I love to explore. I love seeing where one Google search takes me. I love how watching one TED talk by the founder of the Acumen Fund, Jacqueline Novogratz, leads me to find NextBillion.net. In their words, Next Billion is a website and blog bringing together the community of business leaders, social entrepreneurs, NGOs, policy makers and academics who want to explore the connection between development and enterprise. It is a discussion forum, networking space and knowledge base for individuals and organizations interested in the "next billion". Their goal is to highlight the development and implementation of business strategies that open opportunities and improve the lives of the world's approximately 4 billion low-income producers and consumers.
Next Billion bases itself on creating business models that engage low income communities as producers and consumers. While development aid and political reform are essential components in poverty eradication, successful business models can sometimes tackle development challenges more quickly and effectively than government and aid mechanisms.
Next Billion uses the term BoP, an acronym for "base of the (economic) pyramid." This term was first introduced by Professors C.K. Prahalad and Stuart Hart in their 2002 article, "The Fortune at the Bottom of the Pyramid." It has come to designate not the poverty but the potential of the world's poorest citizens as entrepreneurs, employees and discerning consumers. It also refers to the approximately four billion people whose incomes are less than $3000 per year (PPP), based on analysis done at the World Resources Institute.
The site has a blog, research, news and career links all related to this idea of
bringing smart enterprise to low income communities so that they become self-sustaining. I have tagged this site on delicious and am following it on LinkedIn and Twitter. Seems like a great resource.
harp-weaver is an independent philanthropic advisory firm based in Philadelphia, Pennsylvania. Teresa Araco Rodgers, the principal, works with individuals and families to gift to issues that matter in a meaningful way.
Tuesday, January 18, 2011
Monday, January 3, 2011
Night Out With Meaning: Women & Giving
I am thrilled to talk about and promote Night Out With Meaning: Women & Giving; a series of evenings for women to be inspired by the stories of women.
Held at The Philadelphia Cricket Club in February, May and November, each Night Out With Meaning focuses on a topic and features a wonderful storyteller. Night Out With Meaning is for women to connect with others, to learn from extraordinary women through their stories, and to find meaning in personal giving.
Come to one or all of the Nights Out With Meaning and invite a friend so you can continue the conversation!
The second Night Out With Meaning will be held on February 10th at 6:30pm. The topic is "Buidling a Family." Sue Badeau joins as our storyteller. Sue has been working as a child welfare professional for over thirty years. Sue sees a world where every child, regardless of the circumstances or place of birth, race religion, ability or disability has an opportunity to grow strong, deep roots with a family.
The cost of Night Out With Meaning is $65 for dinner including two glasses of wine. To register and pay, go to the Night Out With Meaning page on the harp-weaver website.
Night Out With Meaning is hosted by harp-weaver the firm I recently founded to help individuals and families with their personal giving. I look forward to sharing the Night Out With Meaning with you!
Held at The Philadelphia Cricket Club in February, May and November, each Night Out With Meaning focuses on a topic and features a wonderful storyteller. Night Out With Meaning is for women to connect with others, to learn from extraordinary women through their stories, and to find meaning in personal giving.
Come to one or all of the Nights Out With Meaning and invite a friend so you can continue the conversation!
The second Night Out With Meaning will be held on February 10th at 6:30pm. The topic is "Buidling a Family." Sue Badeau joins as our storyteller. Sue has been working as a child welfare professional for over thirty years. Sue sees a world where every child, regardless of the circumstances or place of birth, race religion, ability or disability has an opportunity to grow strong, deep roots with a family.
The cost of Night Out With Meaning is $65 for dinner including two glasses of wine. To register and pay, go to the Night Out With Meaning page on the harp-weaver website.
Night Out With Meaning is hosted by harp-weaver the firm I recently founded to help individuals and families with their personal giving. I look forward to sharing the Night Out With Meaning with you!
Thursday, December 23, 2010
Aimee's Bulletin
Over the course of the past couple of weeks I have come to know two wonderful women - Abigail Sandler and Sue Hoag Badeau. These two women have worked tirelessly on a much needed piece of Pennsylvania legislation called Aimee's Bulletin.
