I have suffered with MG since September 2021, and been to more hospital a&e visits than I care to remember.
Lack of understanding through the health service has made this journey to diagnosis unnecessarily long and painful.
Alongside a thymoma that I have had recently removed, which can be common with myasthenia gravis, I still have a long way to go in understanding my future and the treatment available to me.
This is a long term disease, it doesn’t just go away, and can be debilitating at its worst.
Help this disease to become more understood, so that diagnosis, treatment and support becomes an easier process to navigate. Thank you x

Kerrie Hewitt