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Every Life Counts
Приєднався 2 сер 2012
Let love shine through. Because every life counts.
This online outreach is a place where parents of children who were diagnosed with a terminal condition can share their memories, their joy, their pain, and their love. It's a place where the lives of our much-loved children are celebrated, and where we can reach out to parents in similar situations.
Every Life Counts aims to be a valuable resource and source of hope for families and their children who, above all else, seek the gift of time.
We also hope to assist parents in establish perinatal hospice services in Ireland immediately.
A perinatal hospice would give parents the gift of time - providing dedicated, loving and supportive services so that they can have precious time with their special children. Parents who are told that their babies will not live long after birth are not currently getting the support and services they need. These parents and their beautiful babies deserve all our love and support.
This online outreach is a place where parents of children who were diagnosed with a terminal condition can share their memories, their joy, their pain, and their love. It's a place where the lives of our much-loved children are celebrated, and where we can reach out to parents in similar situations.
Every Life Counts aims to be a valuable resource and source of hope for families and their children who, above all else, seek the gift of time.
We also hope to assist parents in establish perinatal hospice services in Ireland immediately.
A perinatal hospice would give parents the gift of time - providing dedicated, loving and supportive services so that they can have precious time with their special children. Parents who are told that their babies will not live long after birth are not currently getting the support and services they need. These parents and their beautiful babies deserve all our love and support.
NOAH'S STORY: "Love shouldn't be defined by someone's diagnosis. Trisomy 18 didn't define my son."
NOAH'S STORY: "Love shouldn't be defined by someone's diagnosis. Trisomy 18 didn't define my son."
#everylifecounts
See more here: www.everylifecounts.ie/stories/noah-and-ayla/
#everylifecounts
See more here: www.everylifecounts.ie/stories/noah-and-ayla/
Переглядів: 6 101
Відео
Ayla's Story
Переглядів 9982 роки тому
Ayla's STORY: "Love shouldn't be defined by someone's diagnosis. Trisomy 18 didn't define my daughter." #everylifecounts See more here: www.everylifecounts.ie/stories/noah-and-ayla/
A Letter to My Son Noah, who had Trisomy 18
Переглядів 2302 роки тому
LETTER TO NOAH, Yvonne reads a letter she wrote for her first born son Noah. A raw and beautiful testimony for a life all too short but full of love. #everylifecounts See more here: www.everylifecounts.ie/stories/noah-and-ayla/
Wave of light October 2020
Переглядів 2734 роки тому
We couldn't host a service this year so we made a short video to remember all the babies that didn't get to stay.
A shower for Freya.
Переглядів 1,1 тис.4 роки тому
Baby Freya was diagnosed before birth with Anencephaly, this is a life limiting condition, but her parents Jamie and Erin spent the time they had with Freya making memories that will last a lifetime.
Mums explain how Every Life Counts can help when baby may not live for long after birth.
Переглядів 3844 роки тому
A special day was held in Belfast castle where the mothers from Every Life Counts gathered to remember and talk about their precious babies. Some of these women had never actually met but it was like they were always friends with the amazing bonds that our babies give us to other bereaved mothers. Please feel free to contact us if you need or know someones that needs our support. www.everylifec...
Little Angels Day
Переглядів 2985 років тому
One of our special angel days where families get the opportunity to share stories and memories and to craft remembrances for their babies. Always in our hearts, never forgotten, we love you always... #compatiblewithlife #compatiblewithlove.
Every Life Counts: "My heart is breaking for that baby aborted because of a misdiagnosis
Переглядів 7925 років тому
Vicky Wall spokesperson for Every Life Counts says "My heart is breaking for that baby aborted because of a misdiagnosis and for the family .... I know how it feels to be told your baby is an 'abnormality'".
Meet Baby Faith Wilson: Our beautiful precious daughter born with anencephaly, she lived for 15 days
Переглядів 1,1 млн5 років тому
May is anencephaly Awareness Month and to start that off we would like to share the beautiful story of Baby Faith Wilson, we were honoured to spend time with Faith and her amazing parents. "SHE has done more good in 12 twelve days than I've done in 31 years". So much LOVE in the beautiful story of Baby Faith who lived for 15 days after birth with anencephaly and gave her parents so much joy. #E...
Every life Counts offers support and hope to families who have received a diagnosis for their baby
Переглядів 6365 років тому
If your baby is very sick and may not live long after birth, we in Every Life Counts are here to offer you support, hope and compassion at this difficult time in your families life #gript
March is Trisomy Awareness Month, we in Every Life Counts are here to offer support
Переглядів 3075 років тому
During Trisomy Awareness month, like every month, we been privileged to talk to families who've been told that baby might not live and offer them love and support on that journey, so that they can let love shine through, and make sure their baby knew nothing but love. #everylifecounts
To the mother whose abortion case was raised in the Dáil...
