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Creating change by raising awareness of causes that ensure a better future.

April 19, 2012

Brooke's Blossoming Birthday Wish!

Blossoming Hope ~ Birthday Wish!


On April 27th, Brooke will be 5! After over a year of battling cancer, she has one wish for her birthday... to GIVE. Instead of asking for presents, Brooke wants her friends and family to give to her project, Brooke's Blossoms & Buddies, which is in the process of becoming a full fledged 501(c)3 nonprofit foundation with goals of empowering others, especially kids, to help find cures for all pediatric cancers. If you are unable to donate online, please send a birthday note to Brooke letting her know how you want to make her birthday wishes come true. Brooke's cancer has recenlty been discovered to be progressing so she is in and out of the hospital and care often right now, but her current address will be posted on her special page at:   http://www.caringbridge.org/visit/BrookeHester 

By: Jessica Moore Hester

Brooke is our special little girl so please help us spread the word so she can watch her birthday wish come true to keep sending smiles all over the world to children who so desperately need them! 

"Planting Seeds of FAITH, LOVE, and HOPE for CURES... One SMILE at a time!"

"Thank you for helping to make Brooke's Birthday wish come true!"

-Jessica Moore Hester

To make a donation to Brooke's Blossoming Birthday Wish, simply click on the link below
http://fundrazr.com/campaigns/4IBo7?psid=f467cfdf120f406b8a325b2b75329c81 

Donation amount reflects total at time of this publication.
$2,425 raised
$10,000 goal

Mattel, Inc.: Sell us the bald "friend of Barbie"

Petition for the public sale of the "friend of Barbie"!

Mattel has agreed to produce a "friend of Barbie" fashion doll but they are not going to be available for purchase by the public in retail stores. Here is some of the past updates as the campaign has been ongoing for months between the Facebook group "Beautiful & Bald Barbie! Let's see if we can get it made" and Mattel.  

http://www.facebook.com/BeautifulandBaldBarbie

Mattel's announcement of the production of the "friend of Barbie" fashion doll:

“Play is vital for children, especially during difficult times. We are pleased to share with our community that next year we will be producing a fashion doll, that will be a friend of Barbie, which will include wigs, hats, scarves and other fashion accessories to provide girls with a traditional fashion play experience. For those girls who choose, the wigs and head coverings can be interchanged or ...completely removed. We will work with our longstanding partner, the Children’s Hospital Association, to donate and distribute the dolls exclusively to children’s hospitals directly reaching girls who are most affected by hair loss. A limited number of dolls and monetary donations will also be made to CureSearch for Children’s Cancer and the National Alopecia Areata Foundation.  http://www.facebook.com/Mattel

Thank you to Mattel for agreeing to produce the "friend of Barbie" fashion doll.

Of course, the supporters of the doll are very excited about Mattel's announcement and would be extremely happy to see if available on retail store shelves available to anyone who would like to own it. The Facebook group "Beautiful & Bald Barbie" have asked Mattel to consider this and have created a petition on Change.org in the hopes that the public will sign the petition and be heard. The goal is 15,000 signatures and as of today there are just over 1500. Below is the wording of the petition:

Why This Is Important:

Mattel has made the decision to make a one time production of a bald "friend of Barbie" doll which will be donated exclusively to children’s hospitals and a smaller amount going to CureSearch and the National Alopecia Areata Foundation. Mattel has made the decision not to sell these dolls at retail stores.

Why this doll should be made available for purchase By Mattel beyond the donated ones...

Head Hunters - There will be a high price on her head for recipients to sell her. By donating a limited one time production, while honorable, this will create a high demand for collectors. This leads to other concerns...

Many children who do receive one will not be allowed to even open the box because of the high worth of such a rare Barbie brand doll. This will defeat the whole purpose of donating them to the “sickest children who could benefit from them the most”.

Trichotillomania kids will not qualify for one through this donation process.

Adults with Cancer, Alopecia and Trichotillomania want these dolls too. I have even heard from many men who want one as well. None of which will be able to purchase one as of right now.

A child like my daughter, whose mother loses her hair to cancer treamtments will not qualify for one through this donation process.

Children of a relative, aunt, mother, grandmother, sister, friend with hair loss due to chemo, alopecia, trichotillomania or any other cause, will not be able to have one.

Raising awareness and tolerance for children and women with hair loss will be lost in this effort as it will still be "hidden" by not allowing the sale of them, not allowing them on the shelves of stores.

