As Megan’s Aunt i want to say a huge thank you for all the lovely supportive comments. Megan is 8 now and is doing well. She is a very happy intelligent little girl that goes to main stream school and has lots of Friends that absolutely love her.. We as a family continue to support,love and adore her. She leads us everyday.
My son had cleft lip and palate, not this severe, but bad enough to have 23 reconstructive surgeries on nose, lip, palate and ears! People asked what I did to do this to my baby?! SERIOUSLY!! We just treated him like a regular kid and thank God he was a resilient child. He’s now an airline pilot!! From having the doctor tell us he’d be mentally disabled to college graduate and now flying an Airbus 320. Totally worth all the work!
I'm sorry some people were so awful. I'm sorry he went through so much. I know you suffered with him. What a blessing to have such dedicated parents! It's great to hear how well he's doing. You have every reason to be proud...and you should be proud of yourselves, too.
We all want our children to be so called normal, but life is not like that. It throws us many curve balls that are sounexpected . We are never ready for, and all we can do is stay strong for our children.
I was born with a trilateral cleft & palate in Russia and at the age of 18 months was adopted/saved by the most loving parents I could ask for. Seeing how this family just accepted her as she is really touches me because there are unique struggles that patents and kids with clefts go through and watching this I am taken back to when my mom constantly enstiled in me that I was worthy of love. I relate so much. All the best to your family.
Isn’t she though?! I have watched this documentary 3 times. Every time I watch, I am amazed by the way they make her life fulfilled. With them treating her just like the other kids, I think they are an amazing family. My prayers go out to this beautiful family for a long, happy, and healthy life for Megan❤
I just happened on this video. What had me crying, was after Megan’s birth and her mother stating that she is beautiful. What a remarkable and loving mom! I know without a doubt that Megan will reach her full potential due to her families love and devotion.
I have never seen such a compassionate, loving group of specialists, doctors and nurses. Absolute rockstars! Way to go Ireland! The rest of the world could learn from you. And don’t get me started on this beautiful mom. Such an inspiration. What a picture of strength and love for her baby girl. Such a beautiful story. ❤️
You said what I feel. These doctors and surgeons are the people who deserve awards, not celebrities. I cried like a baby watching that sweet little girl. I hope she has a long, happy life. She couldn't have a better mother.
I feel not enough has been said in the comments about the phenomenal doctors that helped Megan. Especially Dr. Early. Such a compassionate man, looking not just at what Megan needs right now, but considering her whole future. He sees aspects of Megan, like her personality and strength and intelligence, that really made me admire him so very much. THAT'S a doctor! Not deterring from the other doctors on the team by any means, but Dr. Early really made an impression on me. God bless him and keep him in good health so he can keep giving children like Megan the best quality of life possible.
You are right, thank you for noting that. They are legends of their professions. God certainly was watching over them as well as Megan during her surgeries.
And lets not forget to give thanks to al the fantastic nurses and RN's that helped and cared for her every minute of the day when she was in the hospital😘❣ As a RN myself I wish that more praises were given to my profession as well as the MD's 🙏 if we weren't their there wouldn't be any surgeries performed, or any surviving patients for that matter 😘🙈 It takes teamwork to make dreamwork ❤
@@anneahrnell Absolutely true. It is surely phenomenal the team work that goes into the preparation, ensuring the safety and recovery of a little baby needing such major surgery. The parents are also such incredible people, the strength, faith and positivity they showed, never doubting for a minute, just constantly clinging to the belief that Little Megan was going to come through every time with flying colours, and this is exactly what she did. She is an adorable clever intelligent little girl, who is so blessed to have a family and extended family that love her so much, and see the importance of raising her in a very normal way as you would any child. As a grandmother myself, the 6th of whom was born just this Monday last, it truly brings to the forefront how blessed we are with each little one we have been blessed with. God bless you all, and I know that with the amazing network of care from her professional team and her family that Little Megan is going to be just fine. A documentary with a beautiful success ending. Well done to Megan herself and to all involved. ❤️🙏
How could you not fall in love with her. She is so good, and happy. What a trooper. She definitely developed her own personality. God bless her and all the surgeons
She "Megan". Thev corrected much of her face and head, but they will continue for awhile. I saw where her Aunt commented and said she was happy and normal and in regular mainstream school where everyone loves her. 😊🍀
Every child, healthy or otherwise, deserves a mother that is so dedicated and loving despite the circumstances. This woman is an angel and that babies obvious and undeniable smile says it all.
Thank you all for the wonderful supportive messages..Megan read them herself and was happy to know she has many lovely supporters throughout the world..Today is Megan’s 9th birthday 💖She is the happiest little girl and is so loved by all her many friends and family.. she continues to amaze everybody. Happy Birthday Megan
Amy Hanrahan I have shared this with many people and get the same reaction 😥😢😞😭😓 But at the end, it's always 😅😄☺😃😍😘 Tears for a moment and then victorious joy!
My cousin had that. She was one of the first to have it they did all surgeries free as they were experimental. Shes in her 30's, has a son who just graduated high school!
Yes it is wonderful what doctors and nurses can do as a team. Like they say, it takes a village. But yes, specialists like these who are so dedicated and spend so much of their lives and money learning to offer these services is incredible.
even before she had her first surgery, when she was in the bouncy seat and smiled.....she has the cutest smile! what a precious little girl. and she has a very sweet big sis. lovely family. 💛😊🌼
When the mom is playing with her in the waiting room and she waves those little angel hands then squeezes her cheeks with that smile, my heart cried tears of happiness!! She's a blessing and her mom is a Earth Angel
She's a precious baby girl... babies are so resilient and are stronger than we can ever believe. She has such a precious personality, you just want to kiss her little dolly cheeks. Blessings to your family!💖💕
The great love of a mother, the inner strength and faith of a wee bairn, and a team of fine hospital staff who CARE can perform miracles. Faith, of course, helps so very much. So wonderful and joyful. Love to them, and thank to the hospital staff. Bravo and love.
Meghans charm, curiosity, strength, intelligence, determination come from and are fed by the love of her parents, sister, family. Mum and Dad are inspiring , modest, warm and determined to give all to their brilliant children. Thank you for sharing. Respect to you all.
I can’t find the words to describe how Megan’s mum has touched me. What a truly beautiful person. And these doctors are simply awesome, as a med student these are the kind of role models who inspire me to keep going every day. Amazing example of medicine and parenting at it’s best. Megan is just a wonderful little warrior.
@@pecan11 he didn't.. do your research that's happening under Biden now at the border. Biden also using same "cages" that Obama had built but only Trump was criticized for putting to use also..
