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

April 30, 2012

MGA's True Hope dolls ~ Available at Toy's R Us in June!

True Hope line of Bratz and Moxie dolls.

Beautiful and Bald Barbie! Let's see if we can get it made, the Facebook Community announced today: Jane, co-founder, has two sets of the True Hope dolls available for the media to spread the word and bring awareness to these wonderful dolls. Jane is available for questions and information regarding the production of the True Hope line of Brantz and Moxie dolls by MGA. Jane's email address is JaneBingham@gmail.com.


Posted today on Facebook by Jane:
Beautiful and Bald Barbie! Let's see if we can get it made

MGA gave me 2 sets of True Hope dolls. One in package and one out. If the media would like to see these dolls before they come out on shelves in June I would be happy to show them to you so you can spread the word about them. We want everyone to know they will be on shelves in June at ToysRUs! ~ Jane, Contact JaneBingham@gmail.com 

AVAILABLE starting in JUNE at ToysRUs in US and Cananda. We are hoping to get them to other countries in the future as well.

Please visit their Facebook page: 

Help bring awareness to the True Hope Dolls by MGA and tell your friends and family they will be available for purchase at Toy's R Us in the US and Canada beginning this June with $1.00 from each sale going to fund research for finding a cure of Children's Cancer at City of Hope.

The photo on the right is of the True Hope Doll "Cameron" the boy doll of the line. He is very handsome and an inspiration to all the children who suffer from hair loss for many reasons.


Below is a photo of "Sophia" she is a beautiful inspiration as well.


All of the True Hope Dolls by MGA are wonderful and will be a great comfort and esteem builder for so many children who are affected by hair loss due to several medical conditions including Cancer and Alopecia. Beautiful and Bald Barbie of Facebook and MGA hope these dolls to exactly that, help the self esteem of children while raising awareness to the need of research so that a cure can be found immediately. 



Anyone will be able to purchase these dolls beginning June 2012 at Toy's R Us in the US and Canada, $1.00 of each sale will go to funding research to find a cure at City of Hope.

To read the press release from MGA Entertainment see the link below:

April 28, 2012

Michael J. Fox Opens Today's Parkinson's Unity Walk!


Today's Parkinson's Unity Walk was opened by Michael J. Fox!


The 18th Annual Parkinson's Unity Walk (PUW) was held today Saturday, April 28, 2012 in New York City's Central Park. The PUW is the largest grassroots awareness and fundraising event for Parkinson's disease (PD) research in the United States. The event, which has grown from 200 participants in its inaugural year, is expected to unite more than 10,000 participants from across the globe.

"The annual Parkinson's Unity Walk is a powerful way for families, friends, caregivers, research organizations and major Parkinson's foundations to come together," said Martin Tuchman, Chairman of The Parkinson Alliance. "For any individual or family affected by Parkinson's disease who wants to feel the support, strength and compassion of a community – this Walk is where you should be." Currently, more than 1 million individuals in the U.S. are living with PD and 60,000 are newly diagnosed annually. 

Funding for research, for the cause and cure, as well as therapies that will improve the quality of life for those with PD, is critical. The PUW donates one hundred percent of all donations directly to research. As the "unity" in its name implies, the funds raised are distributed evenly among the seven leading Parkinson's foundations in the country: American Parkinson Disease Association, The Michael J. Fox Foundation for Parkinson's Research, National Parkinson Foundation, Parkinson's Action Network, The Parkinson Alliance, Parkinson's Disease Foundation, and The Parkinson's Institute and Clinical Center.

"The National Parkinson Foundation (NPF) is proud to participate in and support the 2012 Parkinson's Unity Walk," said Joyce Oberdorf, NPF President and CEO. "This event truly unifies the whole Parkinson's community behind a common mission—supporting the best, cutting-edge research. It is like no other."

In addition to being able to walk with thousands of members of the Parkinson's community, participants are able to take full advantage of a myriad of available resources at the event, including information about clinical trials, educational material from leading Parkinson's organizations and information on how to become an advocate for the Parkinson's community. This day of community and education also provides individuals who might otherwise have limited access to experts in the field, a chance to speak directly with movement disorder specialists, neurosurgeons, physical therapists, occupational therapists and speech therapists.

Most importantly, whether PUW participants are individuals diagnosed with PD seeking encouragement, family and friends showing support, caregivers desiring to know more, or researchers working toward new therapies, the PUW serves as a source from which to draw strength and build a greater community of support.

"It is by motivating, collaborating, educating and raising awareness of Parkinson's disease that we take important steps toward our goal of improving the quality of life of Parkinson's patients while we continue to work toward a cure," said Tuchman.