Supporters of seeing this doll made from all over the world will not be able to purchase one, although Mattel did tell me that a very small amount will be sent to their offices overseas to be donated, it will not be nearly enough for all the children and people effected by hair loss in the many countries who want to see this doll in their country.

So much money could be raised if they were sold beyond the donated dolls with a portion of proceeds going to cancer research or another worthy cause. As a mother with cancer, I would buy one for my daughter to play with, one for me to remember my victory through chemo, one for my daughter’s friends to play with with her when they come over, birthday presents for my daughter’s friends, a few to donate at the cancer center, etc That would be a minimum of 6 dolls that I would purchase as a mother with cancer. Multiply that by mothers, aunts, grandmothers, friends all over the world and that feel the same way...that’s a lot of dolls! and potential money raised that will be missed out.

In summary, while I love that Mattel has agreed to make this doll and I am very appreciative and think it is honorable that they want to donate them to Children's Hospitals and The national Alopecia Areata Foundation, I fear many of them will end up on Ebay or at other auctions. I fear that many of the children they were intended to benefit will not get to play with them because of their rarity, that children of a relative with hair loss will not be able to have one, that countries besides in North America will not have access to them like they could, that there is a missed chance for raising awareness and funds by Mattel. Yes, I love what they have agreed to and I am encouraging them to do more...to continue to listen us and respond appropriately to these concerns.

Mattel at first responded to us that "they don't take suggestions from outside sources." They changed their mind and listened to the outcry for these dolls. I am encouraging them to continue listening to our suggestions. Will you join me?

Please go to this link to sign the petition and show your support:

April 14, 2012

Parkinson’s Unity Walk (PUW) April 28, 2012!

18th Parkinson’s Unity Walk (PUW), April 28, 2012!

Join us for a gentle 1.4 mile walk in Central Park. Visit informational booths along Margot Zobel Way which will include Ask the Doctor, representatives from our sponsors, and seven major US Parkinson’s foundations.

Walking is optional. Stay and enjoy the day’s activities!

100% of donations go directly to Parkinson’s disease research.

The walk will be on 72nd Street Bandshell, Central Park, New York. Use 72nd Street Park entrance on Fifth Avenue or Central Park West.

REGISTRATION OPEN:      8:30 am to 1:00 pm
BOOTHS OPEN:                              9:00 am to 2:00 pm
WALK KICK-OFF:               9:45 am
WALK BEGINS:                    10:00 am

Registration Information: 

While there is no registration fee, we encourage all walkers to raise funds on behalf of the Walk. Remember, 100% of all donations go to research.

Go to the Registration booth only if you need to do any of the following:
  • Pick up your Unity Walk T-shirt (if eligible).
  • Walkers who donate or fundraise $75 by the day of the Walk and are present at the Walk will receive a T-shirt (for a team, average raised per team member is taken into account).
  • Turn in your donations.
  • Register for the Walk (if you have not done so online or by mail).
Any of our Registrars can help you on the day of the Walk. Go to any seated Registrar; there are no special lines; make only one stop to pick up shirts and turn in donations. All walkers are registered as individuals, even if they are part of a team -- there is only one envelope per walker so you will be sure to get credit as the fundraiser. We recommend that you allow extra time to go through Registration.

2012 PUW Final Registration Times:

Team Registration Deadline:  April 27, 2012 
(Team registrations will not be accepted on the day of the Walk.)

Deadline to Give and Turn in Donations:  May 28, 2012.
All donations received by May 28, 2012 will be credited to the 2012 Walk. 
(Donations where all information is complete and legible will be acknowledged by July, 2012.)

Refreshments:

No need to leave the park for lunch. Have a bite while you are visiting the informational booths along “Margot Zobel Way.” Four food trucks will be selling moderately priced food items throughout the day:  Eddie’s Pizza TruckGorilla CheeseRickshaw Dumpling Bar and The Treats Truck.

Chock Full o’ Nuts is generously donating coffee to all Walk participants. Look for their trucks by the Bandshell, near Registration and further down “Margot Zobel Way.”

Complimentary snacks and bottled water will be served at the Refreshments Booth. Bottled water will also be available at the Water Station by the Bandshell.

Teams:
Use the Team Meeting Area near the Bandshell if you are looking for a place to meet your group. 

Stop by the Team Photo Booth by the Bandshell and receive a printed copy of your photo to take home with you. You can also download a digital copy of the photo from the vendor’s website and forward it to your team members and supporters.