These stories of children with disfiguring abnormalities break my heart and prove that acceptance and love can make a world of difference. Years ago I was working as an inspector for the state of Arizona's automotive emissions control program. I was on one end of the building and looked across and noticed a small girl strapped into a child seat in the rear of an SUV. She had this huge disfigurement which looked like a large dark muffin literally growing off of the side of her face. Her hair was stringy and she looked miserable. I stood staring at her when she suddenly looked up and noticed me looking at her. I gave her as huge a loving smile as I could muster and she cackled out loud to the point where her mother turned around and looked at her and then looked to see who she was looking and laughing at. There I was standing there smiling and waving like she was the dearest thing to my heart. As soon as they drove away I had to excuse myself so that I could go to the men's room and cry. I can't imagine what Magen's mother goes through on a daily basics. God give continue to her strength.
Но почему то никто не задумывается ,как в дальнейшем жить девочке с такой внешностью, сколько психологических травм и травли от сверстников ей придется пережить! Ее жизнь будет адом, т.к. внешность для женщины крайне важна.
I can’t imagine how her parents must have felt when they met a doctor who believed in Megan’s ‘worth’ and potential, decided to treat her and gave them hope for her future for the very first time. That kid’s got a winning personality and disposition, and her determination is off the scale.
why if USA has the best doctors and knows that a baby will born sick so their parents can't to abort because is a big 🤔 sufrimiento , dije que deberian abortar a los inocentes que tienen esas enfermedades o que estan con deformidades porque sufrirán mucho y habra bullying , supongo que en el ultrasonido se sabe que estan enfermos y estados unidos es muy rico mejor tecnología
That baby thrived because of a nationalized healthcare system. The family never had to fight with insurance companies about what would be covered, and worry about how they were going to pay for what the insurance companies would not cover.
This story of Megan really had such an impact on me. It took just one doctor to say "We can do it". He is such a positive man, so gifted in his manner of speaking, he just exudes positivity. Not once did I detect an iota of hesitation, nor any kind of negativity at all. Mostly that he treated Megan as a unique little individual human. An amazing team led by a strong person.
Megan is in my prayers also the family. I have a Grandson with face deformity and the doctor's said he wouldn't live past 2 hours, well he is 26 years old now and is one good looking young man. He has the mind of a 5 year old but like Megan is a very happy child and there both lucky to have the parents that they have. Hugs and kisses to Megan and god bless.
God bless you and your family. I can feel the love you have for your family just through your comment. I wish more people would see how blessed they are to have family before disaster strikes. Jesus is the way. The truth. The life. ♥️
@@April-xq4ll Direct quote: "He has the mind of a 5 year old child" This is insulting and demeaning and ableist to people with intellectual disabilities. The 26 year old MAN is NOT a 5 year old CHILD and should NOT be referred to that way. He cannot be treated exactly the same as a normal adult of course, but there is absolutely no need to demean him like that.
@@tangenty6987 What would be an appropriate term to describe someone's cognitive development? English is not my first language but to me it doesn't sound judgemental, just giving a rough comparison so that people get an idea of someone's cognitive or mental abilities. Like for example, the person is able to talk and knows a few letters but could not read an entire book (because on average, most 5 year olds can't). Again this is just an example.
It’s always good to be supported by family. It was the care and love from them, that made Megan blossom! God bless you Meg’s family and thanks to the amazing team of doctors, for never giving up on the Little one.
WOW! MEGAN'S PARENTS ARE SO STRONG IT BREAKS MY HEART TO SEE HOW STRONG THEY NEED TO BE FOR HER. GOD BE WITH YOU AND MEGAN YOUR VIDEO REALLY TOUCH MY SOUL.
Maria Casas you are so right especially when the world can be so closed minded and hateful. God bless this family. I pray Megan is doing well and will have a blessed life if that’s Gods will.
I watched Megan's story surprisingly with my three and a half year old grandson! He was so concerned with the baby that had the owie and kept saying all the way through the video how beautiful the little baby was. Isn't it beautiful, and a lesson to all of us, that he saw her for her lovely little personality and didn't judge the book by the cover! Best wishes to Megan and her family and her doctors. May God continue to bless her and continue to give her health and strength!!
Actually made me wonder what he saw physically. Being young and not as exposed to cultural norms He may truly physically see something different than we see We are affected by what we've been taught and what we've previously seen. I once met a child That was speaking in complete sentences, But from where I was sitting it was obvious the family did not understand the child. I eventually asked them if they understood and they said no and I said he's speaking in full sentences and they looked at me like I was crazy but I think they were used to hearing him a certain way and I wasn't so I could understand him differently I guess. Anyhow I think it's wonderful that your grandsons thought the baby was beautiful. I just thought you might think that my story was interesting. Beauty truly is in the eye of the beholder. I hope Megan has a wonderful life and I hope your grandson does too.
It's amazing how we all look so ordinary after we've given each other a chance to just be together a few minutes, to know something about each other. This girl is far beyond ordinary, she's stunning in every way and has made me happy. A great family.
Megan's life journey with her amazing parents is so tender and emotional, thank you for sharing with us all. The consultant surgeons were so skilled, and caring! It is quite humbling to see a family go through so much, and Megan....what a joy she brings with her happy nature, loved her blowing kisses and waving at her family. It is a privilege to share this evidence of her first journey...may God bless her always, and Dad and Mum, her big sister and everyone else!
The United States has better technology than Mexico and I suppose that on ultrasound it is known if the baby is deformed, they should abort them because they will suffer a lot and there will be bullying, it is not logical to bring a baby with deformities to the world because there is a lot of physical pain, trauma, stress, teasing and a child deserves to be born healthy
I couldn't stop crying through this whole video. What a precious angel and her wonderful family. I'm glad she is doing so well now. Would love to see an update.
This little girl is such a sweetie! It made me sad to watch, but also so positive about her future. She has a sweet, cheeky personality which completely overrides her appearance. Bless her family for being so positive and loving. They treat her like any other child which is great. I hope she's doing ok!
I would love to see how Megan is doing now. But regardless she is loved and happy, given such a loving family especially her incredible Mom. Happy Mother's Day!
What a wonderful little girl. Megan instantly stole my heart. My goodness she is a fighter with a brave & strong family supporting her. She deserves only good things in life. I'm continually astounded by the medical expertise that strive to make lives better. 🙏🏼
As a fellow mother of a child born with Craniofacial abnormalities, I can really empathize with how Megan’s Mom feels post op. The odd feeling of looking at your child’s face and it being a totally different face. I appreciate that she brought this up, as well as the surgeon’s mention of this. I think it’s so important to discuss the possibility of parents feelings of loss immediately after surgery. For our family, it was a very unexpected feeling, and because it wasn’t mentioned pre op by the surgeon, I felt ashamed of my sudden mixed feelings upon first sight of my child post procedure. This documentary is really well done. Continued blessings for Megan and family.
