Summary
“I am proud to do my little bit to help.” Julie, an LA Family Volunteer Visitor.
My name is Julie. I am a Family Volunteer Visitor with the LA. My role involves speaking to those closest to people facing limb loss. This is a very daunting time; life will be very different going forward. Hopefully, I can use my experience to answer their questions and dispel some of the fears.
My husband Mike is a quad amputee (hands and feet). In 2017, he contracted meningitis, was in intensive care for 10 weeks and spent a total of 6 months in hospital. When he first came home from hospital, the future looked bleak, with so many obstacles to overcome. Slowly, we both adapted until we reached a point, the ‘new normal’, where life is different but good. I love to pass on some of the things I have learned to benefit others.
The carer plays a very important part in rehabilitation after limb loss. Often, they don’t want to share their fears with the person undergoing limb loss. Something I always try to mention is how easy it is to fly and go on holiday. The accessibility scheme at the airport means no more queuing; you are fast-tracked through to your seat. We have used it in many countries without a hitch.
Through the LA, I have had the opportunity to meet some amazing people who take limb loss in their stride. I am proud to do a little bit to help.
