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Keeping you up to date

Thank-you notes

Dear friends, I have finally finished my thank-you emails. They have taken me over a year to write.  I have tried, where possible, to add a personal touch to each one, and it has been very emotional writing them. Apologies that it has taken so long, there have been more than 777! You should be

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July update

Well we’d always like an update to be positive, but that is something I can’t do today. I had a scan last Friday, and unfortunately it shows disease progression. There are two new metastases in my brain (fortunately not in very important bits!) and multiple small nodules in my lungs. One nodule in my lung

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February update

Philosophy You know its funny this preparing to die thing. It feels a lot like normal life. Each day is much like it was in the past. There are some very notable differences. I work less. I spend more time clearing up and clearing out my life – decluttering and simplifying things as much as

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Jo's cancer treatment

Update for December 2020

Well its a long time between blog posts. Cancer update: The chemotherapy protocol I was on initially – eribulin + Keytruda (this is the really expensive immunotherapy one we/you are funding), did not work. I could feel my lymph nodes enlarging, and just prior to finishing prescribed course of treatment (8 x 3 week rounds

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Jo Lauchie Ben Smiling family day

Three rounds of chemotherapy down… more to go.

This week marked the end of my third round of chemotherapy, and also my third dose of Keytruda (“pembro “).

There isn’t a great deal to report medically. I am tracking ok. Few side effects, no nasty autoimmune effects from the Keytruda – taking the brakes off my immune system can lead to my immune system attacking just about anywhere.

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August update on cancer Treatment

The first time I had chemotherapy, I cried. I had to sign a consent form that I understood just what was going to happen to me. Of course, I couldn’t read it. Most of that day was a blur, and my eyes were tightly closed. But the finality of consenting to literally poison being pumped

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Chemotherapy is over

Chemotherapy is over. Officially since mid February. This means I am seven weeks post chemo. My hair is growing back. First my legs have tiny blonde hairs of only a few millimeters. I notice it here first around the tenth of March. I luxuriate in feeling for stubble and hold them up against the light

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I feel like I’m in a cage

I feel like I’m in a cage. A cage with no key. There is no escape. I will always feel the bars. My sister visited. She is perhaps the only one who acknowledges that the odds aren’t good. Everyone else is buoyed with optimism. “You will beat it”, “The odds aren’t good” I say. “I’m

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Hair

My hair is falling out. In drifts and tangles it comes away. Settling on my pillow, in my hair brush, on my collar, like autumn leaves. My head still has hair but it is frizzy and lifeless. The exodus cannot end well. Despite the dreaded cold cap, I am now succumbing. I have finished 12

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I want to live long enough for Lachy and Ben to have meaningful memories of me.
Joanna Griffith