I have had the privilege of teaching three angels with angelman syndrome in Calgary .. beautiful young people. Rhett is lucky to have parents like you!! ❤❤❤
God chose a very special mommy and daddy for a very special boy! Such a sweet soul who, as you mentioned, will never try to hurt another. The world could learn a lot from him. God Bless you both and your precious boys. 🙏
I just want to share with you. They said the same and worse about my sister with Downs Syndrome. Don’t let the Dr’s limits become your own. One day at a time.❤
Wow this brings back memories. My daughter was originally diagnosed with Angelmans syndrome. She had a lot of the symptoms your son has. We went through the mind blowing screams and lack of sleep and flapping of arms etc. turned out she has cerebral palsy with a seizure disorder and non verbal. She was not missing the chromosome. I really feel for you both and funnily enough we are from Calgary as well. Remember to take each day at a time.❤
Such a beautiful family. My heart broke hearing the mom talking. As a speech therapist I've had only one child who was diagnosed with Angelman's Syndrome. She was a girl of three with a single mom. I'll never forget the mom because she was completely exhausted. This poor child would rarely sleep. The little girl was mobile and had a crib. The mom said she never stopped moving, going in continuous circles in the crib as though she were doing laps. I think about that mom even now (20 years later) and wonder how they're doing.
What a Beautiful Story about a Beautiful Family. Bella & Ben told Rhett's story in a way that really showed the emotional roller coaster they've been through & the love they have for their family. Just beautiful.
I'm without words. SO many things i saw is this couple and their attitude i will never forget. Lessons taught in such a deep profound way. God bless precious Rhett and his story. What and amazing story of hope and love.
God gives the right child to the right parents! He knows what is best. God Bless all of you and may God give you the strength and patience to parent Rhett!( you already have the love!)
God bless your family! Prayers for Rhett, you as his parents, and his baby brother, who hopefully doesn’t have the same diagnosis. Rhett is well loved and happy, and that’s a huge blessing! ❤️
How many of us took for granted our children born and raised trouble free. Until I met this family I had no idea. Are they perfect?, ..yes, for Rhett they are. I'm so happy to know they will all be fine 🙂 😘🇦🇺
What 2 BEAUTIFUL BOYS…..I know what it’s like having a Child in My Family that’s Not PERFECT but PERFECT for Us… His Name Is ZEVEN and now is 30yrs Old and Thanks to My BEAUTIFUL SISTER is WHY We still have him…. ZEVEN has less than a 2 yr olds mind and My Sister has to do EVERYTHING for Him and Yes her Husband helps also We are so Blessed to still have him and his Parents are getting older but He dose have a Sister who loves him so Much and can take care of him also…These children are Gifts to Families and should be treated with nothing less…
This young man was so beautiful and smiley and I loved it that he was interacting with other kids in the junior high. It was the right thing to do for this young man.
I have enormous respect for this couple and to use a commonly used phrase “ my heart goes out to them” it truly does . I felt it as I continued the video . As a parent whose child was frequently hospitalized my husband and I saw the many single mothers with sick children whose fathers were unable to cope with it all and left . There are so many aspects involved. Grief for the perilous future of the child you love with all your being , fear of dying before they do ,sorrow and sympathy for the pain and hardship you can do nothing to alleviate and so on . Then there’s your spousal relationship , changed forever to accommodate the little one’s needs . Becoming partners in advocacy for your child, sharing care and fears and still managing to love each other. Out sweet good girl achieved 26 years and devastated us by dying one night with no warning . Fortunately we believe she is better off now in a place of love in which she can flourish as she was not able to in this life .I will say a prayer for you all , and tell you that you are magnificent even if you don’t necessarily feel it , YOU ARE ! ❤❤❤.
I Pray Dear Lord To Heal This Child And That These Parents Have All The Support They Will Need And That You Fill Their Hearts With Joy And Peace And Again Healing For Rhett And All Children Afflicted And I Praise You Lord Jesus In Jesus Name Amen 🙏
I am so deeply sorry & your comment about Rhett will never have bad intentions toward anyone made me think that he is an angel sent from Heaven for some reason to you parents. Lord have Mercy on your family.
