Showing posts with label Gold Ribbons. Show all posts
Showing posts with label Gold Ribbons. Show all posts

Monday, September 30, 2013

Gold with Envy

I was never a girl who was in to pink anyway. These days, I have to really fight to not be bitter about it.

I don’t begrudge them their month. I’m even continually impressed by how many organizations step up and promote the pink.

It crushes me, however, to watch it push into September.

September is for the kids.

September is gold.

Where are those organizations when the kids are involved? Why isn’t my soup can gold, and why aren’t  my favorite receiver’s gloves gold, and where are the gold ribbon displays at the grocery, and the convenience store, and, well, dammit, where is the gold?

I see it here and there, in part because I am looking. Because much of my social network is looking, and we share the images. We celebrate the businesses that support the kids that are fighting. We hunt it out, the gold.

The pink? It’s everywhere. My emails are full of it, my stores are flooded with it. They’ve worked hard for that, and I know we all know someone who has been touched by breast cancer, but I know so many who have been touched by pediatric cancer! I know how drastically underfunded research is where the kids are concerned. I know what the ramifications can be of the limited treatment options that exist for our kids. I’ve seen the young athlete battling his way back from a wheelchair to a walker. I’ve seen the aspiring singer suffer such dramatic hearing loss.  I’ve visited the grave of a little girl who spent more of her short 10 years on this earth fighting cancer than she did living without it.

So, I try to not be bitter, I know that cancer is hard for anyone, but I cannot help but want the gold to be as recognizable as the pink. For it to be as supported as the pink.

I at least want it to get to use its whole month, without being crowded out by the pink….

Wednesday, August 7, 2013

First Day of School, First Impressions

Today was our first day of school. I celebrated by promptly screwing up the bus schedule, and as a result, had to drive my brand new middle-schooler to school.

He was up & dressed, teeth brushed and bag packed in plenty of time. We were hanging out outside, snapping a few photos when the bus went by at the end of our road. Our Wednesday schedule results in students having a later start time than the rest of the week, allowing for collaborative teacher meetings. For the elementary kids, school starts an hour later. For the secondary kids, it’s only 45 minutes. I assumed it was the same hour, thus  the missing of the bus. Oops.

After I got him safely delivered to school, I returned home, sent my husband off to work, checked on the elementary kids (and verified their bus schedule!) and then uploaded a photo from my phone to my Facebook, sharing his “First Day of School” image with friends and family.

It was then that I noticed his shirt.

He’s a Minecraft fan, and we picked up several t-shirts featuring Creepers a few weeks ago. I assumed one of those would be his first day shirt.

I was wrong.

Today, my son wore his St. Baldrick’s shirt.

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His first day in a new, much bigger school, his first chance to make impressions on potential friends and his new teachers, and he quietly made the statement that Childhood Cancer Sucks.

He’s got a gold ribbon on his bag, too. (It’s right under that Chewbacca. Chewie stayed home though.)

It’s enough to burst my heart from my chest. That boy will make waves in the fight against childhood cancers. I’m proud to be his mom.


Linked up with Pour Your Heart Out! Check out the other posts at Things I Can’t Say

Thursday, June 20, 2013

Gamers Giving Back–Mario Marathon 6

Guess what tomorrow is?!

Mario Marathon Header

My kids and I are SO excited – Mario Marathon is back for a sixth year raising money for Child’s Play Charity. Child’s Play raises money to provide games, gaming consoles, movies and more for over 70 children’s hospitals around the world, bringing a little joy to kids facing challenging situations.

Mario Marathon is independently run by a group of friends who play the Mario series of games live online and generally do silly things in the name of supporting Child’s Play. Donations go directly to Child’s Play – these guys spend their own money, use their vacation time, give up hours of sleep, sanity and time with their families to support the great work of Child’s Play. The 5 previous events have raised nearly $350,000 (and if you count their Zelda event in 2008, they’ve hit that!), which is amazing.

