Latex fruit syndrome: The echos of genetics
When I was in 8th and 9th grade, whenever my parents wanted to buy my grandmother something to wear, I had to try it on. That was the age I stopped growing taller, and she and I were the same height. She was a slight women and I was a gangly teen. Thin is not the norm of my family, but as far back as I can remember, grandma was the exception due to allergies. When she was going to visit, finding foods she could actually eat was a trial. Wheat — no. Most fruits — no. Item after item could send her to the hospital, and as a child no one would explain to me what was wrong. She died of cancer when I was in 9th grade, when she was not yet 60 and I was 14.
Looking back from the perspective of adulthood, I see now that my grandmother had celiac disease that was complicated by a Latex allergy and Latex Fruit Syndrome. I had figured out the celiac disease years ago, but it took developing my own latex allergy in 2017 to understand that this slight women really just couldn’t find anything she could eat because she had latex fruit syndrome.
This blog post is the first in what will be a periodic series on my journey in figuring out how to live with a Latex Allergy and includes Latex Fruit Syndrome.
Allergies suck, and we live in a society where allergies cause many to roll their eyes and say “those aren’t real.” Others think that…