I was honored to provide organization support for a mom whose beautiful son was born with Angelman syndrome. It was a huge learning experience for me. I have moved away and haven't visited them for a while... Missing the feeling of profound love & compassion I witnessed. That young man's parents personify service and respect.
Rhett is so lucky to have you both as parents. But your life is so hard 😢. I hope and wish you get plenty of help, because you both and your other child need some normality. Bless you both and ,any god give you the strength to carry on ❤
Incredible story. As a young couple and having your first child ill is devastating. My daughter was ill alot but we were fortunate that she eventually outgrew the illness. But I remember crying holding her we loved her so much . We didn't know anything about babies as she was our first so everything we did likec all first time parents it was a guess and hope that it was right. I feel your pain but your an incredible couple I believe the love you have for each other will and has benefited your Beautiful baby boy. Many couples can't handle the stress and break up. As long as you continue to hold the love and respect for each other he will grow up happy and isn't that all we really want. Good luck to you both. I dont have a doubt in my mind that God gave you this child for a reason and this little angle may have an illness but he's perfect for you both. 😊
Your words and story is so similar to our life. As a mother of 3 boys, with different issues, our past 42 years with our youngest had many of the issues your does. Your heartfelt shared thoughts of hopes and dream ring so true. My sons disorder has cross over traits with developmental challenges, struggles, behaviours, seizures, feeding issues, love but 42 years ago, not the family support nor DNA info but constant trips to doctors, specialist, hospital stays, tests….worry, stress, and making a uncharted future for him. Never gave up but forged forward out of love for him like yourself. Others did not understand. Our life is unique. His joy is our joy. Our world is better as he’s in it. It gave us direction and strength. We are better people, more patient than we would of. We try always to see life through his eyes and yes, it’s hard work. There was no Google for us then in 1980 but we did questions and never gave up. He is unforgettable to all who met him, us not but he has made a mark on this earth, teaches others what a living pure angel walking amongst others. I will keep your story with us. Thank you for sharing yours. There is light at the end of the tunnel. We live differently but love the same.
Thank you for saharing your story, what a beautiful family, i wanted to say as a craniosacral therapist one of my first profound moments in my training was working with a boy with Angleman syndrome and he taught me so much about non verbal communication that it has helped hundreds of my clients since, every human being has a something to say, if we are willing to slow down and listen deeply ❤
Rhett surely loves n enjoys his brother. It's so obvious watching his face n reaching out. A handsome little man for sure. Keep nourishing yourself physically and mentally n for your husband as well. Rhett is doing great. I love how you stated his intentions will always be pure. He will bring you n family untold moments of joy n love. God bless you all. Especially you Rhett.
Heartbreaking but so thought provoking. I have never heard of this j condition and find the strength that these parents have and their willingness to reach out to other parents for info and then pass that on to the less informed is absolutely incredible. You are truly the parents that Rhett was meant to have. May God continue to keep you all wrapped in his love and strength. God bless you, the physicians caring for Rhett and your community of supporters. My prayers and love goes out to all of you.
I understand what you went through. I can't write it all here. I just want you to know I remember how hard it was to be so tired and frustrated. To have a baby that has a condition which is not diagnosed correctly or in a timely manner. I often thought well maybe I'm crazy. But you know in your gut something is wrong. I could go on and on but just want to stress to you how well you spoke of your and your husband's experience. You both obviously love your child dearly. I'm sorry you have had to go through all the pain of it. Please give yourself credit for your guys strength.
