An orphan colt whose mother died shortly after giving birth has a new mom – a mare that had tragically lost her foal – thanks to the generosity of strangers and Washington State University veterinarians playing matchmaker.
Pairing an orphan foal and a nursing mare is a challenging task and one that commonly ends with failure. In this case, the connection was instantaneous.
“The mare had only been without a foal for about 24 hours,” Dr. Lisbeth Matthews, an equine medicine and surgery intern, said. “We walked her into the Veterinary Teaching Hospital and past him. He made a noise, and she went, ‘oh, there’s my foal,’ and started making noises back at him.”
It was a surprise to everyone how quickly the mare, named Shelly but affectionally called Mama by her owners, Roy and Faye Lions, accepted the colt. Equine veterinarian Jenifer Gold, who was helping to care for the foal and to supervise its introduction to the mare, said nursing mares frequently reject orphan foals, and when they don’t, the pairing process often takes days.
“She walked in and started nickering at him like it was her own baby – it was unbelievable,” Gold said. “I’ve been doing this for 20 years, and I have never seen it happen that way.”
The foal, which has been named Laredo, was admitted to the teaching hospital by his owner, Spokane resident Rachel Williams, just days after he was born when he started showing troubling digestive issues. Shortly after the colt arrived in Pullman, Faye Lions placed a call to WSU to see if the equine team was aware of any orphan colts needing a nursing mare.
“Our foal was dead, and nothing was going to bring it back, so we were hoping we could help someone else,” Faye Lions said. “It just so happened there was a foal there.”
A day later, the colt and Shelly were introduced.
“For them to be so willing to basically hand over their animal to a complete stranger after experiencing their own tragedy was pretty phenomenal,” Williams said. “I feel like in this scenario it was the worst of the worst for everybody, but there was a little bit of silver lining to the story.”
Williams is also grateful for the care and treatment she and her foal received at WSU.
“I just can’t even find words to say how great the veterinarians at WSU were,” she said. “They went above and beyond. I am just happy I ended up at WSU. I am so glad we were able to match those two up – it is kind of a miracle.”
Shelly will live with Williams until the colt is ready to be weaned, likely in six months, before she will return to her home in Kamiah, Idaho.
“It will be tough to say goodbye because you just naturally start to bond with animals, and she has kind of been my lifesaver,” Williams said. “It will be bittersweet for sure, but I am sure her owners will be happy to have her back.”
During the spring, the equine team at WSU typically sees at least a handful of orphan foals. Equine medicine specialist Dr. Macarena Sanz said orphan foals can be fed a powdered milk formula designed for horses, but those raised by humans typically develop behavioral issues that can become problematic as the animal matures.
“They turn out to be socially weird, have no understanding of personal space, and they are more difficult to train,” WSU equine veterinarian Macarena Sanz said. “The fact that this orphan foal has a mare is really going to make a difference.”
Sanz strongly encourages owners to immediately call their veterinarian if a foal is orphaned, as early care is critical to the animal’s survival.
A Man Who Was Called “The Tree Man” Was Able to Hold His Daughter Again After Many Surgeries
“The Tree Man” is a man whose life has been defined by a rare malformation in his hands. Once dubbed for his distinctive condition, he has undergone numerous surgeries, overcoming tremendous challenges on his journey. Now, with unwavering determination and the skilled hands of medical professionals, he has reclaimed a simple yet profound joy—holding his daughter once again.
Abul Bajandar has a rare condition called ’Tree Man’ Syndrome.
Abul Bajandar, a man hailing from Bangladesh, is afflicted with an extraordinary and rare condition known as ’Tree Man’ Syndrome. This hereditary condition, though non-contagious, is unfortunately incurable, and surgical interventions offer only temporary relief. Abul is not alone in his struggle, as there are others worldwide grappling with the challenges posed by this syndrome.
This syndrome manifests through the development of wart-like skin growths that bear a striking resemblance to tree bark. These growths, while initially small, have the potential to grow significantly in size, resulting in considerable disability for those affected.
He has it from a young age.
The onset of his condition began during adolescence, with small warts appearing on his body at the age of 13-14. Regrettably, as he advanced in age, the affliction rapidly escalated, affecting various parts of his body.
After 16 surgeries he was able to hold his daughter again.
After undergoing a series of 16 surgeries between 2016 and 2017 at Dhaka Medical College Hospital in Dhaka, Bangladesh, Abul Bajandar achieved a poignant milestone—he could once again hold his daughter. The surgical procedures aimed to remove the bark-like lesions from his hands and feet, offering a glimmer of hope in his battle against Tree Man Syndrome.
Bajandar shared the profound joy he experiences spending time with his daughters, emphasizing, “If I recover from this, I want to work again, to build a small business to help my daughters in her studies and to give them a good life.” These words reflect not only his determination to overcome the challenges posed by his rare condition but also his unwavering commitment to providing a better future for his family.
Throughout Abul Bajandar’s challenging journey with Tree Man Syndrome, he draws strength from the unwavering support of his wife and mother. In the face of the condition’s recurrence, their steadfast presence provides him with comfort and encouragement. Bajandar reflects on the transformative power of fatherhood, sharing, “When my daughter was born, she brought me the hope of life again. I didn’t want to leave her as an orphan. I felt like I must live for her.”
Abul Bajandar’s condition returned but he remains hopeful.
Despite facing the disheartening recurrence of his condition, Abul Bajandar maintains a resilient sense of hope. Doctors, initially uncertain about the possibility of the condition’s return, witnessed its reappearance. Undeterred, Bajandar expresses his unwavering optimism, declaring, “My only dream is to recover from this situation and live a healthy life.”
His poignant words reflect not only the personal challenges he endures but also a universal desire for health and well-being. Bajandar’s enduring hope shines through as he states, “All I can say is that I truly believe and hope that a cure exists for this disease.” In the face of adversity, his spirit remains unbroken, embodying the strength of individuals confronting rare and challenging medical conditions.
Another person born with a rare condition has defied societal norms and emerged as a symbol of extraordinary resilience. Meet the girl affectionately referred to as “Voldemort” due to being born without a nose.
Preview photo credit Tansh / Alamy Stock Photo, ZUMA Press, Inc. / Alamy Stock Photo
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