Please Share it with all healers you know...
Tonight about 12 hours difference here in the States from California....I am requesting all Healers, Reiki any and all Energyworkers to focus with Intention towards all of Iran Unconditional Love and Peace.Calling all angels and Higher Selves and Higher Light Beings and The Creator of all There is....The woman ofIran will enter the Streets tomorrow January 7th and remove all scarves and chardors in order to bring peace back to Iran from the Oppression of the Iranian Government.Please hold the Unconditional Love and Light for all of Iran and be the peace and Love we all know is Possible...support the Energy workers as well in Iran holding the Door of the Creator open for all of them.Iran is one of the planets Greatest Teachers at this moment for the planet True Freedom aligned with the will of the Creator Now..See it and feel it.Thank youPlease tell everyone and post on your sitesThank youWe are all honored to help Jeri, and thanks for telling us.HugsMarlene
Calling All Lightworkers, Energyworkers, Healers and Those Who Work for Love and Light. - My Special Inner Child
Thursday, January 7, 2010
Wednesday, December 9, 2009
Giving Lavi Life
Giving Lavi Life:
"Gift_ Of_ Life_Fundraising is to help 18 months old Lavi who was diagnosed with Canavan Disease at age of 3 months.
Today, at 18 months, Lavi is considered a medical miracle. He is progressing neurologically, he can see and hear -- defying the dire diagnosis, but unfortunately the existing drugs alone will not retard the progression of the disease.
The question for the parents was one: What else can we do to save Lavi?
Yulia and Gili assure that all the money raised will to fund the research.
They hope that each donor will tell Lavi's story to at least 10 friends, and this way, even with small donations they will be able to raise the necessary funds to save their child.Thanks to all the love and support of people like you. All that it takes to save me and many other children is 7,000 more friends who will each give $18 (18 being 'alive', in Hebrew), and inviting 10 of their friends to do the same.
Can I count on your generosity?
Blessings Doreen Cohanim C.Ht
www.HypnoCruise.com"
"Gift_ Of_ Life_Fundraising is to help 18 months old Lavi who was diagnosed with Canavan Disease at age of 3 months.
Today, at 18 months, Lavi is considered a medical miracle. He is progressing neurologically, he can see and hear -- defying the dire diagnosis, but unfortunately the existing drugs alone will not retard the progression of the disease.
The question for the parents was one: What else can we do to save Lavi?
Yulia and Gili assure that all the money raised will to fund the research.
They hope that each donor will tell Lavi's story to at least 10 friends, and this way, even with small donations they will be able to raise the necessary funds to save their child.Thanks to all the love and support of people like you. All that it takes to save me and many other children is 7,000 more friends who will each give $18 (18 being 'alive', in Hebrew), and inviting 10 of their friends to do the same.
Can I count on your generosity?
Blessings Doreen Cohanim C.Ht
www.HypnoCruise.com"
Monday, December 7, 2009
לתת ללביא חיים | give2gether
Giving Lavi Life Doreen Cohanim
Gift_ Of_ Life_Fundraising is to help 18 months old Lavi who was diagnosed with Canavan Disease at age of 3 months. Today, at 18 months, Lavi is considered a medical miracle. He is progressing neurologically – he can see and hear -- defying the dire diagnosis, but unfortunately the existing drugs alone will not retard the progression of the disease. The question for the parents was one: What else can we do to save Lavi? Yulia and Gili assure that all the money raised will to fund the research. They hope that each donor will tell Lavi's story to at least 10 friends, and this way, even with small donations they will be able to raise the necessary funds to save their child. Thanks to all the love and support of people like you. All that it takes to save me and many other children is 7,000 more friends who will each give $18 (18 being "alive", in Hebrew), and inviting 10 of their friends to do the same. Can I count on your generosity? Blessings
Doreen Cohanim C.Ht
http://www.hypnocruise.com/ Edit
Part 1 - Mom and Dad discovering the illness
About Dr. Paola Leone and the CGTC
Paola Leone, Ph.D.
Dr. Paola Leone is an Associate Professor of Neurosurgery and Director of the Cell & Gene Therapy Center (CGTC). As Principal Investigator at UMDNJ-Robert Wood Johnson Medical School for Gene Therapy for Canavan Disease, she leads all research activities at UMDNJ and the affiliated centers. Her research interests have included in vivo neurochemistry of epilepsy and gene transfer approaches for the treatment of neurological disorders. She has published extensively in the field of CNS gene therapy and conducted the first direct gene therapy trial using a liposome-based vector for a pediatric neurodegenerative disorder. In addition to applications of viral vectors and stem cells, Dr. Leone is studying pharmacological approaches in humans and in animal models of Canavan Disease, Amyotrophic Lateral Sclerosis, Tay Sach’s and other neurological disorders.
give2gether is a new way of doing good by simply harnessing your existing friends and social networks.