If you ever hung out with your friends playing Mario in somebody’s basement, you have a pretty good feel for what MM is like. So, you’re officially invited to come hang out with the gang! If you’re so inclined, feel free to donate -you can even do that from right here!

If you’re on other social media, give the gang a shout out. We’ll all be tweeting with the #MarioMarathon tag, and you can tweet @MarioMarathon. You can also find them on Facebook.  Hope to see you there!

Mario Marathon 6 begins Friday, June 21st at 11:00am EST at MarioMaration.com

Saturday, May 11, 2013

Yesterday

It should be such a good week.

It WAS such a good week.

I finally treated myself to a DSLR camera, which I had wanted for a very long time, and just couldn’t justify. It was a want, not a need, and let’s face it moms, wants aren’t typically at the top of our “get” list.

It was finals week, and I was feeling good about my classes, and getting to take a few weeks off before summer session starts.

School is nearly over, and it’s time for the fun, year-end stuff. We’ve been planning a fun trip to an amusement park for the 6th grade, and we’ve had a blast with fundraising. We go on Tuesday, and I’m super-excited.

And then? Yesterday happened.

Part of yesterday I cannot yet talk about specifically. I know that I have friends who are hurting, and that there will be more hurt before healing comes. I’m hurting. A relationship, one that we hoped would grow and flourish, and be wonderful for so many people, is being pulled apart. Not by the parties in that relationship, but by others, higher up, who don’t know. Who don’t understand. It’s painful, and going to get worse.

And after spending time with some of those most directly impacted, wounded by what is coming, I came home and found more bad news.

Naomi, a sweet two year old little girl who lives in my community with her mom, dad, her four year old sister and one year old brother, was just diagnosed with neuroblastoma. Another baby, whose life is now forever changed by the monster that is childhood cancer. Another family, stopped in their tracks, and entering a new normal, on that involves oncologists, MIBG, CT, TPN, DX, stem cell rescue, chemotherapy, radiation, and hopefully sooner rather than later, NED.

It was enough to destroy me last night. I lost it.

Today? It’s enough to strengthen my resolve. Reaffirms for me that, no matter what, I cannot stop fighting for these kids. All the kids.

Tomorrow is a new day, with new challenges and new successes.

I need a few successes for a minute, though. Please.

Sunday, April 28, 2013

The “Why”

Friday night, I was as proud as I could possibly be of my boy.

This guy:
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Became this guy : Jeep's After Picture

And donated this:

