At age 26, Anthony was diagnosed with ALS. Though he will eventually lose the ability to move his body, his loved ones are helping him find ways to continue …
43 Comments
Although it’s strange having my personal life in the public eye, it’s always been important for me to be vulnerable. There is no other way to bring true understanding to a chronic illness like ALS. It’s been almost two years since this was filmed and a lot has changed… Laarne is now on her own journey with life and I wish her love and happiness. I don’t know if I will find love again But I am finding it within myself. This past year has made me a more resilient soul. I don’t plan on giving up.. My mom and I are still fighting together and I am doing my best to continue my photography despite my progression. ALS has brought my voice to a whisper. I got a new feeding tube. Last week. My life is painfully beautiful and I am grateful for every second of it.. I just need to continue to evolve with my circumstances. Thank you My Last Days team for all of your hard work and enlightened souls and my family for your unwavering love and support. I L O V E Y O U.
Maybe some of you would – like me – donate a little bit to Anthony's care, his insurance covers only a small part of it (he s in a worse condition now, as you can see here: https://www.youtube.com/watch?v=FqUAJBd-rKc – There s also a donation link in his youtube account to which my URL eads you…
ALS has taken 2 family member’s, a Father and month’s ago his Son. It does run in families and I cannot imagine what a challenge it must be to wait for that first sign of disease. This beautiful video is inspiring to anyone silently waiting for that first sign. I am truly sorry your struggle but I commend You, Anthony for Your Life and the way you Live it. Your Family is Awesome, just Amazing !
Why can’t the warmongers of the us administration see that this sort of love is what the world needs not their grasping violence and thieving of peoples dreams
Such a beautiful young man… It's not fair… Life can be so cruel with wonderful people… It makes me so angry. Good people usually get the worst and evil people enjoy a splendid life… I don't get it…
My first symptoms of ALS occurred in 2009, but was diagnosed in 2011. I had severe symptoms ranging from shortness of breath, balance problems, couldn't walk without a walker or a power chair, i had difficulty swallowing and fatigue. I was given medications which helped but only for a short burst of time, then i decided to try alternative measures and began on ALS Formula treatment from Herbal Health Point, It has made a tremendous difference for me (Visit ww w. herbalhealthpoint. c om). I had improved walking balance, increased appetite, muscle strength, improved eyesight and others.
My first symptoms of ALS occurred in 2009, but was diagnosed in 2011. I had severe symptoms ranging from shortness of breath, balance problems, couldn't walk without a walker or a power chair, i had difficulty swallowing and fatigue. I was given medications which helped but only for a short burst of time, then i decided to try alternative measures and began on ALS Formula treatment from Herbal Health Point, It has made a tremendous difference for me (Visit ww w. herbalhealthpoint. c om). I had improved walking balance, increased appetite, muscle strength, improved eyesight and others.
I lost a beautiful soul last year due to ALS. i found the most beautiful time was our eye contact towards the end. Her soul is always with me. This video was so human and I love each one of you ❤️?♥️♥️❤️
Our precious friend and a wonderful artist passed away from this disease. God bless you and your journey I pray you know the Lord Jesus because without him eternity is a long time.
Anthony, I'm praying for you, your beautiful wife, your Mother and for a cure for ALS, you are a giant of a man, with a spirit to match, God has a plan for you, wether it is to heighten awareness of ALS, or to show others suffering disease or limitation, that you can fight for life, and never give up. Thank you for giving so much of yourself, send my love and best wishes to your mum & your Angel of a wife.
My first symptoms of ALS occurred in 2011, but was diagnosed in 2013. I had severe symptoms ranging from shortness of breath, balance problems, couldn't walk without a walker or a power chair, i had difficulty swallowing and fatigue. I was given medications which helped but only for a short burst of time, then i decided to try alternative measures and began on ALS Formula treatment from Akanni herbal centre t, It has made a tremendous difference for me (Visit www. akanniherbalcentre .com). I had improved walking balance, increased appetite, muscle strength, improved eyesight and others.
Thank you for sharing your experience. I am very sorry that your wife left you in your time of need. You have a great support system. You are a true inspiration.