Now is the time to inspire your friends
Every one of us can make an impact, help and contribute. Here are a few ways to get involved - five steps on the road to a big breakthrough.
Q&A with Dr. Paola Leone
Question:
What is the Cell and Gene Therapy at UMDNJ/SOM?
Answer:
The Cell and Gene Therapy Center is a Translational Research Center, in which the scientists study in the laboratory methods that can be used in clinical settings using for instance either Stem Cells Therapy or Gene Therapy or both, in order to improve the health of patients affected by Canavan Disease or by other neurodegenerative disorders.
Question:
What are the current methods used to treat Canavan Disease?
Answer:
The current method is a pharmacological approach using a combination of drugs and supplements designed to benefit patients affected by Canavan Disease.The Stem Cell method is still undergoing investigation in the laboratory to test the “proof-of-principle” prior to use it for human applications.
Read More About Canavan Disease & Gene Therapy and Giving Lav's Life by clicking on the link.
לתת ללביא חיים give2gether
Gift_ Of_ Life_Fundraising is to help 18 months old Lavi who was diagnosed with Canavan Disease at age of 3 months. Today, at 18 months, Lavi is considered a medical miracle. He is progressing neurologically – he can see and hear -- defying the dire diagnosis, but unfortunately the existing drugs alone will not retard the progression of the disease. The question for the parents was one: What else can we do to save Lavi? Yulia and Gili assure that all the money raised will to fund the research. They hope that each donor will tell Lavi's story to at least 10 friends, and this way, even with small donations they will be able to raise the necessary funds to save their child. Thanks to all the love and support of people like you. All that it takes to save me and many other children is 7,000 more friends who will each give $18 (18 being "alive", in Hebrew), and inviting 10 of their friends to do the same. Can I count on your generosity? Blessings
Doreen Cohanim C.Ht
http://www.hypnocruise.com/ Edit
Part 1 - Mom and Dad discovering the illness
About Dr. Paola Leone and the CGTC
Paola Leone, Ph.D.
Dr. Paola Leone is an Associate Professor of Neurosurgery and Director of the Cell & Gene Therapy Center (CGTC). As Principal Investigator at UMDNJ-Robert Wood Johnson Medical School for Gene Therapy for Canavan Disease, she leads all research activities at UMDNJ and the affiliated centers. Her research interests have included in vivo neurochemistry of epilepsy and gene transfer approaches for the treatment of neurological disorders. She has published extensively in the field of CNS gene therapy and conducted the first direct gene therapy trial using a liposome-based vector for a pediatric neurodegenerative disorder. In addition to applications of viral vectors and stem cells, Dr. Leone is studying pharmacological approaches in humans and in animal models of Canavan Disease, Amyotrophic Lateral Sclerosis, Tay Sach’s and other neurological disorders.
give2gether is a new way of doing good by simply harnessing your existing friends and social networks.
Now is the time to inspire your friends
Every one of us can make an impact, help and contribute. Here are a few ways to get involved - five steps on the road to a big breakthrough.
Q&A with Dr. Paola Leone
Question:
What is the Cell and Gene Therapy at UMDNJ/SOM?
Answer:
The Cell and Gene Therapy Center is a Translational Research Center, in which the scientists study in the laboratory methods that can be used in clinical settings using for instance either Stem Cells Therapy or Gene Therapy or both, in order to improve the health of patients affected by Canavan Disease or by other neurodegenerative disorders.
Question:
What are the current methods used to treat Canavan Disease?
Answer:
The current method is a pharmacological approach using a combination of drugs and supplements designed to benefit patients affected by Canavan Disease.The Stem Cell method is still undergoing investigation in the laboratory to test the “proof-of-principle” prior to use it for human applications.
Read More About Canavan Disease & Gene Therapy and Giving Lav's Life by clicking on the link.
לתת ללביא חיים give2gether
Wednesday, December 2, 2009
Please Help With This Fundraising To Save Lavi's Life.... - My Special Inner Child
Dear Friends, Please Help Fundraising To Save Lavi's Life....
Dec. 2st, 2009 – Yulia and Gili Ben-Moshe, who live in a small town in Israel, were confronted with every parent’s nightmare: their third child, Lavi then three months old, was diagnosed with Canavan Disease. At the first moment they didn't understand what it means, but after a short while they learned that children with Canavan disease first lose their sense of sight, then their hearing and their motor function. Usually, before age 4, the disease kills off their brain cells and the children die.
