I've recently been diagnosed with ALS and I now realize that there's, so many things I took for granted. For example, walking without stumbling, eating without choking, working, being able to open your hands. I challenge anyone reading this to figure out what you want in life and keep going after it, because life can be short.
RIP young man. Thanks for sharing some of his story with us🙏🏼 My wife was diagnosed May 2022 after her first symptoms (drop foot) began in the summer of 2021. We had just married Halloween of 2020. Her spirit remains bright most days. Keeping a smile on her face and comfortable is the daily goal😊 She’s pretty much wheelchair bound and speech is quickly weakening 😔 We listened to some old voicemails the other day and she cried, having forgot what she use to sound like. We’re going on our second cruise in less then two months, have had many parties with friends and family, traveled to Oregon for a month, all so recently! We knew we were in for journey and adventure and she’s doing everything to go out with a bang. She is my hero🥰
God bless. Time is short. I hope you spend it filled with love and understanding. Eat everything she wants. Go everywhere. Never argue. Always holding each other! ❤
@Science Review Thank you. Ironically, today is 2-27-2021. Her birthday would have been this Monday (3-1-1958). She was diagnosed on May 5, 2005. After her birth, she was placed up for adoption. It wasn't out of selfishness. It was out of love because her birth mother was unable to care for her. My aunt and uncle adopted her when she turned one and brought her into a loving home. She passed that love on to everyone that she ever met and never met a stranger.
I cried my eyes out... what a wonderful spirit he had. I can't wait to see you in heaven one day, Adam! Thank you for sharing your story & making me aware of so much. Your voice is still heard and continues to carry great purpose. ♥✨
The one commonality that I have noticed is that people with ALS can still smile even as the disease progresses. The other is how strong and somewhat accepted they are. Sorry for your loss family and friends.
Adam had great courage to share his story! My twin did not want to nor did she accept she even needed to see a Dr until bedridden and her hands were curling up! NO matter how I begged her...she saw a homeopathic quack and was taking over 100 herbal and other types of pills a day. hyperbaric chamber for 1 1/2 hours a day, infra Red sauna, activated charcoal. Colloidal silver and others...no matter what her very own twin asked her to do with getting diagnosed, I WAS REFUSED! She died miserably in an early chosen "Comfort Care and died quite painfully in two weeks! Unreal....ALS must be diagnosed as soon as possible and those people need the BEST CARE AVAILABLE! I have joined the ALS foundation as I was a care giver on weekends....most devastating loss of my life...tore me apart. I cherish very single day on earth and am at peace with her passing now. Its been 4 years!
"This is where im coming to die" OMGUDNESS.. THAT MADE MY HEART CRY!!! I wish I could HUG CERTAIN PEOPLE THROUGH MY SCREEN!!! TRULY IDO!!! that would be 1 wish I would want to come true!! So many SAD STORIES LIKE HIS ON YOU-TUBE... SO MANY PPL ID LOVE TO COMFORT WITH JUST SOME LOVEEEEEE FROM MY HEART!!!!
@@shawnmcanthony5724 thank you.. but it's just my feelings with the heart the good lord gave me.. I've been told way too many times that I'm way too sensitive.. but I think I'd rather stay that way then be like some people now a days.. know what I mean??...I have so much love in my heart... before I became disabled at 29.i worked in the nursing field..I would bring my children to work with me... my oldest daughter is now a nurse...❣️❣️ to me bringing my Littles with me to work taught them the most kindest of compassion... and a different kind of love ❤️
@@barbaraspieler1222 Barbara my wife is a mid wife an i can tell you she is the sweetest person i have met. Nursing i believe can mold someones personality. She loves what she does.keep on being sweet . Soon at isiah 33:24 it says no one will be sick in jehovah gods new world right here on earth like in the garden of eden.The blind will see again and the disable will run an skip about.
@@ruby4761 nah stop eating non human diet, every thing will be fine. The body heals itself when provided with right diet. See the gospel of peace for perfect human diet.
My father was diagnosed 4 years ago.He can't do anything for himself.He can't walk,his speech is barley understood,he drools alot and just wants to die.He hates the life he lives.It's such an awful disease.I wish he had the "I'm not going to let this disease stop me from living life" attitude but that's not the case.It's so sad and depressing to see him this way day in and day out,as I am his caregiver.I can't begin to imagine how he feels.We need to find a cure for this awful disease!
It absolutely is such a heartbreaking, devastating disease. A positive attitude can only last so long when your body is being taken from you. I pray you have much needed support. Cherish your time together (as I am sure you are).
I can relate, I lost my dad to ALS too. I know the struggle and don't be afraid to ask for help. Caregiving is both emotionally and physically challenging with no breaks, full time, stressful and depression can set in. Do you have anyone helping? Is you father still with us?
I just watched my dad die this weekend over this horrible disease.. My Dad was my hero and he chose they way he wanted to go.. He didn’t want a Vent and it was that time..