Abby's sister, Aimee, was profoundly developmentally and physically disabled. As a result of horrific, detailed circumstances that surrounded Aimee's Group Home care, Abby with others formed Aimee's Team. For the past four years she has worked towards enhancing the end-of-life decision making process for special needs individuals in Pennsylvania. She refers to the document as Aimee's Bulletin, and it will effect literally thousands of special needs individuals, state-wide. This Bulletin provides a clear policy, with guidance and steps that are morally, medically and legally sound to ensure that end-of-life care can reflect the needs, desires, values and beliefs of the individual and their family members. Harrisburg has promised that the Bulletin will be signed by January 15, 2011.
Wayne Badeau is one of the youngest of Hector and Sue Badeau's 22 children, adopted from all over the world with a variety of life circumstances and challenges. Wayne, one of three terminally ill children adopted by the Badeaus, is delightful and charming with a beautiful smile and engaging spirit. He is also dying. Wayne has a rare terminal illness called San Felipo Syndrome, and while he has already out-lived the medically-expected life-span for this disease, he has definitely declined and it won't be long before he is facing his final days. The Badeaus have already experienced the deaths of their sons Adam (11 years ago this week) and Dylan ( just 3 months ago) and they know how deeply moving, and at the same time painful, it is to experience the death of a child. Wayne is much beloved and adored by his parents, all his siblings and others and we all hope and pray that his final days, when they do begin, will be spent surrounded by family with hugs, love and peace. Yet, because of what they experienced near the end of their son Dylan's life just this past September, they are fearful this may not be the case.
Aimee's Bulletin must be signed. Abby and Sue are working to ensure that it will be signed and Sue and her husband Hector are waiting for the go ahead to take their son Wayne to Harrisburg for the signing.
For more information see: http://badeaufamily.webs.com/
Abby's sister, Aimee, was profoundly developmentally and physically disabled. As a result of horrific, detailed circumstances that surrounded Aimee's Group Home care, Abby with others formed Aimee's Team. For the past four years she has worked towards enhancing the end-of-life decision making process for special needs individuals in Pennsylvania. She refers to the document as Aimee's Bulletin, and it will effect literally thousands of special needs individuals, state-wide. This Bulletin provides a clear policy, with guidance and steps that are morally, medically and legally sound to ensure that end-of-life care can reflect the needs, desires, values and beliefs of the individual and their family members. Harrisburg has promised that the Bulletin will be signed by January 15, 2011.
Wayne Badeau is one of the youngest of Hector and Sue Badeau's 22 children, adopted from all over the world with a variety of life circumstances and challenges. Wayne, one of three terminally ill children adopted by the Badeaus, is delightful and charming with a beautiful smile and engaging spirit. He is also dying. Wayne has a rare terminal illness called San Felipo Syndrome, and while he has already out-lived the medically-expected life-span for this disease, he has definitely declined and it won't be long before he is facing his final days. The Badeaus have already experienced the deaths of their sons Adam (11 years ago this week) and Dylan ( just 3 months ago) and they know how deeply moving, and at the same time painful, it is to experience the death of a child. Wayne is much beloved and adored by his parents, all his siblings and others and we all hope and pray that his final days, when they do begin, will be spent surrounded by family with hugs, love and peace. Yet, because of what they experienced near the end of their son Dylan's life just this past September, they are fearful this may not be the case.
Aimee's Bulletin must be signed. Abby and Sue are working to ensure that it will be signed and Sue and her husband Hector are waiting for the go ahead to take their son Wayne to Harrisburg for the signing.
For more information see: http://badeaufamily.webs.com/
Thursday, December 16, 2010
The Need For Philanthropic Advice
New Philanthropy Capital (NPC) and Global Partnership presented the results of a philanthropy survey sent to over 600 single and multi-family offices in the UK between March and May 2010. The results offer insight into the philanthropic nature of some of the UK's wealthiest families. The report titled: Family Philanthropy: rewards and challenges, dives into the philanthropic behavior of high net worth individuals revealing that while the vast majority of such clients like to actively plan their charitable giving there is a clear lack of service providers able to give the full range of advice they require. Wealth management firms largely do not have some provision in place to assist in this planning and are neglecting an important area in clients’ eyes. Fundamental to this planning process is deciding which causes to support and which charities are making an impact. Philanthropists are finding it hard to access the information they need to make informed choices and would welcome input from their advisors.
