LymeNet Flash: Where to donate money

LymeNet on Facebook

LymeNet on Twitter

Follow @LymeDiseaseNet

The Lyme Disease Network receives a commission from Amazon.com for each purchase originating from this site.

When purchasing from Amazon.com, please
click here first.

Thank you.

Dedicated to the Bachmann Family

LymeNet needs your help:
LymeNet 2020 fund drive

The Lyme Disease Network is a non-profit organization funded by individual donations.

»	LymeNet Flash » Questions and Discussion » General Support » Where to donate money

UBBFriend: Email this page to someone!

Author

Topic: Where to donate money

dmbfan
LymeNet Contributor
Member # 11948

posted

Where is the "safest" place to donate money in the name of lyme disease? I know LDA, but what else? Are there specific research foundations?

Thanks

Posts: 368 | From freehold, nj | Registered: May 2007 | IP: Logged |

Tracy9
Frequent Contributor (1K+ posts)
Member # 7521

posted

Dr. Charles Ray Jones Legal Fund
Lyme Aid For Kids
Turn the Corner Foundation

....are my other favorites. If you want more info on any of them just give a shout out.

--------------------
NO PM; CONTACT: [email protected]

13 years Lyme & Co.; Small Fiber Neuropathy; Myasthenia Gravis, Adrenal Insufficiency. On chemo for 2 1/2 years as experimental treatment for MG.

Posts: 4480 | From Northeastern Connecticut | Registered: Jun 2005 | IP: Logged |

Tracy9
Frequent Contributor (1K+ posts)
Member # 7521

posted

Turn the Corner puts a huge amount of money into research, and funds I think most of the research going on.

--------------------
NO PM; CONTACT: [email protected]

13 years Lyme & Co.; Small Fiber Neuropathy; Myasthenia Gravis, Adrenal Insufficiency. On chemo for 2 1/2 years as experimental treatment for MG.

Posts: 4480 | From Northeastern Connecticut | Registered: Jun 2005 | IP: Logged |

LLYME
Member
Member # 18687

posted

The new lyme disease documentary, Under our Skin, really needs money to promote awareness of all the problems in diagnosing and treating lyme.

http://underourskin.com/donate.html

Posts: 92 | From Virginia | Registered: Jan 2009 | IP: Logged |

Tracy9
Frequent Contributor (1K+ posts)
Member # 7521

posted

Yes, another good one!!!

--------------------
NO PM; CONTACT: [email protected]

13 years Lyme & Co.; Small Fiber Neuropathy; Myasthenia Gravis, Adrenal Insufficiency. On chemo for 2 1/2 years as experimental treatment for MG.

Posts: 4480 | From Northeastern Connecticut | Registered: Jun 2005 | IP: Logged |

dmbfan
LymeNet Contributor
Member # 11948

posted

Thanks for the suggestions!

Posts: 368 | From freehold, nj | Registered: May 2007 | IP: Logged |

bettyg
Unregistered

posted

fan, is this in general or in your will?

if it's will, you have to make contact them and get the wording of THAT ORG ON HOW THEY WANT IT LISTED IN YOUR WILL.

i found this out 2 yrs. ago when i updated mine and had lyme charities shown in them! [Smile]

IP: Logged |

LisaS
Frequent Contributor (1K+ posts)
Member # 10581

posted

Places where people can make donations:
http://www.lymenet.org/
http://www.underourskin.com
www.lymefriends.com
http://www.lymedisease.org/news/lyme_disease_events/97.html
http://www.active.com/donate/marinhumanrace09/hrm09C-Batti
http://www.murakamicentreforlyme.org

--------------------
https://www.facebook.com/profile.php?id=1660435643

Posts: 1078 | From Lake Geneva WI | Registered: Nov 2006 | IP: Logged |

Printer-friendly view of this topic

The Lyme Disease Network is a non-profit organization funded by individual donations. If you would like to support the Network and the LymeNet system of Web services, please send your donations to:

The Lyme Disease Network of New Jersey
907 Pebble Creek Court, Pennington, NJ 08534 USA
http://www.lymenet.org/