Micaela Ramón: A Galapagos Islander


Micaela Ramón was born on Santa Cruz Island, one of the many islands that create Galapagos archipelago. She currently lives with her mother, her step father, and older sister her home island. She works in her mother’s business of selling natural medication created from nature. Micaela’s cheerful demeanor would never suggest that she has CF and she did not even know that she had it until the age of 13.  Micaela is the only person with CF in the Galapagos Islands!

Growing up, Micaela had a persistent cough and was repeatedly sick. Her mother called it “the cold that never got cured.” Initially she was diagnosed with bronchitis, so she took medicine for it, but it failed. She was still coughing and at the age of 6, she had her first hemoptysis which she recounts being very scary because no one knew what to do. Doctors prescribed her any and everything to minimize her symptoms and even diagnosed her with tuberculosis, sinusitis, nasal polyps (for which she had 4 surgeries) and allergies. The doctors went even far enough to claim that her mother was crazy and was making her sick! Even though this was not the case, sadly her mother started doubting herself due to the fall out occurring between her and Micaela’s father during that time. Micaela’s mom never saw her daughter low body weight as alarming because everyone was thin in their family.

When she was 13, her mother noticed that she was sicker than normal due to having digestive issues and a cough and took her to a renown children’s hospital, Roberto Gilbert Hospital de Niños. Her doctor, Rosa Briones, informed Micaela and her mom that she had CF and would have to do a month of IV medication every year for the rest of her life, starting immediately. A week later, she met Anthony who had CF and he was required to do same treatments. Being new to CF therapy and very curious, she became friends with him, and he helped her understand the disease. She joked about how they made the nurses follow them around to separate them, but they were still able to remain in close quarters when the nurses were not paying attention.

In her third week of the IV medication, her cheeks pinked up, she became taller and gained 8 pounds. She was breathing easier and from that moment, fell in love with the hospital. However, she was only allowed to be there until she turned 18 and has been jumping from one hospital to another since. This means being taken care of by new and different doctors. As a result, she hasn’t done the month of IV therapy since age 18; Micaela is now 22.

Micaela is full of positivity and joy. Her doctor told her that she has good lung function because she loves to swim. Along with that, she is extremely patient and “takes almost everything in a good way” When Micaela was hospitalized, her mom read to her, another one of her hobbies. She enjoys the natural wonders and beauty of the Galapagos like going to the beach, visiting the farm to see tortoises, farm animals and simply walk around.

When she tells people that she has CF, the first thing that they usually say is, “you seem healthy to me.” She mentioned that in the past year, she has been more open about her condition and has been educating her friends and family about CF. They tend to forget that she is sick, which she takes as a good thing. She values the time that she spends with her community, especially her mother and enjoys cooking with her, helping with dishes or cleaning. She cheerfully said that she’ll even sing and dance around her or they just gossip.

She recounted one of her biggest life accomplishments thus far being when she was 14. Although she was sick, she felt empowered and won a cruise around the Galapagos Islands because of her good grades! The cruise was on the Endeavor ship of National Geographic. She remembers seeing the most beautiful places and enjoyed being on the water. “For 7 days, I was in heaven.”

Having cystic fibrosis has taught Micaela a lot. She has learned to listen and accept people as they are. “We all have something that makes us special and I like to hear that about people.” She describes herself as a “no judge zone” and tries to see the good in everything. She takes nothing for granted, not even a meal, and feels thankful all the time. Even when she has trouble, she reminds herself that she has a good life.

In the future, Micaela would like to own her own business. She’s interested in potentially being an English teacher and doing something related to tourism. She wants the illness to be better known and to see earlier diagnosis of CF like it happens is some other countries. In the end, she hopes for a cure.