May 092012
 

TO  SHE WHOM MUCH IS EXPECTED, MUCH IS GIVEN.

(Visitors: What we have here is a LOVE FLASH MOB. It is a celebration of LIFE and LOVE and HOPE that we Monkees hold once in a blue moon. We come together here to support a Sister, a Sister who might need a reminder that She is Loved and Watched Over.  In short – We Make Magic Happen, Baby.  We do it by showing up, giving what we can (up to a $25 maximum), and trusting that the money raised is the least of the miracles that result. Join us, EVERYONE IS INVITED!)

 Everyone, meet Claudia.

Claudia is a single mama diagnosed with ALS,  also known as Lou Gherig’s disease. She has three children, all of whom have Fragile X syndrome. She currently lives with her youngest son, who has autism, and his caretaker, Amy.

After suffering through a difficult childhood and young adult life, Claudia found her passion in saving the lives of others. For nearly two decades, Claudia served her community in emergency services. She was a volunteer firefighter and EMT, a paid-reserve firefighter, paramedic, Emergency Department RN and helicopter flight medic. Her second full-time job was advocating for her special needs children and other families with similar challenges.

Claudia says:

“I began having slurred speech in October 2004. In August I was diagnosed with ALS. I went from being “gregarious” and “articulate” to being presumed to be mentally impaired. My voice is weak and sometimes I can barely speak above a whisper. I’m frequently very short of breath. I use a wheelchair full time. I’m in near constant pain from my increasing spasticity. I sleep using a breathing machine. All my symptoms are progressive and eventually, while mentally alert and with intact sensation, I will become totally paralyzed.

 My ALS Progression is VERY slow. My slow progression is a blessing and a curse. The blessing is obvious: I have more time with my children and friends; I treasure this time with my children. The curse is that I will pass through the stages of losing function in slow motion. With the loss of functioning comes an increased need for resources that I simply don’t have.  Life is often hard, but I feel blessed. It is amazing to think that coming to the end of my physical, financial, emotional, and relational resources helped me learn to truly rely on God!”

Kay. Well, I  believe God can be depended upon, but I also believe that that God shows up through other people. And today, WE ARE THE PEOPLE, PEOPLE. We’re the ones who are going to show up for Claudia and remind her that God loves her and her family, that the Universe is on her side, that she has not been forgotten, and that We Belong To Each Other.

Here’s how we’re going to do it:

We’re going to buy Claudia a (fully loaded, fully outfitted) handicapped accessible van that will accommodate her special needs as well as those of her youngest son. Right now, Claudia has no vehicle that will hold a wheelchair, so she is not able to attend her son’s frequent doctor’s appointments or even her own. She’s not able to visit her oldest son, who lives thirty minutes away. Amy, the angel caretaker who lives with Claudia, can’t take Claudia to museums or parks or even outside to see the beautiful world that Claudia spent so much of her life saving and loving and serving. Clearly, this is unacceptable.

So the times, they are a changing. Today. Today we raise the money needed to buy a van for Claudia. To give her back some of her freedom, her love of adventure, and her ability to nurture her children – all of which are the stuff that makes Claudia, CLAUDIA.

OH….. ONE MORE THING.

Meet Paul and Mindy and their gorge kiddos.

You’ll remember these folks from this miracle post. Mindy’s family is so beloved by her neighbors that one of them, Matt, sent us a letter asking us to help fix Paul and Mindy’s aging car. Matt told us that he loves Momastery but finds the label Monkee too feminine, so he refers to himself as a Donkee. Donkee went on to explain that Paul and Mindy’s family deserved a break, like, yesterday. You see,  Mindy’s been diagnosed with stage 4 lung, bone, and liver cancer. Matt said that their medical bills get so high that sometimes Mindy and Paul just can’t get their car out of the shop.

Mindy defies her diagnosis. As she told us:  “I have so much to fight for, I don’t plan on dying anytime soon.  My “baby” is 5.  He is full of life and for that I am thankful.  I look at my beautiful children and my wonderful, supportive, and handsome husband, and remember that I too am alive and will be alive….my fight has to be great! I’m not going anywhere!”

And to that we say, No ma’am, not in that clunker, you’re not. So we’re gonna go ahead and buy Mindy and Paul a new van, too. They’ve got enough to handle without car trouble. Just, enough said.

So . . . .Two Vans.  Eighty- five thousand dollars. No problem.

 Here are the Love Flash Mob Rules:

1. EVERYONE IS INVITED.

2. There is a $25 dollar contribution limit per person.

Please remember that the Croyles were sent on a vacation of a lifetime largely due to 5, 10, 15, and 20 dollar donations. Because of all of your five and ten dollar bills, Kristin Croyle, in the wake of her treacherous diagnosis, was able to put her feet in the sand, feel the warmth of the sun on her shoulders, stare out at the big, big ocean, and listen to Lance and her children play in the surf . . . for the first time.

We can do no big things, just little things with great love. Each of our offerings will be little but together, they will become great.

EVERY donation makes a difference. BE the change you want to see in the world. Don’t sit this one out. Jump in. You are worthy. You are powerful. You can change the world. WE ARE THE PEOPLE. YOU ARE THE PERSON. NOW IS THE TIME.

Press the Van-tastic Button on the right of this page to donate to the Claudia/Mindy Van Fund. It has a Monkee and a van on it, and when you press the button it will direct you to our paypal account where you can donate.

I’ll update you frequently as the miracles unfold.

And while you’re at it, think of five friends who have a heart and twenty five (or five)  dollars and invite them to share in this miracle, too.  Share this on Facebook, the car pool line, wherever there is SOMEONE TO INVITE.  Love Flash Mobs are as much for the givers as they are for the receivers – and we want as many human beings as possible to be part of this miracle. We want thousands of souls invested in these families . . . thousands of people praying and sending healing energy and loving on Claudia and Mindy and their families.

Love, LOVE, LOVE!!!!!!  TWMF

(The Whole Monkee Family)

Now…..GO!



Carry On, Warrior
Author of the New York Times Bestselling Memoir CARRY ON, WARRIOR
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  339 Responses to “VAN-TASTIC MOTHER’S DAY LOVE FLASH MOB!!”

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  2. […] and platform to help others in need, including a special purpose school and families who needed an accessible van. How many ways can we love […]

  3. […] the last year I’ve been super-duper inspired by Glennon Doyle Melton leading the charge in raising big bucks for families in desperate need through Love Flash Mobs.  Crowd-sourcing towards *actual* needs is […]

  4. […] wing that brings Momastery readers together to meet each other’s needs. Often it’s a call for lots of people to donate a small amount for a family in great need, but Monkee-See-Monkee-Do, as it’s called, has started to do other projects too. Watch what […]

  5. […] is invited and the maximum donation is $25.  Glennon picks the causes and they vary.  The Love Flash Mobs have given a mother, with a 3%-chance-that-chemo-would-work diagnosis, a once in a lifetime […]

  6. I love being a MONKEE!!! Love wins~

  7. […] You can read about the VAN-TASTIC MOTHER’S DAY FLASH MOB here.  And the Monkee’s amazing response here. […]

  8. […] Read about the VAN-TASTIC MOTHER’S DAY FLASH MOB here.  And the Monkee’s amazing response here. […]

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