It took them 24 hours to start the war to save Lavi. They went online and found Dr. Paola Leone, the leading American expert on Canavan disease. They realized that Dr. Leone, works out of the UMDNJ-Robert Wood Johnson Medical School, is developing innovative treatments for Canavan patients.Ten days later the couple was on a plane on its way to the US. They met with Dr. Leone who put Lavi on her pharmacologic therapies, which resulted in delaying his brain deterioration.
This was the first hopeful sign.Today, at 18 months, Lavi is considered a medical miracle. He is progressing neurologically – he can see and hear -- defying the dire diagnosis.But unfortunately the existing Drugs alone will not retard the progression of the disease. The question for the parents was one: What else can we do to save Lavi?
While staying in New Jersey, they learned that Dr. Leone is conducting basic scientific stem cell research that holds hope for Canavan patients. Since the disease kills off brain cells, Dr. Leone believes that implanting stem cells into the brains of children with Canavan would result in the proliferation of functional brain cells. She is now testing her theory in the laboratory, and intends clinic testing as soon as she scientifically proves the efficacy and the safely of the stem cell treatment. The clinical protocol to use stems cells to treat Canavan patients should be approved within 24 months by the Food and Drug Administration. The subsequent clinical trial would include 15 children with Canavan Disease.
Yulia and Gili Ben Moshe decided to approach Dr. Leone and asked her to put Lavi on the testing group of the new process."Lavi's psycho-motor development has been improving greatly since the pharmacological therapy began,” says Leone. “The therapy is preserving his brain but is not curing the disease.
While Lavi and many other children are struggling to change their prognosis, scientists are working incessantly in my laboratory to bring a cure to fruition. The timing and success of a cure for Canavan Disease fully depends upon the availability of appropriate research funds that would also model the cure for other neurodegenerative diseases.”Dr. Leone’s research is funded only partially by the government. For her research to be completed and approved, she needs an estimated $ 1.5 million.This couldn't deter the courageous parents.
They decided to go fund raising for the complementary funds.They first started in Israel, where they raised the money for Lavi's medical treatments, and then they decided to start an international appeal. They partnered with an Israeli start-up, called give2gether, which developed an innovative platform for micro-philanthropy. They built a website which chronicles Lavi’s life Journey, and enables grass roots fundraising.Yulia and Gili assure that all the money raised will to fund the research. They hope that each donor will tell Lavi's story to at least 10 friends, and this way, even with small donations they will be able to raise the necessary funds to save their child.“It’s a very hard for my wife and me to face this ordeal,” says Gili Ben Moshe, “but Lavi came into this world with a purpose. We believe it’s our privilege to fight for Lavi’s life and for the lives of other children who have this lethal disease.”
Blessings Doreen Cohanim C.Ht
Please join me for Levi's Distance Healing and Prayer by clicking on the inner child link.
http://specialchild.ning.com
Dec. 2st, 2009 – Yulia and Gili Ben-Moshe, who live in a small town in Israel, were confronted with every parent’s nightmare: their third child, Lavi then three months old, was diagnosed with Canavan Disease. At the first moment they didn't understand what it means, but after a short while they learned that children with Canavan disease first lose their sense of sight, then their hearing and their motor function. Usually, before age 4, the disease kills off their brain cells and the children die.
It took them 24 hours to start the war to save Lavi. They went online and found Dr. Paola Leone, the leading American expert on Canavan disease. They realized that Dr. Leone, works out of the UMDNJ-Robert Wood Johnson Medical School, is developing innovative treatments for Canavan patients.Ten days later the couple was on a plane on its way to the US. They met with Dr. Leone who put Lavi on her pharmacologic therapies, which resulted in delaying his brain deterioration.
This was the first hopeful sign.Today, at 18 months, Lavi is considered a medical miracle. He is progressing neurologically – he can see and hear -- defying the dire diagnosis.But unfortunately the existing Drugs alone will not retard the progression of the disease. The question for the parents was one: What else can we do to save Lavi?
While staying in New Jersey, they learned that Dr. Leone is conducting basic scientific stem cell research that holds hope for Canavan patients. Since the disease kills off brain cells, Dr. Leone believes that implanting stem cells into the brains of children with Canavan would result in the proliferation of functional brain cells. She is now testing her theory in the laboratory, and intends clinic testing as soon as she scientifically proves the efficacy and the safely of the stem cell treatment. The clinical protocol to use stems cells to treat Canavan patients should be approved within 24 months by the Food and Drug Administration. The subsequent clinical trial would include 15 children with Canavan Disease.