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to help a child who has lost their hair to a medical condition. He went ahead and raised money for St. Baldrick’s while he was at it, raising over $3,200.
(I gotta be honest. Right now? Still pretty proud.)
I forget sometimes though that people don’t know why we care this much. Why my son, at 9 years old, decided to grow his hair until it would be long enough to donate. Why he smiled through three years of being mistaken for a girl, and endured endless questions about when he was going to cut that hair.  I hope it helped him that his dad and I were so supportive of what he was doing, that we never hesitated to explain to people that we were incredibly proud of what he was doing and why.
You see, our awareness of the reality of childhood cancers began in 2005, when Jeep was just 4. A little girl in his Sunday School class was diagnosed with Stage IV Neuroblastoma, an aggressive cancer of the adrenal system. Her diagnosis came just days before her fifth birthday. Her name is Morgan, and she was our friend. And so? We talked about it. Morgan was sick, and the doctors were going to have to try to make her better. It was going to make her hair fall out, and there would be lots of Sundays that she wouldn’t be at church with us.
When Jeep started kindergarten a little over a year later, Morgan was a first grader at our school, and we saw her after school every day, when she was well enough to be there. You see, the treatment protocol for neuroblastoma involves several rounds of chemo, surgery to remove as much of the solid tumor as possible, maybe more chemo, some radiation, then a bone marrow aspiration in the hopes that they can get clean marrow. Why do they need clean marrow? Because they then attack the body with enough chemical to kill off the marrow still in the body of an innocent child, and then they return the “clean” marrow to the child and hope it sticks.  Then there are days, weeks, months of isolation. The fear of contracting an illness before the marrow has fully recovered is overwhelming. Your bone marrow is what provides you with your immune system, and for a child who is already weakened by chemo, and who has no immune system, a simple cold that inconveniences you or I? It could be a death sentence.
Morgan’s cancer wouldn’t give up, but neither would her family. Her mom and three younger sisters packed up and they went to New York to be part of a clinical trial, hoping that it would be her cure. Lots of times, her scans would show improvement, things would look better and better, and then? A new spot. Another tumor.
Eventually, after fighting for more than half of her life, on October 2nd of 2010, Morgan passed away.
Early in Morgan’s treatment cycle, we connected with another family whose 2  year old was diagnosed with the same cancer, about 2 weeks after Morgan’s diagnosis. The girls underwent essentially the same treatments, just a week or two apart. Colette is a survivor, but the impact of the treatments on her body are still very much an unknown. Her hearing was severely compromised, and she wears hearing aides now. She’s still to young to know for sure what the impact may be for her in regards to her reproductive system, and the risk of secondary cancers as a direct result of the treatments she received are very high.
In 2011, another friend’s son was diagnosed with medulloblastoma, a brain tumor. Again, treatments, surgery, more treatments.
The part that crushes me is that when you see marketing from cancer fundraisers, you frequently will see young kids. What you don’t see, the reality of it is this:
  • There are 12 primary forms of pediatric cancers.
  • 1 in 330 kids will be diagnosed with some form of cancer before they are 20.
  • Most pediatric cancers are treated using lower doses of adult treatments. Research is needed to provide kids with safer treatment options, providing them with a better future.
  • Less than 5% of the federal government’s total funding for cancer research is dedicated to childhood cancers each year.
  • In 2009, the American Cancer Society spent $22 of every $100 raised on fundraising expenses, $6 on management, $14 on research for adult cancers, and spent $0.60 of that same $100 raised on research for childhood cancers. Sixty cents.
  • Worldwide, each day another 720 children are diagnosed with a form of pediatric cancer, and 250 kids lose their battle.
No one asks for cancer. Some make choices that they know carry a higher risk – smoking, sunbathing, etc, but kids?
Kids have done nothing.
Think about the people you know who have been treated for cancer. Think about how sick they were with chemo. The pain in their bodies. The surgeries. The recovery.
Now, imagine that they’re two.
THAT is why we fight. The reality of it is why I’m passionate about it, and Jeep embraced it early on.
Possibly my most favorite part of Friday night was much later, in the quiet of our own home, as we prepared to say goodnight, as I rubbed his fuzzy shorn head, I asked Jeep if he was glad he’d done it.
“Oh yeah.”
Would you do it again?
“Over and over.”

Sunday, April 21, 2013

Home Stretch!

I know I wrote about it a little bit before, but I wanted to throw this out there – we’re just 5 days away from shave day, and have $400 to go to hit our final goal of $3,000!

Incredibly proud of this boy.

www.StBaldricks.org/participants/JeepM

Friday, March 1, 2013

Such a proud momma…

So…

That boy? The one that just turned twelve?

He has insisted on stealing my heart.

I mentioned in his birthday post that he was growing his hair out to donate it. Today he told me this:

On April 26th, we’re going to join some students at Indiana University and he’s going to take part in a St. Baldrick’s event, shaving his head to raise money and awareness for pediatric cancer.

This decision was not one he took lightly, and I’m so impressed with him, I can’t begin to describe it to you. His hair has become such a big part of his identity, and let’s face it, it’s tough being a tween/teen. This was something he slept on, thought about, and decided he was willing to do.

I am so proud of him. I can’t begin to explain it.

Anyway – if you would like to donate, we’d love that, but if you can’t donate, would you consider sharing his donation site via your social media  of choice? Each tweet or FB post reaches out to someone else, and if we raise nothing more than awareness for the kids who are fighting cancer, that’s one more step.

