Comments
FYI. Use the contact info on the flyer.
We have a future Viscardi alum rocking her shirt!!!!
Does anyone have any advice or info on how we can get the vaccine once it's available?
The Henry viscardi reunion new RSVP date is October 18 2019
I graduated from HVS in 2013
check out my website
Fundraiser Aug 2nd. Did you buy your tickets yet? If not please use link to get them. You know how much it means for someone like me to have a service dog. I am trying to give back to the school who works hard to make this happen. Time is running close for the dinner option we need a head count for dinner by Tuesday July 30th. Show tickets should still be available after Tuesday but do not wait.
Friday August 2nd, 7pm
228 Pettit Ave.
Bellmore, NY.
Buy tickets here-
ccicomedynight.eventbrite.com
Come join us as we have gathered some of NYC's top comedians to help raise funds for Canine Companions for Independence. This is sure to be a memorable evening for such a great cause!!
MATURE AUDIENCE SHOW
There are 2 ticket options:
- $50pp includes comedy show and special dinner menu.
- $30pp show only option
There will also be a Chinese auction and 50/50 raffle!!!
Canine Companions for Independence is a non-profit organization that enhances the lives of people with disabilities by providing highly trained assistance dogs at no charge to the recipient. More info on CCI go to their site.
www.cci.org
Hi Everyone
I know someone that is in need of a power wheelchair so if anyone has one please let me know thanks
Hi everyone, When a family receives any kind of devastating diagnosis the first thing they need more is support to know that they are not alone in this world. The doctor visits and hospital stays must take an incredible toll on the baby and the entire family. Life is meant to be lived and enjoyed though. The Linzer family did just that, they lived every moment with Quinn. Many times wit's a diagnosis, we think of all the things our loved ones can't do or won't be able to experience. However, The Quinn Madeleine Foundation helps families to look at it from a whole different perspective. They made every day a cherished memory that they can hold onto forvever. They gave their baby every opportunity to just have every experience she could. Please help other families in similar situations to also have that same support, strength and courage. I will be taking part in The Quinn Madeleine Foundation's 5k on May 19th. Niemann-Pick Disease Type A is a rare disease that cuts extremely young babies, lives short. After reading about the Linzer family and their experiences, I want to help them give others courage and strength to live each day to the fullest, take every chance to go out and do something good for themselves. Please check out about this organize, read the family's blog like I did, realize there are others who are in similar situations and give what you can to help those in need. No amount is ever too small. Help this family be there for others and to give them all the support possible. Thank you!