You have no reason to feel ashamed. My heart goes out to you and all the Mamas and Papas that have sweet angels like Megan. I know I too would feel a loss if my baby's face changed so suddenly. Of course you love their face and you will love what their face becomes too - because it's still them. However telling your heart to let go of that first face must be very difficult.
Dont be ashamed of your feelings. They can be surprising and unexpected. Nothing to be upset for. Your over it now, loving your baby. Just like a wave, a feeling can and will pass.
When you watch things like this it makes your own problems seem insignificant...I have so much respect and admiration for parents who have to deal with things of this nature...so glad to hear from her aunt saying she is doing well,...God bless this family ,and I hope and pray' things will continue to improve so she can enjoy a happy and normal life..🙏🙏🙏🙏
I was born with a bilateral cleft lip and palate and I must say she is incredible! The cleft repair was beautifully done and she is all around stunning
She’s an absolute delight, she’s a fighter, so smart and happy, and she shares a birthday with my youngest son. I look forward to seeing more of her milestones.
@@1961-v9k why? because it's she pronounced it the correct way? It's either mother mom mommy? a mummy is something completely different and ancient history.
Been through similar with my son, but I never had film crew following me. What a mum & human being to be able to cope with it, but you've helped by permitting your precious daughters' life to be shown. What a spirit she has. God bless x
I want to say I can only hope to have a modicum of the dignity and strength this family has. She is a very well loved little girl and I pray they all have a long and happy life. God bless them all.
Such a strong beautiful baby girl.....who gets her strength from her mommy........Thank you to the amazing doctors who make all this possible....much love & prayers sent to you all
What an amazing little girl Megan is with her bright smile 😃 and her determination. Life is to short to wake up every day is a true blessing. I too have had many surgeries but after seeing Megan surgeries i will never complain again. How she bounces back from each surgery with being stronger every time. I wish Megan all the very best and keep up with your true determination & your laughter which is so infectious 💗💗💗.
How beautiful she is with such a bubbly personality. Thank you for sharing her story. I hope it helps other families who may face the same challenges. As parents you were awesome! Mom you showed great strength for your baby girl. Such a beautiful family. God Bless.
🇨🇦 I've watched this documentary 2 to 3 times and each time I've litterally felt the pain from mom and dad. Also, the love and care from the Drs and nursing staff brings tears to my eyes each and every time. This little angels will to live is so strong. She certainly is quite the miracle baby. I know this is an old video and I'm not sure how baby is doing but I pray for her and hope she is a healthy and happy baby. With parents like hers and the remarkable health care team she has looking after her that she's in good hands. 🙏🙏🙏🙏🙏🙏
She deserves the same chances, opportunities, and life as anyone else! Much respect to all who gave her that opportunity, to be her beautiful self! Amazing mom!
She really is so lovely. The whole hospital staff that helped this precious girl deserves a round of applause. The whole family are exceedingly rare and supportive and most of all loving. Kudos to all.
She's almost 11 now last I heard and doing great! Lots of good friends and very well adjusted.. She seems to have a LOT of family and friend support, treating her like she's like everyone else.. Amazing family..
This is Sheri, Paul's wife. I would like to see a picture if that's okay. They truly did miracles with her. My aunt had the cleft palate surgery at 2. She is 83 today. She was always sensitive about her scar but I always thought she was the most beautiful in the family I rarely noticed her scar only when someone mentioned it. I noticed Megan's mouth in that after pictures It appeared to be just a beautiful little mouth anyhow would like to see a picture if you guys are comfortable with it. ❤️🥰😍😘🥳
Meghan is a gorgeous brave dear little girl!! You've all been through so much. Wish you all every happiness in the world. Mum and Dad you are wonderful parents.
Selfish parents here Tell me what kind of a life this poor child will have in a society whom is brutal and will call this poor child a freak,and all the abuse she will encounter from others,Have the parents even thought that through?
Tammy Stockbridge....I totally agree with you....nothing is impossible for and with God.... May God Bless Megan and her family....and may God bless Megan and her siblings with a wonderful and happy and healthy life... She and her sister are soooooo beautiful....one of the most wonderful gifts God can give is the gift of a child.... My prayers will always with you all...
kathy heitchue You are the selfish one. AND WE DON’T CARE ABOUT YOUR EVIL 👿 SELF ABSORBED SICK OPINION. Get back in your cage with the other lions where you belong.
What a precious little girl. She seems so happy and lovable. I’d kiss her little face right off 🥰 she’s just adorable. Way to go Megan! You’ve came a long way. Keep on going and you’ll do great things in life 🥳
So in awe of Megan’s momma, sending her so much momma strength and love. Daddy too. But seeing Megan’s joy is what makes you fall in love with her. This also brings the reality of how lucky I was to have healthy children, and the blessing that every child brings the world. ❤️
god bless this beautiful girl and parents and grandparents that has stuck bside all the way. made me cry watching this cz my grandson had a cleff pallet done to bt insyd the roof of his mouth.and other problems too .soooo thank his mummy whanau n friends for all there support .he has pierce robinson syndrome. id take my hat of to uz all. take caew beautiful xxoo
"how lucky I am to have healthy children" i hate comments like these.. as a mom of 2 special needs kids.. all everyone says is.. im so sorry and im lucky my kids are normal.. well guess what.. you are not the lucky one.. us parents are the lucky ones to have children like we do.. you have no idea what its like for every little thing most take for granted a child does for us is pure joy.. to have a child see the world as perfect and have love for everyone no matter color.. gender.. age..can you imagine if the rest of the world thought like they do what kind of world we would live in.. I'm the lucky one
Oh my lord! That kid is adorable! Her smile turnd me into a puddle. Thank GOD she was born to such amazing parents and in the proximity of such amazing medical staff! Others might have given up and then we wouldn't have that sweet, funny, smart baby in this world. In her first 1.5 years she'd had multiple infections and major surgeries, and she still formed such great attachments and acts like any other toddler, squeezing her cheeks and blowing kisses. HOW?! Well, if I had to guess, it was her own innate brightness and the amazing support of those lovely parents. Thank you for sharing! I needed to see something beautiful today.
Trogdor thank goodness she was born somewhere that has great health care. Here in America those poor parents would have been bankrupt from the cost of all the surgeries and health care. So glad she is a happy, healthy little girl!
This family knows the secret to success, do not treat your child as a victim regardless of what they have or don’t have... it is because of their love and their belief in this child that she can do all that she has done ... beautiful family, beautiful child.
