The 38-year-old photographer based in Calgary, Alberta, Canada had been trying to conceive for eight years with her husband who is also African. They were finally blessed with the most adorable set of twins through IVF, and now at four years old, people have a hard time believing the children are twins because of their different skin colors. The boy, Kamsi, is dark-skinned while the girl, Kachi, was diagnosed with albinism a few days after her birth. However, just like all other babies born out there, the twins are uniquely adorable and thankfully, they don’t see any color differences and are growing up as best friends.
According to Judith, even before the first scan confirmed that she was having twins, she’d already known. She also had several points of worry during her pregnancy and afterward.
“The second scan revealed we’re having twins; I was told the twins might have Down syndrome,” Judith explained.  “At seven weeks Kachi was always behind, was very small, she stopped growing, I remember the doctors telling me she might not make it — I’m so grateful she did. She didn’t cry initially so I was thinking what’s going to happen, how is she going to be? I was shocked. I thought they had handed me somebody else’s baby, I didn’t believe she was mine.”
Albino twins: A rarity as beautiful as any other
In an essay written by Judith for Love What Matters, she admitted she’d been shocked that her baby girl was born an albino because her family didn’t have any history of the condition. She also worried about the girl’s future and how she would cope in an often discriminatory society.
“I loved my princess like every mother would love her baby but worried about her condition,” Judith wrote. “Gradually, worry turned to sadness and I started questioning God, wondering why He would put me in such a situation. I worried about her future, how society would treat her, how she’ll be accepted, etc. I envied other black babies and thought, ‘Why me? Why was I the one to have an albino baby?’ How did I get black and white twins?”
She explains that her husband had also been in denial at first when they learned of the baby girl’s condition, and they later decided to attend counseling. However, they never really got around the feeling of worry and fear until their babies turned one. Judith wrote that she finally began to see the beauty in her baby girl’s condition, “her gold hair, her brown eyes, her pink lips and everything about her.” The fear eased when she noticed how everyone always admired the lovely girl wherever she went. They would often swoon at the sight of her stunning beauty and she’s always the center of positive attention.
Aside from sensitive skin and eyesight, Kachi is a perfectly healthy little girl with a bustling personality and a strong will. Judith explains that she’s using her skills as a professional photographer to showcase the beauty of having twins with dramatically different skin tones. They are perfect in every way, and Kachi’s charming brother, Kamsi, evidently loves and adores her from their photos.
“I always tell her how beautiful she is, because she really is. I wouldn’t trade her condition for a million dollars because she’s perfect to me in every way. Albinism may have its challenges but I’m teaching her to be strong and conquer whatever may come her way. I’m showcasing the beauty in albinism by constantly taking pictures of her and twin brother. I’m not sure she`s aware of her uniqueness at the moment, but eventually she’ll know, and it’s my responsibility to educate her and teach her to love herself no matter what.”
More about albinism
Albinism is an inherited congenital condition characterized by the absence of pigment (melanin) in the skin, hair, and/or eyes.  It occurs when there is a defect in one of the genes that control the production of melanin in the body. Kachi was born with a type of oculocutaneous albinism (OCA), the more common of the two forms of the conditions where the skin, hair, and eyes are totally without pigment.  The other form, ocular albinism, primarily affects the eyes. 
One in 20,000 babies around the world are born with oculocutaneous albinism, and they usually experience a range of eye conditions, usually decreased vision sharpness and strabismus, sensitivity of the skin to light, and increased risk of cancer. 
Albinism is common across Africa and quite rare in the rest of the world.  This is believed to be a result of consanguinity, the inheritance of identical genes by descent. In many parts of Africa, even in this modern-day, albinos are still ignorantly stigmatized, ridiculed, and sometimes abused or even hunted due to countless superstitious myths, and legends about their condition. They are also the objects of intra-racial skin tone discrimination where people from their own races question their true identities.
However, albinism doesn’t make a person any different from everybody else. It should be regarded as a point of uniqueness such as blue eyes or red hair. No one should be discriminated against because of anything, especially not a congenital condition they didn’t choose, one that’s actually really beautiful. All the myths, legends, and superstitions are completely false and should never be taken seriously. People with albinism deserve to be treated equally and with dignity as stakeholders in society.
- “Mum of black and white twins says people don’t believe they are both hers.” Yahoo. Francesca Specter. July 3, 2019
- “Mother of Twins That Appear to Be Different Races Thought There Was a Hospital Mix-Up.” NTD. Colin Fredericson. July 7, 2019
- “Albinism.” Health Line. Rose Kivi and Matthew Sola. September 16, 2018
- “Oculocutaneous albinism.” NIH.
- “Ocular albinism.” U.S. National Library of Medicine.
- “Albinism in Africa: Stigma, Slaughter and Awareness Campaign.” Dermatologic Clinics. Cruz-Inigo et al. 2010.