FL Voices, is the Follicular Lymphoma Foundation’s flexible patient involvement network. Share your experiences, shape research, and make a difference.
People living with follicular lymphoma (FL) have always played a vital role in shaping our work; bringing lived experience to shape research, education and patient support.
My name is Leah and my husband Andrew was diagnosed with Follicular Lymphoma in 2021, in his mid-20’s. It hit us both really hard. Since then, I’ve learned how to support him in the best way I can, while also managing my own emotional health because being the person caring for someone you love comes with its own emotional weight.
