Sponsorship Information and Application

Size: px

Start display at page:

Download "Sponsorship Information and Application"

Flora Black
5 years ago
Views:

1 Sponsorship Information and Application Our Mission: Enhance the quality of life for children diagnosed with rare, life-limiting, and complex medical conditions in Southern Nevada Fax: Little Miss Hannah Foundation is a 501(c)3 tax-exempt nonprofit corporation.

2 Show your support for Childhood Rare Disease Awareness with a 5k and 1 mile fun run! Thank you for your consideration in sponsoring our upcoming event, our Vegas Cares About Rare 5K. This community event is scheduled to take place on February 25, 2017, in Las Vegas, in recognition of World Rare Disease Day. Since our first community fundraising event in 2012, we have raised more than $60,000 to support our mission to help enhance the quality of life for young children diagnosed with life-limiting rare diseases, undiagnosed complex medical needs, and children who have been placed in hospice or palliative care in Southern Nevada. Our goal for this event is to raise $20,000 to continue to help our special families. Our volunteer-staffed organization offers financial assistance for families by way of our Medical and Therapy Equipment Grant program. We also organize support groups and family activities as well as hold various toy and hospitality drives to support local Las Vegas area pediatric hospital units. But we need YOUR help. We can only continue to provide these support services and activities by obtaining the necessary funding. We offer various levels of participation and sponsorship to fit your resources. Please help us provide support and comfort for our local families who live daily with the financial, emotional, physical, and social struggle that caring for a medically complex child can bring. We can t change their inevitability, but we can help them focus on enhancing the quality time they have with their ill child. We can t do it without the support of our community. Attached you will find information regarding our organization and this event as well as sponsorship information. Please contact me at robert@littlemisshannah.org or to discuss the available options. We look forward to your support and hope you join us on this very special day! Robert Ostrea Co-Founder and President Little Miss Hannah Foundation Fax: Little Miss Hannah Foundation is a 501(c)3 tax-exempt nonprofit corporation.

February 25, 2017 8:15 am Race Time Kellogg Zaher Park Show your support for Childhood Rare Disease Awareness with a 5k and 1 mile fun run! Create or Join a Team Save $5!

3 February 25, :15 am Race Time Kellogg Zaher Park Show your support for Childhood Rare Disease Awareness with a 5k and 1 mile fun run! Create or Join a Team Save $5! Join us for an inspirational race in recognition of World Rare Disease Day! 5K-Timed Individual Pricing includes custom medal, T-shirt, and bib $30 8/1 thru 9/30 $35 10/1 thru 11/30 $40 12/1 thru 1/31 $45 2/1 thru 2/23 Team discount pricing available Register today at VegasCaresAboutRare.org Did you know... There are rare diseases that affect children under 18 years old 30% of children diagnosed with a rare disease do not live to see their 5th birthday All proceeds benefit the Little Miss Hannah Foundation, a 501(c)(3) organization committed to enhancing the quality of life for children diagnosed with rare, life-limiting, and complex medical conditions in Southern Nevada. EIN: For sponsorship information, please contact Robert Ostrea robert@littlemisshannah.org /

4 SPONSORSHIP OPPORTUNITIES February 25, 2017 Show your support for Childhood Rare Disease Awareness with a 5k and 1 mile fun run! Your tax-deductible donation via sponsorship will help us support the families of children diagnosed with rare, life-limiting, and complex medical conditions in Southern Nevada. Please contact Robert Ostrea at robert@littlemisshannah.org for more information. Fax: Little Miss Hannah Foundation is a 501(c)3 tax-exempt nonprofit corporation. EIN

Vegas Cares About Rare 5K / 1M February 25, 2017 Las Vegas Sponsorship Form Please return via email to robert@littlemisshannah.

5 Vegas Cares About Rare 5K / 1M February 25, 2017 Las Vegas Sponsorship Form Please return via to robert@littlemisshannah.org or fax to Sponsorships and Gift Bag insertion items should be mailed to: Little Miss Hannah Foundation, S. Eastern Avenue, Suite A847, Henderson, NV Sponsor Information Corporate Name: Sponsor Contact: Title: Address: Phone: Website: Participation Commitment Event Sponsorship (must be received by February 1, 2017 to be included in promotional materials) [ ] Rare Champion - $2,500 [ ] Rare Rockstar - $1,500 [ ] Rare Advocate - $1000 [ ] Finish Line - $750 [ ] Water Station - $500 Payment Options [ ] A check payable to Little Miss Hannah Foundation is attached [ ] A credit card authorization to Little Miss Hannah Foundation is attached [ ] I will be sending a check payable to Little Miss Hannah Foundation Signature: Date / /