Nail on the head. Look up "Big Toe". I met him living in San Diego. He plays the guitar. He doesn't have any arms. He said his parents treated him just like his other siblings. Like when his Mom would tell him to take out the garbage and he'd protest "I don't have arms" she would say.."Oh I didn't notice..take out the trash." Lol he as a result lives like he's perfectly capable.
They have actually taken Megan's head apart, and are rebuilding it as I watch! How incredible that medicine can do that. I am gobsmacked by their skill...Bless all who took part in creating a new life for this delightful little girl!!
She seems a happy child. I can’t imagine how the parent feels to have a child go through so many surgeries. Mom seems admirably, emotionally healthy. I wonder how her older sister feels while all this attention is going to her younger sister.
As Megan’s Aunt i want to say a huge thank you for all the lovely supportive comments. Megan is 8 now and is doing well. She is a very happy intelligent little girl that goes to main stream school and has lots of Friends that absolutely love her.. We as a family continue to support,love and adore her. She leads us everyday.
that little smile in post op was heart warming...thank you to your family for sharing her journey....god speed
What wonderful news. I am so happy to hear she is doing so well. Merry Christmas
Ah I'm so glad I saw you comment all the way through I was wondering how she was doing now, love and blessings to you all xx
Beautiful update I was just looking for an update 👍😀
Amy Hanrahan wow that’s a blessing. Happy for you
My son had cleft lip and palate, not this severe, but bad enough to have 23 reconstructive surgeries on nose, lip, palate and ears! People asked what I did to do this to my baby?! SERIOUSLY!! We just treated him like a regular kid and thank God he was a resilient child. He’s now an airline pilot!! From having the doctor tell us he’d be mentally disabled to college graduate and now flying an Airbus 320. Totally worth all the work!
I'm sorry some people were so awful. I'm sorry he went through so much. I know you suffered with him. What a blessing to have such dedicated parents! It's great to hear how well he's doing. You have every reason to be proud...and you should be proud of yourselves, too.
We all want our children to be so called normal, but life is not like that. It throws us many curve balls that are sounexpected . We are never ready for, and all we can do is stay strong for our children.
That warms my heart. ❤❤
A
How buetyful he is or she 😅
That smile at 35:55 “hi little sweetheart” said it all.
The love within this family is so beautiful to witness.
I was born with a trilateral cleft & palate in Russia and at the age of 18 months was adopted/saved by the most loving parents I could ask for. Seeing how this family just accepted her as she is really touches me because there are unique struggles that patents and kids with clefts go through and watching this I am taken back to when my mom constantly enstiled in me that I was worthy of love. I relate so much. All the best to your family.
All the best to you aswell!❤
God bless you, Emily!🙏❤️
❤❤
Bless you and your loved ones too.❤
A. Mother's heart bless all of you
What a miracle Megan is - but oh, her mother! Her mother is the most magnificent human being I think I’ve ever seen. Words can’t do her justice.
Agreed!❤ Dad is wonderful too! Grandma and aunt are just so caring. Megan and sissy have a lovely family!❤🙏
I agree 100% with everything both of you have said.
Isn’t she though?! I have watched this documentary 3 times. Every time I watch, I am amazed by the way they make her life fulfilled. With them treating her just like the other kids, I think they are an amazing family. My prayers go out to this beautiful family for a long, happy, and healthy life for Megan❤
I just happened on this video. What had me crying, was after Megan’s birth and her mother stating that she is beautiful. What a remarkable and loving mom! I know without a doubt that Megan will reach her full potential due to her families love and devotion.
I have never seen such a compassionate, loving group of specialists, doctors and nurses. Absolute rockstars! Way to go Ireland! The rest of the world could learn from you. And don’t get me started on this beautiful mom. Such an inspiration. What a picture of strength and love for her baby girl. Such a beautiful story. ❤️
Sounds like Bringlish and American are diverging. I can hardly understand this woman.
for sure. her parents are great too
I couldn't have said it better, very touching, absolutely remarkable.
So sweet
You said what I feel. These doctors and surgeons are the people who deserve awards, not celebrities. I cried like a baby watching that sweet little girl. I hope she has a long, happy life. She couldn't have a better mother.
I feel not enough has been said in the comments about the phenomenal doctors that helped Megan. Especially Dr. Early. Such a compassionate man, looking not just at what Megan needs right now, but considering her whole future. He sees aspects of Megan, like her personality and strength and intelligence, that really made me admire him so very much. THAT'S a doctor! Not deterring from the other doctors on the team by any means, but Dr. Early really made an impression on me. God bless him and keep him in good health so he can keep giving children like Megan the best quality of life possible.
You are right, thank you for noting that. They are legends of their professions. God certainly was watching over them as well as Megan during her surgeries.
Well said!
Amen!
And lets not forget to give thanks to al the fantastic nurses and RN's that helped and cared for her every minute of the day when she was in the hospital😘❣ As a RN myself I wish that more praises were given to my profession as well as the MD's 🙏 if we weren't their there wouldn't be any surgeries performed, or any surviving patients for that matter 😘🙈 It takes teamwork to make dreamwork ❤
@@anneahrnell Absolutely true. It is surely phenomenal the team work that goes into the preparation, ensuring the safety and recovery of a little baby needing such major surgery. The parents are also such incredible people, the strength, faith and positivity they showed, never doubting for a minute, just constantly clinging to the belief that Little Megan was going to come through every time with flying colours, and this is exactly what she did. She is an adorable clever intelligent little girl, who is so blessed to have a family and extended family that love her so much, and see the importance of raising her in a very normal way as you would any child. As a grandmother myself, the 6th of whom was born just this Monday last, it truly brings to the forefront how blessed we are with each little one we have been blessed with. God bless you all, and I know that with the amazing network of care from her professional team and her family that Little Megan is going to be just fine. A documentary with a beautiful success ending. Well done to Megan herself and to all involved. ❤️🙏
The Parents are angels that had an angel... she is surviving because she was meant to .. she is a fighter..
People should be aware that this can happen to any one of our children. To those making nasty comments...do you think you are unique?
She is a gift from God! A miracle!!
A huge AMEN to supporting this dear family with encouragement. Everything and everyone is beautiful in their own way....
@@cathharr08 wtf this comment isn’t supposed to be bad idiot
God bless the mother for never giving up on her beautiful baby.
She is not a Monster, so what is your problem?
@MALACHAI SHASHU How dare you! She's a beautiful warrior!
