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Great to see that this trial is finally underway.

thanks all. hope all is well! happy holidays!

Thanks all. Yes, I'm going to tell everyone I come across about this disease - I was scared enough wondering if I had it, I can't imagine those who actually sufferer - such a strong bunch of people- this forum is a testament to that. And as far as what my problem could be - he didn't really...

Haven't posted in over a month. Just wanted to say, finally saw the neuro-muscular specialist, he conducted a nerve conduction and emg and clinical stuff...and it turns out I do not have MND. I've had atrophy, weakness, fascic's, spasticity, over-active reflexes, swallowing difficulties, etc...

finally. awesome news. crossing my fingers as tightly as possible that this is going to prove fruitful. please God, anything at this point is a Success.

well I didn't crack it as in injure it. It just started popping and cracking when I lean back or raise my arms etc. so. will be seeing a doctor about this.

any other people experience this... this is increasing in frequency. it pops/cracks all the time now. sometimes really loud, it feels like the largest pop/crack I've ever felt right in the middle of the chest. it's scary because it's unpredictable now. i just lean back to look at something and...

not really that informative. but still... I hope this disease is slowed down SOON. The brief clips with the Dr. seems encouraging. YouTube- Mario Vella and an ALS research update

thanks guys. I'm waiting for an appt date with Dr. Pierre Bourque (thanks for the recommendation Glen)... hopefully some real answers will finally materialize then.

my weakness + atrophy are progressive. started asymmetrically, now on other side too. also, fascic's, and a host of other problems (i.e. - the aforementioned numbness, drooling, choking, etc., etc. .). Well see. Hope you find a definite answer too.