Attendees are also invited to visit the Abbott booth on Margot Zobel Way to leave their photo and inspirational message on the Messages of Hope™ Wall. For each message, Abbott, a leading global health care and medical research company, will donate $15, up to $15,000, to the PUW in support of research. Additionally, Abbott will invite walk participants to receive ongoing information about treatment and research through an opt-in text message campaign. For each individual who registers, Abbott will contribute an additional $1, up to $10,000, to the PUW.

Video SourcePublished on Apr 28, 2012 by Jessicafrank510

April 22, 2012

April Is Autism Awareness Month!

Autism is worldwide, this is one Mother's story from Australia.

This story tells how your life can change overnight when your child is diagnosed with Autism, told by Karen, a blogger from Australia, see her profile here  . To read more about Autism and for beautiful awareness graphics please visit her blog at  .


April is Autism Awareness month in America. I'm in Australia. We don't have the month long awareness but the 1st of April is World Autism Awareness day. I don't usually post much about my son but today i will share some info.

My son is 19 and was diagnosed with 'classic autism' when he was 2 and a half. He was developing normally up until around the age of two. 

He laughed, played, even said two word sentences and then suddenly he didn't speak, didn't laugh, played in a corner or behind our couch. He lost eye contact and started twisting his hands in front of his face and rocking (this is called stimming and many autistics have some form of it.) He didn't respond when you called him or spoke to him. At first they thought he was deaf, but i knew he wasn't. He did have ear problems and ended up having 3 sets of grommets, but this didn't change how he was. It just stopped his ear infections.

We ended up with Early Intervention for him. He had this for 3 years. The third year he was still hiding under the table when the therapist came. But hey... she just got under there with him. lol.

We used Macaton sign language with him until he was around 6. We had pictures of everything and signs of words on everything. My son, as many autistics, only learns visually. He gets lost on verbal prompts alone. He still does and you have to repeat things over and over sometimes.

He went to a normal school with an aide. He really didn't cope well in that situation, but because his IQ was 72 (70 and under here is an intellectual disability) he was not allowed to go to a special needs school... all because of a stupid 2 points! The first few years were ok, but he just got more and more behind because he just didn't understand what they wanted from him. Plus as the school years go on the teachers use more verbal prompts that visual. This was a huge problem for him. He ended up being very violent. I had so much trouble getting him to school. It ended up he had me in a headlock on the ground (he was bigger than me by then). Sometimes i couldn't breathe and was scared it was the end. He was refusing to go and i couldn't put up with this violence any longer. No one would help me from the school - even though i told them what was happening. So i decided to home school him. The best decision i have ever made! Though it's not for everyone.

I home schooled my son until he was nearly 15. The work was getting way beyond him by then. He was good at maths but only at a primary level. He had a huge problem with English as he responds to the here and now. He has no imagination. He never speaks about the past. But the good thing was that he was starting to smile, he was starting to speak in sentences. Factual, but at least he was speaking.

I had him retested at 15 and they found he does have an intellectual disability with the autism. He now has a Yorallah (a company that help disabled people cope with world) worker.He is very happy now. He is not violent at all... well not unless someone really upsets him. I know what to avoid and now have no problems. Well other than not leaving the house much. He has a phobia of the outdoors. If i'm in the back yard he won't come out. He will bang on the back door to get my attention before he would come out and get me. This is why i got into making graphics. My son is home 24/7 and I have to be here. At least making graphics takes my mind off the boredom of being home looking at the walls. Plus i fell from a window and hurt my back (i have severe nerve damage), so can't do much even if i wanted to, or had the freedom to.

But moving on... My son is now 19, as i said. He has a worker and he's happy. He is on a disability pension as he is far from being able to cope in the work force. He will live with us the rest of his life.. well our life. And i'm happy with that. He is a lovely young man now and i wouldn't change him for the world.

I have some April Awareness tags on my Autism Graphic site. Here is a sample. Just click this link to go to the page.  More Tags Here 

April 21, 2012

Have you ever wondered what the color yellow means?

Yellow is the color of the mind & intellect.


The color yellow relates to acquired knowledge. It is the color which resonates with the left or logic side of the brain stimulating our mental faculties and creating mental agility and perception. Being the lightest hue of the spectrum, the color psychology of yellow is uplifting and illuminating, offering hope, happiness, cheerfulness and fun.

In the meaning of colors, yellow inspires original thought and inquisitiveness.

Yellow is creative from a mental aspect, the color of new ideas, helping us to find new ways of doing things. It is the practical thinker, not the dreamer. Yellow is the best color to create enthusiasm for life and can awaken greater confidence and optimism.