Jeep’s St. Baldrick’s Fundraising Page

Thanks!

Monday, November 7, 2011

A little follow-up

I must extend my thanks to the folks over at BlogFrog -

I tweeted to them, crushed, when voting closed early on the Hero Mom Contest. It was, however, the weekend, and they weren’t on hand immediately.

In the meantime, a kind soul stepped up and offered to cover the cost for Colette’s trip.

Tonight, I was contacted by a representative at BlogFrog.

They acknowledged that an error had, in fact, taken place. Time zone issues, changes from the norm, human error. It happens.

They obviously couldn’t give me that last 30 minutes, couldn’t put me into that top five spot.

They did, however, graciously and humbly apologize, and offer up a $100 gift card, which would have been our “guaranteed” prize for being in the top 5.

That card is, of course, going to be sent to Colette & Tammy, for Colette to use as spending money while in Nova Scotia. (That was our “back-up” plan anyway, just in case we didn’t win the whole enchilada.)

So, while that $2,500 would have been great, and having that nice, big donation for the folks over at Alex’s Lemonade Stand Foundation would have been AWESOME, we’re so blessed. Blessed. Colette’s trip is paid for, she has some spending money, we’ve raised some awareness for pediatric cancer.

Thank you again  to all of you who put up with all my tweets and such begging for your votes, and special thanks to each of you who voted and shared!

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Sunday, October 23, 2011

Hero Mom

She’s no different from any other mom – when our kids are sick, we take care of them. We take them to doctors appointments, dispense medications, cuddle and comfort them.

The difference for her was that her child had cancer. The doctors were oncologists. The medications were injected through a port in her two year old daughter’s chest. Cuddles and comforts were in hospital rooms around IVs. A fever meant an ER trip, not another dose of Tylenol. Holidays were spent in isolation after a stem cell transplant.

That was six years ago now, and today that little girl is going to be nine soon. She’s cancer-free, and full of life. And she wants to share her story.

Allstate & The Blog Frog have an opportunity where we can help.

You don’t have to sign up. No emails, no linking your Facebook or Twitter. You just go to the page & click  the “Vote” button. All we need is to finish in the top five. You can vote once a day, and each and every vote is so valuable.

You see, one of the Hero Moms, one of the top five based on our votes, will win $2,500. My Hero Mom? She’ll get the money they need for her to take her daughter on a mission trip to share her story of faith and her battle with cancer, along with the after-effects of treatment. The remaining money will be donated to the Alex’s Lemonade Stand Foundation to help fund research grants so that in the future, kids will have better treatment options.

Please, click on this image to go vote for my post for my Hero Mom, Tammy, and her daughter Colette.

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I’ll love ya forever!

Momsense Signature

Tuesday, September 13, 2011

Happy Birthday to Me!

It’s my birthday.

You can get me a present.

It’s easy, and it’s free, and I’ll love you forever.

You see, it’s also Childhood Cancer Awareness Day. But people don’t know that. The pink ribbon products for October have already begun creeping in.

Please, don’t misunderstand what I am trying to say. I think support for breast cancer is important, too, but September? September is for our kids.

Kids like Colette.

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This was Colette in 2005. In May of that year, just about 2 weeks after Morgan, Colette was diagnosed with Stage IV neuroblastoma. She was two and a half years old.

Colette endured surgery. Chemotherapy. Radiation. A Stem Cell transplant.

Can I share a little something with you?

Typically, pediatric cancers do not have their own treatment options. What kids get is simply smaller doses of adult treatments. Sadly, these treatments can leave kids with lasting issues. Colette? She now wears hearing aides, as the treatments she endured saved her live, but stole much of her hearing. Secondary cancers are common. So is infertility.

