Cheryl McGregor, a 63-year-old grandmother, and her 26-year-old husband Quran McCain are thrilled to announce they are expecting their first child together. The couple, who have amassed a massive social media following, shared the exciting news with their fans in a recent video.
After facing several hurdles, the Georgia-based couple revealed that their surrogate is now pregnant. “It’s finally happening, we’re starting our family,” McGregor shared in the video, her excitement palpable.
The couple explained that despite McGregor being able to provide a viable egg, they opted for a unique path to parenthood. Their surrogate became pregnant using McCain’s sperm, and the couple plans to adopt the child from the biological mother upon its birth. “We’re very excited about it,” McGregor said, adding, “We can’t wait!”
This new addition will make McGregor a mother of eight – she already has seven children in their 30s and 40s, as well as 17 grandchildren. However, the road to this latest family expansion has not been without its challenges.
Last year, the couple’s initial surrogacy attempt was fraught with heartache after the surrogate allegedly breached their contract by having unprotected sex with her partner while the egg was being fertilised. “It just feels like we’re always getting screwed over,” McCain said at the time.
Reflecting on their journey, McCain noted, “At the moment it does feel like people are reaching out to us for the wrong reasons. We’re completely broke. We don’t get paid for our content. And then the surrogate goes and bleeds us dry.” He shared how they had supported their first surrogate financially, only to have the process fall through.
In spite of their trials, the couple’s relationship has remained strong since they reconnected in 2012. McCain first met McGregor while working in a fast food restaurant managed by her son Chris. Romantic feelings blossomed years later after McCain comforted McGregor when she faced negative comments on a TikTok video.
As news broke about Cheryl McGregor and Quran McCain’s surrogacy journey, social media users expressed a mix of surprise, curiosity, and well-wishes:
- “How is this possible?” questioned one user, echoing the confusion of many about the unconventional pregnancy announcement.
- “Congrats, but how?” another comment read, highlighting the curiosity surrounding the 63-year-old grandmother’s path to parenthood with her 26-year-old husband.
- One follower admitted their shock, sharing, “My jaw dropped….”
- Another fan asked what was on everyone’s minds: “IS THIS REAL?!”
The pair began posting videos together, documenting their relationship milestones — including McCain’s romantic proposal at an Olive Garden restaurant in July 2021. Now, their latest chapter will see them become parents together for the first time.
As the dust settles on this controversial couple’s surprising pregnancy announcement, we’re reminded that love knows no boundaries. Stay tuned for our upcoming feature on 16 famous couples who proved that age is just a number when it comes to matters of the heart.
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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