John Navarro
My name is John Navarro, and I was diagnosed with Multifocal Motor Neuropathy (MMN) in February 2024, becoming Gibraltar’s only known patient with this rare neurological condition. MMN is a chronic, progressive illness that affects the nerves controlling muscle movement, causing weakness and fatigue. Like many others with rare diseases, my journey to diagnosis was long and challenging, filled with uncertainty and numerous medical tests.
Living in Gibraltar, a small region with limited access to specialists, made my situation particularly unique. As the only person in my community living with MMN, I’ve faced not only the physical toll of the disease but also the emotional strain of navigating life without a local support system. Thankfully, regular IVIG infusions have been essential in managing my symptoms and helping me maintain as much of my daily life as possible. After my diagnosis, I became a volunteer with the GBS CIDP Foundation International to raise awareness about MMN and offer support to others facing similar struggles. I’m passionate about improving education and understanding of this rare condition, both locally and internationally.
In Gibraltar, I’m also working toward creating a community for rare disease patients. My mission is to ensure that no one feels isolated or unsupported, regardless of how uncommon their diagnosis may be.
As we mark MMN Awareness Month this February, I hope to inspire others to share their stories and join the effort to bring greater attention to this life-changing condition. Together, we can make a difference by spreading knowledge and building a stronger, more connected community.
