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Captain Caveman nWo's blog: "My blog"

created on 01/28/2007  |  http://fubar.com/my-blog/b49621
First off I want to thank all my old friends and the new ones I have made over the past 2 days. Also a special thanks to the Rating Revolution Crew. I'd never had made it so quick without any of you. Names are too numerous to miss but I'll be sending back the love to as many of you as I can over the next few days. Don't be afraid to message me and ask me to rate if I miss you. 2 1/2 years ago I came to a site called CherryTap. Alot of changes since then. Some good, some bad but always a good place for me to escape the world of real life. I've made many wonderful friends here. I realize there's still a couple more levels but Godfather is all I ever really set my sights on as far as that goes. I'll be simply enjoying my time and rating all my good friends from here on out. Again THANKS TO YOU ALL!!!!!!!

OCTOBER IS RETT SYNDROME AWARENESS MONTH ( A DEBILITATING NEUROMUSCULAR DISORDER) LETS EDUCATE OURSELVES A LIL Rett syndrome is caused by mutations in the gene MECP2 located on the X chromosome. Every five hours a girl is born with Rett syndrome. Rett syndrome is the only Autism spectrum disorder with a known genetic cause. Rett syndrome is the leading genetic cause of severe impairment in females. Rett syndrome affects all ethnic, racial and socio-economic groups; every parent is at risk for having a child with Rett syndrome. THESE ARE JUST A FEW FACTS ABOUT RETTS SYNDROME..... THIS WONDERFUL MOTHER BELOW LIVES EVERYDAY OF HER LIFE WITH IT AND WANTS TO GET INFORMATION OUT THERE FOR EVERYONE. PLEASE GO TO http://www.rettsyndrome.org TO LEARN MORE. ~NorthernAngel~
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@ fubar THIS WOMAN DID NOT ASK ME TO PIMP HER OUT OR EVEN DO THIS BUT AFTER READING HER BLOG, PROFILE AND TALKING TO A FRIEND OF HERS I FIGURED WHY NOT. SHE WANTS TO ADD MORE PICS TO HER PROFILE SEEING AS HER DAUGHTER LIVES WITH RETTS EVERYDAY AND AS A MOTHER SHE WANTS TO FIND OR HELP FIND A CURE. PLEASE STOP BY HER PAGE AND FAN/RATE/ADD AND EVEN BLING HER SOO SHE CAN GET MORE INFO OUT THERE. ME AND A FEW FRIENDS OF MINE AND HERS WILL BE LOVEN HER UP TOMORROW DURING THE DAY, SO PLEASE JOIN US, IT SHOULDNT TAKE LONG AS SHE ONLY HAD 35K TO THE NEXT LEVEL. IF YOU GET THERE AND SHE IS LEVELED ALREADY SHOW LOVE ANYWAYS THE HIGHER LEVEL THE MORE PICS SHE CAN POST. IF YOU HAVE A SOFT SPOT AND YOU HAVE FOURTEEN DOLLARS TO SPARE CONSIDER GETTING HER A VIP..... THATS UP TO 2500 PICS SHE CAN ADD TO HELP PEOPLE UNDERSTAND WHAT SHE GOES THROUGH EVERYDAY. ALSO WHILE YOU ARE THERE PLEASE READ HER BLOG... IT EXPLAINS HER EVERYDAY LIFE. THIS LITTLE BIT OF INFO BROUGHT TO YOU BY DEVIL'S ANGEL....PHANTOM'S QUEEN STALKER
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@ fubar

Hi there

I've been gone for a few months but I'm back. I ve been dealing with alot of issues and had decided to go away for awhile. I regret just disappearing and I know it upset a couple of special people but all I can say is I'm sorry and hope they can forgive me. My daughter has come a long way in the past year. She goes to a special pre-school now for half a day and spends the afternoon in a special daycare. She's learned so much and has come so far. I know in my heart that one day she'll start talking, but for now I take everything I can get.
I wanted to let all my friends know that yes I am alive and well. I needed a break from alot of things and I'm sorry I haven't been around. Those that really know me know that I've been going thru the long and drawn out process of finding out what is wrong with my daughter. After alot of genetic testing she's finally been diagnosed with what is called Rett Syndrome. What is Rett syndrome? Rett Syndrome (RS) is a unique neurodevelopmental disorder which begins to show its affects in infancy or early childhood. It is seen almost exclusively in females, although it can occur rarely in boys. It is found in all racial and ethnic groups throughout the world. What is the outlook for those with Rett syndrome? Despite the difficulties with symptoms, most individuals with Rett syndrome continue to live well into middle age and beyond. Because the disorder is rare, very little is known about long-term prognosis and life expectancy. While it is estimated that there are many middle-aged women (in their 40s and 50s) with the disorder, not enough women have been studied to make reliable estimates about life expectancy beyond age 40. I'm still waiting to have it all fully explained to me but that is it in a nutshell. I want to thank all my friends that have been so supportive of me and I'm going to try my best to be back here on a regular basis.
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