Cri du Chat Syndrome Documentary
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- čas přidán 11. 03. 2017
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Documentary to spread awareness about Cri Du Chat for a benefit concert held in 2013. Author Leah Moore has written a new memoir Loving You Big. The book is available on Amazon. Read more below.
- Contact Leah @ lovingyoubig@gmail.com
- Check out Leah on Instagram @loving_you_big
- Check out Leah's blog @ lovingyoubig.com/
- Check out: fivepminus.org/
Author Leah Moore evokes conversation and change in her powerful parenting memoir, Loving You Big. Moore’s memoir tells the story of her special needs children and navigates both the beauty and hardships of parenting, especially when things don't go as planned. Moore tells the story of her daughter who was born with Cri du chat syndrome, a rare genetic disorder. After receiving this life-altering news, Moore searched for books that would allow her daughter to see herself represented in the pages, however little was available. Moore’s frustration led her to create Loving You Big, a website providing an honest space for parents to create community, conversation, and change surrounding the narrative of individuals with disabilities. When her twins were born four years later, one requiring visits with an oncologist and the other a brain surgeon, Moore realized writing would further her advocacy. “I realized there was a need to reach out to other parents handling the unimaginable fears of parenthood. I wanted to write a book that changed the narrative about individuals with disabilities,” says Moore. She hopes that sharing her story will encourage other parents who have faced similar battles, and combat the stigma surrounding raising a child with disabilities or health issues. “There is a lot of isolation as a special needs parent, and if my writing continues to create community and create societal changes for individuals with disabilities, then all those difficult nights of writing will be worth it.” Loving You Big is a reminder that no one has to navigate the difficulties of parenting alone.
Such a well done documentary. I’m a pediatrician and learned about Cri Du Chat (cry of the cat) in school and residency, but never had had the care for a child with the syndrome in my private practice, because it is rare. My own child developed rheumatoid arthritis and uveitis at age 4. Laura died in 2019 at the age of 32. We gave out packets of Morning Glory seeds at her celebration of life service because they are a beautiful delicate flower but also a tough vine that will find a way over or around obstacles. Laura always found a way to get on with life despite her many medical woes which progressed through her life. We knew we wouldn’t have her forever; she knew it too because she told me one day “mom, I’m not going to live past 40”. So she did as much as she could, cared about people not things, and always had hope. I want to say to the parents that I know how exhausting and frustrating it can be to deal with insurance and doctors and pharmacies, schools, etc. I also know the joy of seeing a milestone achieved that was very hard won. Laura had lovely friends and their families that helped her, but treated her as normally as possible and I was so grateful for these “bonus” families in our lives. I’m so very glad she was my daughter and I miss her every day. I didn’t mean to make this about me, I just wanted to tell the parents that I understand some of what they experience and to remind them to take care of themselves as well. Much love from Laura’s mom. 💕🐝💕🎄🇺🇸
I'm so sorry to hear you lost your daughter, I understand why you wrote about her. It is gut-wrenching sometimes when you have a child with special needs or medical conditions. I understand, I have a child that has juvenile ankylosis spondylitis and juvenile arthritis. He has told me before "mom I don't think I'll be alive past 30". It breaks my heart. Despite his issues, he carries on and pretends nothing is wrong. Thanks for sharing your daughter's story.
That was so kind of you to share, thank you!
Through your own healing you help others heal. Absolutely share about your daughter; and don’t EVER feel guilty about it!!
My daughter has vascular Ehlers Danlos. She is 24. Has arthritis in every joint and the arteries are comprised. My heart felt sympathies are with you and your family.
I was diagnosed w jra when I was 2....I'm 34 now and I can feel my mortality, it's been a very long journey
These parents are an inspiration… to all parents.
Thank you so much! That means a lot to us. She is now 11 years old with twin brothers!
Very inspirational family as I have a daughter with this syndrome as well The Book is amazing as well
I lives with a young woman with cro du chats and she was so much fun. . She didn’t speak but used sing language. She was strong minded and determined . We loved sharing our lives with her . . My children learned sign language from her and she loved them.
It's so strange but very interesting, that they have difficulty walking & talking, yet still learn sign language... I've never even heard of this til just now.
@@elizabethbowie9753 not strange at all. Verbal language is different than visual language. Not being able to vocalize does not mean a lack of verbal understanding. Expressive language vs expressive language. Also walking is gross motor while ASL is fine motor and even if she cannot do all signs and a child may have some fine motor struggles they can still learn ASL with some differences in the way signs are made. Those around the individual learn that persons way to sign much like an accent when someone from the south in the US speaks but someone from the UK understands them
When you say loved instead of love, it means past tense & i began to wonder is she still alive &/or still in your lives?