I pray that no young couple have to go throw this journey with a new born but God only chooses the humans strong enough to handle these babies. If nothing else please get sleep when you can. Love to your family. 💕💝💐
Bless this family! I’ll tell you this: if the Internet existed 40 years ago when I was having children, I probably would not! I had amniocentesis at age 36 when I had my third child and the doctor thought I was nuts. He said I was not at risk for having a Down’s syndrome baby but I knew I would not have proceeded with the pregnancy (not judging those who decide to go forward; I knew that I would not). All of my children were perfect but I’m just in awe of parents who go through the many genetic issues out there. I could not do it. Grandchildren are all here, perfect, and thankfully my kids are done with their families. We’re so lucky! I am just in awe of 😅the parents who go through what these lovely people handle so gracefully.
Down's Syndrome _IS NOT_ exclusive to "older" mothers. I've heard of mothers as young as 18 years old giving birth to babies with Down's, and have personally known a mother who was 28 when her 1st child was born - with Down's Syndrome. I'm SO GLAD that you "listen to your own counsel," as way too many people DON'T do that, then live with regret forever afterwards. (Hugs) from Northern California, from a mother of 3 healthy middle-aged "children," but one who, sadly, has NO grandbabies to worry about. (Frankly, I'm not sure I'd have the chutzpah to worry about grandkids, but my DH would have been THE VERY BEST Grandfather, EVER! For him only, I feel sadness.)
Thank you for sharing! You can see and feel the love you have for each other and your boys! Praying for your little ones and also for you and your continued strength. God bless your family!
I used to care for an adult male with Angelmans. He was a happy person. Could walk, run, eat normally, go out with his housemates. He was no trouble at all. He was one of the lucky ones.
Bless your family. I worked as a aide to care for a set of twin boys with Angelmens. They were 20 years old. One of them had come home from the hospital after a seizure episode. This young man never spoke.. BUT this day I spent the day with him rubbing his head and talking to him and just being there with him. He looked up at me and said "Love you!!!" I couldn't believe it. They are happy young men..
Beautiful lil' boy, beautiful family💕 Were you aware of Colin Carroll's son has AS & he has a beautiful story on him. If you have not seen this, you should watch this. His son is 20 & is an amazing young man. God bless your son & all of his family!
First of all, you all have a beautiful family. Secondly, God gave you this little man because, He trusts you with him. I'm writing this from California. I can tell you this, that if you raise this child diagnosed with Angelman Syndrome, you're definitely amazing and troopers. Even people who haven't experienced AS personally in their families have no clue, including the ones making comments here. You two are definitely not alone. My younger brother has four children. He has his oldest so with Asperger's (doing well in the military), a second son with Angelman's, a little girl (who was stillborn-in heaven), a fourth son who also has Angelman Syndrome. It has been tough all these years on my brother, his ex-wife, who is the mother of these four children, and my parents. My parents are extremely instrumental in the raising of the youngest boy as they've basically raised him, themselves, as well as raising and caring for my older sister, who is also developmentally disabled and has never left home. My parents are amazing and deserve everything for their unrelenting efforts and dedication to raise their daughter and my nephew. We help when we can, but they do it all for sure. The Dr's told my brother and his ex, that "they have a 50% chance of each child having Angelman's if they choose to keep having children." My brother and his then wife had the still born little girl, my niece and she became pregnant a fourth time before specialists told her that the second little boy had AS. It seemed like no Dr. could figure it out, exactly. So, this is why they have two with AS. It is possible that their little girl could also have had AS as well, but we'll never know. So, back then in the 90's, I guess it was said, that out of every 500,000 babies born, there is one born with AS and my brother and his ex wife had two. Love you and God bless.
Thank you for sharing this. I'm a career RN, recently retired, who specialized in the NICU. I had never heard of Angelman's. May God bless your family as they care for your nephews.❤️🙏
Enjoyed your story and you will be an inspiration to many. Our 21 year son was first dx with Prader-Willi Syndrome and finally at 20 months dx with Angelman Syndrome. Hang in there....the sleeping will improve. You have a beautiful family! I really think our son Max has made us better people. Hugs!❤
You have probably seen Its our wonderful life blog. Emily has 6 children One of her twin boys has Anglemans syndrome. That's where I learned about it. Great family!
