How This Works

We have a dear friend of ours that has ALS and every day I pray for a Cure or Miracle.Thanks for this awesome video.Let's turn despair into Hope like it says.
posted by Bernadette Walker on 10/04/07 6:59: PM

I can't get enough of this video! Iam in my 6th year with ALS. My best to Augie and his family. We PALS need to stick together in this fight Best wishes, Christina Moore 40 yrs/old.
posted by Christina on 10/04/07 5:40: PM

Yes, it's time to take this disease down. My father, Mr. J.P. Wadhwa succumbed to ALS on February 24, of 2006 and is missed. JP was of East Indian origin and lived [almost 50 years] and died as an Indo-Canadian. Although thought to be uncommon by many in the ethnic community ALS excludes No-Body; not by reason of Race, Colour, Creed, Age or Gender. And as it devours the majority of those that it afflicts far too hastily it behooves those of us left behind to speak out on their behalves and advance the cause. We, here wish every PAL and their caregivers/loved ones all the best. May God keep you and guide you through your respective journeys. And many thanks, Augie!
posted by Raj Wadhwa on 10/04/07 5:33: PM

THIS IS AWESOME!! i'm 15 years old and my dad died from ALS a little over 3 years ago and we just celebrated his 60th birthday a few days ago. life is completely different with out him....and i wish the best of luck with Augie's Quest.
posted by Mike harris on 10/04/07 5:23: PM

I LOVED this! I have ALS and this was inspirational because it shows that persons with ALS can choose to be happy!
posted by Maureen Garrity on 10/04/07 8:38: AM

I have had bulbar als for 2 years, its bad. I am hoping for a new medician to slow it down.
posted by Tommy Davis on 10/04/07 8:19: AM

GOOD LUCK TO YOU AND YOUR FAMILY. THOUGHTS AND PRAYERS ARE WITH YOU AND ALL THAT SUFFER FROM ALS
posted by debbie on 10/04/07 7:24: AM

I have been a Home Care Nurse for the most loving and sweet woman I have met in all of my years in nursing. Her name is Kathy Radick and she suffers from ALS. Even though I have worked with ALS before, it was only while a person was in the hospital and I didn't get a chance to know them like I have gotten to know Kathy. I have been working with her for several months now and it has brought me SO VERY MUCH MORE empathy for what this devestating disease does to people that are struck with it. I see pictures and videos of Kathy before her diagnosis such a short few years ago and realize how extremely cruel this disease is. Her husband, Keith and only daughter, Amy, have been more of an inspiration to me than they will ever know. I have had some major battles with my own health and getting to know this lovely lady and caring family have given me a new outlook on life. Kathy has done more for me than I will EVER be able to do for her. I HOPE AND PRAY for a cure and my thoughts are with EVERY SINGLE ONE of you out there that this is affecting... May God Bless You All.
posted by Jeri Sumner on 10/03/07 8:38: PM

motor nueron disese is a terrible thing. Let us all do what we can to find help for these people and their families. Let us help to give them hope.
posted by Virginia on 10/03/07 1:17: PM

My family's thoughts and prayers are with you. KIM
posted by Kim on 10/02/07 7:48: PM

Well, after a very long day at work...I needed to see something inspiring like this! I take care of the most incredible man I've ever known, Herbert Ransome, who was diagnosed with ALS in 1984. No, that is not a typo...he is one of the longest living survivors. He is so strong, and fights everyday to hold on. Somedays are better than others, and this weekend has been especially rough. As sad as it sounds, most people have given up on him, given up on believing that a cure can, and will be found. But I will NEVER give up on him. Herbie can no longer speak, and has lost all mobility, but I have never felt so much love from one person. He talks to me through his facial expressions and his eyes. No one seems to understand how I can have such a wonderful relationship with someone who can't say a word to me, but they just don't see what I see. When I look at him I see hope, and strength. One day...there WILL be a cure. I believe that with everything inside of me. Thank you all so much for supporting the desperate search for a cure.
posted by Melanie Gabor on 10/02/07 5:05: PM

May God Bless you in your search for a cure........ Your in my prayers...... My mom passed away 7 years ago from ALS.
posted by Barbara on 10/02/07 3:36: PM

I lost my husband three years ago to this dreadful disease. Thank you for the work and fundraising you are doing for ALS. I want this disease to be recognized as much as breast cancer or other dreadful diseases. I participate in the annual Walk to d'feet ALS to help raise funds and awareness for this disease. Everyone can participate in the annual walk in your area. Just contact your area ALS chapter. I remember to pray for a cure everyday.
posted by Patty on 10/02/07 10:59: AM

I just saw this video and it really brought tears to my eyes. My best friend and husband , Joe, got the official diagnosis 07/06 at the age of 41. We too were amazed at the number of people that this affects. Keep up the good work and hopefully a cure is in the near future. God Bless you and everything you do. Stay Strong!!
posted by pam on 10/02/07 9:21: AM

My Nephew-in-law died in March 2007. he had only been diagnosed with Motor Neurone disease for a very short time. My husband and I noticed something was wrong 2 years before. I advised him to go and see a Dr when they returned to Australia. Many tests were carried out but the outcome was inevitable, his worst fears were confirmed. Lif can be so cruel. As human beings we do not give up with out some sort of a fight but when the realisation dawns that nothing else can be done then we accept our fate. Any disease is a terrible thing but Motor Neurone Disease (ALS) is one of the cruelest. Keep up the good work and may you find a cure one day. Betty Mileham
posted by Betty Mileham on 10/02/07 3:26: AM

This remarkable video should help raise awareness. I don't know anyone with ALS but I was very moved.
posted by Tracey on 9/30/07 7:18: PM

I was diagnosed with ALS in November 2003. This video is truly inspirational and hope that it inspires everyone to join our fight against this horrible disease. Your efforts can make a difference. God Bless.
posted by Kirt Beasley on 9/30/07 3:17: PM

My wife Sylvia has just died after a 2 year fight with ALS. The love of family and friends we never knew we had kept us hopeful to the end. There is in fact a lot of good science happening now as to how ALS works. Finding a cure is possible with the dedication of wonderful people like Augie, the MDA and ALS TDI. I pray every day for a breakthrough. My love to all of you. Bill
posted by Bill Donovan on 9/29/07 9:25: AM

I have had ALS for 18 years. I am also a musician. Beautiful video and song, man. Thank you so much for what you are doing. Big love to you all. Jason Becker
posted by Jason Becker on 9/28/07 1:19: PM

I was diagnosed with ALS about the same time as most of the others shown....and I found the video most inspirational....it showed how so many others are coping with what is a most difficult situation.
posted by dick halpern on 9/28/07 12:42: PM