I have had some beautiful notes and cards from friends, colleagues and students, telling me how I have impacted their lives. I appreciate every one of them. I also have people saying they will pray for my recovery. This is a complicated thing to hear. While I appreciate postive thoughts and people telling me they are thinking of me, the best I can hope for at this stage in my disease is a pain free and long(er) life. My hope is to make it beyond a year from my diagnosis.


I’m finding myself with a lot of questions these days. At school, when I present the kids with a big essential question, I ask them to write as many other questions on the topic that they can think of that might help them answer the big one. For example, the question “Why are the orcas not successful in the Puget sound?” leads to so many more questions and they always come up with big wall of post it note questions!!!
Question: What’s the meaning of life? Here’s Stephen Fry’s response https://www.rte.ie/player/series/the-meaning-of-life-with-gay-byrne/SI0000001819?epguid=IH000322841 and I think it’s an interesting video. Funnily enough the same question came up in an episode of call the midwife https://youtu.be/WiZZ1RBVJMI! At the end of Monty Python’s “Meaning of Life”, the host from “The Middle of the Film” opens an envelope and blandly reveals the meaning of life: “Try and be nice to people, avoid eating fat, read a good book every now and then, get some walking in, and try and live together in peace and harmony with people of all creeds and nations” (and I will add, sexual identity).
I’ve also been thinking a lot about language around cancer. From the start of this, I didn’t want to think of myself as “battling” my cancer. Thinking of fighting against something inside me didn’t feel right. Reading https://powerfulpatients.org/2019/04/24/words-matter-why-cancer-isnt-a-game-of-winners-or-losers/ really connected with me. I’m not waging a way against my tumor, I’m living with it. Doctors tried to quell the growth and advancement of my disease, but no matter how positive I am, my “attitude” and “fight” won’t make a difference. I can, however, enjoy whatever time I have and stay as positive in myself as I have always been. I recommend everyone read the article above completely. It’s an interesting shift in perspective for many people.
Update: I’ve had three (?) rounds of Avastin infusions, every other Tuesday so far. This infusion is not going to halt or reverse tumor growth. Rather, it will help with the symptoms that I’m experiencing from the tumor. Before the Avastin, my arm and leg on my left side had been completely unable to be moved. Since I’ve started these infusions, I’m now able to scratch my head with my left hand! This may seem like a small milestone, but to me it’s really exciting. I’m hoping that the Avastin will continue to help my physical symptoms as I continue to have more infusions
Project risingwild is More than i. Ever hoped for! Such a focus for me as I navigate this journey

Daily routine
-wake up
-meditate and write my gratitudes
Breakfast then pt
Poop! Very important
(Connect with my community supports (mess on social media and whatsapp)
-walk
11 am nap for an hour
Walk
Hang with family
Dinner and bed!
You are so loved . I’m so grateful to know you and how much joy you brought to my parents, Dale &/Sharon
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You are truly amazing Dawn. I have just read this recent blog to Diane. We were talking about how you have both started your journeys at the same time last year along with my sister too. Each journey individual but all individuals are the most amazing people I know! So much learning you are sharing along the way. Wishing you all the very best and sending our love ❤️ xx
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Thank you so much. 💓 each journey is very much individual
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Coucou Dawn, Très contente d’avoir de tes nouvelles, tu sais que je pense très souvent à toi même si je suis très loin, la distance n’efface rien…. Plein de bises
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Just popping in to say hello to a beautiful lady of such wonderful heartfelt knowledge and to say well done!
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You are so kind
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