You two are so loving with each other and with your son. Good luck in the future. I am so sorry this happened to you and made your life so difficult. Sweet little boys.
I don't know why God dies this kids! Makes them suffer! I have a nephew who is very handicapped, can't talk or eat. So sad!! Good luck to you wonderful people!
Why would you say such a thing? I have seven children…the first two were bottle fed a cow milk formula and did great. I learned about breastfeeding and all 5 of my daughters were breastfed for between 2 and 4 years but also had cow milk from a Curt starting at age 2…. no problems what so ever…..ever. None of them have ANY food allergies…..milk and food allergies DO NOT RUN in our families so you really need to walk in other parent’s shoes before you make snotty comments when you are first of all not medically trained and second don’t know everyone’s story. In other words…..quit being a know it all meanie! Geeze.
Oh my gosh, I just saw this, and it was so touching. I'm sure you have heard a lot of inspiring comments and have helped other mommy's and daddy's throughout your journey. I just wanted to say thank you. I've been a nurse for thirty years and have not had knowledge of or experience with this disease. God bless your family through this journey, and remember we don't know His plan or reason's but he made sure this young one had the best parents for the job. Prayers for strength, endurance, and faith. God bless you all🥲❤️🩹🙏
When I got Asperger's too, I stayed at altapointe for 2 weeks and every night I got throwed up in my 🛁🚿 bathroom and since that I got no symptoms inside 💠 my stomach. and "everytime that you see is food" like my mom Mekita Ann said if she said that in that dictionary she will lose me before surgery back in 2022 right before the holidays and the new year as well and back in January of 2023 my old LG Stylo 6 was mess up and not work and couldn't charge well, you may now this, that's a lot of money, but thanks to Kelvin this weekend he got my money and Uncle Steve got me a new phone from Cricket® Wireless, it's called the Cricket® Ovation 2 and back this weekend in April I got a new phone charger the same charger as my new phone, Cricket® Ovation 2.
May God wrap his loving arms around this family.
What a bright, beautiful smile…..so precious. You are doing a fantastic job, Mommy and Daddy!
very touching, what a wonderful pair of people... this child was born to the right parents.
I have had the privilege of teaching three angels with angelman syndrome in Calgary .. beautiful young people. Rhett is lucky to have parents like you!! ❤❤❤
Canada sucks
God chose a very special mommy and daddy for a very special boy! Such a sweet soul who, as you mentioned, will never try to hurt another. The world could learn a lot from him. God Bless you both and your precious boys. 🙏
😅no
God is a made up fantasy
What a beautiful little boy, he’s really a little star ⭐️ bless your family 🙏
God definitely picked the right parents for Rhett. He is a lucky boy and you both are lucky to have him in return! You have got this!!
I just want to share with you. They said the same and worse about my sister with Downs Syndrome. Don’t let the Dr’s limits become your own. One day at a time.❤
Wow this brings back memories. My daughter was originally diagnosed with Angelmans syndrome. She had a lot of the symptoms your son has. We went through the mind blowing screams and lack of sleep and flapping of arms etc. turned out she has cerebral palsy with a seizure disorder and non verbal. She was not missing the chromosome. I really feel for you both and funnily enough we are from Calgary as well. Remember to take each day at a time.❤
Such a sweet little boy.god truly gave you a angel.stay strong
Such a beautiful family. My heart broke hearing the mom talking. As a speech therapist I've had only one child who was diagnosed with Angelman's Syndrome. She was a girl of three with a single mom. I'll never forget the mom because she was completely exhausted. This poor child would rarely sleep. The little girl was mobile and had a crib. The mom said she never stopped moving, going in continuous circles in the crib as though she were doing laps. I think about that mom even now (20 years later) and wonder how they're doing.
What a Beautiful Story about a Beautiful Family. Bella & Ben told Rhett's story in a way that really showed the emotional roller coaster they've been through & the love they have for their family. Just beautiful.