NPC summarizes the reports key findings as follows:
- Giving back to the community and addressing needs are major motivations for family giving, rather than public recognition.
- Most families have had positive experiences of giving, but highlighted some unfavorable aspects including 'tortuous administration' and fear of being 'actively pursued by charities'.
- 85% of respondents with children under 21 involve them in their giving.
- The main criteria for selecting charities are the charity's vision and strategy and whether it is focused on the greatest need.
- Finding information about charities is a challenge, particularly around the measurement of results.
- Nearly 60% of families would find philanthropy advice useful.
There is a growing need for specialized philanthropic advisors offering services to support wealth managers and family offices. Even though this specific report is UK-based, there have been other similar studies in the US. Howard J. Stock wrote an article titled "Clients Lack Charitable Giving Advice" in October of this year. In it he noted a survey which said that only 52% of advisors are proactively reaching out to clients about their charitable gifting. Of the 48% who are not, 31% said it is because they lack expertise to offer guidance.
This is certainly an untapped opportunity for advisors to strengthen client relationships and grow their practices.
NPC summarizes the reports key findings as follows:
- Giving back to the community and addressing needs are major motivations for family giving, rather than public recognition.
- Most families have had positive experiences of giving, but highlighted some unfavorable aspects including 'tortuous administration' and fear of being 'actively pursued by charities'.
- 85% of respondents with children under 21 involve them in their giving.
- The main criteria for selecting charities are the charity's vision and strategy and whether it is focused on the greatest need.
- Finding information about charities is a challenge, particularly around the measurement of results.
- Nearly 60% of families would find philanthropy advice useful.
There is a growing need for specialized philanthropic advisors offering services to support wealth managers and family offices. Even though this specific report is UK-based, there have been other similar studies in the US. Howard J. Stock wrote an article titled "Clients Lack Charitable Giving Advice" in October of this year. In it he noted a survey which said that only 52% of advisors are proactively reaching out to clients about their charitable gifting. Of the 48% who are not, 31% said it is because they lack expertise to offer guidance.
This is certainly an untapped opportunity for advisors to strengthen client relationships and grow their practices.
Monday, November 29, 2010
"It is important for women to inform themselves."
Wangari Maathai founded the Green Belt Movement in Kenya to encourage rural women and farmers to plant trees to protect the environment and promote sustainable development. Maathai won a Nobel Peace Prize in 2004 for her efforts. She speaks of the conditions which led her native Kenya into environment degradation and the impact on women. When farmers plant cash crops they remove vegetation resulting in soil erosion. The soil is carried away to the river and there is no clean water. Women bear the brunt because they are responsible for getting the water for their families.
On the surface Green Belt Movement is about providing incentives to farmers to plant trees and educating them on managing their resources. At a deeper level it is about encouraging women to inform themselves on the impact of bad or lacking government policies.
More information can be found at www.greenbeltmovement.org.
On the surface Green Belt Movement is about providing incentives to farmers to plant trees and educating them on managing their resources. At a deeper level it is about encouraging women to inform themselves on the impact of bad or lacking government policies.
More information can be found at www.greenbeltmovement.org.
Monday, November 15, 2010
Night Out With Meaning: Women & Giving
I just hosted the first Night Out With Meaning: Women & Giving on November 11th. Thirty-four women witnessed Peggy Dolan tell her story. Through family pictures, Peggy told the story of her family and their experiences caring for two of their daughters, Kelly Anne and Kim, as they battled aplastic anemia and a rare form of leukemia. Peggy and her husband Joe turned their tragedy into providing help and hope for families with seriously ill children through the Kelly Anne Dolan Memorial Fund.