Yulia and Gili Ben Moshe decided to approach Dr. Leone and asked her to put Lavi on the testing group of the new process."Lavi's psycho-motor development has been improving greatly since the pharmacological therapy began,” says Leone. “The therapy is preserving his brain but is not curing the disease.
While Lavi and many other children are struggling to change their prognosis, scientists are working incessantly in my laboratory to bring a cure to fruition. The timing and success of a cure for Canavan Disease fully depends upon the availability of appropriate research funds that would also model the cure for other neurodegenerative diseases.”Dr. Leone’s research is funded only partially by the government. For her research to be completed and approved, she needs an estimated $ 1.5 million.This couldn't deter the courageous parents.
They decided to go fund raising for the complementary funds.They first started in Israel, where they raised the money for Lavi's medical treatments, and then they decided to start an international appeal. They partnered with an Israeli start-up, called give2gether, which developed an innovative platform for micro-philanthropy. They built a website which chronicles Lavi’s life Journey, and enables grass roots fundraising.Yulia and Gili assure that all the money raised will to fund the research. They hope that each donor will tell Lavi's story to at least 10 friends, and this way, even with small donations they will be able to raise the necessary funds to save their child.“It’s a very hard for my wife and me to face this ordeal,” says Gili Ben Moshe, “but Lavi came into this world with a purpose. We believe it’s our privilege to fight for Lavi’s life and for the lives of other children who have this lethal disease.”
Blessings Doreen Cohanim C.Ht
Please join me for Levi's Distance Healing and Prayer by clicking on the inner child link.
http://specialchild.ning.com
Please Help With This Fundraising To Save Lavi's Life.... - My Special Inner Child
Dear Friends, Please Help Fundraising To Save Lavi's Life....
Dec. 1st, 2009 – Yulia and Gili Ben-Moshe, who live in a small town in Israel, were confronted with every parent’s nightmare: their third child, Lavi then three months old, was diagnosed with Canavan Disease.
At the first moment they didn't understand what it means, but after a short while they learned that children with Canavan disease first lose their sense of sight, then their hearing and their motor function. Usually, before age 4, the disease kills off their brain cells and the children die.
It took them 24 hours to start the war to save Lavi. They went online and found Dr. Paola Leone, the leading American expert on Canavan disease. They realized that Dr. Leone, works out of the UMDNJ-Robert Wood Johnson Medical School, is developing innovative treatments for Canavan patients.
Ten days later the couple was on a plane on its way to the US. They met with Dr. Leone who put Lavi on her pharmacologic therapies, which resulted in delaying his brain deterioration. This was the first hopeful sign.
Today, at 18 months, Lavi is considered a medical miracle. He is progressing neurologically – he can see and hear -- defying the dire diagnosis.But unfortunately the existing Drugs alone will not retard the progression of the disease. The question for the parents was one: What else can we do to save Lavi?
While staying in New Jersey, they learned that Dr. Leone is conducting basic scientific stem cell research that holds hope for Canavan patients. Since the disease kills off brain cells, Dr. Leone believes that implanting stem cells into the brains of children with Canavan would result in the proliferation of functional brain cells. She is now testing her theory in the laboratory, and intends clinic testing as soon as she scientifically proves the efficacy and the safely of the stem cell treatment. The clinical protocol to use stems cells to treat Canavan patients should be approved within 24 months by the Food and Drug Administration. The subsequent clinical trial would include 15 children with Canavan Disease.
Yulia and Gili Ben Moshe decided to approach Dr. Leone and asked her to put Lavi on the testing group of the new process.
"Lavi's psycho-motor development has been improving greatly since the pharmacological therapy began,” says Leone. “The therapy is preserving his brain but is not curing the disease. While Lavi and many other children are struggling to change their prognosis, scientists are working incessantly in my laboratory to bring a cure to fruition. The timing and success of a cure for Canavan Disease fully depends upon the availability of appropriate research funds that would also model the cure for other neurodegenerative diseases.”
Dr. Leone’s research is funded only partially by the government. For her research to be completed and approved, she needs an estimated $ 1.5 million.
This couldn't deter the courageous parents. They decided to go fund raising for the complementary funds.
They first started in Israel, where they raised the money for Lavi's medical treatments, and then they decided to start an international appeal. They partnered with an Israeli start-up, called give2gether, which developed an innovative platform for micro-philanthropy. They built a website which chronicles Lavi’s life Journey, and enables grass roots fundraising.
Yulia and Gili assure that all the money raised will to fund the research. They hope that each donor will tell Lavi's story to at least 10 friends, and this way, even with small donations they will be able to raise the necessary funds to save their child.
