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@simplyann
dreamers ftw
Faith
Truth
Belief
Power
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The Canary Press is Seeking Short Stories - Pays up to $200/story
Writers have until January 21st to submit their short stories to the 10th issue of The Canary Press (est. 2013), an illustrated literary magazine published in Melbourne, Australia. Each issue showcases stories from emerging writers next to a number of the very best storytellers from Australia and abroad.
The 10th issue has an open call for “general” short stories.
Keep reading
The way that we learn about Helen Keller in school is an absolute outrage. We read “The Miracle Worker”- the miracle worker referring to her teacher; she’s not even the title character in her own story. The narrative about disabled people that we are comfortable with follows this format- “overcoming” disability. Disabled people as children. Helen Keller as an adult, though? She was a radical socialist, a fierce disability advocate, and a suffragette. There’s no reason she should not be considered a feminist icon, by the way, and the fact that she isn’t is pure ableism- while other white feminists of that time were blatant racists, she was speaking out against Woodrew Wilson because of his vehement racism. She supported woman’s suffrage and birth control. She was an anti-war speaker. She was an initial donor to the NAACP. She spoke out about the causes of blindness- often disease caused by poverty and poor working conditions. She was so brave and outspoken that the FBI had a file on her because of all the trouble she caused.
Yet when we talk about her, it’s either the boring, inspiration porn story of her as a child and her heroic teacher, or as the punchline of ableist, misogynistic jokes. It’s not just offensive, it’s downright disgusting.
And no one talks about that teacher being disabled. Anne Sullivan was blind and graduated from a school for the blind. Although she did gain some vision later in life though a series of operations, she was still profoundly visually impaired. She learned sign language because she had a blind and deaf school friend. They developed the methods she would later use with Helen Keller together so that they could communicate. In this story, we have the to quintessential ways that our culture deals with disabled people’s stories. Either their disability is erased, like Anne Sullivan’s and Harriet Tubman’s (She had a seizure disorder sustained when her “owner” gave her a severe head wound) or they are reduced to their disability, as Hellen Keller so often is.
Anne Sullivan’s case is particularly disgusting to me, because it shows a person developing ways to live with her own disability, and the value of female friendships both, and how both that friendship and the skills learned to sustain it in the face of their mutual disability would change the life of one of those friends, and enable her to help someone else.
My mind just gets more and more blown every time I find out just how much disability has been deliberately erased from history–and from daily life, for that matter.
yup yup yup THIS. so much of helen keller’s stories have been so focused on her deafblindess that it ignores awesome stuff like how she wrote books, how she was a socialist, an activist, etc etc. And people took away from these stories that deafblind are to be pitied and treated as a ‘show’. (like, look omg a deafblind person can learn a language and communicate wow what a miracle. it’s not a miracle because deafblinds do that all the time.) Then nowadays people still treat deafblind shitty with low expectation. If we were to truly honor Helen Keller’s life, we’d have treated deafblind, deaf, and blind people better.
Leandra Becerra Lumbreras was the last known survivor of the Mexican Revolution. Artist Nao Bustamante and a small crew made a trip to Zapopan, Mexico to meet her.
Leandra Becerra Lumbreras was the last known survivor of the Mexican Revolution, the last living soldadera. In January, I travelled to Zapopan, Mexico with the artist Nao Bustamante, who has been learning about the women who fought in the Mexican Revolution. In the fall, stories about her longevity appeared in the news – she was then 127 years old, and in these stories, she was identified as the leader of a battalion of Adelitas. The artist took me on her pilgrimage to meet Leandra. I was part of Bustamante’s team: facilitating conversation, translating – language and history – this was my role.
Caribbean, 1979 - Alex Webb Grenada Grenada Barbados Port-au-Prince
Question: Where is the best place to have a work placement? Answer: A Bookshops, always a bookshop… (I got 7 books for free, I’m in heaven guys)
saved by a Palestenian-Jew who allegedly rocked some fly chancletas and washed the soles of people who were literally beneath him, i am jerald and debra's undefeated product of grace.
the writer — blvcker
12 Ways To Say No Gracefully (Without Saying “Maybe Later”)
(Download a printable, poster-sized PDF version of this graphic here.)
Remember: You don’t have to justify your no. Resist the temptation to explain why it’s not a good fit, why you feel stomach-churny, or why you need to build more trust. Avoid making excuses. When you state what’s true about your experience, it’s harder to argue with you. You get to have boundaries. “No” is a complete sentence. When you say what you do want instead, it gives you both something to work from (if you want that.)
Wow. Thank you to whoever made this.
Thanks @acehotel for being an amazing host in Seattle • #vscocam #seattle
The Sisters
Click to Give here: http://www.youcaring.com/medical-fundraiser/help-bisrat-haven-/224911
August 24, 2014
Bisrat (Haven) is 22 a years old young woman who has been hospitalized since April, 2014, for an Autoimmune disease called Lupus. Prior to her diagnose, Haven was a senior fulltime pre-med Neuroscience major student at University of Southern California (USC), Los Angeles. She was supposed to have been graduated on May 16, 2014, and had a plan to apply for a medical school. Instead of taking a break for the summer (2014), Haven was registered to take MCAT courses right after her graduation (May 16), then take the MCAT exam in July of 2014. She was planning to apply for a medical school by September 2014 and to do the research at UCLA.