Accessibility:

Entire Walk route is wheelchair accessible. We do not provide wheelchairs.  Click here for rentals.
Golf Carts are available to pick up walkers who require assistance. Look for waiting areas for Golf Carts if you require transportation.


Some helpful tips:

  • Light snacks and drinks will be provided. Pack a heavier lunch and extra drinks based on your needs.
  • Each participant will receive a tote bag to hold information from our sponsors. If you think you’ll need it, bring a backpack to hold extra items while you walk. PUW Staff can not hold personal belongings while participants walk.
  • Use the Team Meeting Area if you are looking for a place to meet your group.
  • Make a sign in memory or honor of a friend or loved one at the Make-a-Sign Area.
  • Strollers and pets are allowed in Central Park and along the Walk route.  Please be considerate of fellow walkers.  Dogs must on leash starting at 9 am, per Park rules.  General Park information about pets can be found here.
Important links:
For more information on the PUW please see the link below:

April 13, 2012

Team Brennan, Bringing Awareness To Childhood Cancer!

Brennan is almost two years old & has
Stage 4 High Risk Neuroblastoma!


Brennan was diagnosed at 10 months old with Stage 4 High Risk Neuroblastoma. 10 months later he was diagnosed with a secondary cancer which had already metastazised to his liver and lung, and newly his brain. They're calling his secondary cancer " Secondary tumor of highly aggressive Undifferentiated Sarcoma." Brennan is just currently shy of 2 years old and has spent almost exactly Half of his life, fighting for his life. Brennan will turn 2 years old on May 26, 2012.

BRENNAN'S MOTHER CINDY HAS UPDATES & IS ASKING FOR YOUR HELP.

Please find it in your heart to see this tragedy through the eyes of Brennan and his family and help if you can. Thank you for understanding how hard it is for Cindy to ask for help and please share this with your friends and family so that we can get his story told and get him the help he so desperately needs.

I hate to even ask for this, but with everything happening so very fast for our family, and Brennans daddy, Blake Scurlock not having any vavcation to take only relying on FMLA which does not pay during your family leave. I have never asked for anything but prayers, but I have to swallow my pride and ask for help. I want Brennan to know that we have done everything that we could, and that Me (Cindy), blake and his sister Katelyn have and wil continue to be by his side, even as the goes into the arms of Jesus. I have to even know that we have to do this let alone say it. =(

Now Brennan has a fever =( Its so strange that now, given Brennans prognosis we wont be going through the "routine" of blood cultures. Just tylenol. Just seems so strange that now things like this, which are huge in the cancer world just wont be done anymore =( 1 more thing to make my nightmare a reality

There has never been a time I ask ever asked for help, but there isnt a way I cant this time. We have stuggled the last year and with everything now happening so fast, and never having prepaired for this, I have to swallow my pride and ask. =(

Below are links to Brennan's pages and where you can made a donation to his cause, thank you!
http://www.mccowen.net/
http://www.caringbridge.org/visit/brennanscurlock
http://www.facebook.com/events/355971584449476/
http://www.facebook.com/pages/Brennan-Scurlock/214491795231031

April 11, 2012

Childhood Cancer Is Real & Need's A Cure!

More awareness needs to be raised about Childhood Cancer!

It's estimated that just over 11,000 children between infancy and age 14 will be diagnosed with cancer in 2011. Overall, cancer is rare in children (total cancer diagnoses predicted for this year is over 1.5 million), but incidence rates have been increasing slightly by 0.6% every year since 1975.

The good news is that while new cases are increasing, the mortality rate has been cut in half (53%) in that same time-period. This can be attributed to improvements in treatment and the high number of young patients who are participating in clinical trials.


But there is still reason for awareness and diligence in caring for our children's health. Though the mortality rate for childhood cancers is relatively small, only 1,300 children are expected to lose their battles with cancer compared to over 570,000 adults - it is still listed as the second-leading cause of death in children, surpassed only by accidents. One-third of the estimated deaths will be in children who are diagnosed with leukemia.

Early symptoms of cancer in children are usually non-specific. Children should be receiving regular medical checkups to help parents and doctors become familiar with what is "normal" for their health. Any unusual symptoms that persist can be investigated. If there is a suspicion of cancer, it's vital that it is caught early, avoiding a potentially health-threatening delay in diagnosis.