The National Cancer Institute’s federal budget=$4.6 billion. Breast cancer research receives approximately 12% of that funding. Prostate cancer gets 7%. ALL TWELVE major groups of  pediatric cancers COMBINED received less than 3% of it.

Maybe I’m biased. That could be. And that’s ok – this area is my passion, my focus.

I believe our children deserve better. And I think, as we continue to raise awareness of the reality of the issue, there will be a shift.

ColetteThis is Colette 6 years after diagnosis. This summer, she officially hit the “Five Year Cancer-Free” mark, which is huge.

I want more of our kids to see the five year mark.

I want there to be better options. New treatments. Less long-term side effects.

I want people to KNOW.

And that part? The knowing? That’s what I want from you, for my birthday. I want you to help others know. I’ve created a Twibbon that will let you add a gold ribbon to your twitter and facebook images. Would you consider that? Just for today.

It would be a pretty sweet birthday gift.

If you do, please leave me a comment and let me know, won’t you?

Thanks.

Monday, September 5, 2011

Gold

I touch on it when I blog in September.

It’s so very important to me. Especially now, as a mom.

Six and a half years ago, it became real. It wasn’t just a St. Jude commercial, distant and vague. It was Morgan. It was a little girl in our boys’ Sunday School class. It was a face we knew, they were parents we talked to, it was a little sister we saw.

It was cancer.

It was aggressive.

It was already stage 4, and they had just found it.

Literally two days before her fifth birthday.

As they told us in that service, I wept, clinging to my daughter. I shared glances with my friend Bethany, who also held her little girl, both of us afraid to let go. Afraid.

And it wasn’t our child. I can’t begin to fathom the fear in the hearts of Morgan’s mom and dad.

Chemo. Radiation. Stem Cell Transplant. 3f8. Central lines. So much to put such a little person through, and they face it. Every day.

It tears my heart out to think about kids having to face the monster that is cancer. It’s difficult enough for an adult, but adults can understand what’s happening. They can face the repeated sticks for blood draws, the injections, the scans, knowing that it’s to help them get better. How do you explain that to a child?

How do you talk about death, their own potential death, with your child?

We lost Morgan nearly a year ago now. She fought, with her family by her side, for 5 and a half years. She was ten years old.

Ten.

September is Childhood Cancer Awareness Month.

I wear the Gold ribbon for her. For our other friends, those we’ve lost, those still fighting, and those who are NED*.

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*NED is “No evidence of disease. Many pediatric cancers are not declared “cured” until the patient has been NED for 5 years, the typical window of reoccurrence.

Wednesday, December 8, 2010

Blessed, even if I don’t remember it

I’m linking up today with Pour Your Heart Out Wednesday with Shell!

Over the last few days, a woman who I consider a dear, dear friend has been re-living what she dealt with 5 years ago this week.

She was fighting to save her daughter.

Before she was three, Colette had been diagnosed with Stage 4 Neuroblastoma, an aggressive cancer of the nervous system. Her May, 2005 diagnosis led to surgery, months of chemotherapy, and finally, in that first week of December, a stem-cell transplant.

My heart broke for a family, terrified, facing unknown battles. For a little girl, only a few months younger than my own E, who would spend Christmas in a hospital, isolated, while her family prayed the stem cells would graft in, and her body would begin to heal.

As I read over the CaringBridge posts from 5 years ago, I remember sitting in tears at my computer. I remember praying as hard as I had ever prayed for God to heal that little girl.

Blood transfusions. Feeding tubes. Central lines. Stem cell transplants. Chemotherapy. Radiation. Surgeries. All at a hospital 5 hours from home.

She was three. years. old.

For Christmas, they put a sparkly pink tinsel tree in her room. Many of us sent gifts. We left notes of support and prayer on her page.

We loved her.

And we still get to.

This is Colette in October. Notice her hearing aids. The substantial loss in hearing she has is a direct result of the chemotherapy. That’s because pediatric cancer research is sorely underfunded, and often, adult treatments are used to fight childhood cancers.

