That is wonderful Jan Rose Shaub, you said will take everyday and try to find something grateful about that day to make life worthwhile. That is truly wonderful! =)
Thanks to the ALS Foundation for helping those who can't help themselves and to help make a world without ALS.
What type of thyroid condition? Hypo or Hyper. Can this happen to someone that is young? (30 - 50 years old) How long does a patient have Frozen Shoulder, before surgery intervention?
Amyotrophic Lateral Sclerosis (ALS) aka: Lou Gehrigh's disease, is a relentlessly progressive paralyzing disease - most patients die within 2-5 yrs.
ALS is a death sentence w/no end in sight & the only way to further push for research is to get the word out. There is no known cure for ALS, but you can easily bring a thousand people the seed of hope.
PLEASE HELP SPREAD PUBLIC AWARENESS IN THE FIGHT AGAINST ALS AND HELP STRIKE OUT AND DEFEAT ALS.
Astaxanthin (ASTA-ZAN-THIN), the "King of the carotenoids!"
The most potent Antioxidant available to prevent neuro degerative diseases.
I'm so excited about this natural health nutrient I heard from the Dr. Oz Show on TV on 1/18/11, when he interviewed famous/controversial holistic medicine Dr. Joseph Mercola. I will recommend it to all my friends And family and anyone interested.
My Concern Is For The ALS Patients To Be Able To Have Care At Home Whenever Possible And A Nice Sub-Acute Care Nursing Home When Home Care Is Not Possible. I Am Hoping My Fund Raiser By Calling The Media And Getting ALS Patients Who Are Running Out Of Funds For Home Care And Dread Not Finding A Sub-Acute Nursing Home And Will End Up In A Hospital As A Unwanted Outlier. I Want To Know How Often This Outlier Problems Happens And If It Is True? Please Tell Me If It Is True
I Am Talking of Long Turm Care At Home Since Most People Rather Be At Home. Home Care Is Cheaper In Most Cases If It Is Possible To Stay Home. Pluse Their Are Very Few Sub Acute Care Nursing Homes For Specialty Care. Needing Hoyer Lifts, Ventilators, Feeding Tubes That Cost $40,000. to $50,000. A Month For Long Turm Care In Special Nursing Homes. The Sadest Thing Is Some Unlucky ALS Patients Are Left In The Hospital And Hospitals Don't Want Outliers Living At The Hospital At A Loss.
My Grandma had ALS and died of it when I was a child of 4 and then my Grandpa took care of me who died when I was 16. My mother could not take care of my brother and me because she had a mental disability and she lived in a mental halfway house until she was moved to a nursing home and died of old age. My am disabled now with a kidney disease any way thats my story. I am writting to ALS patients and or ALS care takers my plan was to fund raise for ALS patients long turm are needs.
My grandmother died from this disease in February of 1982 when I was just 9 years old. This video has moved me to find out what I can do in my area...thank you...
One of my friends was diagnosed with ALS a few years ago. He is in a wheelchair now, and he can´t speak very well. His arms don´t function properly, either.
guys, to any of you who has ALS, I bumped into a website.. please check it out. I hope it helps in anyway. h t t p : / / w w w . tcmtreatment. c o m / images / diseases / ALS-Report .h t m -- just delete the spaces and go to that URL.
My daddy just passed from ALS 3/1/09 This the hardest thing to deal with I dont no what to do. I still do not believe he is gone I love and miss him so! The advice I can give anyone who is going through this is be strong be prayerful and patience this is a very tough disease for that of who has and that of the family stay strong and spend as much time as possible with that person as possible!
My daddy has the same thing =/ hes still with us tho but is suffering tremendously. and yeah i take ur advice, my advice to you is its ok to cry and be sad but dont feel like your life is done, know that one day ull see ur daddy again just like i know ill see mine when he passes. know hes in a better place now and no longer hurting. <33
My goal here is to educate people on Lyme disease. I don't have ALS but I do have Lyme disease. Many of us within the Lyme disease community believe that some people that have been diagnosed with ALS, ALZHEIMERS, MS, ANOREXIA NERVOSA, ETC... MAY ACTUALLY HAVE LYME DISEASE. Wrote an informative LYME DISEASE BROCHURE with the help of 2 specialists that I will email to anyone.
im only 12 and my dad was diagnosed and i dont know wut to do about it, i no i need to spent alot of time with and help him when i can but my parents are divorced so i dont c him every day
Hi there- I am the one who made this video and my father was diagnosed when I was your exact age. Love him as much as you can, pray and try not to be hard on yourself if you can't be with him.
wow..my dad died from ALS about 5 years ago. it's so hard to watch someone you love get worse and worse by the day..and knowing you cant do anything to stop it no matter how hard you try,.i was only 9, but this is the kind of expeirence that i will never forget,. my thoughts and prayers are with everyone that ALS has or is affecting..rest in peace dad.
my dad has ALS and i am the youngest child of four at home helping my dad,but now its my time, like my siblings, to go away to college. im scared to go away knowing he needs my help. i want to stop this disease and i want to help others with it. my prayers go to the rest of you who are affected by this disease
Tomorrow my dad would have turned 64 if it were not for ALS. My prayers are out to those who have been forced to confront this motherf*cker of a disease. And to those who will. I don't think there is anything that can prepare you for the challenges this disease throws at you.