“It’s a very hard for my wife and me to face this ordeal,” says Gili Ben Moshe, “but Lavi came into this world with a purpose. We believe it’s our privilege to fight for Lavi’s life and for the lives of other children who have this lethal disease.”
Blessings Doreen Cohanim C.Ht
PLEASE HELP!
Save Lavi's Life
Any donation is a blessing, your amount and name will be posted on Inner Child Page
Free Free To contact me via email or via my link below as how you can donate.
Also join us for Distance Energy Healing...
Please Help With This Fundraising To Save Lavi's Life.... - My Special Inner Child
Dec. 1st, 2009 – Yulia and Gili Ben-Moshe, who live in a small town in Israel, were confronted with every parent’s nightmare: their third child, Lavi then three months old, was diagnosed with Canavan Disease.
At the first moment they didn't understand what it means, but after a short while they learned that children with Canavan disease first lose their sense of sight, then their hearing and their motor function. Usually, before age 4, the disease kills off their brain cells and the children die.
It took them 24 hours to start the war to save Lavi. They went online and found Dr. Paola Leone, the leading American expert on Canavan disease. They realized that Dr. Leone, works out of the UMDNJ-Robert Wood Johnson Medical School, is developing innovative treatments for Canavan patients.
Ten days later the couple was on a plane on its way to the US. They met with Dr. Leone who put Lavi on her pharmacologic therapies, which resulted in delaying his brain deterioration. This was the first hopeful sign.
Today, at 18 months, Lavi is considered a medical miracle. He is progressing neurologically – he can see and hear -- defying the dire diagnosis.But unfortunately the existing Drugs alone will not retard the progression of the disease. The question for the parents was one: What else can we do to save Lavi?
While staying in New Jersey, they learned that Dr. Leone is conducting basic scientific stem cell research that holds hope for Canavan patients. Since the disease kills off brain cells, Dr. Leone believes that implanting stem cells into the brains of children with Canavan would result in the proliferation of functional brain cells. She is now testing her theory in the laboratory, and intends clinic testing as soon as she scientifically proves the efficacy and the safely of the stem cell treatment. The clinical protocol to use stems cells to treat Canavan patients should be approved within 24 months by the Food and Drug Administration. The subsequent clinical trial would include 15 children with Canavan Disease.
Yulia and Gili Ben Moshe decided to approach Dr. Leone and asked her to put Lavi on the testing group of the new process.
"Lavi's psycho-motor development has been improving greatly since the pharmacological therapy began,” says Leone. “The therapy is preserving his brain but is not curing the disease. While Lavi and many other children are struggling to change their prognosis, scientists are working incessantly in my laboratory to bring a cure to fruition. The timing and success of a cure for Canavan Disease fully depends upon the availability of appropriate research funds that would also model the cure for other neurodegenerative diseases.”
Dr. Leone’s research is funded only partially by the government. For her research to be completed and approved, she needs an estimated $ 1.5 million.
This couldn't deter the courageous parents. They decided to go fund raising for the complementary funds.
They first started in Israel, where they raised the money for Lavi's medical treatments, and then they decided to start an international appeal. They partnered with an Israeli start-up, called give2gether, which developed an innovative platform for micro-philanthropy. They built a website which chronicles Lavi’s life Journey, and enables grass roots fundraising.
Yulia and Gili assure that all the money raised will to fund the research. They hope that each donor will tell Lavi's story to at least 10 friends, and this way, even with small donations they will be able to raise the necessary funds to save their child.
“It’s a very hard for my wife and me to face this ordeal,” says Gili Ben Moshe, “but Lavi came into this world with a purpose. We believe it’s our privilege to fight for Lavi’s life and for the lives of other children who have this lethal disease.”
Blessings Doreen Cohanim C.Ht
PLEASE HELP!
Save Lavi's Life
Any donation is a blessing, your amount and name will be posted on Inner Child Page
Free Free To contact me via email or via my link below as how you can donate.
Also join us for Distance Energy Healing...
Please Help With This Fundraising To Save Lavi's Life.... - My Special Inner Child
Please Help With This Fundraising To Save Lavi's Life.... - My Special Inner Child
Dear Friends, Please Help Fundraising To Save Lavi's Life....
Dec. 1st, 2009 – Yulia and Gili Ben-Moshe, who live in a small town in Israel, were confronted with every parent’s nightmare: their third child, Lavi then three months old, was diagnosed with Canavan Disease.
At the first moment they didn't understand what it means, but after a short while they learned that children with Canavan disease first lose their sense of sight, then their hearing and their motor function. Usually, before age 4, the disease kills off their brain cells and the children die.
