This is topic MI LLMD? in forum Seeking a Doctor at LymeNet Flash.


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Posted by gardengal (Member # 23094) on :
 
I would like to talk to someone through PM about LLMDs in MI. please.
 
Posted by Lymetoo (Member # 743) on :
 
Information sent!!

Please read in Medical Questions for great information and help:

http://flash.lymenet.org/ubb/ultimatebb.php/forum/1

Each forum also has special links at the top of each page containing information you may find helpful.

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more ways to find a doctor ..

http://flash.lymenet.org/ubb/ultimatebb.php/topic/2/13239
 
Posted by gardengal (Member # 23094) on :
 
Thanks for that Lymetutu.

I'm not new to this and have already read or used all these resources. I was just wondering if any other docs had joined the ranks in my state in the last 1.5 years.

I find it frustrating that we can't talk amongst ourselves about these docs and if any one has any complaints about them. I research everything beyond completely when it come to my health.

Just because someone is an LLMD doesn't mean they are a great doctor. I know we have slim pickings though when it comes to who is willing to treat us and I'm sure thre are some great docs amongst them.

I've kind of lost my faith in the medical community after years of trying to find out what was causing my symptoms that just kept on piling up. But what choice do I have? So I'm going this route. I only know for sure I have connective tissue disease that has caused havoc in many areas of my body. Lyme could have caused it.

Sorry for the long post.
GG
 
Posted by Lymetoo (Member # 743) on :
 
Maybe someone will respond to this. All I have is an old list.

So are you being treated for Lyme??
 
Posted by littlebit27 (Member # 24477) on :
 
I'm not sure if my list is any more recent that Lymetoo's but I will send it to you just in case.
 


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