Niki's Update on Angelina | Living with Lafora Disease | February 2025
Board member and Director of Family Support Niki Markou shares an update on her daughter's battle against Lafora disease. As of February 2025, Angelina's childhood dementia and other symptoms have significantly progressed. Her family is speaking out to help raise awareness and save other children. Give here: www.chelseashope.org/donate - Chelsea’s Hope Lafora Children Research Fund is an IRS 501(c)3 non-profit organization. Our mission is to improve the lives of those affected by Lafora Disease and help accelerate the development of treatments. Learn more: https://chelseashope.org/
▶︎
What are treatment options for Lafora Disease? | Lafora Disease Therapeutic Overview
▶︎
TV ART SLIDESHOW | Abstract Art for your TV | Jené Stephaniuk | 1hour of 4K HD Paintings
▶︎
Redefining status migrainosus: A narrative review
▶︎
A Child with Dementia and her Loving Sister
▶︎
Long Island teen battles rare disease that affects less than 100 people globally
▶︎
WHAT DEMENTIA LOOKS LIKE BEFORE MEMORY LOSS STARTS — Know This to Protect Yourself!
▶︎
My Story | Living with Schizophrenia
▶︎
The Silent Child | Oscar® Winning Short Film
▶︎
Blue gradient background - screensaver, mood lighting, ambiance, TV art, focus, study
▶︎
Healing Success Story: Colton's PANS/PANDAS is Gone
▶︎
Claire | The Documentary
▶︎
Chelsea's Hope Grant.mov
▶︎
Amelia and Makenzie's juvenile Batten disease (CLN3) story.
▶︎
Eva (6) is not allowed to sleep - Living with Ondine's Syndrome | stern TV
▶︎
Angelina's symptoms of childhood dementia
▶︎
25 Personalities.. One Body | Living With Dissociative Identity Disorder
▶︎
Stolen Childhood (2019)
▶︎
Young Woman is Only 1 in AL Currently Diagnosed with Lafora Disease | News 19 at 4:30 p.m.
▶︎
A Kid with a Terminal Disease and the Parents Who Will Love Her Forever (Batten Disease)
▶︎