Having been diagnosed with Myasthenia Gravis (MG) in 2013, I continue to work full time, exercise regularly, travel and live life fully. In September 2014, I had a thymectomy but sadly, like 70% of people who have the operation, my symptoms continue.
In 2015 I posted a blog every day for a year and hope to raise publicity for the condition and also for the charity that has supported me Myaware during this time. I have continued to post blogs after 2015 when I have something new to say and am always willing for guest blogs if you have something to say about living with MG.
Disclaimer: I am not a medical professional. Any advice/tips given on this blog are based on my own personal experiences and should not be treated as medical guidance. You should check any ideas picked up from this blog with your doctor/consultant.
If you would like to get in touch you can reach me on firstname.lastname@example.org.