2016 Alamogordo, NM unite@night walk

2016 Alamogordo, NM unite@night walk

About This Campaign

Attention Walkers: Please register as a team or as an individual. If you are creating a team, please click the register team button. In addition, you must also register yourself within that team. (It does not automatically add you to the team).

unite@night is a one mile casual walk, in various locations around the country. This walk brings together people who are suffering with the devastating effects of Chiari malformation, syringomyelia, and related disorders.  unite@night supports CSF Chapters to provide education and increase awareness while funding research projects that can potentially find answers to help those who are fighting these disorders.

This year's unite@night walks show huge promise in helping those suffering from Chiari malformation, syringomyelia, and related disorders. We are so excited to get out there, have fun with you all, and make a difference at the same time!


Alamogordo, NM unite@night Walk - 9/23/2016
5:30pm - 6:30pm:  Registration
6:30pm:  Walk

For more information, or if you have any questions, please contact one of our unite@night walk Chairs!

Walk Chair
Alexandra Marchand
(575) 491-1234




Location / Venue

  • Address:
  • Alameda Park Gazebo
  • 1321 North White Sands Blvd.
  • Alamogordo, New Mexico
  • 88310, USA
  • Time:
  • Sep 23, 2016 05:30 pm to
  • Oct 31, 2016 08:30 pm
Chiari & Syringomyelia Foundation

Campaign to Support Chiari & Syringomyelia Foundation

CSF: Who Are We?

CSF (Chiari & Syringomyelia Foundation, Inc.) is a 501(c)(3) non-profit organization that was founded in October 2007 with the goal of raising awareness and finding a cure for Chiari malformation (CM), syringomyelia (SM) and related disorders. 

CSF Network of Experts

The CSF Scientific Education & Advisory Board is comprised of several internationally renowned medical doctors, professors, scientists and experts. Further, the CSF Board of Directors and Board of Trustees include community and business leaders, educators, legal experts, families and patients, who have long been advocates in the CM/SM community. Their skills and drive to develop, fund, and oversee CSF programs and research will improve the lives of the over one million families affected by Chiari malformation, syringomyelia and associated disorders in the US, alone. 

CSF: Recognition & Awards

CSF is currently the only organization serving patients with Chiari, syringomyelia and related disorders to have earned all three of the following distinctions: BBB Wise Giving Alliance Seal, Guidestar Gold Seal and the Health On the Net Code. Check us out in the November 2016 issue of USA Today among the other nonprofits deemed as both effective in their missions, and responsible with their donors' dollars

Fundraising Participant Personal Goal Amount Raised
Alex Marchand
Alex Marchand
76000
$760 of $100 (760%)
76000
$760
Mary Noyes
Mary Noyes
5000
$50 of $100 (50%)
5000
$50
Diana Meier
Diana Meier
5000
$50 of $100 (50%)
5000
$50
Randy Schmittle
Randy Schmittle
2000
$20 of $100 (20%)
2000
$20
Daymen Woods
Daymen Woods
0
$0 of $100 (0%)
0
$0
Tammie Reynolds
Tammie Reynolds
0
$0 of $500 (0%)
0
$0
Rachel Winrow
Rachel Winrow
0
$0 of $50 (0%)
0
$0
Mirandy Wood
Mirandy Wood
0
$0 of $100 (0%)
0
$0
Destiny Estrada
Destiny Estrada
0
$0 of $100 (0%)
0
$0
Shannon Woods
Shannon Woods
0
$0 of $100 (0%)
0
$0

Fundraising Teams

Team Abry

$140 raised (28%)
6
Participants

Tammie's Turkeys

Hi! I was officially diagnosed with Chiari Malformation I back in late 2011. I was having some crazy symptoms after my Mitral Valve Heart Surger and they thought I have having mini-strokes. My speak was slurred...but never any rhyme or reason what would bring it on... my gait/walk wou...

$0 raised (0%)
1
Participant
This year's unite@night walks show huge promise in helping those suffering from Chiari malformation, syringomyelia, and related disorders. We are so excited to get out there, have fun with you all, and make a difference at the same time!