Looks like an important amount of medical students including me have found this short documentery while searching for info about the condition. Thank you for sharing this wonderful story. I hope it will spread more awareness among society about CDC syndrome.
This syndrome was missed in my nursing textbook but showed up in a PowerPoint. So here I am researching
I have cri du chat
@@aliceramdom.s I hope things are going well for you. I would like to hear more about your story
Lkkjjj Jim noo
@@aliceramdom.s
I'm sorry to hear that.
I am a medical student. I was looking for something to help supplement my studies. Thank you so much for sharing. You have a very precious little girl. God bless your family.
I am a teacher and just started working with two sisters that have Cri Du Chat. I think they are amazing and beautiful and I wanted hope that they will lead amazing lives where other people will get to see all that they have to offer. Thank you for sharing your story.
why is it called cri du chat? it means cry of the cat... ?
@@OctaviaOG Hi! It's called "cry of the cat" because of a distinct cry that many infants with the syndrome make that sounds like the meowing of a cat
I worked residentially with a kid with cri du chat, another one with angleman syndrome, several trisomy 21 (Down syndrome), several autistics and aspergers. All in the same house unit!!! Most amazing job I had for 10 years. Taught me truck loads.
Mind Mesh you are an amazing person to do that job and to take care of those angels 👼🏻 very curageus : hardest job in the world , lots of respect from a mom with autistic son
As a person with aspergers: thank you.
This condition seems quite similar to Angelman syndrome though this girls seems more high functioning than others I have seen with the same condition
Shows how extremely important therapy is, all these kids should have right to consistent therapy to be able to live to the fullest
@@teijaflink2226 similar trades
I’m a school bus driver and I work with special needs children. Your Video is so powerful positive. Thanks for sharing.
My cousin has this syndrome. She was not walking until multiple surgeries and she was around 7 or later. Your daughter is doing incredibly well. I know how hard it can be. Keep pushing and encouraging her.
Best of luck and maybe my family will see you at the next 5P- conference.
my baby cousin was diagnosed with cri du chat and her parents are completely devastated because we’re from Chile and there are little to no resources for treatment here. Thank you for sharing your story and rising awareness.
dam thats rough
Contact this charity mentioned towards the end of the video, it is for helping parents.
Definitely hit up 5P- community yes its based in the US but it might help you find services nearby to help the cousin grow as best as possible.
Just focus on the progression and getting better/learning. Throw away expectations and just do your best as a family member. Feeding tubes help at earlier ages and sometimes surgeries will be required to walk. Sign language is just as good as the regular languages. The key is being able to communicate with the child as best as possible to ensure they have a happy/good life.
I’m grew up live in rural America. There are absolutely no resources for children/adults with disabilities. Even for the elderly.
You can also visit Leah's website lovingyoubig.com/ to learn more about where to get support.
I just want you to know that your child would not be walking if it was not for your diligence love and compassion for your daughter. So beautiful that she has two parents totally dedicated to her well-being. Most children are lucky to even have one parent that cares so much about their child and take so much time to do everything possible to make their life better. And this beautiful girl has two parents completely dedicated to her🤗 God bless you both!!🤍🤍🤍 Your daughter's future will be bright thanks to your perfect love. ✨
Thank you for your beautiful comment!
I watched their video and totally agree with your comments. I felt and could see, the total love and dedication to their beautiful daughter from her beautiful parents...may god continue to bless you all...
They are saying Chrisean Rock & Blueface’s baby has this syndrome. Very sad 😢
He does: it’s very obvious
I just came from a video with him making cat like sounds. I hope he is able to progress like this wonderful child.
@@NomfundoV8Chrisean is failing to get him any help
@@jenniferatkins3303don’t worry too much if and when baby gets diagnosed Chrisean Rock will be a mama bear to his needs plus she will definitely have a army supporters to help.
I pray she seek help get him diagnosed the sooner the better 🙏🏾
It's nice this child is functioning pretty well. The cases I saw as a nurse were very severely affected. Until I saw this video, I never knew they could be anything but wheelchair bound, unable to communicate, on a feeding tube etc.
