Johnny continues his battle with determination and bravery. Pam is amazing...great attitude with two broken feet and all...and is just trying to cherish every second with her Toad. I am starting to watch you know who struggle (he who won't be named but I am married to him). I see that as my role...to keep it together so others can fall apart when needed. But I need to get out and get out of this funk! Ginger continues to be a rock and our friends are so helpful, strong, and resilient. I am not going to repeat all the information about the major birthday bash and benefit we had for Johnny, but lets just say that Niles, Michigan, despite its warts and blemishes, has some of the most compassionate and hard working, words-can't-describe people living here. The turnout was such a tribute to Johnny, and the entire Brawley family. As more than one person commented, it was the "Brawley Way"...giving to others. One man said to me "you shouldn't be amazed at any of this. Your family has done so much for others and this is our way to pay them back." This was not about me at all, but more about John and Ginger and their fish fries, Grandma's generosity YEARS ago, and all the time the guys have coached, and taught, etc. And, what makes this even better is there are MANY families like this in our little community. So proud to live here.
As always, I become more "involved" in researching MY cancer during the summer months, just because I have time. Still reading a lot about how slow growing it is, but also that almost EVERYONE has mets later in life. I am now three years out and continue to worry about that, but most days, I can shove it out of my mind.
Another friend Becki was just diagnosed with lymphoma and is battling the chemo poison. She is also blogging on Caring Bridge and is a joy to read. This is a woman with tons of energy so this is hard for her. She remains positive and upbeat and I admire her for that.
Again, heart and mind are heavy these days. That is why I visited here today. Hope it helps.
Molly
2 comments:
Sending you whatever support I can through this electronic means, lady, and hoping that it lightens your heart even a bit. Thinking of you and your family. I am 4 years out, and really hoping that everyone gets at least 2 decades after initial diagnosis (even though each one of us is different). Let me know if I can assist you with research - thought you would be interested in my latest post about research on ACC of the breast. Here's to casting shadows with you for MANY years to come! -Cheeky Librarian
Oh Molly - I am so sorry for your family's loss. My heart goes out to you and your brother's family. I wish I had another means to contact you - feel free to delete this comment from your blog - but I wanted you to know you are all in my prayers. Please let me know if iI can do anything from here - honored to do so. teresa.hartman@gmail.com
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