❤❤❤❤❤❤
He is an angel,and they are special,god bless that beautiful family
I am sending out my thoughts and prayers and love to this whole family ❤
I'm without words. SO many things i saw is this couple and their attitude i will never forget. Lessons taught in such a deep profound way. God bless precious Rhett and his story. What and amazing story of hope and love.
God gives the right child to the right parents! He knows what is best. God Bless all of you and may God give you the strength and patience to parent Rhett!( you already have the love!)
He is absolutely adorable and LOVABLE 🙂👍🙂✨🧡🌄🌠✨🌛
God bless your family! Prayers for Rhett, you as his parents, and his baby brother, who hopefully doesn’t have the same diagnosis. Rhett is well loved and happy, and that’s a huge blessing! ❤️
You two are so brave... and so loving.
So glad you found support in your journey! Bliss to you!
You have a beautiful family. God bless you all. I'm Rooting For Rhett 💜🙏
How many of us took for granted our children born and raised trouble free.
Until I met this family I had no idea. Are they perfect?, ..yes, for Rhett they are.
I'm so happy to know they will all be fine 🙂 😘🇦🇺
He’s a BEAUTIFUL little boy! You are a beautiful family, God bless you all!
What 2 BEAUTIFUL BOYS…..I know what it’s like having a Child in My Family that’s Not PERFECT but PERFECT for Us…
His Name Is ZEVEN and now is 30yrs Old and Thanks to My BEAUTIFUL SISTER is WHY We still have him….
ZEVEN has less than a 2 yr olds mind and My Sister has to do EVERYTHING for Him and Yes her Husband helps also
We are so Blessed to still have him and his Parents are getting older but He dose have a Sister who loves him so
Much and can take care of him also…These children are Gifts to Families and should be treated with nothing less…
This young man was so beautiful and smiley and I loved it that he was interacting with other kids in the junior high. It was the right thing to do for this young man.
I have enormous respect for this couple and to use a commonly used phrase “ my heart goes out to them” it truly does . I felt it as I continued the video . As a parent whose child was frequently hospitalized my husband and I saw the many single mothers with sick children whose fathers were unable to cope with it all and left . There are so many aspects involved. Grief for the perilous future of the child you love with all your being , fear of dying before they do ,sorrow and sympathy for the pain and hardship you can do nothing to alleviate and so on . Then there’s your spousal relationship , changed forever to accommodate the little one’s needs . Becoming partners in advocacy for your child, sharing care and fears and still managing to love each other. Out sweet good girl achieved 26 years and devastated us by dying one night with no warning . Fortunately we believe she is better off now in a place of love in which she can flourish as she was not able to in this life .I will say a prayer for you all , and tell you that you are magnificent even if you don’t necessarily feel it , YOU ARE ! ❤❤❤.
God bless Rhett you and husband.
I love your beautiful family. ❤ I am so proud of you. Thank you for sharing your story.
He is such a beautiful boy.
Sending prayers for strength and comfort and healing on his lil body. May God help, lead and direct in decisions tonbe made in his lil life.❤❤
Rhett is a very handsome little lad.
Beautiful young family. May God bless you all N heal your son..prayers!!
I Pray Dear Lord To Heal This Child And That These Parents Have All The Support They Will Need And That You Fill Their Hearts With Joy And Peace And Again Healing For Rhett And All Children Afflicted And I Praise You Lord Jesus In Jesus Name Amen 🙏
I am so deeply sorry & your comment about Rhett will never have bad intentions toward anyone made me think that he is an angel sent from Heaven for some reason to you parents. Lord have Mercy on your family.
I was honored to provide organization support for a mom whose beautiful son was born with Angelman syndrome.
It was a huge learning experience for me. I have moved away and haven't visited them for a while... Missing the feeling of profound love & compassion I witnessed. That young man's parents personify service and respect.