Unfortunately, two weeks before her final exams, she got ill and had to take incomplete for all of her classes, and forced to cancel the MCAT courses and MCAT exam as well.
Lupus is an autoimmune disorder, in which the body’s immune system attacks its own healthy cells and tissues and it is characterized by periodic episodes of inflammation of a joint, tendons, other connective tissues, and organs.
Haven is the type of daughter any mother would love to have. Until the time she felt ill, she was healthy, cheerful and active in school and community activities, including in volleyball, swimming and dance. In fact, if she didn’t have schoolwork or sport practices, she would volunteered at Food Bank or in the Community Health Services. Haven has always been considerate to her brothers and the entire family. She has always been well liked by her teachers and administrators not only for her outstanding school performance but also for her superb social skills. In addition to her top score in SAT exam, it was the combination of these desirable qualities many prestigious universities accepted her application. Haven chose USC where she attended for the last 4 years until she became hospitalized in April 21, 2014.
Even though she was taking full-time pre-med courses and involved in cancer cell research LAB at USC, Haven managed to get involved in other activities including in teaching 4th and 5th grade children in LA. In order to pay her housing monthly bills, she took an RA job at her dorm where she was responsible of managing student residents.
Haven has always spent her spring and summer breaks doing something meaningful. In May 2013, for instance, she joined a program called “Volunteers around the World” and went to Dominican Republic to serve in a hospital.
In summer 2013 she was given medical research opportunity through USC and went to Ethiopia, volunteered at Ayder hospital, Mekelle for two months. As it was her first visit to Ethiopia, she met many medical students, learned the immense medical need of the people and inspired by the selfless medical doctors. This was well documented in the research paper she presented to her University.
During her last semester, Haven experienced acute joint pain in her wrists and ankles for days. On April 7, 2014, she called home at 2 am to tell us she wasn’t feeling good, brought her home and advised her to rest. As her health was not improving we took her to ER several times, but the doctors couldn’t figure out. It was the most horrifying experience for the whole family to witness almost every part of her body was attacked.
On April 21, 2014, she got admitted to the hospital had seizure and aspirated pneumonia involving her right lung and the doctors had be put her in breathing tube. It took almost a month to treat the pneumonia. A team of doctors at UCSD were involved trying to figure out the right diagnose because Lupus is difficult to screen, unpredictable and it can attack any part of the body.
Since then she had been at the intensive care unit (UCSD Medical Center 200 West Arbor Dr. Hillcrest, San Diego California, 92103) for 4 months.
Current Health Issues
Health Issue Date Noted
Mononucleosis 04/16/2014
Anemia 04/16/2014
Seizure 04/25/2014
Positive Coombs test 04/25/2014
Microcytic anemia 04/25/2014
Pneumonia involving right lung 04/25/2014
Lupus cerebritis/autoimmune disease 04/26/2014
Lactic acidosis 05/03/2014 & 05/03/2014
Pneumonia 05/03/2014
Acute blood loss anemia 05/04/2014
Tachycardia 05/08/2014 & 05/08/2014
Acute respiratory failure 05/09/2014
Neuropathy 05/09/2014, 05/12/2014 & 05/19/2014
Dispute all the complication Haven had gone through, the Medical team have done all they could to save her life and now she is out of danger. However, her illness requires the continuous medical care and management, which requires resources.
Currently, Haven is in the hospital receiving therapeutic treatment. Because of the seriousness of her illness, she will require longer therapeutic treatment after she is discharged. Lupus requires continuous attention. As the disease has affected her body, she is unable to move her lower body, which requires 24 hours care. In addition to the therapeutic work, she will have to undergo surgery in the future on three of her fingers that were damaged by the disease.
We have genuine limitation in providing the needed medical, and other supports our daughter needs. For this reason, we have no one to turn our face to but to our community. While we are elated to see our daughter’s health improving, our inability to meet her continuous care has made spend sleepless nights.
The estimated recovery time is between 6 months to a year, which includes many hours of intense therapy. The estimated expenses required to resume her therapy and healthy living after inpatient rehab is $65,952 for a year.
Thank you,
- See more at: http://www.youcaring.com/medical-fundraiser/help-bisrat-haven-/224911#sthash.rZopL0ri.dpuf
Chicago Blue Hour, a photo from Illinois, Midwest | TrekEarth
The start of the school year in Ferguson was pushed back another week, to Aug. 25th. In the meantime, children are able to spend the day at the library or local churches.
The Balance
"I was about to leave for work the other day, so I stopped in her room to wake her up. And the first thing she said was: ‘Dad, I need a surprise.’ I said: ‘You need a what?’ She said: ‘I need a surprise.’ So I ran to the store and got her a doll, brought it to her, and went to work.”
(Nairobi, Kenya)
#DaddyDaughter #LOVE #priceless