My heart aches for your precious and beautiful family , we’ve followed you quietly for so long on your journey and will continue sending you so much love x
So brave of you to do this video! My heart goes out to you. I hope you can achieve as much as you want to while you can. Sending love and strength to you. Xx
The most normal reaction to say in this time is " I'm sorry", but I don't want to say this. The reason why is because I'm going through similar situations as yourself. 12 years ago I got diagnosed with a type of muscular dystrophy, I am now in a wheelchair and on oxygen at home. I got told I would have 10 years max but ive already beaten this and the one thing I hated the most is people saying "I'm sorry". I would always tell people, please don't be sorry, atleast now I know and I know know more than ever that I need to enjoy life to the fullest. I need to live everyday as if it is my last because I don't know if I will wake in the morning. These first few days, weeks and possibly months will be the hardest for sure, but please, if there's one bit of advice that I can give you, it's to tell the people you love, that you love them, multiple times a day, ALWAYS go to sleep at peace with your family and tomorrow when you wake up, enjoy every minute but know "time doing nothing is never wasted" (book by james norbury, big panda and tiny dragon -highly recommend reading). Just being with your family is doing something 💛
Sending u so much love and prayers, your a beautiful and amazing person! Don't give up xxx
I have Als myself. Stay strong mentally and physically. The will to live needs to be stronger than the will not to. Go live my friend.
My heart aches for your precious and beautiful family , we’ve followed you quietly for so long on your journey and will continue sending you so much love x
So brave of you to do this video! My heart goes out to you. I hope you can achieve as much as you want to while you can. Sending love and strength to you. Xx
I have so much respect for you, Sam, for sharing. You are so right about the things that really matter,
Never ever give up, respect for you, our hearts and love goes to you in your battle, but never ever give up, miracles do happen
So, so sorry to hear this mate. Hope this disease hits you as slowly as possible. As I hope you have many year's to live normally as possible 🙏
I’m so so sorry to hear this! Live life to the max xx
Virtual hug 🤗 you have provided me with so much knowledge insight and resources praying for the best for you and your family
Sending you and your family lots of love 💙
I am so sorry to hear this. It can’t have been easy to share. ❤️
I am so sorry for you and your family ❤️
Sending love and hugs to you all xxx
I'm so sorry xx 🧡
The most normal reaction to say in this time is " I'm sorry", but I don't want to say this. The reason why is because I'm going through similar situations as yourself. 12 years ago I got diagnosed with a type of muscular dystrophy, I am now in a wheelchair and on oxygen at home. I got told I would have 10 years max but ive already beaten this and the one thing I hated the most is people saying "I'm sorry". I would always tell people, please don't be sorry, atleast now I know and I know know more than ever that I need to enjoy life to the fullest. I need to live everyday as if it is my last because I don't know if I will wake in the morning. These first few days, weeks and possibly months will be the hardest for sure, but please, if there's one bit of advice that I can give you, it's to tell the people you love, that you love them, multiple times a day, ALWAYS go to sleep at peace with your family and tomorrow when you wake up, enjoy every minute but know "time doing nothing is never wasted" (book by james norbury, big panda and tiny dragon -highly recommend reading). Just being with your family is doing something 💛