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Winona LaDuke

winonababy
Winona LaDuke

 

For those of you who are not familiar with her, Winona LaDuke is the Executive Director of a group called Honor the Earth.

Last week they began a new campaign  called   “Love Water, Not Oil,”  that is vital, no critical,  to all Americans, not  just Native Americans.

What Fracking and Oil pipelines have done and will continue to do to the environment of this country, should be high on everybody’s agenda.

Once our water supplies and land are contaminated, it will take thousands of years to make them safe again.

Hopefully, you will keep this in mind, when you go to the polls to Vote this week and next:

” which candidates are supporting Fracking and Oil Pipelines and which ones are opposed to them? “

The condition of the water and land that you will  have this time next year depends on it.

Here is a brief Bio that I wrote about Winona several years ago.

She was and is,  an amazing woman, that I have the utmost respect for.

A side note that I find interesting about Winona, she and Robert Redford share the same birthday, August 18th!

Winona_duke_dream_reborn
Winona LaDuke at Dream Reborn Conference  April 6, 2008
Picture credit: Eclectek

 

Winona LaDuke, who was born in 1959 and grew up in Los Angeles,  is Anishinabe/Anishinaabekwe – Ojibwe and an enrolled member of the Mississippi Band Anishinaabeg of the Makwa Dodaem – Bear Clan of the White Earth Reservation in northern Minnesota.

Her father, an Ojibwe was a supporting actor in westerns as well as an Indian activist and her mother, a Russian Jew from New York, was an art professor.

As a teenager LaDuke addressed the United Nations on mining issues.

After graduating from Harvard in 1982, she took a position as the principal of the High School on the White Earth Reservation in Minnesota.

LaDuke is a Program Director of the Honor the Earth Fund and works nationally to promote and assist Native Environmental groups.

She is a Founding Director for White Earth Land Recovery Project: a reservation-based non-profit organization focusing on land, cultural and environmental issues.

LaDuke co-chairs the Indigenous Women’s Network and is Program Director of the Environmental Program at the Seventh Generation Fund.

LaDuke ran with Ralph Nader in 1996 and 2000 as his Vice-Presidential candidate for the Green Party and worked to increase Native American voter registration and activism.

She has written on environmental racism and is the author of several books including: Last Standing Woman and  All Our Relations: Native Struggles for Land and Life

LaDuke spoke at the International Women’s Conference in Beijing, China on August 31, 1995.

Read excerpts from her speech

LaDuke teaches courses on Native Environmentalism at the University of Minnesota and other colleges and has campaigned for the reduction of nuclear waste.

In 1994, she was named by Time Magazine as one of America’s 50 most promising leaders under 40 years of age.

She currently lives with her two children on the White Earth Reservation.

 

Places to learn more:

Native Americans Launch ‘Love Water Not Oil’ Ride To Protest Fracking Pipeline

Winona LaDuke – Wikipedia

Honor the Earth Website

Winona’s Facebook Page

Love Water Not Oil

First Nation Ride For Mother Earth Forms Norwegian/Indian Alliance

An Interview with Winona LaDuke

Honor the Earth – Wikipedia

 

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Making Marrow Matches!

navymarrowdrive
Capt. Todd A. Zecchin
June 28, 2006 – Mayport, Florida, during the ship’s Bone Marrow Drive
U.S. Navy photo by Photographer’s Mate 3rd Class Adam Herrada

 

September is Blood Cancer Awareness Month

This is a very difficult subject for me personally to write about, as our beloved Airedale,  Sabrina died of T-Cell lymphoma just three years ago. She was fairly young, at six years and very healthy, it took us by surprise, and went so fast. Her disease and her suffering were unbearable for all of us. Blood cancers don’t only kill people, they kill our beautiful pets as well.If you suspect a symptom with your pet, if you have any questions, or doubts, ask your Vet!”

 

For over ten years, locating a Bone Marrow Organization specifically directed towards assisting Indigenous People, Native Americans, or Alaskan Natives, in this Country has eluded me.

Much needed media attention, hype and hyperbole, was showered on the various Blood Cancer and Bone Marrow Groups, by the recent airing on GMA of Robin Robert’s illness, treatment and eventual Bone Marrow transplant.

She put a public face on a relentless, vicious,  killer disease and gave those also suffering from it, hope!

Robin was one of the lucky ones, as her sister turned out to be a perfect match, but for millions of Americans in this Country, there is/was no happy ending, no perfect match for them.

Many Native People on remote Reservations in America,  have two factors that can delay or detract  from them getting the treatment that they so desperately need,  a local Doctor to recommend them and just basic everyday, ordinary access to them.

Often Native Elders have no access to transportation,  or a local Doctor who is able to refer them to the next level of care, or treatment, on their particular Reservation.

This can make getting the help that they need, nearly impossible.

Right now, there are Native People who are suffering in silence and dying,  without ever getting to the help that they need and that is available to them.

According to a graph on the site below,  once Native Americans do get to the Bone Marrow Organizations, their chance of finding a match is right at 90%.

While this number appears to be quite impressive, please remember that this is, if and when they get there!

After contacting a National Bone Marrow Organization, yes the exact same one that was so vital to Ms. Robert’s recovery,  a phone conversation yesterday with their extremely helpful and dedicated, Marketing Director,  yielded much valuable information, that I am now passing along to you.

If you, or anyone you know, is in need, won’t  you please forward this on them, so that they may have a fighting chance against an insidious disease,  that does not discern between its victims, blood cancer, otherwise known as,  Leukemia, Lymphoma and Myeloma.

Here is the asked for and kindly given,  comment from their Director of Marketing, Tanya Wright:

 

“Every four minutes someone is diagnosed with a blood cancer like leukemia or lymphoma. They desperately hope for a marrow donor who could give them a cure.

Be The Match® connects patients with life-saving donors. And right now, an American Indian or Alaska Native patient in your community likely needs a hero just like you, willing to give a small part of yourself to give someone a cure.

Here are some things you should know:

  • American Indian and Alaska Native patients have a harder time finding a donor than other diverse patients.
  • Patients are most likely to match someone who shares their ancestry, and American Indians and Alaska Natives combined comprise only 1 percent of the registry.
  • American Indian and Alaska Native marrow donors are urgently needed to save patients everywhere.
  • You can be the difference between life and death for someone in need.”

“You can join the national registry now to save a life by visiting BeTheMatch.org, learning more!”

Information about why diversity matters (in relation to marrow transplants)”

http://bethematch.org/Transplant-Basics/Matching-patients-with-donors/Why-race-and-ethnicity-matter/

Thank you!
Tanya Wright Strategic Marketing Specialist, Supervisor

Tanya Wright Strategic Marketing Specialist, Supervisor
3001 Broadway Street NE Suite 100, Minneapolis, MN 55413-1753
Phone: (612) 627-8113  Toll Free: (800) 526-7809 Ext 8113

The cure for blood cancer is in the hands of ordinary peopleSM. BeTheMatch.org.

 

Thank you Tanya, now here are some other places to learn more about these diseases:

National Bone Marrow Transplant Link –   (this is the mother of all Cancer Links, start here)

Event tries to attract black bone marrow donors

The Gift of Life Bone Marrow Foundation – (For Jewish Patients)

The Bone Marrow Foundation

Kinds of Blood Cancer 

American Society of Hematology

Health Resources and Services Administration

Asians for Miracle Marrow Matches

DKMS

 

 

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