Emma Davis

It’s coming to that time of the year again to talk and raise awareness about Multiple Sclerosis (MS)🤍

As most of you know; I was diagnosed with MS nearly 2 years ago. 

MS is a condition that affects every individual differently. Unfortunately for those of us living with MS, there’s no warning signs for when your next attack will be. I am incredibly lucky to have some of the best leading MS specialists and treatments on my side. 

I also feel blessed to have an amazing support network of family and friends - who I honestly can’t thank enough.

MS is defined as a disability; however, it will never define who I am, nor will I allow it to dictate what I can and cannot do.

If you are ever in a position where you might be able to donate and/or have the opportunity raise awareness about MS within your network of people, I urge you to please do so! 

I will be participating in the MS walk 4th of May in Canberra to raise funds, awareness and support my local MS community and programs. 

If you’d like to join me and the team, feel free to register -  our team name is Ginger Ninjas 

https://www.mswalk.org.au/event/canberra/home

Everyone faces challenges throughout their lifetime; so remember to never judge a book by its cover. It’s important to be mindful of others and supportive of one another 🤍 

https://www.mswalk.org.au/s/21805/35154

#msawarness #msaustralia