I am very sorry for your loss. I can’t imagine the pain of witnessing a disease like cancer slowly take away the life of a vulnerable child. I hope you’re continuing to heal to this day. The grief is endless but so is the love.
The child’s suffering is heartbreaking. Sometimes I feel like life isn’t fair, I can’t take it anymore but seeing the child’s struggle and her mother’s incomparable strength and love, I feel like keep going and never give up easily. We are so much more than we think we are.
@Read my channel description That's why the goverment is paying for she's treatment, the parents aren't even needing for donations. Stop believing in western propaganda. The chinese goverment care about human life in a way the US goverment will never, ever do.
“Your life may seem mundane to you, but it’s a life we can only dream of” This words right here just made me realize that I need to stop complaining about silly things and appreciate my beautiful healthy kids that I have Dear Duoduo parents I respect you so much for everything you do, you guys are amazing parents
‘There are other children suffering so we don’t accept donations.’ This, the level of humility even in such a distressing situation just broke my heart. Also Duoduo is the cutest little girl ever
Exactly my thought as well. These parents have such beautiful souls and I really hope a cure can be found one day for all the sick children. As a mother, it really breaks my heart to see other children suffer.
What a gorgeous beautiful little family. The fact that they don't even accept donations either because they think other kids may need it more, just so sweet.
How many of of us wake up every day and say our life isn't fair because I sometimes do but after watching this I feel so blessed just to be able to get out of bed.
@@animallover3904 comparison can help some people be more aware of what they DO have which can help elevate trauma. Comparison can evoke inspiration too. Just don't focus on it too much.
Me too! I found myself talking out loud while watching it all alone, "Awww, look at that smile!" "She's soooo adorable!" "No, Mom, you NEVER give up! Amazingly unexpected things can happen and you'll never know!" (Seems we are a bit like-minded, eh? 😊✌💕)
they are clearly overly emotionally attached to the baby , they should let her go as she's gonna have to spend the rest of her life on a ventilator and unable to walk , it would be like staying in a prison your entire life , sometimes its better to let go
I have a disabled child and I know how hard it is. Never give up they can't talk but they know. I cried all the way through that because I understand Love from the 🇬🇧
As a father of two kids myself, your the true heroes for not giving up. Never give up because holding the baby in your hands is the best feeling as a parent. I wish you the little angel many more happy, healthy and smiling years to come.
Sending love from Kansas, USA. My son Mitchel was born with SMA type 1 back in '92. There was so little known about it then. He loved music and bubbles. And people. He was a happy little guy too, like your precious Duoduo. I wish you all the best. My prayers are with you. And I'm so happy that Duoduo was born at a time when there are treatment options to help extend her life. Though most will not understand, I know exactly what you mean by feeling support and love from her. These are very special tiny humans ❤️
I had a cousin who had a brain aneurism at 19. Remained in a coma for 30 years and finally passed away from an infection. Many people are pro-life no matter what. If the quality of life is severely affected and the person only knows pain and medical procedures, they should be allowed to go with some dignity. I know it's easy for me to say, not being a parent of a child in this state however, I watched family members cling to hope for decades and unable to let go, until the choice was taken from them. Very difficult situation.
There have been cases where parents have gone to extraordinary measures to prolong the lives of children who were born with little more than a brain stem and they always seem a little perverse to me but this little one still seems to be engaging with the world and finding enjoyment from her experiences so I can’t say the parents are being selfish
As a parent myself, nothing can crush my soul than seeing my child suffer. Hope everything works out for this family specially their little angel. Wishing them all the best.
As an ex volunteer( live in) in disabled home , it is extremely stressful & difficult for whoever take care disable child & her condition is extremely hard for the mum. Whether to give up or not is her decision & we need to respect her. My salute to this lady & hope whatever the outcome she shld be proud of herselves. Be strong.
We all feel the same things. It doesn't matter where you live or where you were born. This poor woman is stronger than me. Nobody deserves to live that way.
Wow!! I've NEVER heard that before but you speak the absolute TRUTH!! AMEN!! to that comment. Motherhood is a double edge sword for sure. We love our children SOOO MUCH that we suffer when they are hurting and it's a PAINFUL thing.
Судя по всему, у ребёнка генетическое заболевание или аномалии внутреутробного развития. К сожалению, такие тяжёлые дети редко доживают до совершеннолетия.
I just had a mental breakdown and even thought of ending it all but then I came on to youtube and saw this. I have to keep fighting because I'm privileged justvto be alive. Baby girl is lucky to have such great parents. All the best to her
You hang in there too you hear me? Your life is no less important than hers and to the people who know and love you. If you ever need to talk or help, please reach out darling, ending your life is never the solution. Please remember that you are important, you are loved, precious and most of all STRONGER than you will ever know and no matter how bad life gets, it always gets better.❤ my prayers are with you friend ❤please take care of yourself 😊
I literally have a cousin who is now 10 + years old. She has a condition called cerebral palsy which basically means, her normal developmental milestones are impaired. From simple muscle movement, to speech to swallowing. When she was born, She was immediately put into an incubator because of premature delivery (6months or something) She spent more than 6 months in the neonatal ICU and after that, She had to be hospitalized for another few months for close monitoring. Upon growing up, She literally needs to be fed with special precautions due to very high risks of choking Her mom literally had to give up her career to be her carer 24/7. At some point, my mom would go to their house to assist with my aunt in caring the child. Imagine 10 years of this, Countless hospitalizations, Literally everyday of sleep deprivation on the part of my cousin's parents. A mother's love is indeed immeasurable..... We love the child (my cousin) But I really wished things would have been different with her..... Life is really unfair... But this teaches me to be more grateful of the little things I have in life.....
