Join us now!

Site Navigation

FAQ/Help

ALS For support and discussion of Amyotrophic lateral sclerosis (ALS), also referred to as "Lou Gehrig's Disease." In memory of BobbyB.

ALS/Lyme

Thread Tools

Display Modes

08-20-2011, 03:43 PM

Teacher123 Teacher123 is offline

New Member

Join Date: Aug 2011

Posts: 1

Teacher123 Teacher123 is offline

New Member

Join Date: Aug 2011

Posts: 1

Quote:

Originally Posted by MissClaireee

Hi, just a quick note to let you know that the article in question is written about my husband and myself. I'm happy to answer questions if you are curious about our situation. Even if you think it's all poppycock, my question is this:

If you are diagnosed with a terminal illness with no chance of effective treatment or cure, why on earth would you NOT explore the possibility that the medical establishment just might be wrong?

Cheers,
Claire

Hi Claire,

I was diagnosed with Lymes a few years ago, but now they are teling me that I have ALS. Do you have any suggestions for me?

Thanks,
Beth

Reply With Quote

« Previous Thread | Next Thread »

Posting Rules
You may not post new threads You may not post replies You may not post attachments You may not edit your posts BB code is On Smilies are On [IMG] code is On HTML code is Off Forum Rules

All times are GMT -5. The time now is 07:23 PM.

NeuroTalk Forums

Helping support those with neurological and related conditions.

All posts copyright their original authors.

The material on this site is for informational purposes only,
and is not a substitute for medical advice, diagnosis or treatment
provided by a qualified health care provider.

Always consult your doctor before trying anything you read here.

Site Navigation

NeuroTalk Online Support Groups

ALS/Lyme

NeuroTalk Forums