Fantastic post here.. Lets all contribute and make a change to help those that cant help themselves.
~~VIDEO~~ CureAngelman Point Donation Drive!
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#36Comment -
#37Lets go guys, only 54 entries for tonight so far
How many did we get last yearComment -
#38Maybe people either don't want to ship 200 points, or are focused on the daily tournies?
Are those still going today during the CA tourny?Comment -
#39
it is pretty embarrassing on my behalf but maybe next year I can save pointsComment -
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#41Donating some and gonna put a crazy parlay together tonight to put it all here.Comment -
#4290% of the Forum does not play poker here....If anyone wants to buy-in for the cause you can download the poker client using the link below. No obligation to actually play but your buy-in will count towards donation:
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#43Going Pro now via CureAngelman!Comment -
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#47Can someone help me. I made the donation and forwarded along to SBR.
On the select charity drop down box both options are Make A Wish.
Which do I select? First or second.
ThanksComment -
#48Comment -
#49Comment -
#50Thank you for your donation, jts1207. Can you please forward your donation reciept to this address, forum@sportsbookreview.comand we'll verify the drop down Charity options on the pro application page. Thanks
Sent. ThanksComment -
#51Bigday is one of the best people to ever grace this forum
If I could just offer one piece of advice, I would try to move this to the fall when more people are here and when people have points from BTP
I do realize today is Angelman Syndrome Day, but maybe start the drive in the fall and culminate it with the total amount donated announced today
Just a thought
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#52
fixed now...thank you for becoming a PRO and for contributing to make a difference for this cause.Comment -
#53The poker tourney rocks. I’m part to blame there too as since the 9am tourney went away, I haven’t been in the eyes and ears of the poker community so I completely understand the drop in players.
To be honest, I’m incredibly humbled by 20 people signing up.Comment -
#54Awesome family hope we can kick another disease to the curb,theres my points wish i could give ya more but Icant hit a winner to save my own kids life!!!Comment -
#55Comment -
#56Elk send me some cash!!!!!!!!!!!!!!!!!!Comment -
#57I have been around and friends with many gamblers in my life, probably in the hundreds because of my booking days. Many, many assholes. Many many good guys and a couple good gals. But, usually most of them were fairly generous, especially when they were winning which naturally is not that often.
Good job guys/gals.Comment -
#58Bigday is one of the best people to ever grace this forum
If I could just offer one piece of advice, I would try to move this to the fall when more people are here and when people have points from BTP
I do realize today is Angelman Syndrome Day, but maybe start the drive in the fall and culminate it with the total amount donated announced today
Just a thought
Rudy you are one sharp cookie I don't give a crap what people say.
lol hope you are well my friend.Comment -
#59I have been around and friends with many gamblers in my life, probably in the hundreds because of my booking days. Many, many assholes. Many many good guys and a couple good gals. But, usually most of them were fairly generous, especially when they were winning which naturally is not that often.
Good job guys/gals.Comment -
#60Ok since I feel bad I can only send 2 points as a non-pro, I decided to finally go pro and just made the donation and sent in the app.Comment -
#61Comment -
#62Blew all my points on the Pats, Bigday.
Gave 65, but that’s all I have for now.
Cheers, GLComment -
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#65Great job bigday, keep pushing the hustleComment -
#66
When Amelia Beatty found out her 14-month-old son Orion had Angelman Syndrome in September 2016, she immediately researched all she could about the rare neurological disorder. Within days, she learned that Colin Farrell’s 14-year-old son, James, has the same condition.
She found out about Farrell and his son while watching videos about his story on the website for FAST, the Foundation for Angelman Syndrome Therapeutics, an organization dedicated to funding research on the disorder.
“After my son’s diagnosis I felt kind of helpless and in a way hopeless,” Beatty, 37, tells PEOPLE. “But after finding out about the foundation, the fundraising efforts and this potential cure it was just so exciting to me that I needed to be involved.”
Angelman Syndrome, which affects 1 in 15,000 individuals, can cause severe developmental delays such as a difficulties walking and talking, seizures, and balance issues. The genetic disorder stems from either a mutation, replication or deletion of a gene on the 15th chromosome.[quote=jjgold;5683305]I win again like usual
[/quote]
[quote=Whippit;7921056]miami won't lose a single eastern conference game through end of season[/quote]Comment -
#67[quote=jjgold;5683305]I win again like usual
[/quote]
[quote=Whippit;7921056]miami won't lose a single eastern conference game through end of season[/quote]Comment -
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#69http://people.com/movies/how-colin-f...rare-disorder/
When Amelia Beatty found out her 14-month-old son Orion had Angelman Syndrome in September 2016, she immediately researched all she could about the rare neurological disorder. Within days, she learned that Colin Farrell’s 14-year-old son, James, has the same condition.
She found out about Farrell and his son while watching videos about his story on the website for FAST, the Foundation for Angelman Syndrome Therapeutics, an organization dedicated to funding research on the disorder.
“After my son’s diagnosis I felt kind of helpless and in a way hopeless,” Beatty, 37, tells PEOPLE. “But after finding out about the foundation, the fundraising efforts and this potential cure it was just so exciting to me that I needed to be involved.”
Angelman Syndrome, which affects 1 in 15,000 individuals, can cause severe developmental delays such as a difficulties walking and talking, seizures, and balance issues. The genetic disorder stems from either a mutation, replication or deletion of a gene on the 15th chromosome.Comment -
#70Comment
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