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Today the U.N. panel ruled Wikileaks founder Julian Assange has been arbitrarily detained by Sweden and the UK since his arrest in London in 2010.

In a public statement, the expert panel called on the Swedish and British authorities to end Mr. Assange’s deprivation of liberty, respect his physical integrity and freedom of movement, and afford him the right to compensation.
This is the fund for Julian Assange and WikiLeaks staff's legal expenses. The fund is for legal fees, and does not go to WikiLeaks' core operations. It is therefore unaffected by the banking blockade in force against WikiLeaks.
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Gabby is one of many special needs cats VOKRA cares for each year. Gabby’s a girl with a wobble. The official term is Feline Cerebellar Hypoplasia (CH), and it’s a neurological condition that results in walking and balance problems. The cost of medical care and rehab for these special cats is high and they could use some help.
Gabby is one of many special needs cats VOKRA cares for each year. The cost of medical care and rehab for these special cats is high so we could use your help today. We estimate it will take $2,000 to provide Gabby with the best quality of life possible.
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Amy began by handing out warm clothing and baby food in Greece to refugees making long and dangerous journeys to reach safety in Europe. She soon found out that many people on these journeys are ill-informed about their rights and the risks and dangers ahead. Now she is fundraising to establish a mobile information service for refugees and migrants to help make them safer and better informed.
Thousands of people are travelling across Europe vulnerable to people smugglers, dangerous journeys and exploitation. Our campaign is to establish a mobile information service for refugees and migrants to help make them safer and better informed.
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Sadly, Dave passed away on January 28, 2016, at the age of 41. Classmates of Dave from BHS class of '91 have established an education trust fund for Jacob and Emma, Dave and Isabelle's two young children.
BHS Grads of '91 have established an education trust fund for Jacob and Emma, Dave and Isabelle's two young children. We have fond memories of Dave from school. Let's help Dave's kids create lasting memories from their experience at school.
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OJ is suffering from Pompe disease, a rare multisystem genetic disorder. The disease has reduced OJ’s ability to breath on his own without a ventilator, made it difficult for him to walk, and has confined him to his bed for a little over a year. Thankfully, medication has been found to cure this disease and he is currently waiting for test results to come back before starting treatment. A friend set up a fund so OJ can pay for things he'll need once out of the nursing home (such as rent, furniture, utilities, food, etc.)
Our friend, OJ "Juice” Williams, needs your help to beat a rare genetic disorder called Pompe Disease. Let’s come together as friends and family and give "Juice" the boost he needs to conquer this beast. Your support is greatly appreciated.
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The #Startland initiative plans to raise another $150,000 through the FundRazr crowdfunding platform to provide refugees entering the tech workforce with free workspace, laptops, and smartphones. “We’re in desperate need of new coders,” Armstrong said. “It’s sort of a win-win because the technology sector needs new people, and there is a skills gap.” http://ow.ly/XP6kd
Startland to provide refugees with free coding classes, workspace, laptops and smartphones
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Between 1845 and 1855 over one million people fled starvation conditions in Ireland. Around 100,000 made their way to Glasgow. Coiste Cuimhneachain An Gorta Mór (Great Hunger Memorial Committee) has been formed to build a permanent memorial to those who died of starvation or were forced to emigrate. To find the best design for the long-awaited memorial, CCAGM is launching a design competition open to sculptors and artists at any stage in their career.
To find the best design for our long-awaited memorial to An Gorta Mór, CCAGM will be launching a design competition open to sculptors and artists at any stage in their career. The prize for the winning design is £5,000.
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Last week Flower could not breathe and had to be rushed to the vet for emergency surgery. Flower didn't ask for this life, it was thrust upon her by a greedy breeder who wanted to make miniature bulldogs. What they created was an entire litter of puppies with spina bifida and lifelong challenges. Flower's family just paid a lot of money to save her sister, and are overly extended financially.
Special Needs Baby Miss Flower ( Surgery to save her life)
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Diane's very dear friend Sarah lost her only brother in a tragic car accident. Frank left behind a wife and three young children. Diane has been wanting to do something for this family for some time, so she started this campaign. She has several items that she will hand make in exchange for a donation. You can receive one of her fabulous crafts, and help Frank’s family too.
In June of 2014, my very dear friend Sarah lost her only brother in a tragic car accident. Frank Lyman III left behind a wife and three young children.
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How to help the people of Flint, Michigan. http://ow.ly/XU64g
Flint's drinking water became contaminated with lead in April 2014 after the city, while under the control of a state-appointed emergency manager, temporarily switched its source from Lake Huron water treated by the Detroit Water and Sewerage Department to water from the Flint River, ...
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Hudson has a condition called Tuberous Sclerosis Complex (TSC) which causes tumors to show up in major organs of his little body. He has endured several surgeries and is proven to be a fighter. Sunshine on a Ranney Day is fundraising to create a Dream Therapy Room for Hudson to thrive! The nonprofit organization
renovates rooms to bring joy and light into the home of a child with long-term illness.
Meet Hudson ! Hudson is a six year old with Tuberous Sclerosis Complex a very rare disease that has many unknowns. Sunshine on a Ranney Day is going to create a Dream Therapy Room for Hudson to thrive! YOU can be part of this Super Cool Therapy Room !
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Jeffrey recently had major, life-saving heart surgery. His family met various other struggling families going over the weeks spent in the hospital, and he would like to do everything possible to change these family experiences for the better. That’s why he launched Jeffrey Has Heart, a non-profit charity that seeks to financially assist families of teens undergoing treatment for congenital heart disease.
Jeffrey Has Heart seeks to financially assist families of teens undergoing treatment for congenital heart disease. We are raising funds for these families as well as the kick-off banquet on March 31, 2016. We are a 501(c)(3) non-profit.
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