I can't even imagine the heartbreak one must face when confronted with a disease like this. It feels so unfair that people are robbed of their ability to be independent...thoughts go out to all those with ALS...
Please Sign My Petition To Support The Stem Cell Research Enhancement Act that could help my Brother (and thousands more) With ALS-Lou Gehrigs Disease. There are no Cures for these and many more horrible death sentence of Diseases.
Please Help! Go to i p e t i t i o n s .c o m and searach for als
That is wonderful Jan Rose Shaub, you said will take everyday and try to find something grateful about that day to make life worthwhile. That is truly wonderful! =)
Thanks to the ALS Foundation for helping those who can't help themselves and to help make a world without ALS.
RAINBOWLIZY333 1 month ago
my mom is 2 years into als thank you for this video but it seems like my mom hates life now
EXZ98 3 months ago
This has been flagged as spam show
What type of thyroid condition? Hypo or Hyper. Can this happen to someone that is young? (30 - 50 years old) How long does a patient have Frozen Shoulder, before surgery intervention?
530BigBen 4 months ago
This has been flagged as spam show
Amyotrophic Lateral Sclerosis (ALS) aka: Lou Gehrigh's disease, is a relentlessly progressive paralyzing disease - most patients die within 2-5 yrs.
ALS is a death sentence w/no end in sight & the only way to further push for research is to get the word out. There is no known cure for ALS, but you can easily bring a thousand people the seed of hope.
PLEASE HELP SPREAD PUBLIC AWARENESS IN THE FIGHT AGAINST ALS AND HELP STRIKE OUT AND DEFEAT ALS.
RAINBOWLIZY333 4 months ago
The video was insightful BUT some of the comments had me weeping like a little kid
LeStephane 9 months ago
Comment removed
LeStephane 9 months ago
My dad has als. I try to be strong for him and my mother. I cry when he's not around though.
HellFireKane 10 months ago
I know a man with this and feel so bad for him.
TheCircusfreak777 10 months ago
This has been flagged as spam show
Astaxanthin (ASTA-ZAN-THIN), the "King of the carotenoids!"
The most potent Antioxidant available to prevent neuro degerative diseases.
I'm so excited about this natural health nutrient I heard from the Dr. Oz Show on TV on 1/18/11, when he interviewed famous/controversial holistic medicine Dr. Joseph Mercola. I will recommend it to all my friends And family and anyone interested.
For sale in natural food stores.
GOD BLESS...
RAINBOWLIZY333 1 year ago
The391956 1 year ago
The391956 1 year ago
The391956 1 year ago
My grandmother died from this disease in February of 1982 when I was just 9 years old. This video has moved me to find out what I can do in my area...thank you...
newbiz09 1 year ago
very worth looking into
please send this link to any one you know D X ed with A L S
just delete the spaces and go to that URL to watch the important video
w w w . you tube.com/watch?v=3nIuIF6q8FA
i lost my mom to A LS and i wish i new then what i know now
God speed on getting this to your A L S loved ones
Scott
lsglookout 1 year ago
MY LIFE'S GOAL IS TO FIND A CURE FOR ALS....medschool here i come, hang in there :(, i love all of you!
safarsafar1234 1 year ago
They said that the cure is near.Back in 2004.Mom died 2006.Be as good as you can get!
Kunniatonpaskiainen 1 year ago
@Kunniatonpaskiainen :)
safarsafar1234 1 year ago
My dad had ALS,he died a little over a year ago i miss him so much
i hope they find a cure so that nobody has to go through so much pain
my pryers go out to all those living with ALS and thier familys
vivisloveswaffles23 1 year ago
One of my friends was diagnosed with ALS a few years ago. He is in a wheelchair now, and he can´t speak very well. His arms don´t function properly, either.
And he is the strongest person I know.
I hope a cure is found soon.
SagittarianMe 2 years ago
my dad has it and i o wow i cry wen i say it
edwardfan122 2 years ago
guys, to any of you who has ALS, I bumped into a website.. please check it out. I hope it helps in anyway. h t t p : / / w w w . tcmtreatment. c o m / images / diseases / ALS-Report .h t m -- just delete the spaces and go to that URL.
jasonism123 2 years ago
My Mom passed away due to this horrible disease on 02/06/09. If you would like to donate to the foundation please go to:
alsa org
djknucklez1 2 years ago
I would like to support or donate to this association (ALS) can anyone give me some info?
SaithTheLordMinistry 2 years ago
try googling it. probably alot easier than asking people on youtube. genius.
ariexmae 2 years ago
my hero, or uncle, to whom followed my into Christ furthermore- died 3 days ago from this disease.
buttpoop3 2 years ago
I am very sorry, God bless you and your hero.
