Showing posts with label brave the shave. Show all posts
Showing posts with label brave the shave. Show all posts

Monday, May 7, 2018

April with Team Mallory



I thought I'd do a quick picture update, then 150+ pictures...2 iphone slideshow failed attempts and a computer crash later- here we are. 

April was amazing, busy, wonderful. I can not express how proud I am of my minis. From donating birthday money to St. Baldrick's, to Lily giving almost every class at school presentations on Childhood Cancer and the need to fund research, to the actual bald. Most days I feel like I'm failing miserably- then these bald heads remind me we are doing something right. We can't control circumstances, we can control how we respond to them. 

I am humbled, honored and speechless at the tremendous support we've received this month. From donations, to fundraisers, to sharing all the posts, to wonderful t-shirts, lovingly made by friends(Snarky Cancer is the best), I so appreciate every little and BIG contribution to Team Mallory. I am so grateful for your friendship, love and time. Friends are family that you've chosen, thank you for choosing us. 

Phil and I ventured to Toronto for a long weekend LFS conference. It was the most mutant bang for our buck! There were lots of friends, old friends, new friends, it did my heart good to reconnect in human form. There were so many people I needed to hug, repeatedly. So many who don't like to be touched, who put up with me. I was not on my normal scientific fangirl game, but it was so encouraging to see the LFS community together- hashing away at this mutant p53 problem.  And there were so many pictures I didn't take, friends I didn't get to hug. Plans will be made to rectify this. ***Phil cringes and considers who will employ stage 4 cancer mom to finance this***

As for Phil. He is my lobstah. My best friend. It's been a long haul and he's always supported my need to be a professional volunteer. Which often means his being a professional volunteer and best friend, husband, dad status. None of this would be possible without him. Read that as you will....He is the best person I know. Now on to May- May the odds ever be in our favor!
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Wednesday, March 28, 2018

Team Mallory Takes on St. Baldrick's


There is that spot in my heart that aches when I think of what Lily went through druring chemo. It leaves marks that aren't polite to talk about at parties, but They are there, always. I think of what we all went through. The unknowns. The fear of losing her. The helplessness. The gracious help from family and friends.  We were learning more details about Li-Fraumeni Syndrome, a risk we all carry. I had only met a couple others online at this point who "got it". The Ramers just lost their son Brent last year, after YEARS of cancering. And our hearts hurt. This shouldn't happen. Organizations like St. Baldrick's are making a difference.
Oh monkey. 
Bella Boo- by Lily's side most of chemo



Phillip and Lily's special bond and ELEPHANT!!
sisters. first. forever. 
This is how we feel about Childhood cancer. 
SO in 2014, when Lily said she wanted to shave her curls, well that achey spot lit on fire. By now- I had a mutant posse of friends- each one fighting cancer in their own hell. Ah LFS- we got 53 problems but obviously a tumor suppressor ain't one of them. I had a tight knit group of sistahs, who became my life line as I navigated chemo for the first time. We told our kids about their kids. The Ramers(aka Ramernation) were going through the delights of everything LFS had to throw at them- multiple cancers in multiple children and NO clear path. Their momma Ann is one of few who I would go to to clarify science questions- she knew it all and if she didn't she'd find out. Somewhere in the middle of all of it, we formed living LFS, because we didn't want other families to be without the support we had found. She is one of the fiercest advocates I have ever met.
Living LFS mutant sistahs. 


When Lily shaved her head for St. Baldrick's the first time- all those burning spots of PTSD flared up but mostly we all became empowered to see her - her strength. I was extremely honored that she wanted to honor me, but I have had a beautiful life. My heart aches for our little warriors, through no fault of their own, have their years cut short by cancer.

https://lilykaymonkey.blogspot.com/2014/04/finding-something-she-can-do.html


 I don't always trust odds, numbers, risks. They are guidelines. There is just so much we don't know- so much just plain old LUCK. No one wants to beat cancer more than someone else- we don't want cancer to win.  Yet as we wait yearly for scans, we try to make healthy choices, we try to live. We check in with our LFS friends - Brent and Lauren Ramer who seemed to be wholloped with one rare unicorn cancer or condition after another. The entire time we've known Brent, he'd been in chemo or dealing with a new cancer. Lauren has tumors pop up, they deal, and just keep living, she just finished chemo to have yet another tumor removed. . The odds are an analysis after the fact. We try to make a difference by sharing our stories, our experiences. Maybe one of our weirdisms will help someone else. If not, then there is research. Organizations like St. Baldrick's who fund severely under funded childhood cancer research and treatment protocols.