They aren’t sure if Colette will ever have children, the impact on her reproductive system is unclear at this stage. The risk of secondary cancers for her is high as a function of the treatments she received to fight the neuroblastoma.

Here’s the part where I pour out my heart.

I have three healthy kids. I’m so incredibly blessed, even when they are driving me crazy. There are days when I forget that.  When I yell at them, not because they’re being ridiculous, but because I don’t have the patience for the silliness at that moment. When I’m frustrated that they aren’t trying hard enough on a homework assignment, and I lose track of the fact that they are healthy enough to go to school every day.

I lose sight of how lucky I am.

And then, I feel that much worse when I’m short with them. When I’m impatient. When I’m harsh.

We spend so much time and energy focusing on outward appearances, we lose sight of what we have right here in front of us. We become so overwhelmed by work, chores around the house, social engagements, volunteer work, even things like blogs, we miss the miracles that happen every day.

Or maybe that’s just me.

And that? That’s the part that scares me the most. The part where you go “Am I the only one? Are there other mom’s who feel that way too? Or is it really JUST me?”

And then you get into a spiral of feeling like a mom-failure.

As I re-read Tammy’s thoughts, fears, prayers from those terrifying days five years ago, I am reminded of just how lucky I am. And how much I need to remember that.

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Friday, November 19, 2010

like a lemon

So much to say, and yet no words.

How do you find the words to reach out?

How do you say the right thing? Is there a “right thing?”

You want to help, and yet, not be in the way.

You want to comfort, but not smother.

You want to be available, but not be a constant reminder.

Life changes so quickly. In the blink of an eye, everything you know is different. So different.

This week has sucked. There aren’t any other words that describe it as accurately. It’s just been an emotionally exhausting week. So, I’m glad it’s over, and I’m looking forward to food and family and things that I’m thankful for as we enter the holiday week.

And until then, pray for peace and guidance for me. I’ve got a lot on my plate, and I need to know that I’m handling it all correctly.

Thanks.

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Saturday, October 2, 2010

Still gold…

There is no fairness.

If there was, little children would not have to battle cancer.

Morgan would not have spent more than half of her short, 10 year life fighting to keep it.

Certainly not to lose.

September has passed, and the pink ribbons abound. I support the “girls” too, but for today,

for Morgan,

it still must be gold.

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Morgan Rose ~ May 12, 2000 – October 2, 2010

Fly high, precious angel.

Monday, September 13, 2010

Today

Today is my birthday.

Do you know what else today is?

It’s Childhood Cancer Awareness Day.

You know what I want for my birthday? I was EVERYONE to know that today is Childhood Cancer Awareness Day.

I was a healthy child. My children are healthy children.

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I want everyone to know that there are children who are fighting for their lives.

I want everyone to know that the Gold Ribbon is OUR ribbon.

I want there to be awareness, and support, and a cure.

Would you please consider putting this ribbon on your blog today? :

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Or steal the plain gold ribbon, or find something, anything. Just help spread awareness!

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Wednesday, September 8, 2010

Fighting Mad

I visited a blog today of a mother. This mother has a little girl who has battled cancer. She, too, is using this month to promote awareness for pediatric cancer, fighting for treatments and cures for all kids, including her own baby girl.

She shared information that focused on some of the treatments that exist for our children, on the disparity in treatment protocols, funding and more. I invite you to visit Amber’s blog, in particular this post, and read more about it.

I commented on that post, asking her permission to share it with you, and she graciously and enthusiastically agreed. You see, she’d just come home from the funeral service for a sweet five year old little girl. A little girl who wasn’t ready to give up, but who was out of options.

Five.

A sweet baby who lost  her fight at an age that all of my children have seen come and go. An innocent child who fought for her life for better than two of her five years. Nearly half of her short life was spent battling a monster that ravaged her body.

