentence paragraphs, as there are people on Lymenet who cannot read large blocks of text due to neurological problems from Lyme.

To do that, click the pencil/paper icon, make your changes, then click "Edit Post". Thanks.
 
Posted by Sbright16 (Member # 49902) on :
 
I would like to further broaden my search beyond TX because from my understanding is TX is difficult as well.

I don't want to run across country with my disabled and totally bedridden daughter to the arms of possibly another state similar to what I am running from.

I got a few PMS suggesting Cali. Does anyone have any CALI Lyme Accepting doctors that will accept her medicare insurance so I can start research.

If anyone has a list I would love to review for most congregated doctors to narrow down if the move is a possibility even financial wise. Thank you so much for helping us in our journey in Lyme.
 
Posted by Sbright16 (Member # 49902) on :
 
It doesn't matter to me as far as location in CA or TX because it is something I must do at this point. I will go to where THEY are (hoping that there is an established group to chose from)


I will take her to Natural/holistic/LLMD/MD/Integrative Dr. willing to treat her and knows how to and is not scared of her because of her current state.


She worries doctors because she is "work" as she is bedridden. This is why I will go anywhere at this point. I have to help her in anyway that I can somehow.

Please medicare or the government assistance and if self pay something that can be under $500 initial visit and continued under "$250" if it exists.


I don't know if I can purchase an insurance for her that the doctor will gladly accept but I will go that route too if I need too.
 


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