‘I thought I had a nasty cold, then suddenly I couldn’t walk or talk’

A 17-year-old girl from Oswestry, Shropshire, who initially attributed her tics to a cold found her life drastically altered when she was diagnosed with functional neurological disorder (FND) and functional hyperkinetic movement disorder (FHMD). Amy-Louise Beaumont, now 19, went from being a healthy teen with aspirations of studying law to experiencing daily seizures and requiring round-the-clock care.

Amy-Louise’s family, including her mother Julie, a clinical nurse specialist, and sister Lucy, a nurse, have been assisting her in coping with the debilitating effects of the conditions. They have had to adapt their home and seek equipment like wheelchairs to accommodate Amy-Louise’s needs, having spent significant funds in the process. Lucy has launched a fundraiser for a wheelchair lift to enhance her sister’s independence.

The journey has been challenging for the family, as they navigate the lack of awareness and support for FND within the healthcare system. Amy-Louise’s everyday life is now marked by limitations, seizures, and the need for ongoing therapies. Despite the struggles, the family remains dedicated to providing the best care possible for Amy-Louise.

Aware of the rarity of FND and the lack of understanding around it, Amy-Louise has chosen to share her story to raise awareness and support others living with the condition. The family is striving to secure funds for essential resources, such as the wheelchair lift that could significantly improve Amy-Louise’s quality of life.

As they navigate the challenges, Amy-Louise’s family hopes for a better future where she can regain some independence and normalcy. Their perseverance and unity in the face of adversity shine through as they advocate for better understanding and support for individuals like Amy-Louise living with FND.