Can I tell you that right now, I’m weeping, and I want to punch something. Because it makes me MAD. Mad that Kate, that little girl, left a mother and daddy, and 4 siblings, all wondering why. Mad that my little friend Colette, who began her battle with neuroblastoma before she was three is clear of her cancer, but requires hearing aids because the treatments damaged her hearing. Mad that there are not better answers, better treatments, better options. I’m ready to fight. Are you?

Fighting for our kids,

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Monday, September 6, 2010

No Money? No Problem!

I’ve talked over the last week about pediatric cancer. I’ve linked to a couple of my favorite places to give, but that’s monetary giving.

Folks, I know, it’s hard to give money.

Times are tough.

We’re living paycheck to paycheck, or even worse, unemployment check to unemployment check.

How do we give back now?

Give Blood.

Children who are fighting cancer need blood products – platelets, plasma, whole blood, you name it, it’s VITAL in their fight.

Donating is free. It’s easy. And one pint of your blood could help save the lives of up to three people.

Find your local donation site, or a blood drive near you, by visiting www.RedCrossBlood.org and give the gift of life, without spending a dime.

goldribbon Momsense Signature

Thursday, September 2, 2010

Facts and Funds

First, let me say this: ALL cancers are terrible things. We look forward to the day when cancer is a thing of the past in all forms.

I fully support the need for research funding for cancer as a whole.

This month, however, is dedicated to our children. As a part of that, it’s important for people to understand the shortage of research funding that exists.

Fact: Childhood cancer is the #1 killer disease of our children, more than from asthma, diabetes, cystic fibrosis, congenital anomalies, and pediatric AIDS combined.

Fact: Each year 3,000 children die and 40,000 are in treatment.

Fact: The National Cancer Institute's (NCI) federal budget was $4.6 billion. Of that, breast cancer received 12%, prostate cancer 7%; while all 12 major groups of pediatric cancers combined less than 3%!  

That’s $552 million allocated for breast cancer. $322 million for prostate cancer. And it’s less that $138 million for pediatric cancers. Not one type of pediatric cancer – the 12 major groups of them.

A disadvantage for children facing cancer – only about 20% of adults diagnosed with some form of cancer are diagnosed with a metastatic cancer- one that has spread from it’s source point to other areas of the body. Approximately 80% of children have a metastatic occurrence at diagnosis. (Stage IV cancer.) These kids need the research to fight and treat these aggressive cancers.

They deserve the chance at life.

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Wednesday, September 1, 2010

September

I have always loved September. The temperatures are cooling, the leaves begin to change, my birthday rolls around, and now my younger son’s as well. Let’s not forget that football season kicks off in earnest!

But there is more now to September than I ever imagined.

Now, there are the gold ribbons.

There is awareness.

There is fighting – for better treatments, more research.

For a cure.

You are familiar with the pink ribbon.

You see it, and you know.

Do you KNOW the gold ribbon?

Gold ribbons are for Childhood Cancer Awareness.

This month, September? This month is for the kids.

I’m blessed with healthy children. I thank God for that every day. Over the last five years, I’ve “met” dozens of families fighting for the lives of their children. I’ve wept with those who have lost their sons or daughters to the monster that is cancer. I’ve celebrated, screaming with joy, at clear scans. I’ve prayed for little ones as they’ve suffered through high-dose chemo, and been grateful that they’ve only suffered minor hearing loss.

I am just one voice. One mother. One person in the vast sea that is the internet. But, the reality is, that’s how it begins. One voice speaks. A few listen, and they choose to speak, too. And those who hear, speak. Before long, the one small voice has become a roar, and awareness is born.

I want to be part of the roar. This is my statement to you:

September is Childhood Cancer Awareness Month, and I want YOU to be aware of it! The Gold Ribbon is the Childhood Cancer Awareness Ribbon. Please help make it as recognizable as the pink ribbon. And fight for a cure.

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A few of my favorite Childhood Cancer charities:

Alex's Lemonade Stand Foundation

 

St. Jude Children's Research Hospital