Some symptoms can include:

An unusual mass or swelling in any part of the body;
unexplained paleness and/or loss of energy;
Sudden tendency to bruise;
Persistent, localized pain;
Prolonged, unexplained fever or illness;
Frequent headaches, often with vomiting;
Sudden eye or vision changes; and
Excessive, rapid weight loss.

Major categories of childhood cancer and their respective symptoms can be found on the Ped-Onc Resource Center. As with any cancer, the best defense is a good offense. Know your children and their habits and health histories well, and visit with a doctor if you have concerns about their health.

April 10, 2012

It Might Be Hope!

It's been a while since I felt this
but it feels like it might be
HOPE...


Source:   http://mosthopeful.com/tag/hope-quote/

Brennan Scurlock Needs Prayers For A Cure!

Brennan was diagnosed at 10 month with Stage 4 Neuroblastoma.

UPDATE AS OF APRIL 10, 2012:

Brennans scans showed what we feared.

Brennans sarcoma has progressed through our chemo. the 5mm leaion we found 2.5 weeks ago has grown and there.is a second lesion on.his brain. they have grown and has caused brennans brain to.bleed and cause pressure. every one of his sarcoma tumors have grown. the kidney one, his liver and lung tumors. Brennan cannot continue chemo anymore because its too risky with his hemorrhage. This was not supposed to happen to my son. my heart is shattered. we have chosen to not place a drain because brennan would be unable to move and his comfort would be compromised. ICU is not a place we want Brennan right now. He is comfortable and shows no signs of discomfort. Please pray for my love. 

ABOUT BRENNAN:

10 months later he was diagnosed with a secondary cancer which had already metastazised to his liver and lung, and newly his brain. They're calling his secondary cancer " Secondary tumor of highly aggressive Undifferentiated Sarcoma." Brennan is just currently shy of 2 years old and has spent almost exactly Half of his life, fighting for his life.

Brennan will turn 2 years old on May 26, 2012.

You can donate straight to Brennan from mccowen.net. There is a paypal donation button which you can donate through. The website will also give any information about ALL of Brennan's events as well as a link to download all of out event flyers. Please follow this link to make a donation:  http://mccowen.net/

Brennan was admitted to Texas Children's ER Thursday night, March 31, for an unidentified infection and low blood count. Later we found out there was a large tumor coming from his left Kidney, reaching to his left lung and back toward his spine.

We found out his symptoms were because of a bleed from the vein system inside the tumor.
Doctors say it is showing characteristics of being Neuroblastoma.

Our prayers are that when he makes it into surgery they are able to remove the kidney, tumor and surrounding lymph nodes that are affected.

Please check this site daily for new updates, leave encouraging words for his family and help us pray for this sweet baby.

We have set up an account under Cindy McCowen at Chase for donations for Brennan and family. They do not have paid medical leave to be by his side while he is battling cancer, all donations are appreciated to help pay bills while he is getting treatment, no amount is to small. You can make a deposit at any Chase bank account #965482987.

Thank you so much and God bless!

Please Visit Brennan at his Facebook Page at:

April 7, 2012

In Memory of Thomas Kinkade 1958 ~ 2012!

Thomas Kinkade was born in 1958 & grew up in Placerville Ca.
Artist Thomas Kinkade, whose brushwork paintings of idyllic landscapes, cottages and churches have been big sellers for dealers across the United States, died Friday, a family spokesman said. 


Kinkade, 54, died at his home in Los Gatos in the San Francisco Bay Area of what appeared to be natural causes, David Satterfield said.

Kinkade called himself the "Painter of Light," and his sentimental paintings, with their scenes of country gardens and churches in dewy morning light, were beloved by many but reviled by the art establishment.

He claimed to be the nation's most collected living artist, and his paintings and spin-off products were said to fetch some $100 million a year in sales, and to be in 10 million homes in the United States.

Those light-infused renderings are often prominently displayed in buildings, malls, and on products — generally depicting tranquil scenes with lush landscaping and streams running nearby. Many contain images from Bible passages.

"I'm a warrior for light," Kinkade, a self-described devout Christian, told the San Jose Mercury News in 2002, a reference to the medieval practice of using light to symbolize the divine. "With whatever talent and resources I have, I'm trying to bring light to penetrate the darkness many people feel."


Before Kinkade's Media Arts Group went private in the middle of the past decade, the company took in $32 million per quarter from 4,500 dealers across the country, according to the Mercury News. The cost of his paintings range from hundreds of dollars to more than $10,000.

