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

March 4, 2012

A Special Memory Before Daughter Leaves For US Army!

My sister & niece celebrate leaving for the Army!

It all started a few months ago when my niece Katie decided to join the US Army. After going through all the testing and evaluations she found out she had passed everything and is a Soldier. She leaves for Basic Training this August and my sister Susie has been having trouble with the realization of the fact that her daughter is not only leaving home but is going into the Army, which of course any mother would have these feelings.

Susie is very proud of Katie as we all are, she is an amazing young woman at the age of 19 who knows what she wants to do and is going to give 100% to serving our country and being the best she be. 

Katie is not the first one in our family to join the Army but is the first woman to do so. My father joined the Army in 1964 and served in the Vietnam War as a Platoon Sgt. in Special Forces in 1968 where he received the Bronze Star and many medals for his excellent service.

Katie's father Kenny was also in the Army right around the time Katie was born and served in did a tour in Germany and was deployed to Los Angeles to protect the community and citizens there during the LA Riots.

Today Katie decided to cut her hair so she would have plenty of time to get used to her new "Army" look. Of course she looks beautiful as she always has but what makes her even more beautiful is she and her mother have decided to donate her very long, healthy brown locks to "Locks for Love", what a wonderful way to make a good memory of this life changing event their family is gearing up for.

WHAT IS LOCKS OF LOVE?

Locks of Love is a public non-profit organization that provides hairpieces to financially disadvantaged children in the United States and Canada under age 21 suffering from long-term medical hair loss from any diagnosis. We meet a unique need for children by using donated hair to create the highest quality hair prosthetics. Most of the children helped by Locks of Love have lost their hair due to a medical condition called alopecia areata, which has no known cause or cure. The prostheses we provide help to restore their self-esteem and their confidence, enabling them to face the world and their peers.

Mission Statement
Our mission is to return a sense of self, confidence and normalcy to children suffering from hair loss by utilizing donated ponytails to provide the highest quality hair prosthetics to financially disadvantaged children. The children receive hair prostheses free of charge or on a sliding scale, based on financial need.

For information on how you can donate to Locks of Love see: http://www.locksoflove.org/

Endometriosis Is Real, Painful & We Need A Cure Now!

March is Endometriosis Awareness Month!

Endometriosis is a disease occurring very frequently in women of reproductive age, its prevalence being higher than breast cancer. It is also the most misdiagnosed disease.

Endometriosis is the abnormal growth of cells (endometrial cells) similar to those that form the inside of the uterus, but in a location outside of the uterus. Endometrial cells are cells that are shed each month during menstruation. The cells of endometriosis attach themselves to tissue outside the uterus and are called endometriosis implants. These implants are most commonly found on the ovaries, the Fallopian tubes, outer surfaces of the uterus or intestines, and on the surface lining of the pelvic cavity. 

They can also be found in the vagina, cervix, and bladder, although less commonly than other locations in the pelvis. Rarely, endometriosis implants can occur outside the pelvis, on the liver, in old surgery scars, and even in or around the lung or brain. Endometrial implants, while they can cause problems, are benign (not cancerous).

Who is affected by endometriosis?
Endometriosis affects women in their reproductive years. The exact prevalence of endometriosis is not known, since many women may have the condition and have no symptoms. Endometriosis is estimated to affect over one million women (estimates range from 3% to 18% of women) in the United States. It is one of the leading causes of pelvic pain and reasons for laparoscopic surgery and hysterectomy in this country. Estimates suggest that between 20% to 50% of women being treated for infertility have endometriosis, and up to 80% of women with chronic pelvic pain may be affected.

While most cases of endometriosis are diagnosed in women aged around 25-35 years, endometriosis has been reported in girls as young as 11 years of age. Endometriosis is rare in postmenopausal women. Endometriosis is more commonly found in white women as compared with African American and Asian women. Studies further suggest that endometriosis is most common in taller, thin women with a low body mass index (BMI). Delaying pregnancy until an older age is also believed to increase the risk of developing endometriosis.

What causes endometriosis?
The cause of endometriosis is unknown. One theory is that the endometrial tissue is deposited in unusual locations by the backing up of menstrual flow into the Fallopian tubes and the pelvic and abdominal cavity during menstruation (termed retrograde menstruation). The cause of retrograde menstruation is not clearly understood. But retrograde menstruation cannot be the sole cause of endometriosis. Many women have retrograde menstruation in varying degrees, yet not all of them develop endometriosis.