Gross
Anna Thom damn gross
Richard Bal there was a post above that only a mother could love a monster. But now it is deleted
How could you not fall in love with her. She is so good, and happy. What a trooper. She definitely developed her own personality. God bless her and all the surgeons
Right from the get go, she said look at me. I'm a force to be reckoned with. What a strong, beautiful child. You go girl.
That smile after the surgery brought tears to my eyes. Her personality shines.
Nona Cee yes, that little smile says it all
It sure does!!!
It certainly does shine
@@anniew5277 I'm 56 yrs old.i had a cliff palet when born.my mother had the surgery.been ok since.had a normal life.
What a loving mother. I was moved by her love for her precious daughter.
This child is so beautiful and special. Blessings for darling Megan and her loving family!❤❤❤🙏🙏🙏
Amazing how a child will improve and thrive when it is wanted & accepted & so thoroughly loved by its parents!
Lol at “it”.
Guess I should’ve said he or she.
Caroline your comment was heartfelt....
She "Megan". Thev corrected much of her face and head, but they will continue for awhile. I saw where her Aunt commented and said she was happy and normal and in regular mainstream school where everyone loves her. 😊🍀
I guess ``uh``
This mum is an absolute inspiration, I am in such awe of her. She's the kind of mum I would aspire to be ❤️
Every child, healthy or otherwise, deserves a mother that is so dedicated and loving despite the circumstances. This woman is an angel and that babies obvious and undeniable smile says it all.
j
What a blessed story . Thank you . Heaven sent .
Poor husband is my inspiration....didn't utter a word the entire video.
I feel God knows exactly what mums are needed for disabled children❤️
This precious angel has the best loving mom.
Catherine Hamilton
angels are born from angels
Catherine Hamilton. And Dad
Thank you all for the wonderful supportive messages..Megan read them herself and was happy to know she has many lovely supporters throughout the world..Today is Megan’s 9th birthday 💖She is the happiest little girl and is so loved by all her many friends and family.. she continues to amaze everybody. Happy Birthday Megan
Amy Hanrahan
I have shared this with many people and get the same reaction
😥😢😞😭😓
But at the end, it's always
😅😄☺😃😍😘
Tears for a moment and then victorious joy!
Amy Hanrahan amazing!!!!! Happy #9 to a truly beautiful angel!
This program just makes you appreciate how amazing doctors and nurses are. Little Megan’s beautiful and so glad she has such a caring family 💜
Beautiful?? Only in the most abstract way…
My cousin had that. She was one of the first to have it they did all surgeries free as they were experimental. Shes in her 30's, has a son who just graduated high school!
God blessed her.
@49jubilee you do realize she's not talking about the child in the video
😊That's really nice ❤️
Kay King no she’s not
Wendy - wonderful encouraging comment re yr cousin... wish her well from all here... love positivity...
Isn’t it wonderful what doctors can do now. It is such a blessing for you all. She should have a good normal life. You’re a great Mom.
Candace Roberts
Candace Roberts
AMAZING!
Yes it is wonderful what doctors and nurses can do as a team. Like they say, it takes a village. But yes, specialists like these who are so dedicated and spend so much of their lives and money learning to offer these services is incredible.
PLASHET WARD LONDON
MELATONIN CAPSULES AT NIGHT
FRANCIQUE THEOPHALUS
it's 2020, I'm only 5 minutes in and I'm already in love with this kid and her mum and dad,
Yeas. 5 min and i love her to. And her parents.
2021
Бедная мама! Плачет , наверное, день и ночь.
@@iapplypressure1119 its 2020 for them it was 8 months ago
Me too. God bless this family ❤
even before she had her first surgery, when she was in the bouncy seat and smiled.....she has the cutest smile! what a precious little girl. and she has a very sweet big sis. lovely family. 💛😊🌼
When the mom is playing with her in the waiting room and she waves those little angel hands then squeezes her cheeks with that smile, my heart cried tears of happiness!! She's a blessing and her mom is a Earth Angel
She's a precious baby girl... babies are so resilient and are stronger than we can ever believe. She has such a precious personality, you just want to kiss her little dolly cheeks. Blessings to your family!💖💕
She is quite possibly the cutest little girl I've ever seen But it's her determined spirit that makes the world cheer her on GO MEGAN!!!
She is beautiful little girl she is very determined to have a good life god bless the sweet girl
Your the type of person that finds jellyfish cute huh?
the definition of "cute" and "beautiful" in my dictionary is something else ...
dude she looks like straight out of a horror movie, I'm gonna have nightmares after seeing her face 😣 she's the opposite of cute ffs
She is a beautiful little girl
The great love of a mother, the inner strength and faith of a wee bairn, and a team of fine hospital staff who CARE can perform miracles. Faith, of course, helps so very much. So wonderful and joyful. Love to them, and thank to the hospital staff. Bravo and love.
This woman's picture should be in the dictionary when you
look up the definition of the word mother.
Beautiful. Bless this kewpie doll.
I agree with you wholeheartedly 👌👄
@Cansuꪔ̤̫ I think maybe bc the mum looks just like a very popular doll we have here in America called Kewpie
Kudos to the dad also. That’s a real man.
Really. Fathers often abandone famílies in that situacion. He’s a lovely dad!
Absolutely both parents deserve credit for hanging in there
He's such a wonderful dad. My heart swells up.
@@taniabecker6663 Many run in an everyday situation! She is not a " Baby Momma..she is his Wife and a Mother and he is a true Husband
Megan has wonderful parents! I am impressed with their love for Megan.
Meghans charm, curiosity, strength, intelligence, determination come from and are fed by the love of her parents, sister, family. Mum and Dad are inspiring , modest, warm and determined to give all to their brilliant children. Thank you for sharing. Respect to you all.
The doctor is very honest about her and I like how he doesn't sugarcoat it.
I can’t find the words to describe how Megan’s mum has touched me. What a truly beautiful person. And these doctors are simply awesome, as a med student these are the kind of role models who inspire me to keep going every day. Amazing example of medicine and parenting at it’s best. Megan is just a wonderful little warrior.
“Give her what she deserves”. You got it momma! Every life is precious and deserves to be treated with dignity ❤️
Amén
Absolutely ❤ every last one
Then why did trump think it was ok to abandon and endanger so many with covid
@@pecan11 he didn't.. do your research that's happening under Biden now at the border. Biden also using same "cages" that Obama had built but only Trump was criticized for putting to use also..
@@kristinamartz348 yea he did . Why we have 500k + dead U r one of those cult followers No one is interested 🤮
Her little eyes told how strong and beautiful her spirit is!
The extent of this surgery is mind blowing... a sincere thank you to all the doctors that do this sort of work
My husband was on a craniofacial team. I felt so fortunate to be around such talented people
Megan would be 11 now. Sending her and her family lots of love and blessings this Christmas. May Almighty God’s hand remain over her 💝
I didn't know that she died. That's so sad. How long did she live? What a sweet little angel.