It hurts me and I cry so hard. All these people are gone. All these videos I watch they have all died. Where is the hope? This is the most hopeless disease.
I watched a bout a young woman at the age of 16 trying to fight this awful &’horrid disease. It honestly goes to show, this disease doesn’t discriminate against age, race or gender. Unfortunately this youth died within a year from ALS. But her story will always be embedded in my memory
Dude I’m dying of autonomic neuropathy been sick almost 9 years it’s a Fucking nightmare please try to find the will to not take your life man life is and can be very beautiful if you open your self to it and make it so … yeah it’a not always rainbows and unicorns but the other option is forever no matter what all the Bible beaters say there nothing else after this so live this one hard and compete
![[DRIP] ‘Woke Up In Tokyo (RUKA & ASA)’ PREVIEW](http://i.ytimg.com/vi/QN44lcR_VkI/mqdefault.jpg)
I've recently been diagnosed with ALS and I now realize that there's, so many things I took for granted. For example, walking without stumbling, eating without choking, working, being able to open your hands. I challenge anyone reading this to figure out what you want in life and keep going after it, because life can be short.
🙏🏼🤍
I heard you
Thank you
RIP young man. Thanks for sharing some of his story with us🙏🏼
My wife was diagnosed May 2022 after her first symptoms (drop foot) began in the summer of 2021. We had just married Halloween of 2020.
Her spirit remains bright most days. Keeping a smile on her face and comfortable is the daily goal😊
She’s pretty much wheelchair bound and speech is quickly weakening 😔
We listened to some old voicemails the other day and she cried, having forgot what she use to sound like. We’re going on our second cruise in less then two months, have had many parties with friends and family, traveled to Oregon for a month, all so recently! We knew we were in for journey and adventure and she’s doing everything to go out with a bang. She is my hero🥰
And you sound like the perfect hero husband. Wishing you both lots of love 🩷
God bless. Time is short. I hope you spend it filled with love and understanding. Eat everything she wants. Go everywhere. Never argue. Always holding each other! ❤
Gosh, I wish I could've hugged him. He has a beautiful soul
I lost my cousin to this on December 27, 2007. We all miss you, Pam.
@Science Review Thank you. Ironically, today is 2-27-2021. Her birthday would have been this Monday (3-1-1958). She was diagnosed on May 5, 2005. After her birth, she was placed up for adoption. It wasn't out of selfishness. It was out of love because her birth mother was unable to care for her. My aunt and uncle adopted her when she turned one and brought her into a loving home. She passed that love on to everyone that she ever met and never met a stranger.
@Science Review She was. I wish that everyone could have known her.
I cried my eyes out... what a wonderful spirit he had. I can't wait to see you in heaven one day, Adam! Thank you for sharing your story & making me aware of so much. Your voice is still heard and continues to carry great purpose. ♥✨
The one commonality that I have noticed is that people with ALS can still smile even as the disease progresses. The other is how strong and somewhat accepted they are. Sorry for your loss family and friends.
Adam had great courage to share his story! My twin did not want to nor did she accept she even needed to see a Dr until bedridden and her hands were curling up! NO matter how I begged her...she saw a homeopathic quack and was taking over 100 herbal and other types of pills a day. hyperbaric chamber for 1 1/2 hours a day, infra Red sauna, activated charcoal. Colloidal silver and others...no matter what her very own twin asked her to do with getting diagnosed, I WAS REFUSED! She died miserably in an early chosen "Comfort Care and died quite painfully in two weeks! Unreal....ALS must be diagnosed as soon as possible and those people need the BEST CARE AVAILABLE! I have joined the ALS foundation as I was a care giver on weekends....most devastating loss of my life...tore me apart. I cherish very single day on earth and am at peace with her passing now. Its been 4 years!
"This is where im coming to die"
OMGUDNESS.. THAT MADE MY HEART CRY!!! I wish I could HUG CERTAIN PEOPLE THROUGH MY SCREEN!!! TRULY IDO!!! that would be 1 wish I would want to come true!! So many SAD STORIES LIKE HIS ON YOU-TUBE... SO MANY PPL ID LOVE TO COMFORT WITH JUST SOME LOVEEEEEE FROM MY HEART!!!!
Barbara you're a sweet heart🌹
@@shawnmcanthony5724 thank you.. but it's just my feelings with the heart the good lord gave me.. I've been told way too many times that I'm way too sensitive.. but I think I'd rather stay that way then be like some people now a days.. know what I mean??...I have so much love in my heart... before I became disabled at 29.i worked in the nursing field..I would bring my children to work with me... my oldest daughter is now a nurse...❣️❣️ to me bringing my Littles with me to work taught them the most kindest of compassion... and a different kind of love ❤️
@@barbaraspieler1222 Barbara my wife is a mid wife an i can tell you she is the sweetest person i have met. Nursing i believe can mold someones personality. She loves what she does.keep on being sweet . Soon at isiah 33:24 it says no one will be sick in jehovah gods new world right here on earth like in the garden of eden.The blind will see again and the disable will run an skip about.