Night Out is about learning, connecting and reflecting. It is my hope that attendees take away knowledge that they did not have before about the experiences of families in crisis. It is my hope that attendees will meet someone new or discover something about a friend that brings them closer. And it is also my hope that there are pieces from Peggy Dolan’s story that make attendees stop and reflect about their own lives and experiences.
At the beginning of the year, I decided to take a step back from what I was doing to figure out where I wanted to go professionally and as a mom. I started a journey that began with talking to people. With each conversation, which really was an exchange of stories, I was inspired. And from those conversations, I gained clarity about what would bring meaning to my professional life. The thing I thought would be really fun was working with women in my community around some aspect of charitable giving. I want to inspire women to take the time to think about their personal giving and I want to encourage women to align their passions with their gifts – both financial and non-financial. Then came the internal question - how exactly am I going to do this? I thought about what has given me great satisfaction and inspiration recently and I kept coming back to my meetings with people and hearing their stories.
And so Night Out With Meaning was created. It is pretty simple really, let’s enjoy elements of a typical Girls Nights Out – food, wine and friends – where women can feel comfortable and welcomed. Let’s pick a topic of interest to focus on like understanding the needs of families in crisis or why empowering women is so important to alleviating poverty. And let’s have one inspiring woman stand before us to simply tell her story. Stories, told well, have the power to transport us. Storytelling encourages exploration. It is a nurturing way to remind us that our spoken words are powerful, that listening is important, and that clear communication between people is an art. I am committed to inviting storytellers with different backgrounds and approaches to their chosen issue. I am also committed to helping make connections.
I witnessed women exchanging information, comforting each other, and creating an environment to allow those at the table to speak openly and personally.
My mission is to inspire others by helping them articulate their values and passions to be purposeful givers. Informed philanthropy can bring great satisfaction to a person’s life and has the power to transform communities, organizations and people.
I look forward to sharing future Nights Out with such creative, sensitive and inquisitive women!
Night Out is about learning, connecting and reflecting. It is my hope that attendees take away knowledge that they did not have before about the experiences of families in crisis. It is my hope that attendees will meet someone new or discover something about a friend that brings them closer. And it is also my hope that there are pieces from Peggy Dolan’s story that make attendees stop and reflect about their own lives and experiences.
At the beginning of the year, I decided to take a step back from what I was doing to figure out where I wanted to go professionally and as a mom. I started a journey that began with talking to people. With each conversation, which really was an exchange of stories, I was inspired. And from those conversations, I gained clarity about what would bring meaning to my professional life. The thing I thought would be really fun was working with women in my community around some aspect of charitable giving. I want to inspire women to take the time to think about their personal giving and I want to encourage women to align their passions with their gifts – both financial and non-financial. Then came the internal question - how exactly am I going to do this? I thought about what has given me great satisfaction and inspiration recently and I kept coming back to my meetings with people and hearing their stories.
And so Night Out With Meaning was created. It is pretty simple really, let’s enjoy elements of a typical Girls Nights Out – food, wine and friends – where women can feel comfortable and welcomed. Let’s pick a topic of interest to focus on like understanding the needs of families in crisis or why empowering women is so important to alleviating poverty. And let’s have one inspiring woman stand before us to simply tell her story. Stories, told well, have the power to transport us. Storytelling encourages exploration. It is a nurturing way to remind us that our spoken words are powerful, that listening is important, and that clear communication between people is an art. I am committed to inviting storytellers with different backgrounds and approaches to their chosen issue. I am also committed to helping make connections.
I witnessed women exchanging information, comforting each other, and creating an environment to allow those at the table to speak openly and personally.
My mission is to inspire others by helping them articulate their values and passions to be purposeful givers. Informed philanthropy can bring great satisfaction to a person’s life and has the power to transform communities, organizations and people.
I look forward to sharing future Nights Out with such creative, sensitive and inquisitive women!