@@directioner2870 I didn't say it is easier. The point I'm making is: parents will love their child unconditionally and are willing to give up everything.. Also . Just so you know, My cousin, who is now 11 years old, Never got to experience normal childhood She is literally totally dependent (till now) and for the rest of her life. Her upper and lower extremities never got to develop normally, Even her ability to talk never really improved.. I'm not saying this to complain about how life unfair is But I'm saying this to let you know that not all cerebral palsy case is "easy".
Hi! Your cousin is so strong and brave. Take care and love her more. They are so special that what they need also is a special and unconditional love. Spend more time with her. This may sound silly but I'mma say this: Take pictures and videos together. Each moment is very very special :) I am really hoping and praying that there will be a very efficient and effective treatment for cerebral palsy that will make people who have that disease experience a normal life. I hope that I can do more for them.
I first watched this a year ago…my heart broke for this family. I’m wondering how they are all doing now, and hoping that they are well and happy. Sending love from America ❤❤❤
Oh my heart..... I have tears while watching this child loved by her parents. They are so so strong and deserves a miracle. They don't even request donations. I pray pray Duo Duo can recover and live a normal life or at least will everyday feel her parents love and warmth towards her. It's too tough making decisions like this.
It's hard to say On one hand, they're just prolonging her suffering On the other hand, you can't just let someone die without trying Tough situation to be in
Exactly.. and if her parents to suddenly die, what would happen to her who needs 24 hour care?🥺No one would be as dedicated as her own parents.. I keep thinking about this..
The thing is, for how long? These procedures look expensive, I'm glad that they are able to afford them. But if nothing changes, if she remains the same - choosing the toughest option would be a blessing for her. How would she survive like this when she grows up?
I cried watching this. Thank you to the parents of DouDou who never get tired taking care of her. I wish and pray that DouDou will be healed and all of you will enjoy life altogether.
To the entire team helping this young girl, thank you! You deserve all the goodness coming your way! Looking forward to seeing her make a full come back.
This was incredibly beautiful as well as humbling. I hope with all of my heart that this child and her family experience great miracles and a happily ever after. 💙
Да.современная медицина сильна. Почему не вылечили, или в утробе не определили аномалию. Доктора обещают, если бы государство не платило бы деньги больницам за больных сколько вылеченных было-бы. Везде только бизнес.
Duoduo is a beautiful little girl. She is incredibly blessed to have such wonderful, loving, dedicated parents. Wishing Duoduo a happy pain-free loving life and many blessings. 🙏🥰❤️
I'm a 53yo heavily tattooed old rascal who's been around and been through a lot so in general not much gets to me, but I'm not ashamed to say a couple of big heavy tears rolled down my face watching this. Love is love regardless of all the other negative things in our world.
Me too big guy. I cried my eyes out watching this, the poor innocent little face smiling back at her parents and holding onto what life she can and her parents just fighting to keep her comfortable and alive is shattering.
I have a daughter myself, so blessed that she's healthy. This girl's situation really breaks my heart, no child should have to go through something like this.
Adversities can wake up our inner strength, wisdom and courage. Very touched by this very dedicated couple. The illness aside it looks like Duoduo has grown well. The situation will only get better. All the best 🙏
I bow down to both of you for being loving parents. I am a single mother of 18yrs special child. My mother left me when I was 15 for the sake of her second marriage. For the past 17 yrs, without any family support and lot of financial crisis I didn't leave my daughter bcoz I have undergone the pain of being left for selfishness. My daughter is completely dependent on me. Hats off to you, especially to the father bcoz he has overcome the society and relatives to continue being loyal and caring to his wife which gives her strength to face all these. Nice couple.
Her mother's tears bought tears to my eyes. I'm also a mom to a 3-month old girl and Duoduo has some resemblance to my daughter. Hugs from one mom to another.
I really don't know what to say. If the child has the will to live and wants to live then I say support her. Otherwise I do think her in pain and the poor quality of life is too sufferable for her.
the problem is , a child doesn't have a will , they do not understand anything that's happening , they cry if it hurts , sleep if they are sleep , smile when they are happy , they do not understand what's going on
@@shukrantpatil that's also a moral dilemma. I do believe an individual, at a certain age, children included, are capable in making this life or death decision. As long as they understand what death entails and it is legalized then they should have the right and the decision to continue or end it.
@@onion4464 yes. Exactly. That's why there's a dilemma. A parent's love for her child, hence why her mom can't let go of her child. A parent can only think of saving her child and prolonging the life. But there's also a different perspective...is prolonging the life of a child that is in constant pain and in a very poor quality of life the "right" decision. It's a grey area, not black and white and no right or wrong. It's a debatable question that there is no definite answer to.
@@onion4464 It is easy to say, because the obvious is quite clear to the passerby. As family, people tend to not let go even though they know it may not be the best decision.
The kind of video I could never finish watching. Totally heart wrenching. Her parents are giving it all with no reservations at all. I only wish her family can find peace and acceptance down the road.