AMYOTROPHIC LATERAL SCLEROSIS (A.L.S.). Also known as MOTOR NEURONE DISEASE (MND) or LOU GEHRIGS DISEASE. It kills by causing the death of the neurones in the body that control voluntary muscles. There is no cure. 2 out of 100.000 people get hit with it. 10% of sufferers get it through inheritance and children born from an ALS sufferer have a 50-50 chance of getting the illness.
I'm a 19yold kid who is losing hair. I was so depressed when I find out, I even started to lose wieght. Even my friends start to notice there is something wrong with me. When I see videos like this I feel so stupid and grateful.
Precious video , have you looked into stem cell therapy ? I watched another video the other day where someone got that with your condition and it reversed a lot of the symptoms. God Bless
Anthony. Ok, I have fallen in love with you and your personality. We do have a couple of issues, one being your beautiful and funny wife, and the fact that I am forty years older than you! You are in my prayers, sugar. God bless you.
I was unable to watch the video as it would be too emotional for me. My maternal grandmother and my mother passed away from ALS. It is a cruel, rough way to go and it encompasses my thoughts every day. God Bless this man, my grandmother, my mother and everyone suffering from this horrible disease. The ALS Association was absolutely no help whatsoever and I believe they are truly profiting from this illness.
Although it’s strange having my personal life in the public eye, it’s always been important for me to be vulnerable. There is no other way to bring true understanding to a chronic illness like ALS. It’s been almost two years since this was filmed and a lot has changed… Laarne is now on her own journey with life and I wish her love and happiness. I don’t know if I will find love again But I am finding it within myself. This past year has made me a more resilient soul. I don’t plan on giving up.. My mom and I are still fighting together and I am doing my best to continue my photography despite my progression. ALS has brought my voice to a whisper. I got a new feeding tube. Last week. My life is painfully beautiful and I am grateful for every second of it.. I just need to continue to evolve with my circumstances. Thank you My Last Days team for all of your hard work and enlightened souls and my family for your unwavering love and support. I L O V E Y O U.
????
His mom is so pretty.
Omg I hate hate ALS. My friend Kate has it. She is like Steven Hawkins. Had it over ten years.
Maybe some of you would – like me – donate a little bit to Anthony's care, his insurance covers only a small part of it (he s in a worse condition now, as you can see here: https://www.youtube.com/watch?v=FqUAJBd-rKc – There s also a donation link in his youtube account to which my URL eads you…
I cried though the whole video.
ALS has taken 2 family member’s, a Father and month’s ago his Son. It does run in families and I cannot imagine what a challenge it must be to wait for that first sign of disease. This beautiful video is inspiring to anyone silently waiting for that first sign. I am truly sorry your struggle but I commend You, Anthony for Your Life and the way you Live it. Your Family is Awesome, just Amazing !
God Bless Anthony
I was in Idaho for the total eclipse. It was heavenly – can't put it into words. I'm so glad Anthony got to experience it.
Why can’t the warmongers of the us administration see that this sort of love is what the world needs not their grasping violence and thieving of peoples dreams
So beautiful what a gorgeous guy
Such a beautiful young man… It's not fair… Life can be so cruel with wonderful people… It makes me so angry. Good people usually get the worst and evil people enjoy a splendid life… I don't get it…
Beautiful connections you have made.
AMAZING!!!! LOVE ALL OF YOU!!!
My first symptoms of ALS occurred in 2009, but was diagnosed in 2011. I had severe symptoms ranging from shortness of breath, balance problems, couldn't walk without a walker or a power chair, i had difficulty swallowing and fatigue. I was given medications which helped but only for a short burst of time, then i decided to try alternative measures and began on ALS Formula treatment from Herbal Health Point, It has made a tremendous difference for me (Visit ww w. herbalhealthpoint. c om). I had improved walking balance, increased appetite, muscle strength, improved eyesight and others.
