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» LymeNet Flash » Questions and Discussion » Seeking a Doctor » LLMD (in NY, VT, ME) needed for friend w/ ALS/Lyme

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Author Topic: LLMD (in NY, VT, ME) needed for friend w/ ALS/Lyme
Bobidor
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Member # 14453

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Hi,

A friend of mine just received her IGeneX WB results. She has bands 31+, 34IND and 41+ on both IgG and IgM.

She was diagnosed w/ rhumatoid arthritis 25 years ago, then with MS 10 years ago, and with bulbar ALS this spring.

I want to know if there are good LLMDs out there willing to take such patients. I would have tried with Dr. Martz, but I was told he retired.

Thanks for any help you can give. [Smile]

Julie

[ 09-20-2009, 06:07 PM: Message edited by: Bobidor ]

Posts: 209 | From Montreal, QC, CAN | Registered: Jan 2008  |  IP: Logged | Report this post to a Moderator
bettyg
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hi julie,

what are the closest USA STATES to where your friend lives?

please edit subject line showing 2 USA states in there, and then we'll do some looking for you ok. hugs/kisses


what is bulfar ALS? lou gehrid's i know; just don't know what bulfar is???

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Bobidor
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She lives in the province of Quebec, just above the American border (NY, Vermont, Maine).

ALS can present in what is called the "bulbar form", which first affects the neck, throat, tongue, before affecting the limbs. She can no longer talk, and she swallows with great difficulty. She only eats food in liquid form, and for that reason has lost a huge amount of weight.

I pray that it's not too late for her and that an LLMD can help stop the progression of her disease, and maybe even cure her.

Thank you...

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bettyg
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thx for more info and explaining that to me [Smile] hugs

check your profile for NY, VERMONT, & MAINE llmd info.

best wishes to your friend.

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Bobidor
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That's amazing, precious info, Betty. Thanks a million!
Posts: 209 | From Montreal, QC, CAN | Registered: Jan 2008  |  IP: Logged | Report this post to a Moderator
   

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