I’m so happy she’s doing better and her treatments are working. As soon as the video started playing I broke down like she was my child. I love her strong and her parents encouragement to stay by her side. Geez the love we give our kids ❤❤❤
I’ve seen lots of documentaries about babies and children with life threatening illnesses, but I’ve never cried over them, this one got me, it’s the moms reaction to living with her daughter and saying that maybe our lives are mundane but that’s what they would like, my husband died and I’ve been through so much, but this mom made me realise that my life has and is not as bad as I thought! Kudos mom!! You’re fantastic!!! I’ll pray for you all.
This is inspiring. How much her parents love her and treasure her even through struggle. They're right that we should be grateful for any normalcy in our lives
As long as she is trying to survive and her condition is ok, I think she is having a great life with such a strong mom/family... such a hard decision to make:(
Thank you to these wonderful parents for allowing this video. You've given us all a gift, of thankfulness for what we have. You are a beautiful family and I hope your little darling's life improves. Love from Australia
The parents should receive the "Parent of the year"award, but most likely their satisfaction comes from seeing their daughter enjoying life to the fullest.
"Worst parents of the year award"* that kid is suffering everyday and will even more when they have enough awareness to realize they will never live a "normal" life. Humans were not put on this world to live like this, this is sickening, and should be outlawed. To poor child is living a life of suffering and hardship, simply because the parents can't make the right and loving decision of letting go to stop this. Imagine yourself in this situation.
I know they are trying hard to help her but is she really happy? She is probably in a lot of pain and suffering and I understand it's hard for the parents to end their child it would still make the child hopefully be much happier in heaven, I remember being in hospital really young and I was in so much pain I just wanted to die
There was visual progress, that progress indicates hope, were hope is found it encourages us, gives us strength to continue to be courageous in a overwhelming medical situation, although there burdens are many, its accepted as a labor of love, they care, they are trying to make it the best they can, what the child's future will be like 5 years from now will be hard to guess, where there is hope, one will still try...wishing the family there best, prayers for strength and miracles......
I am in tears watching this, I hope the little baby will survive this catastrophe and be a very strong person in the fure. The parents are a role model too.
Qué importante es valorar lo evidente que no es tan evidente! Gracias a almas como esta niña que viven estas duras experiencias crecemos en AMOR. Qué Dios la bendiga y a toda su familia! 🙏
Your daughter has the most beautiful smile, thankyou for giving her a chance your are truly inspiring. You are not alone out there, we are a large community with children of special needs, every moment we spend with them is a blessing, a true blessing.
I take the time to share these types of real life stories with my tween kids so that are always reminded how blessed they are...and that some of their issues are nothing in comparison. Im not the little girl's mother but i felt so proud and deeply happy seeing her little hands at work. And her smile is priceless...
People asking the caregivers to let their family member suffering from rare or/and serious diseases go probably haven't experienced something like this in their entire lives. As a caregiver of a family member suffering from a very serious rare disease, i can tell everyone here that even if we consider something like that for once, we get scared of actually doing it as soon as we look at their faces. I'll continue to sleep for only four hours for the rest of my life if i could see her face after waking up daily.... It's just that's how much I love her. Even a daughter's love knows no bounds.
My sister is handicapped, my mother has been her caregiver for 40 years. There comes a point we are all ready for her to pass in peace. My mother wants her to pass peacefully when it's her time. If she was on a vent they would of pulled the plug and I would of supported them. Working in healthcare you learn quick what quality of life is and what it isn't.
As someone who had my grandma at home for 10+ years suffering from an illness that is not Alzheimer but a similar and unpopular and not as much researched illness which basically made her an 80 kilo baby while I was growing up, everybody was suffering and it destroyed the familly. I still remember the look on her face when we had to remind her of her late husband and she remembered in one of her rare moments of semi clarity. As you put it people are "scared" to do the right thing, when they are gone already they are already gone. There's a point where the person has to go and the family is the only one holding on not being able to let go only making everyone suffer more.
There is nothing that can break a mother's devotion and love to her child...
Unless she never had any love from the beginning
Do mercy to girl, don't torture her
Or a Father's love
Not always’!
Not for all mothers. Speak for ur self and some but not all.
This is so heartbreaking. Really praying for miracles to happen and this girl will fully recover.
your literally everywhere but i agree this is saddening I hope she will fully recover and have a wonderful life filled with happiness
@Huang Jianhao why what did he do?
Are still watching this channel
@@ariktochowdhury9122 at least he has actual contents unlike Justin Y
Bruh you don’t work ? Every time I have some spare time to watch you tube and check the comments I see you 👀
Just realized how blessed a normal child is. Be safe and healthy everyone.
Благословенны все!!!Тем более Дети.
And remember to always be thankful
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This is NOT A BLESSING, let this child go, no more pain on the other side
Jesus christ will bless her ✝️✝️
I feel the mothers pain😢
I lost my child in cancer,seeing them struggling to live,their sufferings we cant bear..
I am very sorry for your loss. I can’t imagine the pain of witnessing a disease like cancer slowly take away the life of a vulnerable child. I hope you’re continuing to heal to this day. The grief is endless but so is the love.
I am very sorry for your loss 😢
It’s seems really hard ❤
You can do this and it’s okay to be sad
Extremely sorry for your loss. Bless you, I hope you give birth to a healthy child.
