I don’t recall the exact moment I sensed something was different about my son, Juju, but a mother’s intuition often whispers truths before they become evident. Before doctors ever uttered the words “CLN2 disease” (also known as late-infantile Batten disease), I was concerned. Juju, now 8, was a vibrant…
A Mother's Dream to Rise Above
— Cristina Vargas

Cristina Vargas has a strong educational foundation in paralegal studies and an outstanding record of writing as an advocate for rare diseases. Her professional background is focused on activism and legal work that have been boosted by her great writing techniques. At the age of five, her remarkable son Juju was diagnosed with CLN2 Batten disease. She is committed to making a difference in the lives of those impacted by rare diseases. She lives to motivate, uplift, and encourage others! Cristina genuinely enjoys writing and speaking out for causes.
Grief has seasons, but they do not arrive politely. Sometimes the weather, a familiar smell, or a calendar date cracks me open. Late this summer, it found me in aisles filled with backpacks, notebooks, and first-day outfits. For everyone else, back-to-school season meant a fresh beginning, but for me, it…

Among the everyday chaos, I often pause to reflect on what it means to be a caregiver for my son, Juju, who bravely battles CLN2 disease, also known as late-infantile Batten disease. At just 8 years old, he’s not only my child but also a true warrior facing a tough…
This time of year holds a special place in my heart and fills me with gratitude, determination, and a deep sense of purpose. Rare Disease Awareness Month, observed every February, isn’t just a time to reflect on my journey as a mom. It’s also an opportunity to consider how I’ve…
As the new year dawns, I find myself reflecting on the hopes and dreams I hold for my child, who is bravely navigating the challenges of CLN2 disease, also known as late-infantile Batten disease. Each year brings a mix of anticipation and anxiety, and this year is no different.
As the mother of Juju, a brave boy who was diagnosed with late-infantile Batten disease (also known as CLN2 disease) in 2021, I’ve witnessed an incredible journey filled with challenges, resilience, and hope. He’ll turn 8 years old on Dec. 19, and as I reflect on those years, I…
As Thanksgiving approaches, the air is filled with a sense of warmth and an invitation to reflect. This time of year invites us to pause and appreciate the little things that make life beautiful, even amidst the challenges we face. Our family, though small, is tightly knit, and this…
My story begins with my most precious gift: my son. Like any mother, I dreamed that his future would be filled with laughter, adventures, and boundless possibilities. However, our reality took a sharp turn when Juju, my son, was diagnosed with late-infantile Batten disease (CLN2 disease), a rare and devastating…
How can someone maintain a clear vision of their goals when navigating a whirlwind of emotions and striving to be the best mother, wife, and person possible? Life has a unique way of throwing unexpected challenges at us, much like the sudden craving for a sweet treat. Our smiles can…
In the whirlwind of daily life, carving out time for ourselves can feel almost as challenging as seeking a mythical unicorn; it’s like an elusive figment of our imagination. For my husband and me, navigating the fun house mirrors of parenting three children with significant health challenges adds an extra…
My precious son, Juju, took a significant step in his life recently when he started second grade. Earlier this year, Juju became an older brother when my daughter, Serenity, was born with a congenital heart defect called pulmonary atresia. Between this new role, more responsibilities at school, and…
As the mother of a child with late-infantile Batten disease (CLN2 disease), I find myself on a journey that is both heart-wrenching and illuminating. Each day presents unique challenges, and while the emotional toll can be overwhelming, I’ve learned the importance of not allowing those emotions to overshadow my…
My husband and I are parents to two children with rare diseases: CLN2 disease, also known as late-infantile Batten disease, and pulmonary atresia with intact ventricular septum (PA/IVS), a rare, congenital heart disease. We also have a healthy teenage daughter. My vision is to create an ideal temporary…
Recent Posts
- 3D retina model reveals how vision loss may begin in juvenile Batten disease
- Back-to-school season reminds me of the life my son should be living
- Missing my son in heaven brings a unique kind of loneliness
- CBD may delay seizures, shorten their duration in late infantile Batten
- Behind the Batten disease advocate is a grieving mother
- Research takes time that our children with Batten disease don’t have
- Batten disease study from Argentina shows regional data is key
- My son may be in heaven, but I will never stop being his mother
- A mother’s dream for her child with Batten disease, written across heaven
- Low quality of life found for children with juvenile Batten and their parents