Diwatang Byaning

I dedicate this entry for my friend and family that is suffering from a heart disease.

Tomorrow, February 1, is the fifth anniversary of National Wear Red Day. It’s the day to wear your favorite red clothes or accessory - a red blouse, a red dress pin, a fabulous red handbag - put on red lipstick, or sport a red tie and red socks. Go red in your own fashion to show your support for women and the fight against heart disease.

Macy’s, is a proud national sponsor of Go Red For Women, tomorrow Friday, February 1, Macy’s will offer an all-day savings pass for customers wearing red. For those who forget their red, Macy’s is offering an all-day savings pass to those who make a $2 donation in the store to the American Heart Association. All contributions received will benefit the Go Red For Women movement.

Now, what am going to do is find a *red socks, red pants, red shirt, red shoes, red scarf, red lipstick, red make-up, red hat and am ready to go shopping at Macy’s and take advantage of this All-Day shopping pass for an extra 15% off* I am going to paint the town red tomorrow! :::wheeee:::

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A cleft is a gap in a body structure that results from incomplete closing of a specific structure during development. Clefts that occur in the lip and palate (roof of the mouth) are called oral-facial clefts. There are two main types of oral-facial clefts: cleft lip/palate and isolated cleft palate.

Some babies have only a cleft lip. However, many babies with cleft lip have a cleft palate as well. These are called cleft lip/palate. Cleft palate also can occur by itself without cleft lip. This is called isolated cleft palate. Cleft lip/palate and isolated cleft palate are considered separate birth defects.

Here in the United States, clefts occur in 1 in 700 to 1,000 births, making it the one of the most common major birth defects.

The good news is that both cleft lip and cleft palate are treatable birth defects. Most kids who are born with these conditions can have reconstructive surgery within the first 12 to 18 months of life to correct the defect and significantly improve facial appearance.

There are some unfortunate children born with cleft/lip palate who are suffering., Not because they were born with a cleft/lip palate, but because they were born too poor to ever afford a surgery. Being born with a cleft in a developing country is truly a curse. You can help a desperate child not just with a new smile, but a new life.

Make a donation today at your favorite cleft lip/palate organizations.

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I was reading entries from Ambo’s site Pinoyambisyoso.com and found an entry about Kat Yarza it really touched my heart *Promise*! I may look rough and tough at times but I have a soft heart…

The girl used to be a Fine Arts student and is suffering from Neurofibromatosis. She has brain tumor, half of her body is paralyzed already and starting to get blind. She needs to raise 1.5 Million for her get an operation.

She really inspires me. Having this kind of condition, she still manages to make shirts on her own design which she is selling for Php300.00. You can visit Kat at her blog hearyeah.multiply.com.

I am asking all my dear bloggers/fans/readers/followers and enemies , let’s help Kat, let’s spread the word. This is for a good cause.

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What is Neurofibromatosis?

The neurofibromatoses are genetic disorders of the nervous system that primarily affect the development and growth of neural (nerve) cell tissues. These disorders cause tumors to grow on nerves and produce other abnormalities such as skin changes and bone deformities. Although many affected persons inherit the disorder, between 30 and 50 percent of new cases arise spontaneously through mutation (change) in an individual’s genes. Once this change has taken place, the mutant gene can be passed on to succeeding generations.

Is there any treatment?

Treatments for both NF1 and NF2 are presently aimed at controlling symptoms. Surgery can help some NF1 bone malformations and remove painful or disfiguring tumors; however, there is a chance that the tumors may grow back and in greater numbers. In the rare instances when tumors become malignant (3 to 5 percent of all cases), treatment may include surgery, radiation, or chemotherapy. For NF2, improved diagnostic technologies, such as MRI, can reveal tumors as small as a few millimeters in diameter, thus allowing early treatment. Surgery to remove tumors completely is one option but may result in hearing loss. Other options include partial removal of tumors, radiation, and if the tumors are not progressing rapidly, the conservative approach of watchful waiting. Genetic testing is available for families with documented cases of NF1 and NF2. New (spontaneous) mutations cannot be confirmed genetically. Prenatal diagnosis of familial NF1 or NF2 is also possible utilizing amniocentesis or chorionic villus sampling procedures.

What is the prognosis?

In most cases, symptoms of NF1 are mild, and patients live normal and productive lives. In some cases, however, NF1 can be severely debilitating. In some cases of NF2, the damage to nearby vital structures, such as other cranial nerves and the brainstem, can be life-threatening.

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We can fight poverty! Do your part and send an electronic greeting now to your friend that is in need.

Education is empowering. It strengthens individuals, families and communities. I believe that working to improve education is one of the best investments we can make in the effort to overcome poverty.

You can help by donating. Your involvement with The Fairie enables poor women to create lasting change for themselves, their families, and their communities and ultimately for the world we all share.

NOTE: Sana walang mang bato sa akin, hindi po ako nangungutang. Ako po’y nanghihingi lamang ng kaunting tulong mula sa inyong malalambot na puso. Hindi sa isa o dalawang partikular na tao ngunit sa inyo pong lahat!

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If Britney Spears can do it, why can’t i?!(mailto:*%^#$@$% *Oh yeah i am competitive!* Who the fcunk she thinks she is?

I am no longer a Brunette! I am gonna be re-born as a Ginger!

So i decided to have my own auction at EBay tomorrow starts at noon. [And since I am so awesomely fabulously generous 90% of the proceeds will go to my favorites! Yes your reading that right!]

I am gonna have a one-woman empire. I didn’t go to Business School for NOTHING!

[I am not gonna be left behind by Her Majesty Reyna Elena and My Boss Chuva. That’s how competitive I AM! Yes they have thier own Internet Stores already. Feel free to visit them.]

*Okay Reyn and Chuva this endorsement is not free! I have to have a percentage on the sales that you guys gonna make.* He he he…

I am still BITTER about Google AdSense-NON-Sense accusations!!! [I am definitely not bovverd thou!] *This BITTERNESS is never-ending*

Since I am Ethnic, I love animals and supports PETA. [People Eat Their Animals.]

I don’t eat animals! But my tribe does! LOL.

Well I am Asian enough. So I decided to give something to ASIA CS! [Aids Services In Asian Communities.] For the benefit of my people who are suffering from the disease.

If YOU are one of my avid readers yes YOU will know Kori! Yes it is a bit over year now, but ahh i just can’t help it. I STILL HEART HER! Yup i don’t really have the balls to tell her that! *And who says that i have balls? I am a woman eh?*

Of course i will also shower Kori some of the earnings! Since she’s the love of my life! Awww

LOL.

See the proof? I ain’t greedy. IShare! =)

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