My sincere condolences to you, melodykipgen5. I cannot imagine the pain and sadness you’ve experienced. ❤️🩹
little girl couldn’t ask for better parents then this couple, all my respect and I wish lot’s of beautiful moments for this family!
🙏🙏♥️♥️♥️♥️
Better parents? ?
❤️
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@@bluecolor555They mean more better than them
The child’s suffering is heartbreaking. Sometimes I feel like life isn’t fair, I can’t take it anymore but seeing the child’s struggle and her mother’s incomparable strength and love, I feel like keep going and never give up easily. We are so much more than we think we are.
@Al Haqiqi LIVE | HAALAN bruh
@Al Haqiqi LIVE | HAALAN هل نستطيع ألا نفعل؟
The mother needs to let the child go. The child cannot live like this
@@phole1100 That’s like saying that an Autistic person needs to be put down due to the inability to communicate, cut the BS!
@@neverangel24officialytchan87 are you really comparing a child who cannot breathe or even move on their own to an autistic person?
Its easy to say "let go" when its not your child. Shes a mother and no matter what loves her baby the most. Its damm sad
Ok, but she is thinking Just about her pain, and not in the child, that's selfish.
@@tophi5358 man you have a point there. Imagine the amount of pain the child is experiencing
@@tophi5358 i hope you never get a child
@@naikiklis I won't. I would never be that selfish.
@@tophi5358 it's easy to say, when it's not your baby or happens to you. It's a dilemma situation for this one not all the answer is black and white.
the parent's love and willingness to care for their daughter no matter what is amazing
When that baby smiled, i cried. Cant hold it. Hang in there lil angel
same here 😭
Same here
@Read my channel description That's why the goverment is paying for she's treatment, the parents aren't even needing for donations. Stop believing in western propaganda. The chinese goverment care about human life in a way the US goverment will never, ever do.
I know how you feel.
cam on ban chia se
I couldn’t sleep when my toddler was having a fever. I can’t imagine the pain this mom and baby are suffering. I wish them all the best of the best!💕
Definitely Im sure she has anxiety now
😘
Ela é linda demais Jesus abençoe essa criança anjos de Deus
@@elieneportugal2124 Why bless after cursing them? They already decided what they wanted for the child...
Me too
Heartbreaking. Courage and strength to the family.
Thanks
@Noogle Noodle That's rude
@Noogle Noodle No. Eat halal meat 👍
@Noogle Noodle But,the prophet of Muhammad SAW, Never teach to us about bullying to other people who we don't know about.
@Noogle Noodle Look man, Im not Chinese alright, im From Indonesia 🇮🇩. And i'm Muslim
I started crying I hope this baby gets even better than she is now ❤️
DIOS LOS BENDIGA.
NADA ES IMPOSIBLE PARA DIOS.
@@isabelramirezsancho2547god is not keeping her alive, machines are.
U r a noble soul
She isn't going to be A valuable one here,she will just remain the part of the system that can be replaced
@@SoJangHo37Why would you ever say that??
“Your life may seem mundane to you, but it’s a life we can only dream of”
This words right here just made me realize that I need to stop complaining about silly things and appreciate my beautiful healthy kids that I have
Dear Duoduo parents
I respect you so much for everything you do, you guys are amazing parents
Beautifully expressed.💗
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U r Right dear sister 💞
@@calihipechik7657 ❣️
And ALL THIS TIME SHE IS SUFFERING BADLY F*THE DOCTOR OF CHINA JUST GOT TO CARE ABOUT PATIENTS
‘There are other children suffering so we don’t accept donations.’ This, the level of humility even in such a distressing situation just broke my heart. Also Duoduo is the cutest little girl ever
They probably dont need a donation
She is sooo cute bless her soul .. I wish I could make her a happy healthy child and remove her pain and suffering.
indeed
Exactly my thought as well. These parents have such beautiful souls and I really hope a cure can be found one day for all the sick children. As a mother, it really breaks my heart to see other children suffer.
💔💔
What a gorgeous beautiful little family. The fact that they don't even accept donations either because they think other kids may need it more, just so sweet.
How many of of us wake up every day and say our life isn't fair because I sometimes do but after watching this I feel so blessed just to be able to get out of bed.
Don't compare dude. That's not how trauma works
@@animallover3904 comparison can help some people be more aware of what they DO have which can help elevate trauma. Comparison can evoke inspiration too. Just don't focus on it too much.
Life is never fair, there's always people above you, then there's those who are below you.
@@animallover3904 comparing doesn't invalidate others' problems, but it gives them perspective
Unzufriedene Menschen müssen einen Monat im Krankenhaus arbeiten, dann sind sie dankbar❤🙏
When she smiled I smiled. Going through all that and she's still smiling! She's adorable. Never give up lil angel. That's the spirit ☺️♥️
💓💓
Me too! I found myself talking out loud while watching it all alone, "Awww, look at that smile!" "She's soooo adorable!" "No, Mom, you NEVER give up! Amazingly unexpected things can happen and you'll never know!" (Seems we are a bit like-minded, eh? 😊✌💕)
Yup me too 💗 and I said high baby 💗💗💗💗 As if I was there with her 💗💗💗
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I don't know what to say... but I can only say that I'm glad that she has loving parents 😢 I really, really wish her all the best in her life.
