Monika Abdullai is my cousin, and until last spring, she was a healthy and vibrant young woman. Everything changed when she began experiencing odd neurological symptoms that no one could explain. After seeing a neurologist and undergoing an extensive workup, all the tests came back negative. Despite this, Monika’s symptoms continued to worsen. She developed limb weakness and her speech became impaired, making daily life increasingly difficult and frightening for her family.

Desperate for answers, Monika traveled to the Mayo Clinic, where she was ultimately diagnosed with Rasmussen’s encephalitis—a rare and devastating neurological disease that affects only 1 in ten million individuals. The diagnosis brought some clarity, but also a wave of uncertainty. Very little is known about the course of this disease, and the future is extremely unclear. What we do know is that Monika’s quality of life will be forever altered. She is now on disability, unable to speak coherently, and her ability to swallow has been affected.

We are raising funds to help Monika with her mounting medical expenses and daily living costs. The support will also help prepare for any future care she may need as her condition progresses. Our family is deeply grateful for any help you can offer during this incredibly challenging time. Your generosity will make a real difference in Monika’s life and help her face the uncertain road ahead with a little more hope.