Wow so this is my first post about MS since my own diagnosis in December 2018.

After a turbulent 11 months of pains, aches and confusion I am now living my new life of painkillers, injections and a fuzzy mind! 😋

I am still learning so much about this illness but what I've learned is how it is invisible to so many people and no two people's symptoms are the same. I may look fine but if you look closely at times I may look confused or tired or disorientated! I'm hoping these symptoms get less severe as I get used to the treatment. 🤞  

The mini marathon in June is giving me a goal to achieve. It would be so easy for me to just sit here and wallow in self pity because of this disease I have for the rest of my life but what's the fun in that... 

With 2 very active kids I need to find my mojo and get it back!!  

Please donate to a worthy cause x