Переглядів 4975 років тому
"TO the mother whose abortion case was raised in the Dáil, I know getting this news is so scary because I was told my daughter would die. I'm not here to judge or persuade you, just to let you know that if you'd like to talk, I'm a mum who has been through this too and I'm here to listen if that would help."
Rainbows from Líadán: Vicky remembers her precious daughter diagnosed in the womb with Trisomy 18
Переглядів 29 тис.7 років тому
Vicky Wall is from Dungarvan, Co. Waterford. In 2014, 23 weeks into her pregnancy, her baby was diagnosed with Trisomy 18, a life-limiting condition also known as Edward’s Syndrome. On 17th August 2014, at 32 weeks she delivered her little baby girl, who was born sleeping. Vicky named Michael named their little girl, Líadán. “Líadán is our precious daughter. Her short life taught us all so much...
Mary Butler TD, Waterford, speaks on the term fatal abnormality
Переглядів 4867 років тому
Mary Butler TD for Waterford said she wanted to ask “what determines a fatal foetal abnormality” and explained that her 15-year old cousin had CDLS Syndrome. “She has never spoken, she has never walked, but she is a joy to behold. She’s tube fed every day and she has the love of her mother, her father and her brother and her extended family, and why should she be denied the right to live? That’...
Our baby Shane Michael: Dan & Jenna tell the story of their son - the 'bucket list baby'
Переглядів 170 тис.8 років тому
When Dan and Jenna were told their baby boy, Shane, would not live for long after birth, they decided they would bring him on a 'bucket list' of adventures - before he was born. He became known as the 'bucket list baby' and his story was followed by millions worldwide. The courage and love in their beautiful story together touched hearts everywhere, and changed how we see babies like Shane, pre...
Baby Noah was diagnosed in utero with Trisomy 13. His favourite song was Wake Me Up by Avicii
Переглядів 20 тис.8 років тому
Baby Noah was diagnosed in utero with Trisomy 13. His favourite song was Wake Me Up by Avicii
Sarah Nugent speaking of perinatal care on Morning Ireland, 11 August 2016
Переглядів 2598 років тому
Sarah Nugent speaking of perinatal care on Morning Ireland, 11 August 2016
Sarah Nugent speaking about Isabella and the need for perinatal care, RTE, 10 August 2016
Переглядів 4268 років тому
Sarah Nugent speaking about Isabella and the need for perinatal care, RTE, 10 August 2016
Prof Jim Dornan on the term 'fatal, foetal abnormality' : 'It's not a medical term'
Переглядів 4,5 тис.8 років тому
Prof Jim Dornan on the term 'fatal, foetal abnormality' : 'It's not a medical term'
Tracy Harkin: Every Life Counts on PrimeTime: Our children's lives are precious
Переглядів 5638 років тому
Tracy Harkin: Every Life Counts on PrimeTime: Our children's lives are precious
Gemma and Tracy, Every Life Counts, speaking on BBC Newsline, 11th May 2016
Переглядів 3018 років тому
Gemma and Tracy, Every Life Counts, speaking on BBC Newsline, 11th May 2016
Medicals practitioners and experts give their testimonies at the Geneva Conference
Переглядів 739 років тому
Medicals practitioners and experts give their testimonies at the Geneva Conference
Incredibly brave mothers tell the UN: The term ‘incompatible with life' must be discontinued
Переглядів 11 тис.9 років тому
Incredibly brave mothers tell the UN: The term ‘incompatible with life' must be discontinued
Compatible with life and love. Parents speak about their children with life limiting conditions
Переглядів 43 тис.9 років тому
Compatible with life and love. Parents speak about their children with life limiting conditions
Our babies were compatible with life and love. Leo Vardkar: Please withdraw hurtful comments
Переглядів 42 тис.10 років тому
Our babies were compatible with life and love. Leo Vardkar: Please withdraw hurtful comments
Every Life Counts Launch Project Love at Stormont Assembly
Переглядів 16 тис.10 років тому
Every Life Counts Launch Project Love at Stormont Assembly
Baby Lillie - My Special Star. Tanya's beautiful testimony about her baby who had iniencephaly
Переглядів 50 тис.10 років тому
Baby Lillie - My Special Star. Tanya's beautiful testimony about her baby who had iniencephaly
Kathleen Rose: Trisomy 13: How Our Beautiful Girl Surprised us all!
Переглядів 210 тис.10 років тому
Kathleen Rose: Trisomy 13: How Our Beautiful Girl Surprised us all!