https://www.stbaldricks.org/blog/post/the-girl-who-beat-the-odds-lilys-story


In 2016, I had just been diagnosed with brain metastasis. The clock ticked loudly. We hunkered down. Just like Phil had the overwhelming need to take Lily to football games and disney, we needed to go to Europe. We never had a honeymoon, we are always day to day. That trip gave us so many memories and completely recharged us. We facetimed Lily fo her shave. It was not about me- it was about her doing what she could to help. She lost friends too, Haley, Abriana, Elikia. So many more were still fighting cancer, like Brent. Years of chemo and fighting and nonstop cancering. living cancer LFS style. but kicking ass and taking names- Chuck Norris style.

Lily rocking it after shave 2.
Photo credit:Debbie Leanne. 

http://lilykaymonkey.blogspot.com/2016/03/lilys-second-shave-for-brave-st.html

So here we are - 2018. Lily signs up for her 3rd Shave. Not phased that she's now 13, that middle school crowd is kinda tough.  Yet she is a force to be reckoned with. The little ginger haired toddler who napped almost exclusively in hospital rooms, is now almost a teen and last week says- I'm gonna shave for St. Baldrick's! Ok, why. For Lily. Ok then. We can all shave. Ok, see if Phillip and Kiera will. And of course when the youngest asks- the eldest teens say- yeah- that's a great idea and it suddenly becomes a competition as to who can raise the most money. They all set up their own pages and have told their friends. I had many many happy proud tears and big hugs of my mini mutants.

So I realize we ask a lot for help with fundraising. I appreciate our friends' and family's generosity. If this is a cause near to your heart- please pick a monkey and donate. If you can't decide, we've all agreed that Lily can be the default! All money goes to St. Baldricks!If you would be so kind as to share this blog, any of the kids' pages wide and far-we'd appreciate it!  If you would like to join us (no shaving required) the event is April 22, 2018.  If you'd like to hire out kids to do cleaning or lawn work or whatnot for donation- Mallory kids are at the ready. Bella already is helping make leis for me to earn $ for the shave.

Thank You for continuing to support Team Mallory and our Many Adventures, Especially adventures that Fight Childhood Cancer!


Bella's Page



Jen's Page






Tuesday, March 8, 2016

Lily's Second Shave for the Brave- St. Baldrick's Event April 24

Lily's 1st St. Baldrick's 2014


Remember 2 years ago when Lily wanted to shave her head? It was an amazing experience for her  and in the process raised almost $5000 for childhood cancer research through St. Baldrick's. I had recently lost my hair due to treatment and many of the emotions were overwhelming.  She said at the time she was going to wait a year and then do it again. Not every year, maybe every other year. I nodded and said Ok because we were very deep in the uncertainty of my cancer treatment. Secretly I just hoped to be around in 2 years.

Well here we are. And not only am I here- Lily is no longer the only one in the family with fabulous curls. She is very proud to tell people that I have HER curls. In January she started reminding me she was going to shave her head.  Phil and I had just made plans to be off island and wouldn't be here for the event. Lily says- it's OK mom- I want to do this. You were there last time. I have so many mixed feelings, but the dominant one is pride. And to see her take the lead and do this for her is beautiful. We started talking about a fundraising plan. Part of me wanted to see if I made it more her responsibility, maybe the novelty would wear off. Silly Jen. I'll say one thing- that kid is mine. She sets her mind on something and good luck changing it.
This is what I say to cancer. 

In a world where I spend an inordinate amount of time trying to talk my children through situations where adults are behaving badly, children behaving badly and over all nonsense- there is this beacon of hope. As the dishes sit unattended in the sink, Phillip is composing songs and teaching himself to play the guitar. Kiera is supporting classmates who are having a tough time adjusting and fitting in while dealing with bullying and poor leadership. Bella soaks everything up like a sponge and then wrings it out and does shit her own way anyhow. And Lily, she feels intensely and struggles to fit in because in her almost 11 years, she's been through a lot. I look how well they are dealing with the past 3 years of my being sick and in constant treatment and although it hasn't been easy, they are remarkable. We are not perfect, but I try very hard to give them tools for happiness and to try and be the best they can be. So when she says she wants to shave off her beautiful curls to help people, we make a plan.