Loving parents? Or torturing baby?
they are clearly overly emotionally attached to the baby , they should let her go as she's gonna have to spend the rest of her life on a ventilator and unable to walk , it would be like staying in a prison your entire life , sometimes its better to let go
@@merahnaga1651 Don't say like that 😒
@@Misty_Tomboy_Mermaid he is right
@@Misty_Tomboy_Mermaid tbh honest just think about it. It's actually better to not let the baby aswell as the parents suffer
glad the medicine is more affordable for them now. it’s a hard life on not only the child but the other people around her also. best of luck to them.
It is not medicine. Just some kind of experimental drug. Only love and nutrition can help her improve the condition.
@@Tekhelet75 >some kind of experimental drug
Thats what medicine is
@@Tekhelet75 Yeah, not the experimental drug, it's actually love and nutrition that is improving her condition
Zdrowy człowiek nigdy nie zrozumie jakie szczęście go spotkało .
Pozdrawiam z Polski .
Jak wielki szacunek dla Was tak wielkie współczucie.
Have you people ever heard of a friggin' vowel???
@@ShortFuseFightingimagine getting upset about another language. Troll
I have a disabled child and I know how hard it is. Never give up they can't talk but they know.
I cried all the way through that because I understand
Love from the 🇬🇧
Srdečný pozdrav zo Slovenska ❤️❤️Veľa šťastia, síl a lásky Celej rodinke prajem 🙏🙏🙏❤️❤️❤️
ua-cam.com/video/1GJ0aj9yD1Q/v-deo.html
More power to you 💪 ✨ 🙌
As a father of two kids myself, your the true heroes for not giving up. Never give up because holding the baby in your hands is the best feeling as a parent. I wish you the little angel many more happy, healthy and smiling years to come.
Sending love from Kansas, USA. My son Mitchel was born with SMA type 1 back in '92. There was so little known about it then. He loved music and bubbles. And people. He was a happy little guy too, like your precious Duoduo. I wish you all the best. My prayers are with you. And I'm so happy that Duoduo was born at a time when there are treatment options to help extend her life. Though most will not understand, I know exactly what you mean by feeling support and love from her. These are very special tiny humans ❤️
How your son is now ? Well ?
@@prabalmohanta9775 He referred to his son as “was”. Rest In Peace.
@probal.....he died at 9 1/2 mos.
RIP dear Angel.
@@shannonakins5752 im so sorry for your loss
He's in a better place now♥️
And im sure he loves you with all his heart
I had a cousin who had a brain aneurism at 19. Remained in a coma for 30 years and finally passed away from an infection. Many people are pro-life no matter what. If the quality of life is severely affected and the person only knows pain and medical procedures, they should be allowed to go with some dignity. I know it's easy for me to say, not being a parent of a child in this state however, I watched family members cling to hope for decades and unable to let go, until the choice was taken from them. Very difficult situation.
I agree
Мы не в праве забирать жизнь, это большой грех, если тебе суждено нести крест, нужно его нести
True man, its better to give them peace and let them go
There have been cases where parents have gone to extraordinary measures to prolong the lives of children who were born with little more than a brain stem and they always seem a little perverse to me but this little one still seems to be engaging with the world and finding enjoyment from her experiences so I can’t say the parents are being selfish
I agree. It would be the hardest thing a mother ever had to do. I would have to let her be free.
As a parent myself, nothing can crush my soul than seeing my child suffer. Hope everything works out for this family specially their little angel. Wishing them all the best.
Que dieu protège cet enfant
And what would you do Allow them to carry on suffering waiting for a miracle that's never going to happen
How bout when the Tony Danza show got canceled?
As an ex volunteer( live in) in disabled home , it is extremely stressful & difficult for whoever take care disable child & her condition is extremely hard for the mum. Whether to give up or not is her decision & we need to respect her. My salute to this lady & hope whatever the outcome she shld be proud of herselves. Be strong.
Thank you for your contribution to society,it is people like you who make the world a better place
We all feel the same things. It doesn't matter where you live or where you were born. This poor woman is stronger than me. Nobody deserves to live that way.
When it comes to a mother & her child, you find strength you never knew you had.
Боже какая борьба за жизнь....
Полнейшего выздоровления малышке....сил и терпения родителям...
Какая совершенная медицина в Китае
being a mother ( parent) is the greatest and worst feeling. I understand this statement even more with this story.😭
@Noogle Noodle the baby has never eaten pork u fool
This is why people should not be shamed for not having kids - it is a choice that they would have to live with for life.
@Noogle Noodle brother, ik you're a Muslim, pls stop, it's not about pork,
not a parent myself, but I live with my nephews and nieces. Every time one of them fall sick, I feel like somebody just punch my stomach.
Wow!! I've NEVER heard that before but you speak the absolute TRUTH!! AMEN!! to that comment. Motherhood is a double edge sword for sure. We love our children SOOO MUCH that we suffer when they are hurting and it's a PAINFUL thing.
Сердце разрывается смотреть на страдания этого малыша!!! Пускай случится чудо, и болезнь отступит.
Ame
Судя по всему, у ребёнка генетическое заболевание или аномалии внутреутробного развития. К сожалению, такие тяжёлые дети редко доживают до совершеннолетия.
Сердце не качает?.....
Amém, que suas palavras sejam cheia de poder
Tenho certeza que eles pedem todo dia por esse milagre, só falta vir
So heartbreaking! I wish she would walk and talk one-day! Kudos to the parents.