6 One Time Credit Card Payment Authorization Form Sign and complete this form to authorize the Little Miss Hannah Foundation to make a one time debit to your credit card listed below. By signing this form you give us permission to debit your account for the amount indicated on or after the indicated date. This is permission for a single transaction only, and does not provide authorization for any additional unrelated debits or credits to your account. Please complete the information below: I (full name) authorize Little Miss Hannah Foundation to charge my credit card account indicated below for $ (amount) on or after (date). This payment is for. Billing Address City, State, Zip Phone Account Type: [ ] Visa [ ] MasterCard [ ] AMEX [ ] Discover Cardholder Name: Account Number: CVID: Expiration Date: / / SIGNATURE DATE I authorize the above named business to charge the credit card indicated in this authorization form according to the terms outlined above. This payment authorization is for the goods/services described above, for the amount indicated above only, and is valid for one time use only. I certify that I am an authorized user of this credit card and that I will not dispute the payment with my credit card company; so long as the transaction corresponds to the terms indicated in this form

Offering Hope, One Child At A Time We work with families of children with life-limiting

neurologic, metabolic, and genetic conditions.

LITTLE MISS HANNAH S MISSION: To enhance the quality of life for children diagnosed

Organization We are a volunteer-staffed Vegas-based nonprofit created by the family of

of 3. Equipment Program We provide programs and services to hundreds of local families

complex kids such as our: PICU Care Bags Program Medical and Therapy Equipment

Disease Advocacy - Vegas Cares About Rare Kids Family and Community Activities and

rare diseases that affect children 30% of children diagnosed with a rare genetic

medical expenses not covered by insurance Get Involved!

7 Offering Hope, One Child At A Time We work with families of children with life-limiting rare diseases, undiagnosed complex medical needs, and kids with debilitating neurologic, metabolic, and genetic conditions. Contact us for info on how to become a LMHF family! LITTLE MISS HANNAH S MISSION: To enhance the quality of life for children diagnosed with rare, life-limiting, and complex medical conditions in Southern Nevada Our Organization We are a volunteer-staffed Vegas-based nonprofit created by the family of sweet Little Miss Hannah Ostrea who passed away from an ultra-rare disorder at the age of 3. Equipment Program We provide programs and services to hundreds of local families that do not have proper support and resources to care for their rare and medically complex kids such as our: PICU Care Bags Program Medical and Therapy Equipment Assistance Program Hospital Pediatric Intensive Care Unit Care Bags Childhood Rare Disease Advocacy - Vegas Cares About Rare Kids Family and Community Activities and Events Be the Sunshine Campaign Childhood Rare Disease Facts There are more than 3,500 rare diseases that affect children 30% of children diagnosed with a rare genetic condition will not live to see their 5th birthday 55% of families will incur direct medical expenses not covered by insurance Get Involved! Maximizing a child s happiness and enabling families to enjoy time with their child is impossible without your support. Be the Sunshine in a Child s Life and join the Little Miss Hannah community today! * Volunteer * Host a Donation Drive * Become a corporate sponsor Vegas Cares About Rare Family Activities Find us online! Little Miss Hannah Foundation is a 501(c)3 tax-exempt nonrofit corporation - EIN#

2015 Child Impact Report Thank you Southern Nevada for helping us

life-limiting, and complex medical conditions.

car seats 4 special needs tricycles 5 special needs bathing chairs 3

special needs chairs Worked with 112 families with children diagnosed

annual Rainbows in the Wind Festival Fundraiser in July 2015 Delivered

2015 Participated in Rare Disease Day in Washington D.C.

activities, and RARE Patient Advocacy Summit for childhood rare disease

2 % Equipment Grant Family Activities Operations 2015 Expenses 57.

8 2015 Child Impact Report Thank you Southern Nevada for helping us enhance the quality of life for local children diagnosed with rare, life-limiting, and complex medical conditions. As we look back at 2015, we can see what an amazing and productive year we have had! Since 2012, we have: Raised over $50,000 to help local children and families 2.9 % 4.7 % 4.7 % Purchased 50+ new pieces of equipment including: 5 special needs car seats 4 special needs tricycles 5 special needs bathing chairs 3 communication software programs 6 special needs feeding chairs 10 special needs chairs Worked with 112 families with children diagnosed with 40+ rare diseases Welcomed over 1250 people at Town Square for our annual Rainbows in the Wind Festival Fundraiser in July 2015 Delivered 125 care bags to local area pediatric intensive care hospital units in 2015 Participated in Rare Disease Day in Washington D.C., Nevada Disabilities Conference, School World Rare Disease Day activities, and RARE Patient Advocacy Summit for childhood rare disease awareness and advocacy % 15.2 % Equipment Grant Family Activities Operations 2015 Expenses 57.7 % Rare Disease Advocacy Misc. Programs Marketing / Outreach Expenditures for Medical/Therapy Equipment Grant Program We are a family-run, 100% volunteer supported organization! Find us online! Little Miss Hannah Foundation is a 501(c)3 tax-exempt nonrofit corporation - EIN#

CCC Bike Tour Fundraising Materials Guide

2017 CCC Bike Tour Fundraising Materials Guide [Type the document subtitle] photo credit: Nick Agelidis CCC 17 Fundraising Materials Guide Version 1 11/21/2016 Sample Letter 1 Date Name Street City, State,