I told her I would post on Facebook for her, but that I wanted her to write the info for her St. Baldrick's page and write the email thank you's. We again were flabbergasted that within a couple of weeks she had already made it half way to her goal of $5000. We know so many generous, caring people. At times I feel like all we do is ask for our causes, so Lily and I had conversations about other ways she could raise money outside of just asking friends.  She decided on Kool-ade stands and making invitations for her friends at school to attend the event. We talked about awareness and how although action is really important, so many people are not aware of St. Baldrick's and what it is about. Then it occurred to me- the 6th graders do IB exhibition projects. It's a self-directed inquiry that is largely based in a community service project. The kids identify a problem, research it, and work towards a solution. I started asking around at school if as a 5th grader, Lily might be able to do an exhibition project about St. Baldrick's.  Lily finally had to be the one to make a formal request. We sat down and I let her write her request, guiding only to help her clarity and format. We talked about which IB attitudes she was using, she even drew a mock up of her posterboard. We came up with a shamrock and gold cancer awareness ribbon.

Dealing with administrative red tape on the school level is not new for us. I try to be as active in the kids' education as possible. It was much easier years ago when I was not employed as a full time cancer fighter. Many parents work very hard during school hours and cannot actively participate, I always felt like it was a privilege to be present and involved at school. We have been lucky to have some sincerely supportive teachers in our time. Many I now call friends. It is a really nice side effect of helping at school, you get to spend time with quality educators who are very passionate, because otherwise I have no idea how they deal with all the added nonsense.

I also know it is not a common occurrence for a lower grade child to ask to do an extra project, but that really is what the exhibition and International Baccalaureate attitudes and learner profiles are all about. Unfortunately I fully expected for Lily to be told no, just not for the reasons that were given. I expected her to be told that she missed the Exhibition deadline and that it is a process therefore it would be too late for her to set up a presentation at the 6th grade Exhibition night. Personally- I feel it's like a curriculum fair and her presence would neither help nor detract from the other students' efforts- it is more of a community venue for Lily to independently discuss her experience with childhood cancer, the lack of funding and a present a call to action. It wouldn't undermine the efforts of the 6th graders and as she was not being graded or given any credit for the project, what is the harm? She would not be asking for donations. That is not what her presentation would be about. It is about getting others involved and letting them know about a local event.


The reason given was that the DOE guidelines would not allow it. Also that if Lily was allowed to do it, they would have to allow other students to do it as well. It was made very clear they could not endorse Lily or her cause in any way, but she would be allowed to speak about it during non instructional time. In a week where there was a gun threat at my teen's high school and a subsequent bomb threat today, I think our efforts would be better spent celebrating and highlighting community service efforts of children. To live in a community where the kids clamor to their teachers requesting special permission to make the world a better place and solve problems with big impacts, that's the community I am trying to foster.

Lily will be 11 on Monday March 14th. Monday is also the day of 6th grade exhibition. She wanted to spend her birthday honoring the cause she has chosen and spreading awareness. She is not asking for presents or a party this year which is ultimately ironic. Instead she is asking for donations to St. Baldrick's, so other kids can be as lucky as her.  None of us are guaranteed birthdays, yet here she when so many forces have stacked against her.  I cringe as adults celebrate entire birth months with extravagance and here we are- so grateful for each bonus birthday we are given and her willingness to use it to help others makes me proud beyond measure. She is allowed to present information to her grade level and we are trying to coordinate that with teachers as it has to be on non instructional time. She is also allowed to hand out ribbons before they leave for break.

Please consider sharing about the event, Lily's St. Baldrick's page or just commenting below with a Happy Birthday message for Lily, it would mean a lot to me. If you feel inspired to donate, that is also really appreciated. Lily's St. Baldrick's Page Thank you for taking time to read this.


Lily Kay Monkey

Lily Kay Monkey
November 2008 Photographed by Shelley Detton (7 Layer Studio)