I love how despite all her suffering she's still trying to turn over and cause mayhem she's such an angel :')
I just had a mental breakdown and even thought of ending it all but then I came on to youtube and saw this. I have to keep fighting because I'm privileged justvto be alive. Baby girl is lucky to have such great parents. All the best to her
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You hang in there too you hear me? Your life is no less important than hers and to the people who know and love you. If you ever need to talk or help, please reach out darling, ending your life is never the solution. Please remember that you are important, you are loved, precious and most of all STRONGER than you will ever know and no matter how bad life gets, it always gets better.❤ my prayers are with you friend ❤please take care of yourself 😊
Amazing parents I'm glad that the medicine she needs is now free for her.
I literally have a cousin who is now 10 + years old.
She has a condition called cerebral palsy which basically means, her normal developmental milestones are impaired.
From simple muscle movement, to speech to swallowing.
When she was born,
She was immediately put into an incubator because of premature delivery (6months or something)
She spent more than 6 months in the neonatal ICU and after that,
She had to be hospitalized for another few months for close monitoring.
Upon growing up,
She literally needs to be fed with special precautions due to very high risks of choking
Her mom literally had to give up her career to be her carer 24/7.
At some point, my mom would go to their house to assist with my aunt in caring the child.
Imagine 10 years of this,
Countless hospitalizations,
Literally everyday of sleep deprivation on the part of my cousin's parents.
A mother's love is indeed immeasurable.....
We love the child (my cousin)
But I really wished things would have been different with her.....
Life is really unfair...
But this teaches me to be more grateful of the little things I have in life.....
Your comment reads like a prose poem,
Like Leaves of Grass by the great Walt Whitman.
@@Food-Dharma don't know if that's a bad thing.
But I didn't mean it that way.
Cerebral palsy is easier than SMA
@@directioner2870 I didn't say it is easier.
The point I'm making is: parents will love their child unconditionally and are willing to give up everything..
Also .
Just so you know,
My cousin, who is now 11 years old,
Never got to experience normal childhood
She is literally totally dependent (till now) and for the rest of her life.
Her upper and lower extremities never got to develop normally,
Even her ability to talk never really improved..
I'm not saying this to complain about how life unfair is
But I'm saying this to let you know that not all cerebral palsy case is "easy".
Hi! Your cousin is so strong and brave. Take care and love her more. They are so special that what they need also is a special and unconditional love. Spend more time with her.
This may sound silly but I'mma say this: Take pictures and videos together. Each moment is very very special :)
I am really hoping and praying that there will be a very efficient and effective treatment for cerebral palsy that will make people who have that disease experience a normal life. I hope that I can do more for them.
I first watched this a year ago…my heart broke for this family. I’m wondering how they are all doing now, and hoping that they are well and happy. Sending love from America ❤❤❤
Oh my heart..... I have tears while watching this child loved by her parents. They are so so strong and deserves a miracle. They don't even request donations. I pray pray Duo Duo can recover and live a normal life or at least will everyday feel her parents love and warmth towards her. It's too tough making decisions like this.
It's hard to say
On one hand, they're just prolonging her suffering
On the other hand, you can't just let someone die without trying
Tough situation to be in
I think most people choose what they want though not what’s best for the child. It’s not easy
But since the medicine is included in insurance now it should be better for her
Exactly.. and if her parents to suddenly die, what would happen to her who needs 24 hour care?🥺No one would be as dedicated as her own parents.. I keep thinking about this..
The thing is, for how long?
These procedures look expensive, I'm glad that they are able to afford them. But if nothing changes, if she remains the same - choosing the toughest option would be a blessing for her. How would she survive like this when she grows up?
@@thanatos2288 well, while it is true
I cannot say any opinion to what that child's best option besides their loving parents action
Просто плачу. Малыш солнышко. Пусть Боженька даст тебе здоровья. Так хочется чтоб ты бегал и улыбался как все здоровые детки.
Боже!!!Ты так всемогущ и всевидящ!!!Ну вот кааак ты это допускаешь???Зачем???За что???🤦😰😭
Это точно! Дай Бог ему здоровья!!!
@@ЕленаМареева-ф6м не дал... жалко что-ли... Бледный ангел и его родители
Amen!
@@tayakrasa7144 потому что не надо верить во всякий бред
She is so very precious! As parents you are doing an amazing job! Sending nothing but love and positive thoughts 🙏🏼💕
I cried watching this. Thank you to the parents of DouDou who never get tired taking care of her. I wish and pray that DouDou will be healed and all of you will enjoy life altogether.
To the entire team helping this young girl, thank you! You deserve all the goodness coming your way! Looking forward to seeing her make a full come back.
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This was incredibly beautiful as well as humbling. I hope with all of my heart that this child and her family experience great miracles and a happily ever after. 💙
This really hit me hard, and mommy is so amazing in making sure her baby gets to experience as much as she can.
Her eyes show so much emotion and love.. even if nonverbal:)
Господи, пусть все детки будут здоровы💓Надеемся, что малыш поправится и современная медицина поможет, насколько только это возможно...
А если нет,кому он нужен после их смерти?
🤲🤲🤲
Да.современная медицина сильна. Почему не вылечили, или в утробе не определили аномалию. Доктора обещают, если бы государство не платило бы деньги больницам за больных сколько вылеченных было-бы. Везде только бизнес.
