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Summer Solstice at the Needle In Honor of Tessa Shevlin for the Benefit of The Cure JM Foundation

The Shevlin Family and Cure JM

Tuesday, June 21, 2011 from 6:00 PM to 10:30 PM (PDT)

Summer Solstice at the Needle    In Honor of  Tessa She...

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Ticket Type Sales End Price Fee Quantity
Summer Solstice at the Needle In Honor of Tessa Shevlin for the Benefit of The Cure JM Foundation Ended $50.00 $3.49

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Event Details

 

Summer Solstice at the Needle


In Honor of

Tessa Shevlin

for the Benefit of

The Cure JM Foundation

Tessa


Join us for an evening party celebrating

The Cure JM Foundation

and help us find a cure for

Juvenile Myositis.

 

 

Summer Solstice at the Needle

 

Where:

Seattle Space Needle Skyline Level,

Access to the top of the Needle (observation deck) included with ticket.


When:

Tuesday, June 21st, 2011, 6:00pm-10:30pm.

Observation deck open until 11:00pm.


What:

Appetizers, JM presentation, desserts, silent auction, friends, cash bar available.


Dress:

Cocktail Attire


Babysitting:

Please send us an email if you are interested in babysitting options.

jshevlin76@gmail.com

 

Parking:

Valet parking is available at the Space Needle entrance for $8.00.

Street parking is free starting at 6:00pm.

Multiple pay-to-park lots are in the area.

Seattle monorail open until 11pm for commute from/to Westlake Center.


 

If you are unable to attend please consider a donation.

Contribute to Cure JM through Tessa's fundraising website:

www.firstgiving.com/tessacurejm

All donations are tax-deductible.

Please ask if your company will match your donation!

 

Have questions about Summer Solstice at the Needle In Honor of Tessa Shevlin for the Benefit of The Cure JM Foundation? Contact The Shevlin Family and Cure JM

When & Where


Seattle Space Needle
400 Broad Street
Seattle, WA 98109

Tuesday, June 21, 2011 from 6:00 PM to 10:30 PM (PDT)


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Organizer

The Shevlin Family and Cure JM

Tessa Shevlin

Tessa Shevlin is a 6 year old girl from Lake Stevens, WA who was diagnosed with Juvenile Dermatomyositis (JDM) at 4 years of age. JDM is one type of Juvenile Myositis that has attacked Tessa's muscles and skin.

Tessa has been undergoing treatment for 2 years and is still waiting for the disease to go into remission.

Juvenile Myositis (JM) is an autoimmune disease in which the body's immune system attacks its own cells and tissues. For many children with JM, it's a challenge to simply stand up or sit down. This rare disease affects approximately 1-4 children out of a million.

The Cure JM Foundation

Cure JM Foundation is an all-volunteer foundation created and managed by families of children with Juvenile Myositis. Cure JM Foundation's mission is to provide support for families coping with JM, raise awareness of JM, and fund research that will ultimately lead to a cure.

The Foundation's aspirational goal is to never, ever let another child suffer with Juvenile Myositis. With your help, this goal may be well within reach some day.

To learn more about the Cure JM Foundation, please visit our web site at www.curejm.org

  Contact the Organizer

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