2843 E. Grand River Avenue – #230 East Lansing, MI 48823 [email protected] 303-783-0924

Get Involved-Help Fund Leiomyosarcoma Research

 


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Reaching for the cure-fund leiomyosarcoma researchTogether!

 

 “Purpose drives everything we all do together!”

PARTICIPATING-VOLUNTEERING-CONTRIBUTING TO FUND LEIOMYOSARCOMA RESEARCH ARE ALL WAYS TO “INVEST”  IN THE FUTURE OF PROGRESS IN  “REACHING FOR THE CURE – TOGETHER!”
* ATTEND PATIENT EDUCATION PROGRAMS – held throughout the year.   Check Patient Education page for calendar updates.
* BE A VOLUNTEER FOUNDATION AMBASSADOR –  Help the Foundation with a small project. Initiate a project you feel passionate about doing, based on your time / availability.  The Foundation has  at least 50 fundraising ideas to share. Students and young professionals can also be Ambassadors to help raise awareness and LMS research funding.
*THINK OF A PROJECT AT CHURCH, SCHOOL, WORK, CLUB AFFILIATION, in connection with a holiday to make it a             festive fundraising effort.   Fall is a great time to launch a fundraising project.
JULY 15 IS LMS AWARENESS DAY –  A fundraising event on this day would highlight awareness of LMS.
Contact  Annie at 303  783-0924 or email at:  [email protected] for the Ideas List to share with you.
* BE A FACEBOOK/TWITTER PARTICIPANT –   Connect with patients/supporters/Foundation board members. See information updates posted about research articles/news/updates.
*  CONTRIBUTE – Invest in the future of surviving LMS.  It is all about the present and the future of Leiomyosarcoma research breakthroughs to advance treatment options and extend survival for patients.

 

WAYS TO CONTRIBUTE:

Remembering  those touched by Leiomyosarcoma and who have special meaning in our lives – honor them with an Leiomyosarcoma research contribution.

Your tax deductible  “investment” contribution is directed to LMS Research projects.

1.  Personal Donation – monthly, quarterly, semi-annual, annual contributions – automatic through PayPal or by check;  

Automatic PayPal makes it easy!
Donate

By Check;

Make your check payable to the NLMSF:
2843 E. Grand River Ave., Suite  230 East Lansing, MI  48823

For questions or help to get started:  contact Annie Achee at 303 783-0924 or [email protected]l.com

You are the “donor in the driver’s seat” – to select any or all LMS research projects being supported through the Foundation.
A “directed donation” to certain or all research projects is welcomed!
The Foundation will continuously support promising LMS research for the advancement of treatment breakthroughs.
The need never stops, ongoing efforts to raise funds to support the much-needed research is imperative.  65% of LMS-diagnosed patients live five years. Therefore, patients do not have the luxury of time on their side.

2.  Planned Giving –   Think about a “lasting impact” on the future of LMS research efforts through wills, trusts, annuities.

3. ASK YOUR EMPLOYER about a MATCHING GIFT PROGRAM

Ask your employer about your corporate/company program to possibly double or triple your donation(s).

Increase the amount of your gift by using your Employer’s Gift Match Program.  Many companies offer matching gift programs to encourage employees to contribute to charitable organizations.

Check with your employer or Human Resources Manager to determine if your company participates in a Gift Match Program.

4.  Honor /Tribute /SURVIVOR / THRIVER FUND

If you want to establish a memorial/ tribute fund for a loved one, please visit the establish a tribute page below:

Establish a Tribute

NATIONAL LMS AWARENESS DAY began on  July 15, 2016.  The Foundation will continue to work with legislators annually to ensure each year includes this special day . . . a special time to honor survivors and those that would want to be remembered for a life lived with grace and courage while facing this rare cancer journey.

For more ways to contribute, visit our shop online page and build LMS awareness on your community page

 A fund in observance of this day through crowdfunding such as IGIVE.com,  YOUCARING.com, GOFUNDME.com, etc., is a great way to have others join you to help fund research, perhaps even through a matching donation!

We are ALL “Stakeholders” in accelerating LMS research efforts/advancements/results to extend survivorship.  We have to stand behind the LMS Researchers –  it’s up to all of us – Together!

Your Tax Deductible contribution/investment to fund lifesaving research means so much to patients currently fighting this rare cancer. Please donate today and you will receive Foundation acknowledgment for tax record purposes and a personal message from the Foundation President, with a purple ribbon to wear or NLMSF silicone wristband.
 
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Inform – Inspire – Empower

Our Mission is our Passion:

“What we can do today can affect what happens tomorrow”

  • Annual Patient/family/ Caregiver LMS Education/Advocacy Programs
  • Annual LMS research funding for promising LMS research projects
  • Founded by the NLMSF: The Annual International LMS Research Roundtable
    Think Tank of the Sarcoma Research Community in support of advancing
    LMS-specific precision research initiatives
  • Continuously bridging partnerships/collaboration with organizations to increase/strengthen resource assistance support
“The information in the NLMSF’s three websites helps shape the journey and build hope.”
Foundation Resource/Support Contact:
Annie Achee (303)  808-3437 or (303)  783-0924  Email: [email protected]

The National LeioMyoSarcoma Foundation (NLMSF) is a 501(c)(3) Non-Profit Charitable Organization and a member of the GuideStar Exchange.

National LeioMyoSarcoma Foundation – NLMSF

2843 E. Grand River Avenue – #230
East Lansing, MI 48823

Sarcoma Coalition Member Seal

Sarcoma Coalition – We are here for you.

The Sarcoma Coalition brings together advocacy groups throughout the United States,
to build bridges of collaborative resource advocacy and support and Sarcoma Research
Community alliances.

By working together, the Sarcoma Coalition members extend their advocacy strength
and provide a united presence for patients and their families/caregivers.

“Achieving More Together!”

Disclaimer

Information provided on the NLMSF website and Facebook page as well as any referenced information links are provided for informational purposes only and do not represent medical advice or opinions. All information provided has a referenced source indicated for further access to the information being provided to followers. Followers are responsible for interactions with this website, the Facebook page, and any links relative to the medical information offered/posted.

Q & A Patient / Clinician Disclaimer:

Please be advised that only general questions may be directed to a volunteer clinician, and to only expect a general response – one that does not take the place of your medical care team/oncologist’s guidance and care.

Please do not include personal information such as your full name, date of birth, personal medical information in any emails sent through the Foundation’s open Facebook group or webpage on its website. No one can diagnose your condition from email or any other written communication and communication via the Foundation’s Facebook group / website cannot replace the relationship you have with your health care provider(s).

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