I have cri du chat
So close to home. My son was diagnosed with Cri du chat in 2004 . God has truly blessed us with an AMAZING medical team at the Kennedy Center, Montefiore and Blytedale. They're times when we felt lost and discouraged because his condition was so rare which makes it very hard to get services but through it all, they're some medical professionals like Dr. Lisa Schulman🙏, Tammy Fried and Nicole Martinee who made sure our son was not just a number. They exhaust every option possible to provide my son with the services he needed to have a functioning life today at 15 years of age. Today Brandon walks, run, communicate his needs and a lend the length of his tongue if need be😂.
Thanks for sharing your story.
God bless you and your family🙏💞
💖💞💖
I worked as a direct therapy service provider for people with developmental disabilities for many years, and as an administrator in a State/federally funded Early Intervention Program with an emphasis on support for families and community-based resources. I moved into Older Adult services at a point- different and similar, too. Now retired, and so delighted to hear your daughter is thriving and your family's story and promotion of Early Intervention resources to others.
Look at these mighty people. Their love is so strong!! They see the worth in this magnificent child. What a gift: they shared their story with the world.
Every child deserves parents like you 2. Your daughter is a beautiful reflection of your love & dedication to making her world a better place. It’s amazing to see how far she’s come. ❤
What a remarkable story! The parents advocated for her and reaped the benefits. May all involved be blessed this holiday season!
we have a little boy - with CDC - and he looks like your "baby" - really -
we have also experienced so many positive surprises - it is very exhausting, but also such a great feeling.
Our little one can now also speak and at school he learns simple arithmetic and writing - so great!
a lot greetings from Dresden / Germany
God bless him
Bless this beautiful child and her loving, dedicated parents, as well as determined therapists and other professionals. Great!
Thank you for creating this video. I thought Cri Du Chat was just a high pitched cry or so, but this changed my mind completely and now I understand.
as far as I know all children including me with cri du chat are born like cry like a cat.
its kind of the thing with cri du chat.
we lose the cat cry a few months afterwards and it is all different for every person
I teach special education at a low income elementary school in Texas. The majority of our students get an hour of speech or OT therapy or less per month that’s provided by the school district. The case loads our therapists have is ridiculous. Most of our kids are on a waitlist for speech or other therapy outside of school. We never stop trying to teach our students new skills or give up hope. Sadly, in many cases how far a child progresses depends on how much money the families have to pay for outside therapy. It’s truly heartbreaking.
Thank you for sharing that! I agree. That’s why we are trying to raise awareness and do more advocacy work on a federal level
We need more support for parents to support their children at home. Therapists can provide great resources but too many sessions can be exhausting for the child.
@@windybeach2184 I absolutely agree. Many of our daily challenges in our classrooms could be minimized if parents were more aware and involved. It’s important to advocate for your child. Many of my parents believe teachers and therapists can work magic without them putting in any work at home. If I had one dream to come true it would be for parents to be forced to take educational classes on how to parent and navigate life with a special needs child if their child receives special education services. Sadly, many of my parents believe their child isn’t capable of learning and knowing how to follow rules because of their disability so they put little to no effort into teaching them. It’s sad all around. 😔
Your school is out of compliance with IDEIA. I wonder if the state is complying with providing required state funding.
I have an enormous soft spot for kids. I'm sitting here trying not to cry as I watch this sweet little baby achieve so much...
She's absolutely gorgeous.
Parents are very patient and strong. These conditions would be very tough for them.
My Granddaughter has cri du chat. She was diagnosed at about 3 weeks old. She's now. We're in Australia and we couldn't even find a doctor that has ever seen a cdc child. She started walking independently at around 3 yo. My daughter has a blog called the honest pirate, melanie stephens. I know she has people from all over the world reading it, some are parents of cdc kids. Worth checking out.
who diagnosed her?
People like these parents, through having to face such tough challenges because of having to raise a developmentally delayed child, find such resources of strength, love, compassion and tenacity within themselves. In order to allow their kid to reach their full potential, they've had to persist and be determined, day after day, week after week, for years without losing hope, just so that their child could eventually reach the milestone of walking, which most other parents can take for granted will happen when their child is around a year old. I do have great admiration for them. The fact that they dug even deeper, and raised money to help other children receive the care that they needed too, is absolutely remarkable and is very worthy of admiration as well. Their little girl gets a lot of enjoyment out of life and can appreciate all the beautiful things that our world has to offer, which of course is very gratifying to see.
Jordan is beautiful!!! She looks just like her dad. God bless your beautiful family.