These stories of children with disfiguring abnormalities break my heart and prove that acceptance and love can make a world of difference. Years ago I was working as an inspector for the state of Arizona's automotive emissions control program. I was on one end of the building and looked across and noticed a small girl strapped into a child seat in the rear of an SUV. She had this huge disfigurement which looked like a large dark muffin literally growing off of the side of her face. Her hair was stringy and she looked miserable. I stood staring at her when she suddenly looked up and noticed me looking at her. I gave her as huge a loving smile as I could muster and she cackled out loud to the point where her mother turned around and looked at her and then looked to see who she was looking and laughing at. There I was standing there smiling and waving like she was the dearest thing to my heart. As soon as they drove away I had to excuse myself so that I could go to the men's room and cry. I can't imagine what Magen's mother goes through on a daily basics. God give continue to her strength.
Those are real humbling moments when you "stop and stare" makes you appreciate what you do have.
That is a beautiful story and you brought her so much joy, she probably was thrilled you didn't run away. I hope she is somewhere happy and you too,
Но почему то никто не задумывается ,как в дальнейшем жить девочке с такой внешностью, сколько психологических травм и травли от сверстников ей придется пережить! Ее жизнь будет адом, т.к. внешность для женщины крайне важна.
I can’t imagine how her parents must have felt when they met a doctor who believed in Megan’s ‘worth’ and potential, decided to treat her and gave them hope for her future for the very first time. That kid’s got a winning personality and disposition, and her determination is off the scale.
Oh my
why if USA has the best doctors and knows that a baby will born sick so their parents can't to abort because is a big 🤔 sufrimiento , dije que deberian abortar a los inocentes que tienen esas enfermedades o que estan con deformidades porque sufrirán mucho y habra bullying , supongo que en el ultrasonido se sabe que estan enfermos y estados unidos es muy rico mejor tecnología
MX Female This is in the UK, not the USA.
@@gabe-po9yi sorry still I can't understand English totally 😢
@@evilevil15 hush
That baby thrived because she was surrounded by love❤Hope she is doing well
And science
Jennifer Blevins so true!!!!!
@@homeskillet7423 and God.
@@homeskillet7423 Yes, brilliant and good doctors.
That baby thrived because of a nationalized healthcare system. The family never had to fight with insurance companies about what would be covered, and worry about how they were going to pay for what the insurance companies would not cover.
What a strong little girl! And she is so lucky to have such a AMAZING family! Bless them!
This story of Megan really had such an impact on me. It took just one doctor to say "We can do it". He is such a positive man, so gifted in his manner of speaking, he just exudes positivity. Not once did I detect an iota of hesitation, nor any kind of negativity at all. Mostly that he treated Megan as a unique little individual human. An amazing team led by a strong person.
Megan is in my prayers also the family. I have a Grandson with face deformity and the doctor's said he wouldn't live past 2 hours, well he is 26 years old now and is one good looking young man. He has the mind of a 5 year old but like Megan is a very happy child and there both lucky to have the parents that they have. Hugs and kisses to Megan and god bless.
A 26 year old is ***not*** a "happy CHILD". A happy GROWN UP PERSON, intellectual disability or no.
@@tangenty6987 You need to read the comment again. It never stated that the grandson is a 26 year old child. God bless you.
God bless you and your family. I can feel the love you have for your family just through your comment. I wish more people would see how blessed they are to have family before disaster strikes. Jesus is the way. The truth. The life. ♥️
@@April-xq4ll Direct quote: "He has the mind of a 5 year old child"
This is insulting and demeaning and ableist to people with intellectual disabilities. The 26 year old MAN is NOT a 5 year old CHILD and should NOT be referred to that way.
He cannot be treated exactly the same as a normal adult of course, but there is absolutely no need to demean him like that.
@@tangenty6987 What would be an appropriate term to describe someone's cognitive development? English is not my first language but to me it doesn't sound judgemental, just giving a rough comparison so that people get an idea of someone's cognitive or mental abilities. Like for example, the person is able to talk and knows a few letters but could not read an entire book (because on average, most 5 year olds can't). Again this is just an example.
Her little hand clapping makes me want to cry it’s sweet! Baby smiles so big when she claps her tiny little hands.
It’s always good to be supported by family. It was the care and love from them, that made Megan blossom! God bless you Meg’s family and thanks to the amazing team of doctors, for never giving up on the Little one.
WOW! MEGAN'S PARENTS ARE SO STRONG IT BREAKS MY HEART TO SEE HOW STRONG THEY NEED TO BE FOR HER. GOD BE WITH YOU AND MEGAN YOUR VIDEO REALLY TOUCH MY SOUL.
Maria Casas you are so right especially when the world can be so closed minded and hateful. God bless this family. I pray Megan is doing well and will have a blessed life if that’s Gods will.
Catherine Montalbano-Harris what if god made her and wanted her to be ugly tho?
@@cheechscrazychannel8947 she not ugly in my eyes that child is an angle gb her & family x
They are selfish.
@@markburke1919 an angle? Peculiar compliment .....
This sweet girl was blessed with the perfect parents ❤
She really was🙏
Precious baby, precious family. My hat is off to all the wonderful people in her life. It's evident that she's cherished absolutely.
Her wee hands clapping are adorable. What a sweetheart 💕
Phew!!! Post-surgery... what a huge difference already!!! SO amazing what these brilliant doctors can accomplish... that little smile ....
Her staring at the doctor like he was God and she knew he was gonna make her so much better health wise was amazing
I watched Megan's story surprisingly with my three and a half year old grandson! He was so concerned with the baby that had the owie and kept saying all the way through the video how beautiful the little baby was. Isn't it beautiful, and a lesson to all of us, that he saw her for her lovely little personality and didn't judge the book by the cover! Best wishes to Megan and her family and her doctors. May God continue to bless her and continue to give her health and strength!!
Great grandson , from a terrific grandmother.
Yea, it's astonishing kids as young as 3 are more kind than a lot of adults
@@carmenmitchell1377 loop no hi
Actually made me wonder what he saw physically. Being young and not as exposed to cultural norms He may truly physically see something different than we see We are affected by what we've been taught and what we've previously seen.
I once met a child That was speaking in complete sentences, But from where I was sitting it was obvious the family did not understand the child. I eventually asked them if they understood and they said no and I said he's speaking in full sentences and they looked at me like I was crazy but I think they were used to hearing him a certain way and I wasn't so I could understand him differently I guess. Anyhow I think it's wonderful that your grandsons thought the baby was beautiful. I just thought you might think that my story was interesting. Beauty truly is in the eye of the beholder. I hope Megan has a wonderful life and I hope your grandson does too.
