{ LINE OF OFFICE MOUSE PADS ADDED }

LOOK BUSY MOUSE PAD by rfraz20

Tweet This

{ PERSONALIZED HOLIDAY CARDS ADDED }

I know the holiday season inst for a few months,

but for those of you that don't like to procrastinate, check out the new holiday cards added.

There will be many more to come, this is just the start of the holiday season so be sure to check back as time goes on....

view more holiday cards here! click me

Tweet This

{ BACK TO REALITY }

-from time to time you are gonna come across a blog or two or five about my favorite reality shows and my thoughts on "what were they thinking" moments.... It's too hard NOT to have a discussion about these people and their lives

a few words on the Jersey Show episode from last night

#1:   I had to look away when that blonde girl was in bed with The Situation and started rubbing his belly after they finished, like she was reinacting a scene from Twilight laying in a feild of flowers, we knew what was coming next.... "I called you a taxi, when you're dressed I'll walk you to the door" .... classic.

#2:  Mike, that clearly was a dude you made out with, what girl would go out wearing sheer gloves up to her biceps and a choker from 1991.

Tweet This

{ AVA WEDDING COLLECTION }

TO VIEW THIS COLLECTION WEDDING - CLICK HERE

Tweet This

{ NEW TEE'S ADDED }

Tweet This

{ HELP US RAISE AWARENESS }

As you may not be aware, Sickle Cell Disease directly affects my family. As a wife of a husband who has this disease and a mother of a daughter who is the carrier of the trait, I find it extremely important to help spread the word of this incurable illness.


Sickle cell disease is an inherited blood disorder present at birth that affects red blood cells. People with sickle cell disease have red blood cells that contain mostly hemoglobin* S, an abnormal type of hemoglobin. These red blood cells become sickle-shaped (crescent shaped) and have difficulty passing through small blood vessels. When sickle-shaped cells block small blood vessels, less blood can reach that part of the body. Tissue that does not receive a normal blood flow eventually becomes damaged. This is what causes the complications of sickle cell disease. There is currently no universal cure for sickle cell disease.

Sickle cells are destroyed rapidly in the body of people with the disease causing anemia, jaundice and the formation of gallstones. The sickle cells also block the flow of blood through vessels resulting in lung tissue damage (acute chest syndrome), pain episodes (arms, legs, chest and abdomen), stroke and priapism. It also causes damage to most organs including the spleen, kidneys and liver. Damage to the spleen makes sickle cell disease patients, especially young children, easily overwhelmed by certain bacterial infections.

Periods of pain are commonly referred to as pain crises, which vary in their severity, how often they happen, and how long they last. Whereas one person may have only one sickle cell pain crisis a year, another may experience them more often. Crises may be brief, or may last hours, days, or even weeks. Pain can be severe enough to require treatment in the hospital. Symptoms can develop in any body organ or tissue and include aching arms, legs, hips, and shoulders. When people with sickle cell disease get acute chest syndrome, they may have severe chest and abdominal pain, fever, cough, and trouble breathing.


Those affected with sickle cell have a shortened life span of approximately 40-48 yrs of age. However, some people with this disease live longer then the average life span and some live under the average.
Who Is At Risk for Sickle Cell Anemia? 

Sickle cell anemia is most common in people whose families come from Africa, South or Central America, Caribbean islands, Mediterranean countries (such as Turkey, Greece, and Italy), India, and Saudi Arabia. In the United States, it’s estimated that sickle cell anemia affects 70,000–100,000 people, mainly African Americans. The disease occurs in about 1 out of every 500 African American births. Sickle cell anemia also affects Hispanic Americans. The disease occurs in 1 out of every 36,000 Hispanic American births. About 2 million Americans have sickle cell trait. The condition occurs in about 1 in 12 African Americans.


Researchers continue to look for new treatments for sickle cell anemia. These include gene therapy, improved bone marrow transplants or cordblood stem cell transplant.


*Please help spread awareness of Sickle Cell Anemia. Educate and inspire others and give hope to the families effected by this life threatening disease! Visit my website at www.zazzle.com/rfraz20* to purchase customized sickle cell clothing and products.



Tweet This

{ HAPPY 2 MONTH B-DAY AVA }

Today our little Ava ( aka Ava Bean, Ava-tar,Avi-ator ) turns 2 months old !
She's growing up so fast, by next month she'll be driving and graduating from highschool.

We love you Ava Bean,

Love Mom & Dad Tweet This