As you can probably tell by the image and title of the post, this is the official announcement of Maxapalooza. Melissa has been working day and night to pull this together and we have been wanting to wait for the headliner band to be found and signed and this just happened on Friday (while we were at Legoland with the kids on a "surprise visit" no less). We have signed The English Beat (with Dave Wakeling and Ranking Roger for all those who remember) and are happy with the outcome. We looked at a lot of bands and The English Beat were very accommodating and easy-to-work-with, a big plus since this is our first event and are still learning.

So, what's all this for? Where does the money raised go? It goes to fund an innovative neuroblastoma (and it's close cousin medulloblastoma) research consortium headed by Dr. Giselle Sholler and HQ'd at the University of Vermont/Vermont Cancer Center. Most of you know Dr. Sholler from our blog so I won't go into much detail here. Here is a PDF describing how your money is used to help save kids from this common yet overlooked cancer. However, I also wanted to let you read a letter from another angel parent, Bob Piniewski who started an effort called People Against Childhood Cancer or PAC2. The context of the letter doesn't matter here. What does matter is his message, which he has graciously allowed me to use on Maxapalooza.com (thanks Bob) and which I include here as well:

Childhood cancer is considered "rare". Rare has two meanings in this case: Happening to your child or someone else’s. One in 300 children will be diagnosed with cancer before age 20. That’s 46 kids every school day. 12,500 diagnosed every year. 3,000 kids, or 1 in 4 or 5 will not survive. It is the #1 killer disease of our children today, more than from asthma, diabetes, cystic fibrosis, congenital anomalies, and pediatric AIDS combined. Each year 35-40,000 are in treatment. Childhood cancer has a huge societal impact - 180,000 potential years of life are lost to it EVERY year! Does that sound RARE?

Right now, two major fundraising organizations for childhood cancer research are St. Baldrick's Foundation and Alex's Lemonade Stand. They rely on parents to shave their heads or sell lemonade to raise money for childhood cancer research. To save the lives of the children being raised in the richest nation on earth. Think about that.

And the medical industry even agrees! And write about it! (Cure Today – Picking up the Pace - Igniting progress in the cure of children with cancer)

To paraphrase - “we must enlist friends and families of children with cancer to secure funding for research.”


While it sounds like a bad comedy, it is a national tragedy. What are the last 2 national tragedies? When the shuttle went down, did we ask the astronauts families to figure out the problem with the O-rings? After 9/11 did we ask the victims’ families to "help us out with this war thing?" Yet it's our approach for dealing with the #1 killer disease of our children today!

And don’t believe that research into adult cancers is transferred to our kids. Right now the treatments are “down-sized” adult doses. And the results? 60% of survivors develop secondary cancers, infertility, major organ damage, developmental problems or other issues.

We are so grateful for those that have helped us get where we are, and will be there to help make sure Maxapalooza is a success. As you may have noticed, Maxapalooza is much more than an ordinary fundraising event that just so happens to be raising money to fund neuroblastoma research. In a way, it's a living tribute to Max. Which makes it difficult at times to "settle" for things - it also likely makes us difficult to work with but luckily we have surrounded ourselves with fantastic people who like us, are inspired by Max and what he represented and so work on our behalf in a way that is consistent with our beliefs and desired outcomes. Some of those people include Leo Benevidez at YMI, Chris at Grind for Life, Grant at Sport About, Elizabeth Wainwright-Alkhas, and Craig and Nelson at Premier Jet. Also some the committee making this all happen and supporting Melissa including Alessandra, Andrea, Kristi, Lisa, Lori, and Marcina & Neil, and Randee. Thank you so much - all of you - for your help and support in getting us where we are today! There's much more to do, it's just started, but without your help Maxapalooza would have never even gotten off the ground.

Tomorrow, we leave on a little vacation. It's nothing extravagent. We're going back to South Dakota to visit with Melissa's family. We'll be saying on a lake the whole week, the kids will have a blast fishin' swimmin' & boatin', and hopefully Melis and I can slow down for a few days to catch our breath. We also are planning on meeting Donna Ludwinski (mom to Erik: 23 and still kicking NB's ass) and whatever of her clan are able to make it to Minneapolis to attend an NB fundraiser.

This summer - as I presume all summers will be - has been tough. Bookending the start and end of summer are Max's birthday (June 30) and his angel day (August 31). With "the year" mark approaching rapidly, I cannot believe it has been this long that we have been without our perfect little boy. Each day, I find myself missing more and more of him and what I would give to have him back if only for one more day.


Bree said...

Have a fun (relaxing) time in S.D. Wish we were going too! Miss everyone.

Anonymous said...

Yah for Chris Conway! I'm so happy he was able to hook you all up! The poster looks great btw. Enjoy your vacation. xolisa

Anonymous said...

Enjoy your vacation... you deserve a little getaway! Can't wait for Maxapalooza!!! Holly

Dennis Pyritz, RN said...

Great Blog! I have added you to my blogroll, “Cancer Blog Links” with almost 500 other cancer blogs at www.beingcancer.net, a cancer networking site featuring a cancer book club, guest blogs, cancer resources and more. Please stop by and visit. If you like the site, please consider adding Being Cancer to your blogroll.
Take care, Dennis

Deck Ape said...

Just wanted you guys to know that I am thinking of you.... Kudos on the "Touch a Truck" fundraiser. You have some great ideas..

Take care...

Vickie said...

Are you back? Can't wait to hear about your trip.

Dennis Pyritz, RN said...

Each Wednesday at Being Cancer.net we feature a Guest Blog. This week we are highlighting neuroblastoma with two guest posts. The first is by Connie Powell, mother of Miss Madelyn, who recounts what the experience of diagnosis was for her and her family. In the second a twenty-four year old NB survivor, Erik Ludwinski, reflects on how cancer has affected his young life. I know that neuroblastoma has a strong blogging family. So thought you might be interested in visiting. Also please visit the “Neuroblastoma” section of our blogroll, Cancer Blog Links, to see if your site is listed. www.beingcancer.net
Take care, Dennis

Anonymous said...

Wow. This. event. looks. so. AMAZING! Having fun and helping such a worthwhile cause--beyond cool!


Anonymous said...

This looks so very cool. Another way you continue to honor Max. I sent this to my family in SD who sent it to a bunch of people who are so excited to come. I hope it is a great success.
Carrie Palmer

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