❤️ warming, * I have a daughter born with Cru du chat .she's now 23 ** always so happy ..yes theirs struggles, but we all got em.. honestly she seems so happy * always .God 🙏 has all of us Truly..she had early schooling threw our local regional center, at 8 month to 3 years then went to special needs school from 3 to 18 , and she also young adult program from 19 to 21, after 18 years of school .* One morning she woke up and refused to go **! Lol so I'm giving her a year break**!! Soon as covid 19 is cleared up . I will find get another program to enjoy .
Came across this video whislt studying for my Psychology degree. Thank you for sharing your inspiring story! God Bless your wonderful family.
This changes people in so many ways. Great effort and sacrifice of such parents and unconditional love for these amazing children is a testament to so many things. 💜
what a gorgeous gorgeous little girl. how joyful and intelligent she is. I truely admire you both as parents, getting to grips with a child with an inpairment of any kind is so difficult I know. I grieve for the energy I don't have anymore. my mind is like a big cotton wool ball. please take care of yourselves along the way, take time to reconnect with each other and do thinngs that you enjoy together. it is so so important.
I thank God u have such amazing resources. And such a beautiful child. So cute😍
Such dedicated, loving parents.
Not many would be able to do what u guys are doing.
God bless u💜
I just want to say thank you for this video. My son is 6 months old and has cri du chat and this video has really given me hope. Your story has inspired me.There isn't a lot of information out there as you know and I just want to thank you again.
Hi Danielle, please reach out anytime if you would like to discuss more. We are working on making another video to showcase her progress, but in the meantime there is so much we as parents can support each other with. I write about the journey at www.lovingyoubig.com. Stop by to say hi.
Thank you for reaching out. It is a long road but there are so many of us here to help. Please reach out if you ever have questions. You can find me at my blog www.lovingyoubig.com
@@leahmoore6957 i gave a baby girl of 2.3 years suffering from the same but i dont find any way for her progress.plz help me if u can
trust e you're such an mazing strong mother
Thank you Kristen! We are so glad you saw the film and could meet Leah, Zac and Jordan!
How wonderful that this beautiful child has such intelligent, loving and patient parents to give her the best possible chance in life. I hope Jordan is doing well 5 years on.
I wish my parents can see this... see how hard it is to be a parent.. All the love to them, Jordan and the generous people who has helped them.
Thank you for this documentary and especially the comments about the therapists. My son has Agenesis of the Corpus Callosum, another condition with wildly differing prognoses, and thinking back to the therapists who worked with him in Early Intervention, we were so blessed... The memory of their hard work & kindness makes me tear up.
We have a little boy with cri du chat, i'd just like to say thank you for this video. She's absolutely magical :) our boy makes the same faces and laughs sound identical. much love x (edited for the spelling police)
*identical
Thank you for sharing your story. This little girl is a miracle! And the strength I see in your little family, encourages my heart to keep moving forward and never lose hope
I remember when my little sister with cri du chat learned to walk, it took a long time and she worked soooo hard and I am so proud, like the first time she said “I love you” she was like 9 or 10 years old I cried so hard. I remember the first time she said mom and my mom sobbed. My sister loves to paint and she loves to draw, her drawing has improved so much in the past year she can draw faces now
You two are amazing parents! She will reach the stars with you both building her up, and you’ve gotten her every help in every way. Wish you all many many blessings! She is a beautiful little girl.
Thanks for sharing this, I’d never heard of it !
I was studying genetics and discovered about cridu-chat syndrome ( deletion of short arm of chromosome 5).....she's so beautiful...lots of love from india..
My son has not been diagnosed with this exact syndrome, but he is autistic with a profound speech delay and so much of what these parents had to say could have come straight from my and my husband’s mouths. The immeasurable joy and love, but then there’s the hard parts too. I really appreciate their honesty, every child is different, but to hear from parents I can really relate to is so valuable.
Such a beautiful child. A smile can communicate a thousand words. Thanks
Thank you so much for allowing us to come into your home and see your beautiful family. May the lord bless you guys!
These parents heart for their child, and other families dealing with this same challenge, is a beautiful thing to see. Participating in this documentary has surely brought awareness to Cri du Chat
Thsnk yiu so much for sharing your journey. I had never heard of Cru Du Chat… Your little daughter is absolutely adorable…She has her Daddy’s curly hair… it is so clear that this precious child has briught joy to yiur lives. She is so,lucky to have so much therapy..and living, intelligent parents. Watching her learn, walk, and communicate made me smile… God bless you all. ❤❤❤
You are amazing parents, just incredible.
lots of love for her.. She will grow strong and beautiful InshaAllah..
