Hi Steve, My name is Cathy and my brother (also named Steve) is living with ALS. After hearing your story, I'm compelled to express my gratitude. What you've done is remarkable and inspiring. After researching long-term care, I've been filled with despair as the options have become clear... Ironically, Steve was once a caregiver for senior citizens. He worked in a nursing home and was so popular with residents and their families, they offered him private work in their homes. He LOVED and cared for his patients. Sadly, sometimes more than their own children. I can't bear the thought of him lying in bed staring at the ceiling. I submitted an application to the Leonard Florence Center. It's a long shot, I know... Even if it's not feasible for him to live there, I'm so glad you're in the world. And I'm profoundly grateful for what you've accomplished for ALS patients everywhere.
Thank you Steve for your wonderful story with your powerful creative solutions to a living hell for so many.. I have watched your video several times and will show it to house visitors I have ALS though we call it in MND in Europe as you know. An initiative by media studies students in Dublin University resulted in the production of a video about my life. It's titled : MND my part in its downfall. I wrote a fantasy novel titled 'The Marshlander Chronicles.' which in one year has raised $5,500 for the Irish Motor Neuron Disease Association. I met all the publishing costs and kept no money for myself. I wish you and your family and friend all the very best life can offer.
neurotherapy is the only treatment of MND its stops the progression of mnd about 90% and you will feel better and able to do all works like eating walking etc.......My father has diagosned mnd and he had loss his muscles and his legs got paralises but he took treatment neurotherapist and now he will do all the works and walking again for some steps........its a new treatment plz atleast try this.........neruotherapy center tilak nagar new delhi india...🤗
I attended high school with Steve and remember his being an absolute computer junkie. So much so that, without him, I never would have passed the Intro to Computer Programming class. I remember our 20th high school reunion was a week after Steve got his diagnosis. We all thought that it may be the last one he would ever attend. HA! Meanwhile, 12 years later... I am proud to say that I have known a man who REFUSED go gently into that good night and, as a result, has changed THE WORLD for so many people who would otherwise be locked into Hell on Earth. Steve, there are few people who can say they have changed the world. You have, my friend. So honored to know you.
Such an amazing story Steve. SO much progress in such a short time. The disabled world is greatly improved because of your generosity and strength of spirit. Godspeed friend.
My boss was diagnosed in July with bulbar onset ALS. He is an older man in his 70's and is overwhelmed and depressed. I applaud your attitude, determination and accomplishments!!! God bless you for not only finding a productive way to live even with joy but also, thank God, you have also been able to give others with ALS a more abundant life. You are nothing short of amazing and you sure did use God's gifts to glorify Him. You used your wisdom to help yourself and others. I am sure your son is very proud of his fine Father.
You may want to consider that this god of yours (a god who watches horrific suffering with folded arms) is completely imaginary (or a sadistic thug). ruclips.net/video/FChIoVg2Nu4/видео.html
Wow, what an amazing life story. Thank you so much for sharing it: you are very inspiring to all! Hope to see one of 'your homes' in Quebec Canada one day...it's a dream for now but we can make it come true, as you demonstrated it so well! Big hug to you! Yes, life is good...
My ma died of ALS. I can't understand why someone would pray for someone you do not know. What are you praying for? Cure? What his/hers god is "the wrong one". This is the reason I became atheist when I was 15.
Hi Steve, My husband was just diagnosed with ALS on 5/4/20. Without doubt, your highly ambitious plan among the most ground-breaking designs for public and private constructions for ALS patients. My hat's off to you, Steve. Thank you so much for sharing your inspirational story. Love it.
Wonderful and touchy story Steve...It most be God's plan to use you to help many others, who are imprisoned by this disability. I am sure many of them doesn't know, there is a place like this exist. So accomplish your mission by reaching out and help them out...Good Luck.
als is is because fascia position adjustment mechanism which is energy consuming. When fascia move body gets asymmetrical. Adjustment mechanism eventually start for energy saving and kills muscle cells or more precisely neurons responsible for muscle control. It is much about recently discovered circulation in fascia.
@@classybooty that's horrible that our government won't help people in need of I were you know would keep fighting call attorneys etc but I'm sure you thought of that God bless
@@classybooty I'm 62 I 2017 my doctor told me I have als and they give my medicàre same day because als it's don't have treatment it's the reason you can have Medicare medical they can't denied
Hi Steve, My name is Cathy and my brother (also named Steve) is living with ALS. After hearing your story, I'm compelled to express my gratitude. What you've done is remarkable and inspiring. After researching long-term care, I've been filled with despair as the options have become clear... Ironically, Steve was once a caregiver for senior citizens. He worked in a nursing home and was so popular with residents and their families, they offered him private work in their homes. He LOVED and cared for his patients. Sadly, sometimes more than their own children. I can't bear the thought of him lying in bed staring at the ceiling. I submitted an application to the Leonard Florence Center. It's a long shot, I know... Even if it's not feasible for him to live there, I'm so glad you're in the world. And I'm profoundly grateful for what you've accomplished for ALS patients everywhere.