@@ИнгаПшемецкая ну явно ни вам дорогуша
Иншааллах
Respect to the parents for recognizing Duoduo's strong will to survive. Hope she gets better soon. Sending love and prayers 🙏
Duoduo is a beautiful little girl. She is incredibly blessed to have such wonderful, loving, dedicated parents. Wishing Duoduo a happy pain-free loving life and many blessings. 🙏🥰❤️
Thank you for sharing your love for your daughter. You are such an inspiration.
Really sad. No words can express my sympathy.
Stay strong and all the best wishes especially for a miracle for full recovery.
As a mother to a newborn I can literally feel the mother's pain to see her baby go through this... I'm crying my heart out
I’m so sorry; this family is incredibly strong. I hope things get better - I hope a cure is found. Hugs from BC, Canada
I'm a 53yo heavily tattooed old rascal who's been around and been through a lot so in general not much gets to me, but I'm not ashamed to say a couple of big heavy tears rolled down my face watching this. Love is love regardless of all the other negative things in our world.
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Me too big guy. I cried my eyes out watching this, the poor innocent little face smiling back at her parents and holding onto what life she can and her parents just fighting to keep her comfortable and alive is shattering.
And you just made me cry 😢 🥺
Such a gentle hearted man you are💕
You have a heart ♥
I have a daughter myself, so blessed that she's healthy. This girl's situation really breaks my heart, no child should have to go through something like this.
El amor de los padres no tiene fin, que hermosa familia, muchas bendiciones y mucha fuerza para todos
Wish her a speedy and full recovery.
Это ж сколько сил у мамы, дай Бог им сил и здоровья! 🙌💕папа , папа поддержал семью не убежал как это делают часто мужчины... Блага семье🤗
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Adversities can wake up our inner strength, wisdom and courage. Very touched by this very dedicated couple. The illness aside it looks like Duoduo has grown well. The situation will only get better. All the best 🙏
I bow down to both of you for being loving parents. I am a single mother of 18yrs special child. My mother left me when I was 15 for the sake of her second marriage. For the past 17 yrs, without any family support and lot of financial crisis I didn't leave my daughter bcoz I have undergone the pain of being left for selfishness. My daughter is completely dependent on me. Hats off to you, especially to the father bcoz he has overcome the society and relatives to continue being loyal and caring to his wife which gives her strength to face all these. Nice couple.
Your humility and dedication put me to shame; may the rest of us be half the parents to our healthy children that you two are to your sweet baby.
Деточка, как ты борешься за жизнь! Это просто до слёз....
Где же наш справедливый м сильный Господь....😭такая неправедливось и боль крошкам 🤦😰
give up?! no! every life is precious, no matter how insignificant one might think. let us respect their decision
Дай боже здоровья малышке, и скорейшего выздоровления 🙏🙏🙏
Her mother's tears bought tears to my eyes. I'm also a mom to a 3-month old girl and Duoduo has some resemblance to my daughter. Hugs from one mom to another.
Дай Бог сил родителям!И здоровья малышу
Amen
@@stirfry4215🙏
Amen 🙏
Ameen
Amen 🙏
I really don't know what to say. If the child has the will to live and wants to live then I say support her. Otherwise I do think her in pain and the poor quality of life is too sufferable for her.
the problem is , a child doesn't have a will , they do not understand anything that's happening , they cry if it hurts , sleep if they are sleep , smile when they are happy , they do not understand what's going on
@@shukrantpatil that's also a moral dilemma. I do believe an individual, at a certain age, children included, are capable in making this life or death decision. As long as they understand what death entails and it is legalized then they should have the right and the decision to continue or end it.
Easy to say so since she isn’t your baby
@@onion4464 yes. Exactly. That's why there's a dilemma. A parent's love for her child, hence why her mom can't let go of her child. A parent can only think of saving her child and prolonging the life. But there's also a different perspective...is prolonging the life of a child that is in constant pain and in a very poor quality of life the "right" decision. It's a grey area, not black and white and no right or wrong. It's a debatable question that there is no definite answer to.
@@onion4464 It is easy to say, because the obvious is quite clear to the passerby. As family, people tend to not let go even though they know it may not be the best decision.
The kind of video I could never finish watching. Totally heart wrenching. Her parents are giving it all with no reservations at all. I only wish her family can find peace and acceptance down the road.
My heart is broken for this sweet little child. Life is so unfair.
A mother’s love is everything. I can’t imagine how painful this is for her
I’m so happy she’s doing better and her treatments are working. As soon as the video started playing I broke down like she was my child. I love her strong and her parents encouragement to stay by her side. Geez the love we give our kids ❤❤❤
Будь здоров малыш, ты ещё всем покажешь как надо и можно жить🙏🏻
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This story came just at the right time in my life. Baby I hope you will be healed.
Mother's love and Father's support is immortal
The love from parents is irreplaceable.
Выздоравливай поскорее🙏🙏🙏.Мое уважение родителям.Дай бог вам и вашему малышу здоровья🙏🙏🙏
I’ve seen lots of documentaries about babies and children with life threatening illnesses, but I’ve never cried over them, this one got me, it’s the moms reaction to living with her daughter and saying that maybe our lives are mundane but that’s what they would like, my husband died and I’ve been through so much, but this mom made me realise that my life has and is not as bad as I thought! Kudos mom!! You’re fantastic!!! I’ll pray for you all.