I forgot to say this isn't Paul this is Paul's wife Sheri just so you don't get worried about who's paying attention.
I can’t get over how Dear and Sweet she is when so young! She finds joy! And love!
It's amazing how we all look so ordinary after we've given each other a chance to just be together a few minutes, to know something about each other. This girl is far beyond ordinary, she's stunning in every way and has made me happy. A great family.
OMG, how could anybody resist this tough, resilient little baby-doll? What a precious girl! 💕
What a darling little girl and when she blew her mother a kiss - makes your heart melt.
Strong and brave baby with a loving family.Thank you to the team too
Megan's life journey with her amazing parents is so tender and emotional, thank you for sharing with us all. The consultant surgeons were so skilled, and caring!
It is quite humbling to see a family go through so much, and Megan....what a joy she brings with her happy nature, loved her blowing kisses and waving at her family. It is a privilege to share this evidence of her first journey...may God bless her always, and Dad and Mum, her big sister and everyone else!
She’s lucky to have such a lovely family, as they are lucky to have such a brave loving intelligent child. This really moved me.
The United States has better technology than Mexico and I suppose that on ultrasound it is known if the baby is deformed, they should abort them because they will suffer a lot and there will be bullying, it is not logical to bring a baby with deformities to the world because there is a lot of physical pain, trauma, stress, teasing and a child deserves to be born healthy
@@evilevil15
We heard ya the first time, okay? Quit repeating yourself like a broken record, damn it.
@@evilevil15
Ya what about it? Got nothing to do with the video so stfu, simpleton.
I couldn't stop crying through this whole video. What a precious angel and her wonderful family. I'm glad she is doing so well now. Would love to see an update.
This little girl is such a sweetie! It made me sad to watch, but also so positive about her future. She has a sweet, cheeky personality which completely overrides her appearance. Bless her family for being so positive and loving. They treat her like any other child which is great. I hope she's doing ok!
Wow.God bless her parents and give them long lives to go on protecting her.
I would love to see how Megan is doing now. But regardless she is loved and happy, given such a loving family especially her incredible Mom. Happy Mother's Day!
What a wonderful little girl. Megan instantly stole my heart. My goodness she is a fighter with a brave & strong family supporting her. She deserves only good things in life. I'm continually astounded by the medical expertise that strive to make lives better. 🙏🏼
As a fellow mother of a child born with Craniofacial abnormalities, I can really empathize with how Megan’s Mom feels post op. The odd feeling of looking at your child’s face and it being a totally different face. I appreciate that she brought this up, as well as the surgeon’s mention of this. I think it’s so important to discuss the possibility of parents feelings of loss immediately after surgery. For our family, it was a very unexpected feeling, and because it wasn’t mentioned pre op by the surgeon, I felt ashamed of my sudden mixed feelings upon first sight of my child post procedure. This documentary is really well done. Continued blessings for Megan and family.
You have no reason to feel ashamed. My heart goes out to you and all the Mamas and Papas that have sweet angels like Megan. I know I too would feel a loss if my baby's face changed so suddenly. Of course you love their face and you will love what their face becomes too - because it's still them. However telling your heart to let go of that first face must be very difficult.
Mud Fish &. 👍👍😇😍🇺🇸
Dont be ashamed of your feelings. They can be surprising and unexpected. Nothing to be upset for. Your over it now, loving your baby. Just like a wave, a feeling can and will pass.
Meagans mum is a beautiful human being and an inspiration to all mum's in the world ...God bless their family to hold on ...
When you watch things like this it makes your own problems seem insignificant...I have so much respect and admiration for parents who have to deal with things of this nature...so glad to hear from her aunt saying she is doing well,...God bless this family ,and I hope and pray' things will continue to improve so she can enjoy a happy and normal life..🙏🙏🙏🙏
What a beautiful little sweetheart!!! Her personality shines right through!!! 💕
I was born with a bilateral cleft lip and palate and I must say she is incredible! The cleft repair was beautifully done and she is all around stunning
She is stunning indeed
It is just so adorable when she smiles, melts my heart ♥️
She’s an absolute delight, she’s a fighter, so smart and happy, and she shares a birthday with my youngest son. I look forward to seeing more of her milestones.
Did a mummy ever love her baby like this mummy does. It resonates off the screen and in to my heart. God bless them all.
.... you mean a mother?
@@makalahgrimes2950 No, I meant mummy.
@@makalahgrimes2950 bet you’d start an argument in an empty room
@@1961-v9k why? because it's she pronounced it the correct way? It's either mother mom mommy? a mummy is something completely different and ancient history.
@@sylviasanchez5646 ok if you want to be pedantic where I come from it’s mummy, mum, mammy, or Mam, but does it freaking matter ? Jeeezuz🤣
I am AMAZED at how well that repaired her cleft. She is a precious little bug. Never give up, Megan!
Been through similar with my son, but I never had film crew following me. What a mum & human being to be able to cope with it, but you've helped by permitting your precious daughters' life to be shown. What a spirit she has. God bless x
I want to say I can only hope to have a modicum of the dignity and strength this family has. She is a very well loved little girl and I pray they all have a long and happy life. God bless them all.
Such a strong beautiful baby girl.....who gets her strength from her mommy........Thank you to the amazing doctors who make all this possible....much love & prayers sent to you all
What an amazing little girl Megan is with her bright smile 😃 and her determination. Life is to short to wake up every day is a true blessing. I too have had many surgeries but after seeing Megan surgeries i will never complain again. How she bounces back from each surgery with being stronger every time. I wish Megan all the very best and keep up with your true determination & your laughter which is so infectious 💗💗💗.
You have those who think they have it tough, then you see this beautiful little baby. I think we can all learn from this family
Listen to her talking away! Such a sweetie my heart melted this whole video! 💖🌟
How beautiful she is with such a bubbly personality. Thank you for sharing her story. I hope it helps other families who may face the same challenges. As parents you were awesome! Mom you showed great strength for your baby girl. Such a beautiful family. God Bless.
Her cleft palate repair looks amazing. You can't really tell that was an issue. She has great doctors.
Omg seriously. The scarring is virtually nonexistent and so nicely flushed with everything else.
Oh wow I just saw the reasoning why her head scar was zigzag. Absolutely brilliant!!!
and the younger you are, the better and faster you heal.....shes on her way!!!!
@@prihaps p
@@marykaybrancheau7759 p
Poor sweet baby girl. She's incredible as are her parents and doctors.