Tuesday, November 2, 2010
Chasing Miracles
Last night I had the opportunity to watch the movie Extraordinary Measures and meet John Crowley, activist and entrepreneur. Extraordinary Measures is the story of the Crowley family and their quest to find a treatment and ultimately a cure for a rare genetic disorder known as Pompe disease. Two of John and Aileen Crowley's children have this disease. Their names are Megan and Patrick. In 1998 there was no treatment for this often fatal neuromuscular disorder. John Crowley started his own biotech firm over an 18 month period and sold it to Genzyme, one of the world's largest biotech companies. After the efforts of hundreds of people they finally discovered and produced a medicine to treat Pompe disease.
Following viewing the movie, Crowley made a few remarks and took questions from the audience. He answered the questions he always gets asked. First, how did the movie come to be? And second, how are Megan and Patrick doing? In 2003, the Wall Street Journal published an article written by Geeta Anandon on its front page about the Crowleys. Harrison Ford read the article, was struck by it and contacted producers to get the wheels in motion to make a movie. Crowley's message: If you are written about in the Wall Street Journal and Harrison Ford calls, do not hang up! Megan and Patrick are both doing well. They are still confined to wheelchairs and ventilator dependent, but they are thriving 8th and 7th graders. They receive the enzyme treatment once every two weeks. Thankfully this can be administered at home otherwise the children would have to spend a full day in the hospital and be exposed to germs that could compromise their respiratory systems. Crowley says that this is the biggest risk the children face. He continues to work on treatments - better enzymes to combat the sugar in their bodies which debilitate muscles and organs.
The Crowleys have written a book called Chasing Miracles. It is divided into 3 parts: Strength, Hope, and Joy. The book intimately chronicles the journey of the Crowley family and profiles all those who have helped along the way. If you are interested in learning more about this family, they have a website - www.crowleyfamily5.com. If you are interested in supporting charities which address the needs of families with rare, orphan diseases, the Crowleys include 4 links to charities on their website: The United Pompe Foundation, The Make A Wish Foundation, The Muscular Dystrophy Association, and Children's r.a.r.e. Disease Network.
John and Aileen Crowley did whatever it took to help their children survive. This is an inspiring story. It is about learning to ask for help, about not losing faith, about coping with challenges, and about the kindness of others. Stories like this one inspire, energize, and encourage self-reflection. I was honored to hear pieces of this story directly from John Crowley. The movie and book have really given him the opportunity to spread his message. It is a powerful one.
Following viewing the movie, Crowley made a few remarks and took questions from the audience. He answered the questions he always gets asked. First, how did the movie come to be? And second, how are Megan and Patrick doing? In 2003, the Wall Street Journal published an article written by Geeta Anandon on its front page about the Crowleys. Harrison Ford read the article, was struck by it and contacted producers to get the wheels in motion to make a movie. Crowley's message: If you are written about in the Wall Street Journal and Harrison Ford calls, do not hang up! Megan and Patrick are both doing well. They are still confined to wheelchairs and ventilator dependent, but they are thriving 8th and 7th graders. They receive the enzyme treatment once every two weeks. Thankfully this can be administered at home otherwise the children would have to spend a full day in the hospital and be exposed to germs that could compromise their respiratory systems. Crowley says that this is the biggest risk the children face. He continues to work on treatments - better enzymes to combat the sugar in their bodies which debilitate muscles and organs.
The Crowleys have written a book called Chasing Miracles. It is divided into 3 parts: Strength, Hope, and Joy. The book intimately chronicles the journey of the Crowley family and profiles all those who have helped along the way. If you are interested in learning more about this family, they have a website - www.crowleyfamily5.com. If you are interested in supporting charities which address the needs of families with rare, orphan diseases, the Crowleys include 4 links to charities on their website: The United Pompe Foundation, The Make A Wish Foundation, The Muscular Dystrophy Association, and Children's r.a.r.e. Disease Network.
John and Aileen Crowley did whatever it took to help their children survive. This is an inspiring story. It is about learning to ask for help, about not losing faith, about coping with challenges, and about the kindness of others. Stories like this one inspire, energize, and encourage self-reflection. I was honored to hear pieces of this story directly from John Crowley. The movie and book have really given him the opportunity to spread his message. It is a powerful one.
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