My first symptoms of ALS occurred in 2009, but was diagnosed in 2011. I had severe symptoms ranging from shortness of breath, balance problems, couldn't walk without a walker or a power chair, i had difficulty swallowing and fatigue. I was given medications which helped but only for a short burst of time, then i decided to try alternative measures and began on ALS Formula treatment from Herbal Health Point, It has made a tremendous difference for me (Visit ww w. herbalhealthpoint. c om). I had improved walking balance, increased appetite, muscle strength, improved eyesight and others.
I lost a beautiful soul last year due to ALS. i found the most beautiful time was our eye contact towards the end. Her soul is always with me. This video was so human and I love each one of you ❤️?♥️♥️❤️
God Bless You ❤️
I literally cried during the video since this was so sad…
You are amazing! God bless you and your wonderful family.
Our precious friend and a wonderful artist passed away from this disease. God bless you and your journey I pray you know the Lord Jesus because without him eternity is a long time.
His wife is so beautiful such a rock for him and a great care giver. But he is walking still. He should walk more often.
Its a generational curse that needs to be broken in JESUS CHRIST name amen.
Everyone should go subscribe to Anthony’s YouTube page, he is worth watching.
Anthony, I'm praying for you, your beautiful wife, your Mother and for a cure for ALS, you are a giant of a man, with a spirit to match, God has a plan for you, wether it is to heighten awareness of ALS, or to show others suffering disease or limitation, that you can fight for life, and never give up. Thank you for giving so much of yourself, send my love and best wishes to your mum & your Angel of a wife.
Beautiful!!
Family first ✊?
What an absolute braveheart! Sending prayers and love from Liverpool, England x
Compassion..you are great example in teaching others.. illness sucks..
You are awesome Anthony. Thank you for bringing us the awareness of ALS. You are an amazing young man and everyday I will hope for a cure.
My first symptoms of ALS occurred in 2011, but was diagnosed in 2013. I had severe symptoms ranging from shortness of breath, balance problems, couldn't walk without a walker or a power chair, i had difficulty swallowing and fatigue. I was given medications which helped but only for a short burst of time, then i decided to try alternative measures and began on ALS Formula treatment from Akanni herbal centre t, It has made a tremendous difference for me (Visit www. akanniherbalcentre .com). I had improved walking balance, increased appetite, muscle strength, improved eyesight and others.
Thank you for sharing your experience. I am very sorry that your wife left you in your time of need. You have a great support system. You are a true inspiration.
Thank You Mr. Anthony Carbaji. Thank You.
I admire your courage and your appreciation for living your life each day with purpose and joy.
They’re amazing ♥️beautiful couple ♥️
https://youtu.be/WblazNv83Yw do I have als
AMYOTROPHIC LATERAL SCLEROSIS (A.L.S.). Also known as MOTOR NEURONE DISEASE (MND) or LOU GEHRIGS DISEASE. It kills by causing the death of the neurones in the body that control voluntary muscles. There is no cure. 2 out of 100.000 people get hit with it. 10% of sufferers get it through inheritance and children born from an ALS sufferer have a 50-50 chance of getting the illness.
I'm a 19yold kid who is losing hair. I was so depressed when I find out, I even started to lose wieght. Even my friends start to notice there is something wrong with me. When I see videos like this I feel so stupid and grateful.
So sorry that you broke up with your wife, true love happens once and should last, I wish you the best of life, living for the moment is a game winner
Deceo con todo mi corazon ,que seas liberado en El nombre de Jesus y tu bella madre !
Absolutely beautiful. ❤️❤️❤️
Precious video , have you looked into stem cell therapy ? I watched another video the other day where someone got that with your condition and it reversed a lot of the symptoms. God Bless
Anthony. Ok, I have fallen in love with you and your personality. We do have a couple of issues, one being your beautiful and funny wife, and the fact that I am forty years older than you! You are in my prayers, sugar. God bless you.
I was unable to watch the video as it would be too emotional for me. My maternal grandmother and my mother passed away from ALS. It is a cruel, rough way to go and it encompasses my thoughts every day. God Bless this man, my grandmother, my mother and everyone suffering from this horrible disease. The ALS Association was absolutely no help whatsoever and I believe they are truly profiting from this illness.