Living with Muscular Dystrophy: Blake's World
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- čas přidán 25. 07. 2016
- Limits have been put on Blake Leitch ever since he was born... initially he wasn't expected to live past the age of 6. He looks at life through a different lens, Now 21, he offers his personal insights into the world.
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Thank you so much for sharing your story, it really means a lot to see someone struggling with the same condition be as positive as can possibly be... So inspired by your motivation and will to live and want more for yourself. God bless you
Hes so inspiring, I shed a tear. And his siblings are supportive and wonderful too.
I absolutely love those smiles you can't see those smiles and not smile I adore them
Thanks for your kind words! Hope you enjoyed the episode!
These documentaries are all awfully touching and very well made. Hope to see more on the future. x
Thanks for your kind words Annie, hope you enjoyed the episode!
Attitude it's cool that you post this cause I have a type of leukodystrophy
annie w I agree wow Annie w you still have an account?
My expiration date was 28 yrs old,,, I’m 44 cuz only God knows when my time will come. N I’m also ok with that.
My son was born with type LAMA-2 muscular dystrophy.
Just watching some stuff cause I worry about him growing up, he's 2.
Utterly amazing human being...thanks for your positivity Blake...best wishes
Thank you for sharing Blake. 🙏🏽💚
I really enjoyed watching this
You are a very strong man, and I would like to congratulate for your path. You are a huge example for every one of us....totally agree with your opinions. God bless you and keep on having this amazing life. Thank you.:))
Great Job Blake!! 🙏🏽
Thanks so much for sharing Blake, You have a great personality.
Thank you for the problematizing the definition of disability and why that is an issue and for spreading this as knowledge
SysteMatic365 you can find me on CZcams as Yanet Cortez hope you enjoy like comment n subscribe so when I post your notified, p.s this sucks but I’m trying so hard cuz just like this genialmente I’ve been through so much frustration. Hope your ok god bless🙏🏼😘
I wish you all of the peace, love and happiness in the entire universe, good sir. You are a an amazing human being! ❤
Very good documentary.
I wish you the best sir
What aan incredible young man! Where can I find his music here om CZcams? He said he has his own channel.
Also me, I really love the music playing, so touching. He is amazing
Thanks this was interesting.
Thanks Bec!
Awesome guy with an awesome family.😊
Thank you for this documentary! I have spinal muscular atrophy and i'm always positive in life, about life but sometimes i do have negative days too. I have one more disabled sister too. She's 23 years old and has epilepsy and she's like 3 years old baby even she's 23 years old. And i'm worrying about what would/will happen if my parents gone because in Turkey there's no other person to take care of us except my parents. I'm so afraid of it. And i'm 20 years old and i want to be successful in life. I have big dreams. I hope one day i'll able to do it. I usually don't say these words and i don't know why am i doing this. Sorry. Anyways... Thank you again attitude for this nice documentary!
Thanks for watching Seda! Glad to hear you enjoyed the documentary 😊
Seda believe in allah.and always prey to allah.
May Allah bless and your family.
Amazing video. I understand what you are going thu I have the exact same as you, hang in their you're doing well. Your friends are lovely they have good hearts ❤
Thanks for watching Jamie!Hope you enjoyed our channel!
I love you Blake.
Thank you for sharing. So inspiring! ❤️
Thank you for watching Lori Watson!
My grandad had a muscular disease too. lived till 85 and had a lot of kids and grandkids. He didn't have a severe form of it but the asshole doctor told him he would for sure and die at 30 also. He actually was a pianist also.
Very attractive and smart
plzzzzz tell me whats the name of this song he made and where i can down load it
My son ,9 years diagnosed duchane muscular dystrophy out of frame deletion ,multiple exons 45-50 missing.......
The 7 people who disliked this video needs to be ashamed of themselves
So true I too have muscular dystrophy most people just don't get it and never will 😑😊
Bodene Davies I too have it n your right unless you going through it no one will ever know what we go through on the daily not only physically but mentally good days bad days happy moments sad moments n people want to get frustrated with us lol crazy but I don’t only think n pray for myself but for everyone 🙏🏼❤️ why can’t more people just b nice? Well I’ve decided to turn my condition into something that just is n there’s nothing I can do to fix it except vlog my story my struggles n good times in hopes that others sick or not can see that no matter what you going through you will get through it just pray n believe n I would like to invite anyone reading this to plz come visit me on CZcams, you can find me as Yanet Cortez, I hope you guys like comment n subscribe 😀thanks in advance
Justice Carter yes they should but maybe they thought thumbs down meant like they didn’t like the situation 🤷🏻♀️ sadly who knows unfortunately these days u never know, would you like to come visit my channel? I have MD too I’m 44 n we all have a purpose in life we just have to get through the hard times knowing that god is in control n our suffering will not b in vain, we all matter until recently I went through a serious depression tried suicide but God is good cuz both times someone walked in, thank god today I’m good enough to turn my story into something positive or atleast try to bring alittle bit of me to you guys,unfortunately my future doesn’t look like it’s getting easier but I’m not giving up! Make a 💪🏼 god bless oh my channel name is Yanet Cortez hope to see you over there,, and my instagram is Yanet.cortes.5 hugs kisses in advance hope you like comment n subscribe I will b making fun videos soon!🙏🏼😀
Hi am misty How s are you doing today I thank you show thank for your you show people who family my
How is your health now
Kya.muscular.distrophy.me.stemcel.traansplaant.karne.se.bimaari.thik.hoti.hai.pless.sahi.jaanjaari.de.plesss.pless
Any body of your known who was In Trials of exondy 51 or have used it does it really help ..........
can a person suffering from FSHD take protein supplements like whey or creatine?
Their muscles don't get any bigger, and with a lack of excersise it wouldn't have too much of an affect, it would probably just leave his system
I thought he and his brother Ryan lived in a flat wit friends/caregivers. Has that changed?
Hello , I am rajat ,delhi India can we talk
Do you take heart meds. And steriods.
People with disabilities i believe God made them carry the load because they are strong people. God bless you
Thanks for watching Mary, we hope you enjoyed the episode!
Mary Cook shut up.
the condemned fucked up world you seem bitter. Just because you have a chip on your shoulder doesn't give you the right to be rude to people. That's something you have to get over.
Why does there have to be a load. Is there an allotment for horrible afflictions some god has to upon us for their sick fantasy or something?
Hi am misty am I like.nice show I love you very much show I I have a happy ok nice do fun ADHD I like
Hope you enjoyed the episode Carri! Thanks for watching!😀
Looks like a discord mod
Grow up