It took them 24 hours to start the war to save Lavi. They went online and found Dr. Paola Leone, the leading American expert on Canavan disease. They realized that Dr. Leone, works out of the UMDNJ-Robert Wood Johnson Medical School, is developing innovative treatments for Canavan patients.
Ten days later the couple was on a plane on its way to the US. They met with Dr. Leone who put Lavi on her pharmacologic therapies, which resulted in delaying his brain deterioration. This was the first hopeful sign.
Today, at 18 months, Lavi is considered a medical miracle. He is progressing neurologically – he can see and hear -- defying the dire diagnosis.But unfortunately the existing Drugs alone will not retard the progression of the disease. The question for the parents was one: What else can we do to save Lavi?
While staying in New Jersey, they learned that Dr. Leone is conducting basic scientific stem cell research that holds hope for Canavan patients. Since the disease kills off brain cells, Dr. Leone believes that implanting stem cells into the brains of children with Canavan would result in the proliferation of functional brain cells. She is now testing her theory in the laboratory, and intends clinic testing as soon as she scientifically proves the efficacy and the safely of the stem cell treatment. The clinical protocol to use stems cells to treat Canavan patients should be approved within 24 months by the Food and Drug Administration. The subsequent clinical trial would include 15 children with Canavan Disease.
Yulia and Gili Ben Moshe decided to approach Dr. Leone and asked her to put Lavi on the testing group of the new process.
"Lavi's psycho-motor development has been improving greatly since the pharmacological therapy began,” says Leone. “The therapy is preserving his brain but is not curing the disease. While Lavi and many other children are struggling to change their prognosis, scientists are working incessantly in my laboratory to bring a cure to fruition.
The timing and success of a cure for Canavan Disease fully depends upon the availability of appropriate research funds that would also model the cure for other neurodegenerative diseases.” Dr. Leone’s research is funded only partially by the government. For her research to be completed and approved, she needs an estimated $ 1.5 million.
This couldn't deter the courageous parents. They decided to go fund raising for the complementary funds.
They first started in Israel, where they raised the money for Lavi's medical treatments, and then they decided to start an international appeal. They partnered with an Israeli start-up, called give2gether, which developed an innovative platform for micro-philanthropy. They built a website which chronicles Lavi’s life Journey, and enables grass roots fundraising.
Yulia and Gili assure that all the money raised will to fund the research. They hope that each donor will tell Lavi's story to at least 10 friends, and this way, even with small donations they will be able to raise the necessary funds to save their child.
“It’s a very hard for my wife and me to face this ordeal,” says Gili Ben Moshe, “but Lavi came into this world with a purpose. We believe it’s our privilege to fight for Lavi’s life and for the lives of other children who have this lethal disease.”
Blessings Doreen Cohanim
PLEASE HELP!
Save Lavi's Life
https://www.paypal.com/cgi-bin/webscr?cmd=_s-xclick&hosted_button_id=10181857
Any donation is a blessing, your amount and name will be posted here....
Free Free To contact me via email or via my website.
Also join us for Distance Energy Healing...
Please Help With This Fundraising To Save Lavi's Life.... - My Special Inner Child
Dec. 1st, 2009 – Yulia and Gili Ben-Moshe, who live in a small town in Israel, were confronted with every parent’s nightmare: their third child, Lavi then three months old, was diagnosed with Canavan Disease.
At the first moment they didn't understand what it means, but after a short while they learned that children with Canavan disease first lose their sense of sight, then their hearing and their motor function. Usually, before age 4, the disease kills off their brain cells and the children die.
It took them 24 hours to start the war to save Lavi. They went online and found Dr. Paola Leone, the leading American expert on Canavan disease. They realized that Dr. Leone, works out of the UMDNJ-Robert Wood Johnson Medical School, is developing innovative treatments for Canavan patients.
Ten days later the couple was on a plane on its way to the US. They met with Dr. Leone who put Lavi on her pharmacologic therapies, which resulted in delaying his brain deterioration. This was the first hopeful sign.
Today, at 18 months, Lavi is considered a medical miracle. He is progressing neurologically – he can see and hear -- defying the dire diagnosis.But unfortunately the existing Drugs alone will not retard the progression of the disease. The question for the parents was one: What else can we do to save Lavi?
While staying in New Jersey, they learned that Dr. Leone is conducting basic scientific stem cell research that holds hope for Canavan patients. Since the disease kills off brain cells, Dr. Leone believes that implanting stem cells into the brains of children with Canavan would result in the proliferation of functional brain cells. She is now testing her theory in the laboratory, and intends clinic testing as soon as she scientifically proves the efficacy and the safely of the stem cell treatment. The clinical protocol to use stems cells to treat Canavan patients should be approved within 24 months by the Food and Drug Administration. The subsequent clinical trial would include 15 children with Canavan Disease.