According to his website, Kinkade's paintings have been reproduced in hand-signed lithographs, canvas prints, books, posters, calendars, magazine covers, cards, collector plates and figurines. The website touts his Disney collection and offers a gallery locator, where fans can find nearby dealers.

Its online store offers a wide range of works and products with Kinkade images including artworks, prints, and coffee mugs.

His artistic philosophy was not to express himself through his paintings like many artists, but rather to give the masses what they wanted: warm, positive images, Ken Raasch, who co-founded Kinkade's company with him, told the Mercury News.

"I'd see a tree as being green, and he would see it as 47 different shades of green," Raasch said. "He just saw the world in a much more detailed way than anyone I've ever seen."

A biography on the website said Kinkade rejected "the intellectual isolation of the artist" and instead, made "each of his works an intimate statement that resonates in the personal lives of his viewers."

"I share something in common with Norman Rockwell and, for that matter, with Walt Disney, in that I really like to make people happy," he said.

He called Rockwell his earliest hero. "I remember my mom had a big collection of copies of (Saturday Evening Post) magazines, and that was really my introduction to those great illustrators," he said.

Kinkade was born and raised in the Placerville, Calif. He studied at the University of California at Berkeley and the Art Center College of Design in Pasadena.


He said art was a major outlet growing up.

"I was always the kid who could draw," he said. "I had this talent, and it was the one thing that gave me some kind of dignity in the midst of my personal environment."

As a young man, Kinkade traveled by boxcar from California to New York with fellow fledgling artist, James Gurney, sketching the American landscape along the way.

The site says that with these sketches in hand, the two were able to get published The Artist Guide to Sketching in 1982, a book that helped land him a job creating background art for animated films.

Also that year, he married his childhood sweetheart, Nanette, to whom he frequently paid tribute to by hiding her name and those of his four daughters within his paintings.

"Thom provided a wonderful life for his family," Nanette said in a statement. "We are shocked and saddened by his death."

There was no immediate word on an official cause of death. Calls to the coroner's office were not immediately returned.

The newspaper said friends and family on Friday began planning a private service and were weighing a public celebration for a later date.

http://www.usatoday.com/life/people/obit/story/2012-04-07/thomas-kinkade-painter-obituary/54088992/1 

Thomas Kinkade was America's most-collecteda living artist.
Combining realism with idealism, grand perspectives with minute details, his artworks reflect the love in his heart for God, for family, for Nature, and for simple idyllic life. In his paintings, we can see majestic mountains, winding rivers, lakes and forests, sea and lighthouses, cozy cottages and rustic chapels, beautiful gardens and peaceful Christmas night. Fresh and uplifting, they radiate with warmth and hope, in which one cannot fail to identify his longings for love,faith and a simple life close to God and Nature.

Thomas Kinkade was born in 1958. He grew up in the small town of Placerville in California.


In 1976, Kinkade attended the University of California and began to receive his formal art training at the Art Center College of Design in Pasadena. He spends the summer after graduation on a sketching tour with college friend, James Gurney. Together the two produced the best-selling instructional book, The Artist's Guide to Sketching. The success of the book landed the two young artists at Ralph Bakshi Studios to create background art for the animated feature film Fire and Ice. It was also during this time that Kinkade began to explore light and imaginative worlds with abandon.

After the film, Thom earned his living as a painter, selling his originals in galleries throughout California.

In 1982, he married his childhood sweetheart, Nanette. Together they raised 4 daughters. Kinkade is a devoted husband and doting father at home. He creatively hid the letter "N" in his paintings as "love notes" to his wife, Nanette. His daughters also find their own messages of love from their father as their names and images often appear in his paintings.

Kinkade is a devout Christian. He credits the Lord for both the ability and the inspiration to create his paintings. His goal as an artist is to touch people of all faiths, and bring peace and joy into their lives through his art.

While admiring his paintings, we can't help feeling the call of love and Nature, and sometimes a nostalgic feeling for simpler life of faith in old time America.

Rest in peace, Mr. Kinkade, you will be missed by everyone and especially by your home town of Placerville, California.

In addition to his beautiful and famous paintings, Thomas Kinkade also created many very inspiring sculptures, ornaments, centerpieces and heirlooms that will be forever in the homes of millions of Americans and worldwide.

See More of Thomas Kinkade's Artworks

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