Hugs and prayers
You guys did a great job
💋🙏🌹Sois bénit petit ange !
Lovely family.
RIP baby Shane !!!!
Defectful people! The chosen ones!
I lost my grandson in 2017 with trisomy 13 it absolutely devastated us he was 22 months old and I will love him until my final days your daughter is absolutely beautiful and I will continue to pray for her❤
Thank you for your gentle words. You are not alone I struggle to find the words to comfort my daughter, thank you for your loving words and for Noah. You honor him
My grand daughter anecephaly baby was born on may 23,2024 10:37am died may 23,2024 3pm
@@JasmineHurry so sorry for your loss
You are an amazing mommy and person ❤ wow!! I had an early stillborn at 22 weeks 2 years ago and chose to hold and kiss the little tiny fetus after the birth, never regretted that! It's so sad like you said but you'll always be the mom of that precious little Noah . I hope and wish you enjoy raising your adorable little girl and G-d Will give you strength!!
Wow! I’m so sorry for your loss but I’m so glad you choose life 🧸
Thank you for sharing your story. Your love shines through! Blessings 💕
I carried my daughter to term as well. We were going to donate her organs but she died an hour before she was born. She would have been 38 this December. Take care.
💔❤️
So sorry for your loss. Beautiful words.
I’m so sorry for the loss of your precious Noah
Precious soul may she rest in peace❤great momma and daddy
What a beautiful story. If only more people in the field of medicine were compatible and sympathetic with the love a mother feels for her child, no matter what. ❤
I used to be a family assistant to a baby/child with Trisomy 12 Pallister Killian Syndrome. It was such a privilege to be available to care for her alongside her mother. She lived to be 8 years old.
They say that these babies don't feel, can't hear, and aren't conscious of their being. But I don’t believe that. I'm sure they feel the love from their parents and siblings. They know what it is to be hungry and need a nappy change. Every life matters. They deserve the best.
She will be home with Jesus soon. Amen ❤😢
May God bless your family always. Amen ❤😢
Remember that Jesus loves her. Amen ❤😢
She's beautiful❤
Congrats to your baby. You lots are heroes. I admire your efforts and hearts.
💖💖💖
These video companies realy know how to sell
❤😢❤😢❤😢❤
So very sorry for the loss of your precious son 😢 💔
Bless you for caring so much , wishing you everything you want
Tiny angel gone too soon x
A short life filled with love, dignity and peace gives a holy gift to mom and dad forever. God bless you all.
You will see her again shes waiting in heaven when your time comes to meet her again
A beautiful baby 💕💕 Wonderful inspiring parents💕💕
Beautiful ❤️❤️❤️
She's so lovely, precious.
This mother is amazing
She is beautiful
❤
Such beautiful, loving parents. What a blessing their daughter is to their family. Nine years on I wonder whether she is still with us, how she is doing? Would love an update on this lovely, caring family.
😢💔🙏👼💖💖💖
Awwwww Faith is so precious & beautiful..I'm so very sorry for ur guys lose, just remember baby Faith despite not being here on earth she will forever be in ur guys heart🫶💖
Pequeña hermosa bendiciones 😍🙏
Reminds me of my baby girl that died q8 yrs ago yesterday. She had very severe heart defects and other defects, and this is one of the syndromes she was tested for. This and trismoy 18 and 21. All chromosomes were normal. They told me at the time of testing, when o was pregnant, that if she had trisomy 13 or 18, they wouldnt do any life saving surgeries, like on her heart. She did have surgery, but bc of the complexity of her heart malformations, she was just too small to take on such a long surgery. She was on the heart-lung bypass machine for 111 minutes, so she went into total organ failure. But my point is, they tried to get me to terminate my pregnancy with her bc they didnt thi k she'd even survive it. She showed them. She had open heart surgery at 10 days old and went to heaven 11 days later. I miss her tremendously and will love and cherish every moment Inhad with her in those 3 weeks she was here. I don't regret for a second not terminating.
So very sorry for your loss
Shame on the doctors who said she wouldn't feel hungry. What a horrible thing to say and imply.
Your sweet girl is adorable and I love how her siblings interact so sweetly with her. Many blessings to her and your beautiful family.
sweet parents wich have prepared a beautiful, cozy room for their little baby. i hope they will have another baby, to who they can give all the love that they have 😪💝💝💝
🙏🙏🙏🙏
I just went this week to an ultrasound appointment to find out my baby was diagnosed with anencephaly😭 they also asked me if I wanted to abort my child and no way am i going to do that! I pray I get to meet my little man!
Sending you so much love right now feel free to email us if we can help
Thank you for sharing your story. You have a beautiful family. Lots to be proud of. My sister had a special needs child gave her 19 years of happiness. God bless