Yulia and Gili Ben Moshe decided to approach Dr. Leone and asked her to put Lavi on the testing group of the new process.
"Lavi's psycho-motor development has been improving greatly since the pharmacological therapy began,” says Leone. “The therapy is preserving his brain but is not curing the disease. While Lavi and many other children are struggling to change their prognosis, scientists are working incessantly in my laboratory to bring a cure to fruition.
The timing and success of a cure for Canavan Disease fully depends upon the availability of appropriate research funds that would also model the cure for other neurodegenerative diseases.” Dr. Leone’s research is funded only partially by the government. For her research to be completed and approved, she needs an estimated $ 1.5 million.
This couldn't deter the courageous parents. They decided to go fund raising for the complementary funds.
They first started in Israel, where they raised the money for Lavi's medical treatments, and then they decided to start an international appeal. They partnered with an Israeli start-up, called give2gether, which developed an innovative platform for micro-philanthropy. They built a website which chronicles Lavi’s life Journey, and enables grass roots fundraising.
Yulia and Gili assure that all the money raised will to fund the research. They hope that each donor will tell Lavi's story to at least 10 friends, and this way, even with small donations they will be able to raise the necessary funds to save their child.
“It’s a very hard for my wife and me to face this ordeal,” says Gili Ben Moshe, “but Lavi came into this world with a purpose. We believe it’s our privilege to fight for Lavi’s life and for the lives of other children who have this lethal disease.”
Blessings Doreen Cohanim
PLEASE HELP!
Save Lavi's Life
https://www.paypal.com/cgi-bin/webscr?cmd=_s-xclick&hosted_button_id=10181857
Any donation is a blessing, your amount and name will be posted here....
Free Free To contact me via email or via my website.
Also join us for Distance Energy Healing...
Please Help With This Fundraising To Save Lavi's Life.... - My Special Inner Child
Please Help With This Fundraising To Save Lavi's Life.... - My Special Inner Child
Dear Friends, Please Help Fundraising To Save Lavi's Life....
Dec. 1st, 2009 – Yulia and Gili Ben-Moshe, who live in a small town in Israel, were confronted with every parent’s nightmare: their third child, Lavi then three months old, was diagnosed with Canavan Disease.
At the first moment they didn't understand what it means, but after a short while they learned that children with Canavan disease first lose their sense of sight, then their hearing and their motor function. Usually, before age 4, the disease kills off their brain cells and the children die.
It took them 24 hours to start the war to save Lavi. They went online and found Dr. Paola Leone, the leading American expert on Canavan disease. They realized that Dr. Leone, works out of the UMDNJ-Robert Wood Johnson Medical School, is developing innovative treatments for Canavan patients.
Ten days later the couple was on a plane on its way to the US. They met with Dr. Leone who put Lavi on her pharmacologic therapies, which resulted in delaying his brain deterioration. This was the first hopeful sign.
Today, at 18 months, Lavi is considered a medical miracle. He is progressing neurologically – he can see and hear -- defying the dire diagnosis.But unfortunately the existing Drugs alone will not retard the progression of the disease. The question for the parents was one: What else can we do to save Lavi?
While staying in New Jersey, they learned that Dr. Leone is conducting basic scientific stem cell research that holds hope for Canavan patients. Since the disease kills off brain cells, Dr. Leone believes that implanting stem cells into the brains of children with Canavan would result in the proliferation of functional brain cells. She is now testing her theory in the laboratory, and intends clinic testing as soon as she scientifically proves the efficacy and the safely of the stem cell treatment. The clinical protocol to use stems cells to treat Canavan patients should be approved within 24 months by the Food and Drug Administration. The subsequent clinical trial would include 15 children with Canavan Disease.
Yulia and Gili Ben Moshe decided to approach Dr. Leone and asked her to put Lavi on the testing group of the new process.
"Lavi's psycho-motor development has been improving greatly since the pharmacological therapy began,” says Leone. “The therapy is preserving his brain but is not curing the disease. While Lavi and many other children are struggling to change their prognosis, scientists are working incessantly in my laboratory to bring a cure to fruition. The timing and success of a cure for Canavan Disease fully depends upon the availability of appropriate research funds that would also model the cure for other neurodegenerative diseases.”
Dr. Leone’s research is funded only partially by the government. For her research to be completed and approved, she needs an estimated $ 1.5 million.
This couldn't deter the courageous parents. They decided to go fund raising for the complementary funds.