Another possibility is that areas lining the pelvic organs possess primitive cells that are able to grow into other forms of tissue, such as endometrial cells. (This process is termed coelomic metaplasia.)

It is also likely that direct transfer of endometrial tissues during surgery may be responsible for the endometriosis implants sometimes seen in surgical scars (for example, episiotomy or Cesarean section scars). Transfer of endometrial cells via the bloodstream or lymphatic system is the most likely explanation for the rare cases of endometriosis that develop in the brain and other organs distant from the pelvis.

Finally, some studies have shown alternations in the immune response in women with endometriosis, which may affect the body’s natural ability to recognize and destroy any misdirected growth of endometrial tissue.

http://blogs.mcgill.ca/gradlife/2012/03/01/endometriosis-awareness/

March 2, 2012

Happy Birthday, Dr. Seuss!

Children’s Author, Dr. Seuss Turns 108!

Today marks the 108th birthday of Theodor Seuss Geisel more famously known as Dr. Seuss.

A wonderful children’s author, Dr. Seuss may have written in a type of English that didn’t always make perfect sense, but his universal appeal is unmistakeable. His 46 children’s books have been loved by pretty much any child and adult who picked one up. Today the good doctor would have turned 108. He passed away in 1991 after a battle with throat cancer and years of poor health.

His books are packed with imaginative characters and playful rhymes, some of his most celebrated titles include best-sellers like Green Eggs and Ham, The Cat in the Hat, One Fish Two Fish Red Fish Blue Fish, Horton Hatches the Egg, Horton Hears a Who!, and How the Grinch Stole Christmas!

Dr. Seuss had a way with words that is for sure but his words had a way of changing his reader's lives and inspiring, encouraging and helping fans of all ages to feel good about themselves as they grew up reading his wonderful quotes. Here is a collage of 30 Dr. Seuss quotes that can change your life and a list of seven interesting facts about Dr. Seuss you probably did not know, enjoy!

7. Born Theodor Seuss Geisel in Springfield, Massachusetts on March 2, 1904, where the future bestseller’s German immigrant father worked in a brewery until it was closed during the Prohibition. As an adult, Dr. Seuss made his childhood neighborhood a household name in his first children's book, And To Think That I Saw It On Mulberry Street.

6. The literary legend’s pen name was born from an illicit drinking session! Geisel studied at the prestigious Dartmouth College and first tried his hand at journalism in the humor magazine Dartmouth Jack-O Lantern, where he rose to the ranks of Editor-In-Chief, until he got busted for drinking gin with some classmates in his room and was banned from all extracurricular activities. Determined not to give up his creative comical outlet, Ted began writing under the pen name, Seuss, which was both his middle name and his mother’s maiden name. Trying to fulfill his dad’s dream of him being a college professor, Ted traveled to England to study at Oxford University but quickly grew bored of the pomp and circumstance and opted instead to travel around Europe with pretty fellow student Helen Palmer, who went on to become his first wife. The couple was married in 1927 and Ted returned to the U.S., with a new bride but without a degree from Oxford.

5. After publishing humorous articles for magazines such as Vanity Fair and Life, Geisel’s first career of creating advertising campaigns for Standard Oil, NBC and General Electric lasted 15 years until the onset of World War II shifted his focus to bigger issues and he began contributing weekly political cartoons to liberal publication PM magazine. He then joined the Army in 1943 as a Captain and Commander of the Cartoon Department of the First Motion Picture Unit, where he fell in love with the art of animation, developing a series of training films featuring a character called Private Snafu.

4. A collection of children's sayings called Boners led to his big break in children’s literature with the eventual publication of And To Think That I Saw It On Mulberry Street, after it was rejected a whopping 27 times by Vanguard Press. Geisel and Helen moved to La Jolla, California, and he penned If I Ran the Zoo, Horton Hears a Who! and If I Ran the Circus. Next came the title that would mould the dreams of generations of children to come, when Houghton Mifflin asked Seuss to write and illustrate a book with just 225 "new-reader" vocabulary words and challenged him to "bring back a book children can't put down,” and The Cat In The Hat was born in 1957 to phenomenal success and rave reviews. It was closely followed by How The Grinch Stole Christmas and Green Eggs and Ham, and his latest to make it to the big screen,The Lorax in 1971.

