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Welcome to Dennis & Jennifer's Page
Dennis & Jennifer O'leary
Dennis & Jennifer O'Leary
Hello Friends and Family!
We are excited to be participating in the 20th Anniversary Brewer's Ball! We invite you to join us at the event at the Wharf on June 14 for a night of beer/wine/cocktail tasting, local food stations, live music and, most importantly, the opportunity to help cure Cystic Fibrosis!
The O'Leary family has been involved with this great fundraiser for 19 years. During that time, we have seen monumental strides made for treatments for CF. Drugs are now available to over 90% of the CF population that are extend their life expectancy by decades and their quality of life infinitely. These drugs are made possible largely through donations to the CF Foundation at events like Brewer's Ball.
Our son Casey is unfortunately in the 10% of CF patients who cannot take these drugs. He is still waiting for his miracle drug or, even better, a real cure for CF.
We are very hopeful that a CURE for CF is on the horizon. Early results from a mRNA based therapy that be a real cure for all CF patients are very positive. We sill not give up "until it's done"!
Thank you in advance for your support and participation in this event. Please join us on June 14 or make a donation to this important cause and help make a difference for Casey and other people living with CF!
Cheers!
Dennis & Jennifer
We are excited to be participating in the 20th Anniversary Brewer's Ball! We invite you to join us at the event at the Wharf on June 14 for a night of beer/wine/cocktail tasting, local food stations, live music and, most importantly, the opportunity to help cure Cystic Fibrosis!
The O'Leary family has been involved with this great fundraiser for 19 years. During that time, we have seen monumental strides made for treatments for CF. Drugs are now available to over 90% of the CF population that are extend their life expectancy by decades and their quality of life infinitely. These drugs are made possible largely through donations to the CF Foundation at events like Brewer's Ball.
Our son Casey is unfortunately in the 10% of CF patients who cannot take these drugs. He is still waiting for his miracle drug or, even better, a real cure for CF.
We are very hopeful that a CURE for CF is on the horizon. Early results from a mRNA based therapy that be a real cure for all CF patients are very positive. We sill not give up "until it's done"!
Thank you in advance for your support and participation in this event. Please join us on June 14 or make a donation to this important cause and help make a difference for Casey and other people living with CF!
Cheers!
Dennis & Jennifer
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