Please dont be discouraged! She is doing great! I know nothi ng about this condition but my grandson is 4 and a half and is in speech therapy. He doesnt have any specific conditions just needs help with speech and from what ive seen with him and your daughter she is very smart and doing very good for her age!!
Wow, what amazing parents. Their dedication and love obviously made all the difference. A beautiful family.
Thank you so much!
You both are absolutely amazing parents. Iam a mother myself can't imagine how much heart it takes to accept that, your child is different from others yet believe in the fact that different is beautiful. Thank you so much for sharing. Iam an early years teacher and studying further and this will definitely be going into my research into different areas of early development. ❤️❤️❤️❤️❤️❤️❤️❤️
You guys are amazing parents. Your child seems happy healthy and well loved. So precious. This video was uploaded 7years ago please could you give an update of her development to date. I appreciate you sharing this.
Incredible story, I had never heard of this genetic disorder, thank you for sharing your story.
A friend had a baby born with this in 1985. He is still alive.
Absolutely amazing video. Thanks for sharing. I'm doing a presentation on cri du chat for my peds class tomorrow and watching this gave me so much more insight.
Wonderful. Hope you get an A!
such a beautiful documentary. the happiness in the eyes of the mother, Leah, when she talks about the day Jordan walks the first time...
Your little girl is so sweet. You have done a wonderful job caring for her. I wish you the best of luck moving forward. May she have a bright future.
This little angel should be about 7 now . I wonder how they are all doing ❤️ God bless this family always
Thank you for watching our film! Jordan is much older than that! She was born in 2011. Visit Leah's website lovingyoubig.com/ to learn more about how the story continued!
This is why we need universal healthcare so all families so children can get therapy
She's precious
Thank you for sharing your experience with your loving child.
Thank you so very much for sharing with us your daughter’s story. I wish you all the best. ❤
Precious parents!! You have made life happen for you and your dear daughter! Hugs for you all…
She is such a precious little girl! God bless you.
wow those parents👏🏻 also such a lovely child!
WOW i m so happy for them that she is walking!! Love and prayers to this beautiful family
This is a truly inspiring and heartwarming story. Seeing people work together like this is so wonderful. This is how we make things happen ... make things better. This is the true power of people working together.
We are getting so many views and comments recently on the video. Would you mind sharing how you came to find the film on CZcams? Thanks!
@@emilydombroffvideos I can’t speak for lifecloud, but it kind of randomly showed up on my feed. You have an amazing family, thank you for sharing!
@@emilydombroffvideos A youtube suggested video. I had never heard of this before and I was interested to find out about it.
Thank you for sharing your story about your child.Thank god your daughter was blessed to have you guys as parents.
Never heard it.. until I researched it for my medical exams.. and laaaa.. came across this wonderful documentary.. i understood it so well.. not because they described it very well but because it made me understand and feel the pain and happiness of the parents... Thnq so much for this wonderful video.... hope lil Jordan is doing well
i don’t know how parents of children with these kinds of problems do it. i can’t imagine the kind of love, emotional trauma, and disappointments they must deal with. they are totally amazing and wonderful people. i have so much respect and emotional support towards them. 🌹🌱
Thank you for your response! I wrote a book, Loving You Big, about our experience to talk about this more! Spread the word to change the narrative about how individuals with disabilities are seen in society.
Good work with this little girl ! I have seen cri du chat kids who were not doing any of this, but they were abandoned by parents, so no one to help them. It makes the difference. Hi from France.
Was studying and came across this term, thank you so much for this wonderful, touching video ♥
My grandson is non verbal, on the spectrum, and was so like this. They had early intervention and such great help and hundreds of therapies. But I have never heard of this.
I feel for this couple, knowing that their daughter will be needing them well into adulthood.
She’ so adorable!! Thank you so much for sharing this great video!
So many challenges we have never been made aware of. Thank goodness there are great support providers to help us in need. Years ago these precious children would have been locked away in an institution. We should never think of what they can't do but rather on what they can do and overcome. These parents are blessed and challenged but our challenged gifts to us enrich our lives in ways you couldn't imagine. It is not easy or always pleasant dealing with some of the challenges presented but nothing in life is truly easy and filled with roses.
What a sweet family! Sending love and prayers for continued success.💕
restore my faith in humanity
As a parent with a daughter who has cdc very nice video. Makes me smile.
I have cri du chat as well
What a beautiful family! Thank you for sharing your story! ❤
Wonderful parents, and also well done kid!! May God bless you all.
I'd love to see an update on your beautiful little girl! 💕
I am so happy for you all! God has blessed you with this wonderful child!