They first started in Israel, where they raised the money for Lavi's medical treatments, and then they decided to start an international appeal. They partnered with an Israeli start-up, called give2gether, which developed an innovative platform for micro-philanthropy. They built a website which chronicles Lavi’s life Journey, and enables grass roots fundraising.
Yulia and Gili assure that all the money raised will to fund the research. They hope that each donor will tell Lavi's story to at least 10 friends, and this way, even with small donations they will be able to raise the necessary funds to save their child.
“It’s a very hard for my wife and me to face this ordeal,” says Gili Ben Moshe, “but Lavi came into this world with a purpose. We believe it’s our privilege to fight for Lavi’s life and for the lives of other children who have this lethal disease.”
Blessings Doreen Cohanim C.Ht
www.HypnoCruise.com
PLEASE HELP!
Save Lavi's Life
https://www.paypal.com/cgi-bin/webscr?cmd=_s-xclick&hosted_button_id=10181857
Any donation is a blessing, your amount and name will be posted here....Free Free To contact me via email or via my website.Also join us for Distance Energy Healing...
Please Help With This Fundraising To Save Lavi's Life.... - My Special Inner Child
Dec. 1st, 2009 – Yulia and Gili Ben-Moshe, who live in a small town in Israel, were confronted with every parent’s nightmare: their third child, Lavi then three months old, was diagnosed with Canavan Disease.
At the first moment they didn't understand what it means, but after a short while they learned that children with Canavan disease first lose their sense of sight, then their hearing and their motor function. Usually, before age 4, the disease kills off their brain cells and the children die.
It took them 24 hours to start the war to save Lavi. They went online and found Dr. Paola Leone, the leading American expert on Canavan disease. They realized that Dr. Leone, works out of the UMDNJ-Robert Wood Johnson Medical School, is developing innovative treatments for Canavan patients.
Ten days later the couple was on a plane on its way to the US. They met with Dr. Leone who put Lavi on her pharmacologic therapies, which resulted in delaying his brain deterioration. This was the first hopeful sign.
Today, at 18 months, Lavi is considered a medical miracle. He is progressing neurologically – he can see and hear -- defying the dire diagnosis.But unfortunately the existing Drugs alone will not retard the progression of the disease. The question for the parents was one: What else can we do to save Lavi?
While staying in New Jersey, they learned that Dr. Leone is conducting basic scientific stem cell research that holds hope for Canavan patients. Since the disease kills off brain cells, Dr. Leone believes that implanting stem cells into the brains of children with Canavan would result in the proliferation of functional brain cells. She is now testing her theory in the laboratory, and intends clinic testing as soon as she scientifically proves the efficacy and the safely of the stem cell treatment. The clinical protocol to use stems cells to treat Canavan patients should be approved within 24 months by the Food and Drug Administration. The subsequent clinical trial would include 15 children with Canavan Disease.
Yulia and Gili Ben Moshe decided to approach Dr. Leone and asked her to put Lavi on the testing group of the new process.
"Lavi's psycho-motor development has been improving greatly since the pharmacological therapy began,” says Leone. “The therapy is preserving his brain but is not curing the disease. While Lavi and many other children are struggling to change their prognosis, scientists are working incessantly in my laboratory to bring a cure to fruition. The timing and success of a cure for Canavan Disease fully depends upon the availability of appropriate research funds that would also model the cure for other neurodegenerative diseases.”
Dr. Leone’s research is funded only partially by the government. For her research to be completed and approved, she needs an estimated $ 1.5 million.
This couldn't deter the courageous parents. They decided to go fund raising for the complementary funds.
They first started in Israel, where they raised the money for Lavi's medical treatments, and then they decided to start an international appeal. They partnered with an Israeli start-up, called give2gether, which developed an innovative platform for micro-philanthropy. They built a website which chronicles Lavi’s life Journey, and enables grass roots fundraising.
Yulia and Gili assure that all the money raised will to fund the research. They hope that each donor will tell Lavi's story to at least 10 friends, and this way, even with small donations they will be able to raise the necessary funds to save their child.
“It’s a very hard for my wife and me to face this ordeal,” says Gili Ben Moshe, “but Lavi came into this world with a purpose. We believe it’s our privilege to fight for Lavi’s life and for the lives of other children who have this lethal disease.”
Blessings Doreen Cohanim C.Ht
www.HypnoCruise.com
PLEASE HELP!
Save Lavi's Life
https://www.paypal.com/cgi-bin/webscr?cmd=_s-xclick&hosted_button_id=10181857
Any donation is a blessing, your amount and name will be posted here....Free Free To contact me via email or via my website.Also join us for Distance Energy Healing...
Please Help With This Fundraising To Save Lavi's Life.... - My Special Inner Child
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