International Children's Heart Foundation

Where Hope Comes to Life

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February 17, 2015

Patient Story ~ Rood Kerry

Rood Kerry was diagnosed with a heart defect at 2 months of age when his mother, Kerline, took him to the hospital with “rapid breathing.”  She said she knew something was wrong because along with breathing quickly, he did not eat very well and seemed to have stunted growth.

Over a period of a year and half, Kerline took her son to 14 different hospitals and clinics, searching for an answer. Rood had X-rays, EKGs, echocardiograms, blood work, and received many different medications.

Rood Kerry PhoneShe eventually received a diagnosis for her son; however, no one could offer a solution to the problem. She was told, “He has a hole in his heart, but we cannot fix it. He will not live long without surgery.” She was referred from hospital to hospital in towns all over Haiti, and even one in the Dominican Republic, but no one could perform the surgery he needed to give him a normal, healthy life.

Being the determined woman she was and searching for any hope for her son, Kerline eventually found the help she was looking for. With the help from Haiti Cardiac Alliance, Rood was brought to an ICHF surgical mission trip in Santo Domingo, Dominican Republic.

Rood Kerry Sleeping PostOPWhen asked how she felt when she heard he would finally receive the life-saving surgery her son needed, Kerline said, “Wow! I felt sad, but I let them do what they needed to do. I was also relieved that I received the answer I had been looking for. And I thank God for that.” The sadness, she explained, was because “surgery is not easy, and I heard only 30 percent of people survive surgery.”

Rood Kerry going homeRood had surgery to repair a ventricular septal defect, or VSD. He did exceptionally well and was discharged from the ICU the following day and went home two days later. His mother was by his side the entire time. After years of constantly traveling across the island searching for an answer, they returned to their extended family in Cap-Haïtien, Haiti.

Kerline’s wish for Rood is that he will start developing and eating better. To the team that made this possible, she wanted to say,

“Thank you, because without you, it would not be possible. I hope you continue to do this work because it is a good work, and you are a blessing from God.”

Filed Under: Patient Stories

February 16, 2015

Waiyl Ali Ibrahem’s ICHF story

Show your #hearts4hearts this February to support ICHF patients across the globe!

February is National Heart Awareness Month, and specifically Feb. 7 to 14 is Congenital Heart Defect Awareness Week. We thank you for your support of ICHF patients and hope you will continue to make more life-saving surgeries possible in February by joining our #hearts4hearts campaign.

Waiyl Ali Ibrahem’s ICHF story

In addition to being born with Down Syndrome and Hypothyroidism, Waiyl Ali Ibrahem was diagnosed with Complete Atrioventricular Canal (CAVC) and Patent Ductus Arteriosus (PDA), causing the majority of his blood flow to go to his lungs instead of the rest of his body. This resulted in rapid breathing, making it difficult for him to eat, which led to his severe malnourishment.

Waiyl Ali IbrahemAt 7 months old, he had the same weight as some newborns and most 1-month-olds. Healthy babies should double their birth weight in the first 6 months of life (5-7 oz per week). Born full term weighing 7 lbs 4 oz (3.3 kg), he had only gained 1 lb 4 oz. Waiyl was a textbook example of what a congenital heart defect can do to the body when it is not repaired soon enough.

A team of ICHF volunteers and local hospital staff were able to perform a complete repair of his CAVC and PDA ligation, giving him the chance grow and develop normally now.

Help us to continue saving the lives of more children like Waiyl this month by…

  • Sharing #hearts4hearts on social media to support CHD awareness and healthy hearts for all children.
  • Giving to the #hearts4hearts campaign this month by texting HEART to 91999 or by visiting https://www.babyheart.org/donate/
  • Become a #hearts4hearts Ambassador by launching your own fundraising page! All you have to do is text HEARTS to 71777. You will receive a text response that will prompt you to set up your own page. Once your page is setup, you can share your personal campaign link with friends and family via text, email and social media!

Also, look to stay updated with ICHF by getting periodic updates sent to your mobile phone. Text Baby to 51555 to sign up today!

It is your continued support that allows ICHF to bring the skills, technology and knowledge to cure and care for children with congenital heart disease in developing nations. Thank you for all you do!

Filed Under: Patient Stories

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Mission Statement

The mission of the International Children’s Heart Foundation (ICHF) is to bring the skills, technology and knowledge to cure and care for children with congenital heart disease in developing nations.  ICHF does this regardless of country of origin, race, religion or gender. Our goal is to make the need for ICHF obsolete. We work toward this goal through our medical mission trips, where we operate on children and educate local healthcare professionals.

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