Well hello there it's been a while since my last post,things have been busy i've moved house and life is good.Even though it was a long boring night i loved volunteering at the pink ribbon walk so much so that i did a bucket collection at the glasgow fort on saturday there and i loved it! My sister says i was born to talk rubbish to the public (i think there was a compliment in there somewhere) and also that my mum would be proud.Although i came on here thinking about my mum and her loss and to volunteer in her memory i am now struck by the amount of people afected by this disease and the wider impact of it all.The people i have met have been awesome whether there volunteers,family or battling this disease.There are sadly people lost everyday to this disease but the wider family is so much bigger! To everyone out there stay strong you are not alone 🙂 until next time x
Happy New Year Craig, and welcome.
I lost my mother to this horrible disease when I was in my early 20s but she had been ill since my teens. A cruel and indiscriminate disease and I still feel angry at mum being taken so early, for what she lost as well as the life we would have gone on to have together. Definitely worth talking about. I didn't realise until I was diagnosed myself, how much of that hurt and anger was still bottled up inside of me and have - in great part thanks to the wonderful friends on here - been able to talk it through. I never think it is good to keep these things bottled up. How lovely that you now have your own son. Your mum would be so proud of you and her grandchild. Hope 2017 is an excellent year for you. Mary Grace
Hi Craigy, I'm so sorry you lost your mum at such a young age. It's so good you are now able to talk about it and come on here and write about it. You sound like such a lovely guy I'm sure your mum would be so proud of you. I have a 44 year old son so I know what I'm talking about!
Happy Birthday
All the best for the future,
Pat xx