Please LISTEN to MY STORY here and SHARE THIS LINK & TALK ABOUT Myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) so we can improve research, funding, understanding and compassion around this condition.
I’m grateful to Nick, Jess and Ducko from Hit 106.9 Newcastle radio station for sharing my story to raise awareness for this very important global awareness day.
Please listen with your ❤ with empathy and with an open mind about this extremely misunderstood condition.
There was a lot more I would love to share with the world about my journey, treatments, and golden nuggets I have learnt from having a blind illness for 13 years.
I’m very lucky🌞, my symptoms are little compared to others, and I ❤ MY LIFE. Yes, I struggle every day, however I’m learning every day to nourish my body & be grateful.
Did you know that:
🦋1 in 100 Australians are estimated to have ME/CFS
🦋25% of people with ME/CFS are housebound/bedbound
🦋 it has 50 yrs of recognition as a neurological disorder by the World Health
🦋There is limited funds and services to assist financially so many families, like mine end up being on 1 wage and out of pocket $10-20K annually for medical treatments with no subsidy!
🙏Thanks in advance for #spreadingtheword and SHARING THIS STORY
Remember share it with ❤, never feel sorry for me, that’s never my intention! Just send love and positive healing powers
Much ❤ to you all