Excellent documentary. The parents & medical team are tremendously in
Thank you for teaching us.
What a beautiful story. Inspiring. What dedicated and loving parents.
big thanx for sharing this,, so inspired and helpful as a physiotherapy student
So thankful that parents are trying to help children who have learning delays when it comes to movement. One of our grand twins (fraternal) has had Low Muscle Tone and did not walk until over 2 years old. Yes, he is walking and he has had physical therapy and now they are working with speech therapy. Our son and daughter-in-law are helping with both speech and sign language as one of the twins was born with low muscle tone whereas the other twin has no struggles.
I had some developmental difficulties for which I was mocked by my parents and siblings, I was called “defective”. Calling a name was so much easier than trying to make an effort. Our one son who had some learning delays, I took him everywhere, got him in Head Start and worked with a nutritionist. I never once told anyone he was “defective”. I even was being told this as a teenager too. I have a high IQ, that I was ever treated this way is very hurtful.
My brother heard these words too and though it was about him, he was born with an inguinal hernia and he committed suicide when I was 22, just before my birthday. He was a very talented and bright person.
I have self-worth issues to this day because of the heartless upbringing I endured. Love your child and get them all the help they need. They are worth it.
That beautiful smile says a lot about who she is, and who she will be.
Thank God you were diligent with Jordan’s PT. Awesome documentary, but you guys are awesome parents so that makes all the difference.
What a beautiful child and family. All the best to you.
This is really well done! Kiddos with this and other genetic disorders are so sweet. While attending a program for blind teenagers, I worked at a summer camp for kids with various disorders. They are some of the best folks I had the privilege of meeting.
What a beautiful family in so many ways.
May God bless your beautiful family!
I had my son at such a young age, 17 days before my 21st birthday, to be exact. My son develops and reached his milestones on schedule, but all of that changed when he was about 20 months old.
I had worked with my mother, who was a preschool teacher, and I had spent about 10 years babysitting just about every single kid in our neighborhood.
When I turned 15, my dad asked me what I would like to do to celebrate my birthday because it was going to be just me and him that day. I told him that I wanted to go and buy a specific piece of clothing at the mall, and then I wanted to go see the movie Rain Man, which was a new release at the time.
I remember feeling so sad for Dustin Hoffman‘s character, end it brought to mind some of the not so kind people that went to my high school who teased some of the special needs kids.
Well, at 20 months I was absolutely positive that my son was regressing in his development. If it hadn’t been for my mother, I never would have known what to do, and I never would have gotten the diagnosis that my son needed. When he was diagnosed at about four years of age, it was just called “autism,“ and not “autism spectrum disorder.“
Nothing hurts more than watching your own child be treated like he or she is less than human by other children, particularly children who are old enough to know better.
My son is well aware of his disability, and he is now almost 28 years old. Hardly a day goes by that I don’t feel sorry for both of us because I was too scared to have anymore children, if it weren’t for my mother I would have raised him by myself, and I would, and still do, get very angry at adults who use the “R word“ as if it was as common as the word “the.“
Having been a single mother for the first 10 years of his life was very exhausting for me, and life continues to be a big challenge for him every day.
This likely won’t sit well with some people, but nearly every day I find myself asking God, or whatever higher power there may be, “why would you do something like this to a human being?“ “Why did you choose him and me?“ “What did I do that was so terribly wrong that you felt you needed to make my already difficult life even more difficult, because that’s not fair to him either?“
I’ve been told too many times to count that “the good Lord never gives you more than you can handle.“ I have to admit that that particular statement is utter nonsense. I know that my son deserves a better mother than I can be.
I could go on and on, but I won’t. I am sure that my comment will evoke A completely mixed bag of emotions, and possibly comments.
Don’t get me wrong, I absolutely love my son, but I don’t love all of the things that he does. Now that he is an adult, the meltdowns that come with autism are much more violent and leave me and my mother with several bruises. We called 911 once, and we will never do that again. A young autistic man does not belong in jail for 2 1/2 weeks among the general population. I didn’t sleep a wink the entire time.
For the second time, I should wrap this up. Even though there is so much more to say, it won’t solve anything.
“She despised the walker” she got this! 😊
Hello! We have been getting a lot of traffic and comments on the video the past week. Can I ask how you came across it?
What a beautiful family and what amazing parents that little girl has. ❤
Love Love Love this beautiful story! Currently in OT school .
Jordan is so lucky to have these particular parents. May she pass more milestones! And it appears that she inherited her father's hairdo!
Great video!