Rhett is so lucky to have you both as parents. But your life is so hard 😢. I hope and wish you get plenty of help, because you both and your other child need some normality. Bless you both and ,any god give you the strength to carry on ❤
God gave this Precious little boy to you very special parents. He is in the best hands possible. May God bless you and your family today and always! 💕
what a beautiful family and that boy is so cute
Incredible story. As a young couple and having your first child ill is devastating. My daughter was ill alot but we were fortunate that she eventually outgrew the illness. But I remember crying holding her we loved her so much . We didn't know anything about babies as she was our first so everything we did likec all first time parents it was a guess and hope that it was right. I feel your pain but your an incredible couple I believe the love you have for each other will and has benefited your Beautiful baby boy. Many couples can't handle the stress and break up. As long as you continue to hold the love and respect for each other he will grow up happy and isn't that all we really want. Good luck to you both. I dont have a doubt in my mind that God gave you this child for a reason and this little angle may have an illness but he's perfect for you both. 😊
Your words and story is so similar to our life. As a mother of 3 boys, with different issues, our past 42 years with our youngest had many of the issues your does. Your heartfelt shared thoughts of hopes and dream ring so true. My sons disorder has cross over traits with developmental challenges, struggles, behaviours, seizures, feeding issues, love but 42 years ago, not the family support nor DNA info but constant trips to doctors, specialist, hospital stays, tests….worry, stress, and making a uncharted future for him. Never gave up but forged forward out of love for him like yourself. Others did not understand. Our life is unique. His joy is our joy. Our world is better as he’s in it. It gave us direction and strength. We are better people, more patient than we would of. We try always to see life through his eyes and yes, it’s hard work. There was no Google for us then in 1980 but we did questions and never gave up. He is unforgettable to all who met him, us not but he has made a mark on this earth, teaches others what a living pure angel walking amongst others. I will keep your story with us. Thank you for sharing yours. There is light at the end of the tunnel. We live differently but love the same.
Brought tears and smiles to me, sending you all love and prayers. Kia Kaha! 💜💜
Blessings
May God bless you as you love your beautiful son!
Thank you for saharing your story, what a beautiful family, i wanted to say as a craniosacral therapist one of my first profound moments in my training was working with a boy with Angleman syndrome and he taught me so much about non verbal communication that it has helped hundreds of my clients since, every human being has a something to say, if we are willing to slow down and listen deeply ❤
God bless you all
What a beautiful little boy God bless your family
This was such a kind way to share with others by these wonderful parents that they may help other children.
Rhett surely loves n enjoys his brother. It's so obvious watching his face n reaching out. A handsome little man for sure. Keep nourishing yourself physically and mentally n for your husband as well. Rhett is doing great. I love how you stated his intentions will always be pure. He will bring you n family untold moments of joy n love. God bless you all. Especially you Rhett.
Heartbreaking but so thought provoking. I have never heard of this j
condition and find the strength that these parents have and their willingness to reach out to other parents for info and then pass that on to the less informed is absolutely incredible. You are truly the parents that Rhett was meant to have. May God continue to keep you all wrapped in his love and strength. God bless you, the physicians caring for Rhett and your community of supporters. My prayers and love goes out to all of you.
I understand what you went through. I can't write it all here. I just want you to know I remember how hard it was to be so tired and frustrated. To have a baby that has a condition which is not diagnosed correctly or in a timely manner. I often thought well maybe I'm crazy. But you know in your gut something is wrong. I could go on and on but just want to stress to you how well you spoke of your and your husband's experience. You both obviously love your child dearly. I'm sorry you have had to go through all the pain of it. Please give yourself credit for your guys strength.
Such a beautiful family ❤ & gorgeous children ❤🇦🇺
God bless you all for your precious little boy
I pray that no young couple have to go throw this journey with a new born but God only chooses the humans strong enough to handle these babies. If nothing else please get sleep when you can. Love to your family. 💕💝💐
Bless this family! I’ll tell you this: if the Internet existed 40 years ago when I was having children, I probably would not!
I had amniocentesis at age 36 when I had my third child and the doctor thought I was nuts. He said I was not at risk for having a Down’s syndrome baby but I knew I would not have proceeded with the pregnancy (not judging those who decide to go forward; I knew that I would not).
