Meet Lynne

It’s heart wrenching when you love someone and have  to watch them going through the vomiting and fatigue  of living with FCS. At times, I could feel my husband’s sense of hopelessness, but he was such a trooper despite all of it. I used to get so mad at the illness and the situations it put us in. We really found it helpful to join a support group. Hearing from other patients and caregivers about their experiences – and sharing our feelings and fears – helped provide a sense of hope that there is a future and a life ahead.

My advice to anyone living with FCS –and their family–is to not give up. How you feel today isn’t how you’re going to feel for the rest of your life.
– Lynne, FCS Caregiver

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