Thank you Steve for your wonderful story with your powerful creative solutions to a living hell for so many.. I have watched your video several times and will show it to house visitors I have ALS though we call it in MND in Europe as you know. An initiative by media studies students in Dublin University resulted in the production of a video about my life. It's titled :
MND my part in its downfall.
I wrote a fantasy novel titled 'The Marshlander Chronicles.' which in one year has raised $5,500 for the Irish Motor Neuron Disease Association. I met all the publishing costs and kept no money for myself.
I wish you and your family and friend all the very best life can offer.
hello bro.......you should try neurotherapy it stops the progression of mnd about 90% and you will be able to do all works
neurotherapy is the only treatment of MND its stops the progression of mnd about 90% and you will feel better and able to do all works like eating walking etc.......My father has diagosned mnd and he had loss his muscles and his legs got paralises but he took treatment neurotherapist and now he will do all the works and walking again for some steps........its a new treatment plz atleast try this.........neruotherapy center tilak nagar new delhi india...🤗
I attended high school with Steve and remember his being an absolute computer junkie. So much so that, without him, I never would have passed the Intro to Computer Programming class. I remember our 20th high school reunion was a week after Steve got his diagnosis. We all thought that it may be the last one he would ever attend. HA! Meanwhile, 12 years later... I am proud to say that I have known a man who REFUSED go gently into that good night and, as a result, has changed THE WORLD for so many people who would otherwise be locked into Hell on Earth. Steve, there are few people who can say they have changed the world. You have, my friend. So honored to know you.
Lol
Wow I think you have just, out done my respect for anyone else
Such an amazing story Steve. SO much progress in such a short time. The disabled world is greatly improved because of your generosity and strength of spirit. Godspeed friend.
Hello, this Silvia Murray. I enjoyed your story. Peac is a wonderful use for AlS.I am interested. I am 1 year into bulbar als in Texas.
Steve thank you for sharing your compelling story!
What a blessing you are sir. My very good friend was just diagnosed and will certainly pass this along.
Absolutely, Terrific!
My boss was diagnosed in July with bulbar onset ALS. He is an older man in his 70's and is overwhelmed and depressed. I applaud your attitude, determination and accomplishments!!! God bless you for not only finding a productive way to live even with joy but also, thank God, you have also been able to give others with ALS a more abundant life. You are nothing short of amazing and you sure did use God's gifts to glorify Him. You used your wisdom to help yourself and others. I am sure your son is very proud of his fine Father.
You may want to consider that this god of yours (a god who watches horrific suffering with folded arms) is completely imaginary (or a sadistic thug).
ruclips.net/video/FChIoVg2Nu4/видео.html
Wow, what an amazing life story. Thank you so much for sharing it: you are very inspiring to all! Hope to see one of 'your homes' in Quebec Canada one day...it's a dream for now but we can make it come true, as you demonstrated it so well! Big hug to you! Yes, life is good...
What an amazing man. What a blessing he was to a lot of people and helped others in so many ways... truly a man of courage
Keep up the wonderful work honey you are doing more than you know! God Bless You And Your Team!
You are awesome Steve!
Thank you Steve for sharing your story and God bless you.
My ma died of ALS. I can't understand why someone would pray for someone you do not know. What are you praying for? Cure? What his/hers god is "the wrong one". This is the reason I became atheist when I was 15.
Yeshua (Jesus) saves.
Life is good. Thank you for all the information.
You're awesome!!!
Your talents are worldly to the disable and to their families.Your inner beauty is amazing.
Thank you
You are an inspiration
What an amazing man.
Your story is amazing cousin. Huggs
Hi Steve,
My husband was just diagnosed with ALS on 5/4/20. Without doubt, your highly ambitious plan among the most ground-breaking designs for public and private constructions for ALS patients. My hat's off to you, Steve. Thank you so much for sharing your inspirational story. Love it.
You are amazing, sir
amazing
Respect
Wonderful and touchy story Steve...It most be God's plan to use you to help many others, who are imprisoned by this disability. I am sure many of them doesn't know, there is a place like this exist. So accomplish your mission by reaching out and help them out...Good Luck.
als is is because fascia position adjustment mechanism which is energy consuming. When fascia move body gets asymmetrical. Adjustment mechanism eventually start for energy saving and kills muscle cells or more precisely neurons responsible for muscle control. It is much about recently discovered circulation in fascia.
My mom was just diagnosed at 87. And this is wonderful
Thanks
Love u
You are pretty awesome 💚💛💜
Melanie
How are you
👏👏👏👏❤❤
#Steve I am a care giver to a patient, please assist him with the technology, I'll appreciate thanks.
That costs a lot of $$$$$$ and wear and tear on loved ones if there your primary caretakers. Would Medicare pay for all these interventions
I have ALS and no If you are younger than 65 and haven’t worked for 5 years no Medicare no disability. I don’t get no help after working 35 years
@@classybooty that's horrible that our government won't help people in need of I were you know would keep fighting call attorneys etc but I'm sure you thought of that God bless
@@classybooty I'm 62 I 2017 my doctor told me I have als and they give my medicàre same day because als it's don't have treatment it's the reason you can have Medicare medical they can't denied
god bless
use cannabis
dude, god bless you. But how did you get ALS?
Thank You