3. Dr. Seuss’ signature style is based on anapestic tetrameter, a poetic meter used by many poets. It consists of four rhythmic units each composed of two weak beats followed by one strong beat, and often the first weak syllable is omitted, or an additional weak syllable is added at the end. A classic example is found in the story, Yertle The Turtle. "And today the Great Yertle, that Marvelous he “Is King of the Mud. That is all he can see.” When it comes to his fabulous illustrations, Dr Seuss’ characters such as the Grinch and the Cat are known for their familiar round and droopy shapes, as are his buildings which melt and bend around free-standing staircases, ramps and platforms.

2. Geisel’s life story wasn’t all about brightly drawn pictures and rhyming verses, it was also marred by tragedy and scandal. After fighting a long battle with cancer and the emotional trauma of her husband’s affair with Audrey Stone Dimond, his wife Helen committed suicide in October 1967, her ‘mourning husband’ married his former mistress six months later. Despite two marriages and a bibliography full of children’s classics, Dr. Seuss never had children of his own, instead living by the motto, "You have 'em; I'll entertain 'em." After several years of bad health, Seuss died of throat cancer on September 24, 1991 at age 81. He was cremated in La Jolla and Dr. Seuss Enterprises was left in the careful hands of ‘Mrs. Seuss,’ Audrey, including the rights to 44 books that had been translated into 15 different languages and sold more than 200 million copies. During his career, he was honored with two Academy Awards, two Emmys, a Peabody and the Pulitzer Prize.

1. Dr. Seuss’ legacy continues to live on in countless modern-day versions of his work, from eleven TV speicals, the Broadway musicals Seussical and The Grinch, to Hollywood blockbusters, The Cat in the Hat with Mike Myers, and How The Grinch Stole Christmas with Jim Carrey, and CGI animated works Horton Hears A Who, and opening Friday, The Lorax. Fans who want to jump into Dr. Seuss’ fantasy world feet-first can visit Seuss Landing at the Island Of Adventures theme park in Orlando, Florida.

February 29, 2012

Lillia Rose Whittle Needs Our Support & Prayers!

At the age of 22 months Lillia was diagnosed with cancer!

Lillia has Retinoblastoma (RB), a fast growing eye cancer of early childhood. This cancer develops in the cells of the retina, the light sensitive lining of the eye. In the UK about 98% of children survive retinoblastoma; this is true for both unilateral and bilateral disease. Nearly all of those with unilateral disease survive without further tumour.

Natalie and Craig Whittle, Lillia's parents are on a mission to raise awareness of this rare childhood cancer that is diagnosed in only 40 to 50 children in the UK each year. If this aggressive eye cancer is caught early enough the child's life can be saved.

Lillia was diagnosed with unilateral (one eye) Retinoblastoma in her left eye at the age of 22 months. It was picked up by the squint and white reflex in her eye. If caught at a late stage a child may face loosing their eye.

Lillian's, her parents as well as myself want to tell her story to the world and raise awareness in the hopes of helping other children with symptoms to be tested in order to catch the cancer in it's earliest stage to save children from losing an eye or their lives. You can join our mission to raise awareness by clicking on the links listed below to show your support for Lillia and children around the world affected by childhood cancer.

A note from Lillia on her website at: http://lilliaretinoblastoma.co.uk/about-me

My name is Lillia Rose Whittle, I was born on 13th January 2010 at Kettering General Hospital. I weighed 3.135 kg (6lb 14oz). My life was relatively normal until 26th October 2011 when my life was about to change. 

A note from Lillia's parents from her website at: http://lilliaretinoblastoma.co.uk

This website is all about Lillia, who was diagnosed with a rare childhood cancer called Retinoblastoma when she was only 22 months old. Retinoblastoma is an aggressive cancer or the eye. She is currently having Chemotherapy to preserve her eye and save her life.

The website is in its infancy and we will try to make it bigger and better as Lillia's treatment progresses.

To give me an idea of who's been visiting here, you can write in the guestbook.

We have been working hard to raise awareness of Retinoblastoma and have taken part in TV, Radio and Newspaper interviews. To see more click here

Please help us raise more awareness of Retinoblastoma and 'Like' our Facebook page. Click Here

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