Read the latest update on Pseudomyxoma and me on my blog at the link below....
Read the latest update on Pseudomyxoma and me on my blog at the link below....
Hey Cavecrawler, it's really good to hear from you!
Thanks so much for sharing the latest installment on your journey - I won't add any spoilers here for those who are yet to read your blog :)
Take care and keep in touch,
Helen
Cancer Chat moderator
Just read your update, fantastic news! I think most of us can empathise re the looming check-ups and scans and the waiting afterwards - I always seem to have so many aches and pains just prior to mine, but once the results are in they mostly disappear.
I am so pleased for you, and wish you another wonderful year of adventure.
Hazel xx
I’m living in a similar state, life goes from one scan to the next, in chunks.
Great blog, and great that your treatment going so well! You write superbly, by the way. And it sounds to me like Basingstoke really is a world class institution, and that you are in the right place. I wish you all the luck in the world for the future. Harry
Hi Harry, thanks for your kind words. The team at Basingstoke are indeed world class. They are a centre of excellence and educate surgeons from around the world on Pseudomyxoma and its treatment. We are so lucky to have them and the team at the Christies here in the UK who can treat people like myself. There are many countries around the world where the expertise and care is just not available. We are so lucky to have our NHS to be there when we need them most despite the pressures they are all under. I can't praise them enough.
Dave
Hi Angela, I hope you are well?
Love to all at Survivor
Dave
Yes, thanks, Dave. Are you coming to the patient event?
Hi Angela, not sure as yet. Have a lot of work commitments at the mo. Would definitely like to be there though so going to try to get there.
Dave