The color yellow loves a challenge, particularly a mental challenge.

Within the meaning of colors, yellow is the great communicator and loves to talk. Yellow is the color of the networker and the journalist, all working and communicating on a mental level. Yellow is the scientist, constantly analyzing, looking at both sides before making a decision; methodical and decisive. Yellow is the entertainer, the comic, the clown.

Yellow helps with decision making as it relates to clarity of thought and ideas, although it can often be impulsive. Yellow helps us focus, study and recall information, useful during exam time. The color yellow can be anxiety producing as it is fast moving and can cause us to feel agitated. Yellow has a tendency to make you more mentally analytical and critical - this includes being self critical as well as critical of others.

Yellow is non-emotional, coming from the head rather than the heart. Yellow depends on itself, preferring to not get emotionally involved. Yellow is related to the ego and our sense of self worth, to how we feel about ourselves and how we are perceived by others. Yellow is the most highly visible of all colors which is why it is used for pedestrian crossings. Take note of the crossings which are marked in white - they are less easy to see than those marked yellow, particularly on wet and cloudy days.

If you are going through a lot of change in your life you may find you can't tolerate the color yellow very well  this will usually pass. It just means that you are having trouble coping with all the changes at the moment and yellow vibrates too fast for you, making you feel stressed. Introduce green or a soft orange into your life for a while to balance and restore your energies. Many older people don't respond well to large amounts of yellow because it vibrates too fast for them.


Positive Traits of the Color Yellow:
Positive keywords include: optimism, cheerfulness, enthusiasm, fun, good-humored, confidence, originality, creativity, challenging, academic and analytical, wisdom and logic.

Negative Traits of the Color Yellow:
Negative keywords include: being critical and judgmental, being overly analytical, being impatient and impulsive, being egotistical, pessimistic, an inferiority complex, spiteful, cowardly, deceitful, non-emotional and lacking compassion.

Yellow Represents: Mind and intellect: From a color psychology perspective, yellow stimulates our mental faculties; it activates the left or analytical brain. Happiness and fun: Yellow is uplifting to the spirits; yellow helps create enthusiasm for life and can awaken greater confidence and optimism.

Communication of New Ideas: Yellow is related to the expression and integration of new ideas and thoughts.

Creative: The color of new ideas, yellow helps us find new ways of doing things.

Quick decisions: Yellow helps with clear thinking and quick decision-making but it can also be impulsive.

Anxiety producing: Yellow is fast moving so too much time in its presence can agitate and lead to nervousness and emotional instability.

Critical: Yellow makes people more mentally analytical and self critical of both themselves and others.

Non-emotional: Yellow relates to the head not the heart.

To read more about the meaning, symbolism & properties of the color yellow see this link:

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

April 5, 2012

Prayers For Jasmine!

Jasmine is three years old with Cancer and needs our prayers.

A Facebook page and fund has been set up by her Grandmother, Debra Cimics David. Here are some words from Debra and the links to the pages. Please visit Jasmine at her pages and if you can please donate to her Cancer fund. Thank you.

From Debra, 

This page is dedicated to my grand-daughter Jasmine age 3, who is fighting cancer! http://www.facebook.com/pages/Prayers-For-Jasmine/177710882329258

Mission: 
To let people know about Jasmine and her battle with cancer!

Jasmine has recently been diagnosed with Cancer. This page will allow people to follow the progress of her treatment and how she is doing in general. Jasmine had kidney cancer that has spread, a 4lb Wilms Tumor had a crack in it that spread the Cancer to both of her lungs and small tumors have formed. Cancer cells have been spotted on the one kidney she has left. We have come close to losing her a few times. She has stage 4 cancer. She is fighting, and so are we!

Jasmine's Cancer Fund: 
This fundRazr is for my 3 year old grand-daughter Jasmine who is fighting cancer. My daughter Ann, Jasmines mother, is a single mom who is struggling emotionally and financially. This has been alot for my daughter Ann to bear. Jasmine's dad is not in the picture so my daughter has had to do it all. With Jasmine fighting cancer and her mom Ann, my daughter, having had a heart attack and stroke not long ago, it has been a lot for both of them. 

I am doing this for Jasmine to help bring donations to her cause. Any donations would be greatly appreciated. I hope that you can help a very worthwhile cause. All donations will go to my daughter for Jasmine. Please, if you are able to donate and find it in your heart, Jasmine and Ann would be very greatful. When cancer strikes it affects the whole family. Jasmine is currently under going radiation treatments which make her very ill and has months of chemo to go through. Thank you and God Bless everyone for any donations you can make!

Please see the link below to make a donation:

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