Welcome to my blog created on Mother's Day 2010, after receiving a Stage3 BC diagnosis. If you are a new member of the Sisterhood of Cancerous Breasts, I bow to you Sister, you may want to read from the beginning. If you are already a Follower, thank you Dear Reader, for your sweet company. Come in, make yourself comfy, and I will tell you a story. 2018: I’m part of a new sorority now. Always wanted to go to Club Med, not Club Met! It’s back and so I’m back!
Saturday, July 21, 2012
Wednesday, July 18, 2012
Farewell Y-Me, sad sad sad
I am very sorry to say that a significant resource for me during and after cancer treatment has closed after 30 years due to lack of funding.
Chicago based Y-Me, aka Network of Strength, was a huge help to me in the early days after diagnosis, during treatment and beyond. I regularly visited their website to participate in chat forums with other breast cancer survivors to discuss a huge range of topics online. It was such a comfort and resource to me, and I made many friends there. Many of you read my tribute to a Sister who was very important to me, Kimberly. The Y-me forum is where we met and started corresponding.
I can't imagine my journey without it! I am so so sad, especially for the newbies, that this resource is gone! There were many days I spent hours on the forum, talking with my Sisters, getting love and encouragement and wisdom wisdom wisdom from ladies who been there done that!
If you are a Sister who frequented Y-Me, please come visit me here, I am looking into a way to add a section to my blog that would allow for chat.
I made a luminary last year for the Sisters that I frequently chatted with, and I'm so thankful that at least some of us exchanged email and snail mail addresses, but for many, I have no idea how to contact them.
If you are a Sister who is a regular to my blog (Hello Faith&Hope, Jill, Debra, Bobbiejayne, Pat and Jane Marie), please spread the word, and let's keep the conversation and love and support going.
Thank you thank you so much Y-me for all your years of support and dedication to breast cancer survivors, like me.
I'll be making another luminary for my Sisters this year too. I thank all of you Sisters, I hope those I'm not in contact with find me.
Thank you Y-me. Thank you.
Chicago based Y-Me, aka Network of Strength, was a huge help to me in the early days after diagnosis, during treatment and beyond. I regularly visited their website to participate in chat forums with other breast cancer survivors to discuss a huge range of topics online. It was such a comfort and resource to me, and I made many friends there. Many of you read my tribute to a Sister who was very important to me, Kimberly. The Y-me forum is where we met and started corresponding.
I can't imagine my journey without it! I am so so sad, especially for the newbies, that this resource is gone! There were many days I spent hours on the forum, talking with my Sisters, getting love and encouragement and wisdom wisdom wisdom from ladies who been there done that!
If you are a Sister who frequented Y-Me, please come visit me here, I am looking into a way to add a section to my blog that would allow for chat.
I made a luminary last year for the Sisters that I frequently chatted with, and I'm so thankful that at least some of us exchanged email and snail mail addresses, but for many, I have no idea how to contact them.
If you are a Sister who is a regular to my blog (Hello Faith&Hope, Jill, Debra, Bobbiejayne, Pat and Jane Marie), please spread the word, and let's keep the conversation and love and support going.
Thank you thank you so much Y-me for all your years of support and dedication to breast cancer survivors, like me.
I'll be making another luminary for my Sisters this year too. I thank all of you Sisters, I hope those I'm not in contact with find me.
Thank you Y-me. Thank you.
Sunday, July 15, 2012
Vallejo Relay Rocks!
This video is from the Vallejo Relay for Life Ice Cream social for survivors, held at Merrill Gardens in Vallejo. Thank you so much Glenda Petterson, this year's Vallejo Chair, for inviting me to speak. It was great fun, and the ice cream was good too!
Thank you Glenda for all the love and support of my blog! |
My great kid. |
Vallejo Relay Committee Members and ACS Staff Partner, Ashley Chappell |
Special thanks to my videographer and techi guy Zac! I love you Zac, aka Robin here on the blog. I never would have survived the long summer of chemo without you Son, while Daddy was at work and Adam was on tour,
you were the man of this house,
taking care of Mommy.
If you are a cancer survivor, I can't say enough about what Relay for Life did for me. Visit the Relay for Life website to find one near you.
I've raised $340 of the $1,500 I set as my goal. Every little bit helps. Click here to visit my Relay page and donate online for me, my home Relay is August 4 in Vallejo!
Tuesday, July 10, 2012
Relay 2012 and other musings
On my way to Concord Relay |
I replied "at least I wasn't texting."
I really enjoyed myself at the Concord Relay last Saturday morning, and I thank you very much Cathy Guzman, Survivor Chair, for requesting me to be your survivor speaker. It was getting hot early out there, but that didn't stop the wonderful enthusiasm on the field and track at Concord High that morning.