This is inspiring. How much her parents love her and treasure her even through struggle. They're right that we should be grateful for any normalcy in our lives
Lots of love ❤️ and courage to the little one. Get well soon.
As long as she is trying to survive and her condition is ok, I think she is having a great life with such a strong mom/family... such a hard decision to make:(
Dios mío que fuerte tienes que ser para soportar ver a tu hijito así , mi admiración y muchas bendiciones para está mamá y su pequeño
Es NIÑA.
Thank you to these wonderful parents for allowing this video. You've given us all a gift, of thankfulness for what we have. You are a beautiful family and I hope your little darling's life improves. Love from Australia
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Дай Бог малышке здоровья! И Родителям тоже терпения и здоровья
The parents should receive the "Parent of the year"award, but most likely their satisfaction comes from seeing their daughter enjoying life to the fullest.
Do you think she is enjoying her life?
@@LS-zo3cr She doesn’t know any better.
"Worst parents of the year award"* that kid is suffering everyday and will even more when they have enough awareness to realize they will never live a "normal" life. Humans were not put on this world to live like this, this is sickening, and should be outlawed. To poor child is living a life of suffering and hardship, simply because the parents can't make the right and loving decision of letting go to stop this. Imagine yourself in this situation.
I know they are trying hard to help her but is she really happy? She is probably in a lot of pain and suffering and I understand it's hard for the parents to end their child it would still make the child hopefully be much happier in heaven, I remember being in hospital really young and I was in so much pain I just wanted to die
Poor little girl, I hope and pray that she gets better. I feel sorry for her parents too, but they are winning with their love and care.
It's true that special children are given to special parents. More power to this amazingly strong family!
Пусть бесконечная любовь родителей поможет данному ангелочеку выздороветь
There was visual progress, that progress indicates hope, were hope is found it encourages us, gives us strength to continue to be courageous in a overwhelming medical situation, although there burdens are many, its accepted as a labor of love, they care, they are trying to make it the best they can, what the child's future will be like 5 years from now will be hard to guess, where there is hope, one will still try...wishing the family there best, prayers for strength and miracles......
Amin♥️♥️
Амин🙏🙏🙏🙏🙏🙏🙏🙏
I am in tears watching this, I hope the little baby will survive this catastrophe and be a very strong person in the fure. The parents are a role model too.
看到這個小女孩發生的事情真是令人難過。 祝福小豆豆和她的家人未來一切順利！
Só tendo amor de verdade para saber cuidar . Muita força para os pais e pra essa criança .
Qué importante es valorar lo evidente que no es tan evidente! Gracias a almas como esta niña que viven estas duras experiencias crecemos en AMOR. Qué Dios la bendiga y a toda su familia! 🙏
Feel sad for Duduo's condition but infinitely moved by her parents' amazing love and devotion to keeping her alive. I wish them all the best. ❤️
She’s a beautiful little girl and I wish this family all the luck in the world! She has an amazing mother and father!
Your daughter has the most beautiful smile, thankyou for giving her a chance your are truly inspiring. You are not alone out there, we are a large community with children of special needs, every moment we spend with them is a blessing, a true blessing.
The love these parents towards their daughter is nothing short of amazing. Bless them all.
This is so heartbreaking. Hope DuoDuo would enjoy life as much as she could, and her parents to be strong as much as they could
Jesus cover this beautiful baby with your holy blood. Bless her parents.
Warum sieht niemand den Schmerz in den Augen dieser gequälten Seele! Ich kann nur hoffen, dass die Natur/Gott gnädig ist und dieses Kind erlöst. 😢
What devoted and loving parents. Duoduo’s smile is precious ❤️ Wishing you all peace and courage from Canada.
Love from Pennsylvania💜
I take the time to share these types of real life stories with my tween kids so that are always reminded how blessed they are...and that some of their issues are nothing in comparison. Im not the little girl's mother but i felt so proud and deeply happy seeing her little hands at work. And her smile is priceless...
People asking the caregivers to let their family member suffering from rare or/and serious diseases go probably haven't experienced something like this in their entire lives. As a caregiver of a family member suffering from a very serious rare disease, i can tell everyone here that even if we consider something like that for once, we get scared of actually doing it as soon as we look at their faces. I'll continue to sleep for only four hours for the rest of my life if i could see her face after waking up daily.... It's just that's how much I love her. Even a daughter's love knows no bounds.
My sister is handicapped, my mother has been her caregiver for 40 years. There comes a point we are all ready for her to pass in peace. My mother wants her to pass peacefully when it's her time. If she was on a vent they would of pulled the plug and I would of supported them. Working in healthcare you learn quick what quality of life is and what it isn't.
As someone who had my grandma at home for 10+ years suffering from an illness that is not Alzheimer but a similar and unpopular and not as much researched illness which basically made her an 80 kilo baby while I was growing up, everybody was suffering and it destroyed the familly. I still remember the look on her face when we had to remind her of her late husband and she remembered in one of her rare moments of semi clarity.
As you put it people are "scared" to do the right thing, when they are gone already they are already gone. There's a point where the person has to go and the family is the only one holding on not being able to let go only making everyone suffer more.
I have watched this a year ago but never got to comment, I hope the baby is doing okay and one day by a miracle , she will be saved. Prayers for her