All of my children were perfect but I’m just in awe of parents who go through the many genetic issues out there. I could not do it.
Grandchildren are all here, perfect, and thankfully my kids are done with their families. We’re so lucky!
I am just in awe of 😅the parents who go through what these lovely people handle so gracefully.
Down's Syndrome _IS NOT_ exclusive to "older" mothers. I've heard of mothers as young as 18 years old giving birth to babies with Down's, and have personally known a mother who was 28 when her 1st child was born - with Down's Syndrome. I'm SO GLAD that you "listen to your own counsel," as way too many people DON'T do that, then live with regret forever afterwards.
(Hugs) from Northern California, from a mother of 3 healthy middle-aged "children," but one who, sadly, has NO grandbabies to worry about. (Frankly, I'm not sure I'd have the chutzpah to worry about grandkids, but my DH would have been THE VERY BEST Grandfather, EVER! For him only, I feel sadness.)
Thank you for sharing! You can see and feel the love you have for each other and your boys! Praying for your little ones and also for you and your continued strength. God bless your family!
Did you know that every time you fart, it's a little piece of your soul escaping your body? Have fun in stinky hell :)
I used to care for an adult male with Angelmans. He was a happy person. Could walk, run, eat normally, go out with his housemates. He was no trouble at all. He was one of the lucky ones.
You are wonderful people your children are a credit to you both x
God bless you and your family the lord is there with you all.God Bess.
God Bless this family.😢
Bless your family. I worked as a aide to care for a set of twin boys with Angelmens. They were 20 years old. One of them had come home from the hospital after a seizure episode. This young man never spoke.. BUT this day I spent the day with him rubbing his head and talking to him and just being there with him. He looked up at me and said "Love you!!!" I couldn't believe it. They are happy young men..
I am so very sorry that this happened in your family.
Your beautiful Angel Rhett and his darling little brother are precious little gifts from God in Heaven 💙 💙 🙏
Beautiful lil' boy, beautiful family💕 Were you aware of Colin Carroll's son has AS & he has a beautiful story on him. If you have not seen this, you should watch this. His son is 20 & is an amazing young man. God bless your son & all of his family!
God bless your family.
First of all, you all have a beautiful family. Secondly, God gave you this little man because, He trusts you with him. I'm writing this from California. I can tell you this, that if you raise this child diagnosed with Angelman Syndrome, you're definitely amazing and troopers. Even people who haven't experienced AS personally in their families have no clue, including the ones making comments here. You two are definitely not alone. My younger brother has four children. He has his oldest so with Asperger's (doing well in the military), a second son with Angelman's, a little girl (who was stillborn-in heaven), a fourth son who also has Angelman Syndrome. It has been tough all these years on my brother, his ex-wife, who is the mother of these four children, and my parents. My parents are extremely instrumental in the raising of the youngest boy as they've basically raised him, themselves, as well as raising and caring for my older sister, who is also developmentally disabled and has never left home. My parents are amazing and deserve everything for their unrelenting efforts and dedication to raise their daughter and my nephew. We help when we can, but they do it all for sure. The Dr's told my brother and his ex, that "they have a 50% chance of each child having Angelman's if they choose to keep having children." My brother and his then wife had the still born little girl, my niece and she became pregnant a fourth time before specialists told her that the second little boy had AS. It seemed like no Dr. could figure it out, exactly. So, this is why they have two with AS. It is possible that their little girl could also have had AS as well, but we'll never know. So, back then in the 90's, I guess it was said, that out of every 500,000 babies born, there is one born with AS and my brother and his ex wife had two. Love you and God bless.
Thank you for sharing this. I'm a career RN, recently retired, who specialized in the NICU. I had never heard of Angelman's. May God bless your family as they care for your nephews.❤️🙏
A
My great nephew has Angelman Syndrom.
They are in Okotoks.
His parents are the best.
Bless you.