@@shawnmcanthony5724 🦋🙏❣️🙏🦋
extremely sad story, however it is one that we need to hear. so sorry for your loss.
ALS took him quickly. I too have ALS. i am still around. I am by myself.
So sorry to hear
I'm sorry to hear that.My father to has ALS.Hang in there and take it one day at a time.
God bless you
Donnie Raveling , me too. Diagnosed this past October, right now just my left arm and some of my right arm are affected. 🙏💕💕
ALS is a terrible diagnosis. I am sorry you have received it.
3 Canadians a day are diagnosed. 😲. Wow that blew me away. That's too many people. I wish we could find out how to cure this horrible disease. 😞
Stop vaccines and you could stop this.
@@ruby4761 nah stop eating non human diet, every thing will be fine. The body heals itself when provided with right diet. See the gospel of peace for perfect human diet.
Thinking of this horrible disease 😓. I’m wishing for a cure. And will try to support this important research for the cure. Love always. ❤️🙏🏻
@@ruby4761 most Stupid comment ever.
@@vishveshtadsare3160this has nothing to do with your diet.
My father was diagnosed 4 years ago.He can't do anything for himself.He can't walk,his speech is barley understood,he drools alot and just wants to die.He hates the life he lives.It's such an awful disease.I wish he had the "I'm not going to let this disease stop me from living life" attitude but that's not the case.It's so sad and depressing to see him this way day in and day out,as I am his caregiver.I can't begin to imagine how he feels.We need to find a cure for this awful disease!
you can get rid of it with the help of Dr Ayes medication
@@lindamarcia8481 You are an ignorant bottom feeder.
It absolutely is such a heartbreaking, devastating disease. A positive attitude can only last so long when your body is being taken from you. I pray you have much needed support. Cherish your time together (as I am sure you are).
It seems like people either fight like hell or let the disease determine everything. So sorry for your loss!
I can relate, I lost my dad to ALS too. I know the struggle and don't be afraid to ask for help. Caregiving is both emotionally and physically challenging with no breaks, full time, stressful and depression can set in. Do you have anyone helping? Is you father still with us?
This disease took him so quickly, it's really horrible.
God bless you Adam ❤️
My gosh this disease is cruel. Rest in peace Adam. It progress so fast. May god give you wings to fly
I just watched my dad die this weekend over this horrible disease.. My Dad was my hero and he chose they way he wanted to go.. He didn’t want a Vent and it was that time..
Too many are taken from us because there is still no cure.
I am so sorry.
I am so sorry.
So sorry for your loss! Only 10% of patients choose to do a trach.
It hurts me and I cry so hard. All these people are gone. All these videos I watch they have all died. Where is the hope? This is the most hopeless disease.
well that was tough to watch ... RIP good man
R I P god bless you adam❤😪😪😪
I didn’t know about als. Somehow I watched the video on TH-cam. This is heartbreaking.... we have to find the cure!
I watched a bout a young woman at the age of 16 trying to fight this awful &’horrid disease. It honestly goes to show, this disease doesn’t discriminate against age, race or gender. Unfortunately this youth died within a year from ALS. But her story will always be embedded in my memory
What a sweet man 🩷x
That's shocking god bless you ⚘🙏
I am being evaluated for ALS due to classic symptoms I am experiencing.
I'm pretty worried. If I am diagnosed, I will begin the MAID process asap.
Как вы?
How are you now? Did you get the diagnosis?
What totally sucks for me is how the beautiful... good people suffer . Sometimes I think I deserve to take their place.
Adam was an amazing person.
lastcall170 , we all get a cross to carry!!🙏🙏💕💕💕
Nobody deserves ALS. I know how you feel though.
I get you, and me too.
RIP Adam😢
Rest in peace
Very touching story, ❤️
R.I.P.
Horrible disease . RIP Brother
Praying for u😢
this is very sad I dont understand how he died from ALS in only a year
May Jehovah sustain you! Courage!
You must be a Jehovah's Witness to use the almighty's name found at psalms 83:18.
What an id10t comment. Take your religious buIIsh1t out of here
this is hard to watch
❤
Remarkable human. Had I been given the option I’d have traded my health for his. I fantasize about suicide. This man wanted to live. Life isn’t fair.
Don't give up.
Dude I’m dying of autonomic neuropathy been sick almost 9 years it’s a
Fucking nightmare please try to find the will to not take your life man life is and can be very beautiful if you open your self to it and make it so … yeah it’a not always rainbows and unicorns but the other option is forever no matter what all the Bible beaters say there nothing else after this so live this one hard and compete
@@GMHG777 isiah 33:24 says soon no resident will say i am sick in Jehovah gods new world right here on earth like in the garden of eden.
😭
Imagine thinking god has plans for all of us and then you get this disease. Like how you live a meaningful life?
But what if it is still meaningful though
God? 😂😂😂
R.I.p bro