I always try and add a little something new to each speech I give. This time I started by recalling the day I sat waiting, on the edge of my bed, for the phone call. I had my mammogram earlier that day, and I knew right away something was really wrong, because they took so many photos. I sat on the edge of my bed, staring at my phone.
Primary care doctor called "Yes, there is something suspicious... I am going to order an MRI and biopsy for you, and I'll call you back with the details." We hung up.
I sat.
Deep breaths.
Trying not to pant.
I was scared.
This couldn't be happening.
Maybe it's all a mistake.
I called Doctor back. "Dr., I'm a best case scenario, worst case scenario kind of girl, was there anything else the radiologist said, or any other information you might have for me? The waiting is killing me."
There was a very long pause.
"Debbie, the radiologist told me that in his years of evaluating mammogram films he would be very surprised if this is not breast cancer..."
That was April 7, 2010,
and two weeks later,
on April 21, 2010,
I was diagnosed with Stage III lobular carcinoma, breast cancer in my left breast.
One of the first phone calls that my Husband made was to the American Cancer Society, and that was the beginning of my family's relationship with ACS.
This is one of the reasons why I participate in Relay for Life, not only on a team raising money, but this year as an ACS Hero of Hope. It's really important to me, and kind of my way of paying back all the support I got from them.
Heroes of Hope for California, 2012 |
My hopefulness is supercharged.
The rest of the day at Relay is almost like a fun fair or carnival, with all kinds of events and entertainment for the whole family.
My favorite part of Relay is the Luminary Ceremony, which is usually about 9pm, when it gets dark. The lights are dimmed, and the whole place is lit only by luminarias made in honor of those fighting and surviving cancer, and in memory of those lost to cancer. I was the Luminary Speaker at last year's Vallejo Relay, and what a magical, spiritual, blessed night that was for me.
These are the Luminaries I made for Mom and me. |
I've got my work cut out for me a couple weekends from now, when I will be the opening speaker at the Oakland Relay on Saturday July 28th, then later that night at Belmont as their Luminary speaker, wait, I'm not done yet, then the next morning, I'm heading to Novato as their Fight Back speaker.
24 hours of Relay but in three different cities! Talk about Relay hopping! I'm excited about this marathon coming up for me, and I'm pushing myself to speak at as many events as I possibly can that I get requested for. Every single time I speak at a Relay or other survivor event, I pray that just one person will be comforted and realize they aren't alone in this. Something magical happens every time.
I've been blessed by bear hugs from survivors and caregivers, and often brought to tears by the sacred quiet things people say to me. Like at the Berkeley Relay for Life, when a young girl, probably about 12 who had also lost her Mama to cancer like me, hugged me and whispered "I was only five..."
UC Berkeley Relay for Life:
Cute coeds who wanted a photo with this old lady. |
Hi Brittany, sweet girl! We are FB friends now! |
My son Zac, known here on the blog as "Robin" |
Then a gentleman named Manny approached me, he had someone in his family recently diagnosed with breast cancer and he was looking for any suggestions I might have, so I gave him my blog address and my cell to give her in case she wanted to call me.
At the Willow Glen Relay, I met another breast cancer survivor Marie, and also an older gentleman, who told me what a good job I did, and he really appreciated that I made people laugh and cry. In fact, after my speech at Concord, the survivor chair Cathy said "Hey that wasn't in your contract, to make us cry!"
Last year I raised almost $1,100 for Relay, and so this year, I set my goal for $1,500.
I'm only a month away from my home Relay in Vallejo, and thanks to my generous friends I've raised $290.00 so far, but I've got a long way to go!
I'm hoping that between my family and friends, my FB friends, and also with the help of my blog, I will be able to reach my goal.
If you, Dear Reader, would like to help, here is the link to my Relay page. You can donate online and even a $5 donation is appreciated. Every little bit adds up. If you can do more, then of course, PLEASE DO, and I thank you in advance.
RFL FY12 CA Vallejo CA: Ms. Deb Clay | The American Cancer Society - 2012 Relay For Life of Vallejo CA
I never thought I would need the services of the American Cancer Society, but I did, and they were there when I needed them, and continue to be.
I have noticed that several of my old blog posts are being read, so I am assuming another newbie Sister has found me. Hello Sister. Welcome. Please comment, I would love to hear from you. There there now. Just a reminder, the American Cancer Society has a 24 hour hotline, just call 1-800-ACS-2345.
Thank you again everybody following Cara's story, and praying for her. I thought you'd enjoy these recent photos she shared with me.
Our doggies, Muffin, Hallie and sister Cassie, waiting for popcorn |
This girl makes neutropenic fashionable. |
My son Adam, aka Batman, is currently on tour with the world champion Concord Blue Devils, for his fifth and final season marching drum corp. I love and miss you Adam.
Batman, in the middle. |
Snare extraordinaire, that's my Son. |
Peace to you Dear Reader.
Peace.
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