SaithTheLordMinistry 2 years ago
Thank you.
buttpoop3 2 years ago
rip to your uncle
god bless
OSA503 2 years ago
great vid.. God bless
cautionblue22 2 years ago
My daddy just passed from ALS 3/1/09 This the hardest thing to deal with I dont no what to do. I still do not believe he is gone I love and miss him so! The advice I can give anyone who is going through this is be strong be prayerful and patience this is a very tough disease for that of who has and that of the family stay strong and spend as much time as possible with that person as possible!
thebaddest005 3 years ago
My daddy has the same thing =/ hes still with us tho but is suffering tremendously. and yeah i take ur advice, my advice to you is its ok to cry and be sad but dont feel like your life is done, know that one day ull see ur daddy again just like i know ill see mine when he passes. know hes in a better place now and no longer hurting. <33
mshecksxtc 2 years ago
HI great vid! my Mom died from als in 2002 ,,,thank you for the post
stephanoz 3 years ago
My best wishes to everyone with ALS . My favorite guitarist Jason Becker has ALS
punketron 3 years ago 3
I knew Jason had a disease, but not this, I got one of his cd's..
SaithTheLordMinistry 2 years ago
SIR STEPHEN HAWKING > ALS
whaththeeee 3 years ago
Hello everyone,
My goal here is to educate people on Lyme disease. I don't have ALS but I do have Lyme disease. Many of us within the Lyme disease community believe that some people that have been diagnosed with ALS, ALZHEIMERS, MS, ANOREXIA NERVOSA, ETC... MAY ACTUALLY HAVE LYME DISEASE. Wrote an informative LYME DISEASE BROCHURE with the help of 2 specialists that I will email to anyone.
Elaine in VA
ecftube 3 years ago
ALS sucks :(
KirstenRaeW 3 years ago 3
im only 12 and my dad was diagnosed and i dont know wut to do about it, i no i need to spent alot of time with and help him when i can but my parents are divorced so i dont c him every day
laxbeargoalie 3 years ago
Hi there- I am the one who made this video and my father was diagnosed when I was your exact age. Love him as much as you can, pray and try not to be hard on yourself if you can't be with him.
ziggyzalewski 3 years ago
This has been flagged as spam show
@laxbeargoalie hello im 13 years old my mom was diagnosed with it as well 2 years ago i am in the same boat
EXZ98 3 months ago
wow..my dad died from ALS about 5 years ago. it's so hard to watch someone you love get worse and worse by the day..and knowing you cant do anything to stop it no matter how hard you try,.i was only 9, but this is the kind of expeirence that i will never forget,. my thoughts and prayers are with everyone that ALS has or is affecting..rest in peace dad.
millyrock 3 years ago 2
My dad died from ALS!!! :( RIP DAD 06/12/07
singerstar678 3 years ago
my dad has ALS and i am the youngest child of four at home helping my dad,but now its my time, like my siblings, to go away to college. im scared to go away knowing he needs my help. i want to stop this disease and i want to help others with it. my prayers go to the rest of you who are affected by this disease
sccrplayainda916 3 years ago
my uncle died from similar disease which called GBS, very similar symptomp
Megadeth72 3 years ago
My father passed away last March(07) from this disease. He was 64. Hope there is a cure found for this disease. Thanks for the video and support.
Styxfansite 3 years ago
Tomorrow my dad would have turned 64 if it were not for ALS. My prayers are out to those who have been forced to confront this motherf*cker of a disease. And to those who will. I don't think there is anything that can prepare you for the challenges this disease throws at you.
turp63 3 years ago
ALS is so frustrating....im verry sorry for those people who got this disease..i hope they find a cure very soon...
cheers
skarbanan 3 years ago
I can't even imagine the heartbreak one must face when confronted with a disease like this. It feels so unfair that people are robbed of their ability to be independent...thoughts go out to all those with ALS...
stickyshooZ 4 years ago
You can say that again. My grandmother has ALS.
languagenut5 3 years ago
very touching...
DrumsHappen297 4 years ago
That is an AWESOME VIDEO!!!
FOBNOW2008 4 years ago 4
My dad has this, and its bad. My prayers go out to all of you who are affected by this.
I Love you dad.
SocDog72 4 years ago 5
Thanks for the response...continue fighting for a cure. My father also passed away from ALS. Prayers to you.
ziggyzalewski 4 years ago
My dad has ALS, too. Stay strong and know you aren't alone.
Kochi999 3 years ago
Excellent video!
bethandbill 4 years ago 3
great video... I miss you mom...
Goku4369 4 years ago 7
Love you mom and miss you!
iratic 4 years ago 4
my mom passed to because of this when i was in 5th grade!
this is terrible! they need to have a cure! i miss you soo much mom and love you!!! i know your smiling down on me!
swimlove28 4 years ago 4
Come join us on the Ride to Defeat ALS on 9/30 in Napa,ca.
deltahouse 4 years ago 4
Please Sign My Petition To Support The Stem Cell Research Enhancement Act that could help my Brother (and thousands more) With ALS-Lou Gehrigs Disease. There are no Cures for these and many more horrible death sentence of Diseases.
Please Help! Go to i p e t i t i o n s .c o m and searach for als
fightingforals 4 years ago 5