🇨🇦 I've watched this documentary 2 to 3 times and each time I've litterally felt the pain from mom and dad. Also, the love and care from the Drs and nursing staff brings tears to my eyes each and every time. This little angels will to live is so strong. She certainly is quite the miracle baby. I know this is an old video and I'm not sure how baby is doing but I pray for her and hope she is a healthy and happy baby. With parents like hers and the remarkable health care team she has looking after her that she's in good hands. 🙏🙏🙏🙏🙏🙏
She was 8 when you commented so she’s nine now in ‘23
She deserves the same chances, opportunities, and life as anyone else! Much respect to all who gave her that opportunity, to be her beautiful self! Amazing mom!
She really is so lovely. The whole hospital staff that helped this precious girl deserves a round of applause. The whole family are exceedingly rare and supportive and most of all loving. Kudos to all.
She's lovely I like her squishy cheeks
She has shown she is a clever girl
My best wishes to you all
I love how the family kept fighting for her survival. Love will make her grow❤️
So happy this little girl could get help. Amazing what the doctors have been able to accomplish.
Another definition of beauty, I swear this angel is perfect in her imperfections. Thankyou and all the best for this wonderful family.
Sharon Barnes I love the way you put that.she is beatiful.i liked hearing her giggle and clap.
So beautiful
We need an update about this adorable little girl and her amazing,loving parents!
She's almost 11 now last I heard and doing great! Lots of good friends and very well adjusted.. She seems to have a LOT of family and friend support, treating her like she's like everyone else.. Amazing family..
@@Swnsasy q
This is Sheri, Paul's wife. I would like to see a picture if that's okay. They truly did miracles with her. My aunt had the cleft palate surgery at 2. She is 83 today. She was always sensitive about her scar but I always thought she was the most beautiful in the family I rarely noticed her scar only when someone mentioned it. I noticed Megan's mouth in that after pictures It appeared to be just a beautiful little mouth anyhow would like to see a picture if you guys are comfortable with it. ❤️🥰😍😘🥳
@@Swnsasy du
@@Swnsasy Thank God for the family & friends support. God bless you, your family & those that helped. Amen
Megan is living proof that every child deserves a chance, and what wonderful parents she has
Meghan is a gorgeous brave dear little girl!! You've all been through so much. Wish you all every happiness in the world. Mum and Dad you are wonderful parents.
Selfish parents here Tell me what kind of a life this poor child will have in a society whom is brutal and will call this poor child a freak,and all the abuse she will encounter from others,Have the parents even thought that through?
I agree 100%
Tammy Stockbridge....I totally agree with you....nothing is impossible for and with God....
May God Bless Megan and her family....and may God bless Megan and her siblings with a wonderful and happy and healthy life...
She and her sister are soooooo beautiful....one of the most wonderful gifts God can give is the gift of a child....
My prayers will always with you all...
kathy heitchue You are the selfish one. AND WE DON’T CARE ABOUT YOUR EVIL 👿 SELF ABSORBED SICK OPINION. Get back in your cage with the other lions where you belong.
What a precious little girl. She seems so happy and lovable. I’d kiss her little face right off 🥰 she’s just adorable. Way to go Megan! You’ve came a long way. Keep on going and you’ll do great things in life 🥳
So in awe of Megan’s momma, sending her so much momma strength and love. Daddy too. But seeing Megan’s joy is what makes you fall in love with her. This also brings the reality of how lucky I was to have healthy children, and the blessing that every child brings the world. ❤️
god bless this beautiful girl and parents and grandparents that has stuck bside all the way.
made me cry watching this cz my grandson had a cleff pallet done to bt insyd the roof of his mouth.and other problems too .soooo thank his mummy whanau n friends for all there support .he has pierce robinson syndrome.
id take my hat of to uz all.
take caew beautiful xxoo
The benefit of national healthcare.
God bless this child and her family and doctors and nurses.Unconditional love which we all deserve.
"how lucky I am to have healthy children" i hate comments like these.. as a mom of 2 special needs kids.. all everyone says is.. im so sorry and im lucky my kids are normal.. well guess what.. you are not the lucky one.. us parents are the lucky ones to have children like we do.. you have no idea what its like for every little thing most take for granted a child does for us is pure joy.. to have a child see the world as perfect and have love for everyone no matter color.. gender.. age..can you imagine if the rest of the world thought like they do what kind of world we would live in.. I'm the lucky one
Oh my lord! That kid is adorable! Her smile turnd me into a puddle. Thank GOD she was born to such amazing parents and in the proximity of such amazing medical staff! Others might have given up and then we wouldn't have that sweet, funny, smart baby in this world. In her first 1.5 years she'd had multiple infections and major surgeries, and she still formed such great attachments and acts like any other toddler, squeezing her cheeks and blowing kisses. HOW?! Well, if I had to guess, it was her own innate brightness and the amazing support of those lovely parents. Thank you for sharing! I needed to see something beautiful today.
Trogdor thank goodness she was born somewhere that has great health care. Here in America those poor parents would have been bankrupt from the cost of all the surgeries and health care. So glad she is a happy, healthy little girl!
Awww cute they are hood parents
She has a smile that goes right into my heart, precious little girl and wonderful Mum❤️❤️❤️
Gita Schweitzer yes ❤️
You’re right about that. Mine’s melting!
What a beautiful story of love and strength this family has displayed. God Bless you all!
This family knows the secret to success, do not treat your child as a victim regardless of what they have or don’t have... it is because of their love and their belief in this child that she can do all that she has done ... beautiful family, beautiful child.
Nail on the head. Look up "Big Toe". I met him living in San Diego. He plays the guitar. He doesn't have any arms. He said his parents treated him just like his other siblings. Like when his Mom would tell him to take out the garbage and he'd protest "I don't have arms" she would say.."Oh I didn't notice..take out the trash." Lol he as a result lives like he's perfectly capable.
im crying. mother is the beautiful creature ever living in this earth !
One thing that stands out a mile in this program is the strength of pure love Megan,s family have for her,it's beautiful,just like her.
Aww.. She is still beautiful Mommy! Forget
what other people say or think just stay
close to her .God bless 💝⚘😊
When megan smiled at her mama after her surgery i started just bawling my eyes out.. shes such a beautiful an smart baby
They have actually taken Megan's head apart, and are rebuilding it as I watch! How incredible that medicine can do that. I am gobsmacked by their skill...Bless all who took part in creating a new life for this delightful little girl!!
She's so precious
She seems a happy child. I can’t imagine how the parent feels to have a child go through so many surgeries. Mom seems admirably, emotionally healthy. I wonder how her older sister feels while all this attention is going to her younger sister.
I'm sure she would rather her sister get better.