Enjoyed your story and you will be an inspiration to many. Our 21 year son was first dx with Prader-Willi Syndrome and finally at 20 months dx with Angelman Syndrome. Hang in there....the sleeping will improve. You have a beautiful family! I really think our son Max has made us better people. Hugs!❤
Worked for Disability Services QUEENSLAND and supported 3 individuals with Angelina's.
You have probably seen Its our wonderful life blog. Emily has 6 children One of her twin boys has Anglemans syndrome. That's where I learned about it. Great family!
Lovely people and I wish them so well. P.S. She looks so much like Taylir Swift!
God bless you!
Queef 🤤
Sending ❤ and prayers
Blessings to your family. You are wonderful parents. 🙏🏻🙏🏻🙏🏻
What a story!!!!
You two are so loving with each other and with your son. Good luck in the future. I am so sorry this happened to you and made your life
so difficult. Sweet little boys.
I wish you would turn the Guitar off!
Attentive parents 🙏
Get him a touch talker. Most AS are very intelligent.
I was employed by a junior high years ago and there was a young man there with angelman syndrome
One day at a time. And if that's too much, one minute at a time.
All 3 of my brothers have children with Angelmans. They are the happiest kids and areAngels Lent to us
Do the doctors say its congenital?
❤🙏🏻
Have anyone ever thought marijuana therapy for the seizures? I did hear that there was some research about this. My prayers are with you❤
This is really great
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🙏🏻
Never heard of this, is it genetic? I see you have another baby, a boy or girl? May God bless your family.❤
It is a genetic condition related to a chromosome.
I don't know why God dies this kids! Makes them suffer! I have a nephew who is very handicapped, can't talk or eat. So sad!! Good luck to you wonderful people!
God didn't do this. If things were perfect we'd be in heaven.
Omg how can you say that ????
No closed captioned ?
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My kids both have dup15q syndrome
My daughter was also allergic to milk protein had to be on nutramagen
They should take equal turns talking back and forth. Husband just sits there for long stretches. And yes , the guitar is distracting
This may be harsh, but I can’t believe even first time parents could be so oblivious to their child’s suffering. I’m astonished.
Oh my….irritating background sound…couldn’t watch the program.
...........😪
Colin Farrell.
Anyone who feeds themselves or a child cows’ milk or any other animal product is highly irresponsible.
Why would you say such a thing? I have seven children…the first two were bottle fed a cow milk formula and did great. I learned about breastfeeding and all 5 of my daughters were breastfed for between 2 and 4 years but also had cow milk from a Curt starting at age 2…. no problems what so ever…..ever. None of them have ANY food allergies…..milk and food allergies DO NOT RUN in our families so you really need to walk in other parent’s shoes before you make snotty comments when you are first of all not medically trained and second don’t know everyone’s story. In other words…..quit being a know it all meanie! Geeze.
From a “cup”…lol…not a Curt.
Oh my gosh, I just saw this, and it was so touching. I'm sure you
have heard a lot of inspiring comments and have helped other mommy's and daddy's throughout your journey. I just wanted to say thank you. I've been a nurse for thirty years and have not had knowledge of or experience with this disease. God bless your family through this journey, and remember we don't know His plan or reason's but he made sure this young one had the best parents for the job. Prayers for strength, endurance, and faith. God bless you all🥲❤️🩹🙏
When I got Asperger's too, I stayed at altapointe for 2 weeks and every night I got throwed up in my 🛁🚿 bathroom and since that I got no symptoms inside 💠 my stomach. and "everytime that you see is food" like my mom Mekita Ann said if she said that in that dictionary she will lose me before surgery back in 2022 right before the holidays and the new year as well and back in January of 2023 my old LG Stylo 6 was mess up and not work and couldn't charge well, you may now this, that's a lot of money, but thanks to Kelvin this weekend he got my money and Uncle Steve got me a new phone from Cricket® Wireless, it's called the Cricket® Ovation 2 and back this weekend in April I got a new phone charger the same charger as my new phone, Cricket® Ovation 2.
lol