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Pretty Smiling Multiethnic Young Adult Woman with Eyes Up and Over Isolated on a White Background. All plans come as a Standard license, and can be upgraded to an Enhanced license at any time. Travel north from Bridgeport through Fairfield to Sport Hill Road in the small, upscale town of Easton, Connecticut and you eventually come to Helen Keller Middle School. That there’s no marker at the house is a bit surprising, for there was a time when Keller was one of the most famous people in the world, better known even than presidents and kings.
Born in 1880 in Alabama with sight and the ability to hear, Keller lost both senses at 19 months due to disease, most likely scarlet fever or meningitis.
In 1887, an extraordinary young woman named Anne Sullivan traveled to the Keller home to be her teacher. Just twenty years old when she arrived in Alabama, Sullivan began a remarkable relationship with Keller that lasted five decades. Shocked members of the scientific and teaching communities studied Keller and Sullivan’s innovative techniques.
Some sought to portray Keller’s situation as an unfortunate but ultimately holy burden delivered from on high. Sullivan and her lover John Macy were both radicals and Keller learned a great deal from them. As a Wobbly, Keller walked picket lines, organized support for strikes and, after learning to speak, addressed rallies and forums around the country about the need for a revolutionary transformation of society. Along with millions around the world, Keller recoiled in horror at the butchery of the Great Imperialist War.
Whatever Keller’s overly trusting nature or occasional naivete, they are trivial points compared to her accomplishments. But those who relegate Keller to perpetual childhood do her legacy and themselves an injustice, for the day Anne Sullivan reached through the darkness was the turning point of Keller’s life, not its end.
Bridgeport native Andy Piascik is a long-time activist and award-winning author who has written for Z Magazine, The Indypendent, Counterpunch and many other websites and publications. Neet Danes - Neet RescuEJohn and Cynthia NeetA  We are thrilled to collaborate with other dedicated rescue organizations. Determined to find answers, Vivian reached out to a family friend who is a cardiologist in the United States.
In June 2015, Vivian came to Mayo Clinic's campus in Rochester, Minnesota, for an evaluation and diagnosis.
Vivian underwent surgery in September 2015, supported by a rotating cadre of family members and friends, including her loving mother, Ruby.
The high-quality care Vivian received is made possible through the generosity of benefactors who previously gave to hypertrophic cardiomyopathy research and education. The family's gift, in honor of Vivian's parents Paul and Ruby Tsai, recognizes medical excellence and innovation at Mayo Clinic.
Learn more about the Division of Cardiovascular Diseases and the Division of Cardiovascular Surgery.
These treatments could help correct the severe spinal curve that had developed quickly during a growth spurt, her doctors said. The Christophersons learned about Camden's condition shortly after a family move put her in a different school district. Designed to treat moderate to severe scoliosis, vertebral body tethering typically is recommended for adolescents during puberty who are still growing. Teresa's investigation took her and Camden to the Philadelphia Shriners Hospital for Children. In Philadelphia, Camden and Teresa met with surgeons that had pioneered vertebral body tethering. Although it's possible vertebral body tethering may be the last treatment Camden needs for scoliosis, the long-term results for the surgery aren't clear yet because the procedure is so new. From Teresa's perspective, it wasn't an easy road, but the effort to find an alternative solution for her daughter was well worth it.
For 33-year-old Tara Brigham of Jacksonville, Florida, living with a heart condition since birth wasn't something that was going to get in the way of living an active normal life.
A Minnesota native, Tara was diagnosed with enlargement of the heart during a routine checkup when she was 1 year old. Tara's heart was monitored closely by her doctors at Mayo Clinic and later a hypertrophic cardiomyopathy specialist at the University of Minnesota. Despite the scare and a challenging recovery, Tara resumed her life, finishing high school, attending college and graduate school, and getting married. Tara is grateful that her transplant has enabled her to experience so much more of her life.
Audra Popp has a rare tumor – anaplastic pleomorphic xanthoastrocytoma, also known as anaplastic PXA. Audra had 20 proton beam therapy sessions to try to destroy fast-growing cells possibly left behind after surgery. After Audra's fourth surgery, her surgeon initially suggested radiation therapy, but that wasn't in the cards. After Audra's most recent surgery, her Mayo Clinic team had a new weapon in their arsenal – proton beam therapy.
A registered nurse, Audra lives in Royalton, Minnesota – a three-hour drive from Rochester.
Audra had proton beam therapy in the summer – her favorite season – and took full advantage of her time in Rochester.
Raegan Cury didn’t worry at first when she developed a cough in early 2002 that wouldn’t go away. Even her husband, a pulmonologist, wasn't too worried, until she received a surprising diagnosis. Raegan, who lives in Atlantic Beach, Florida, had surgery to remove the cancer and woke up with just one lung, due to the extent of the disease. But they also headed to Mayo Clinic's campus in Florida to explore the possibility of lung transplantation.
A lung restoration center under construction on Mayo Clinic’s Florida campus could change that by making many more donor lungs viable for transplant. Growing up on a farm in central Florida, Paige Douglas enjoyed a unique childhood, caring for a menagerie of animals, horseback riding, even barrel racing at local rodeos. But, when she was 10, Paige inadvertently hit her left knee while bouncing on a trampoline.
Her knee became so sensitive that the slightest touch or inadvertent bump would “bring excruciating pain, sending me to the ground, screaming and crying,” she recalls. Paige visited countless doctors near her home in Ocala, Florida, trying different medications, topical treatments and steroid injections. The team developed a customized treatment plan for Paige aimed at not only removing the cancer but saving her leg. To help bring awareness to others about sarcoma, Paige created “Team Paige,” an online support group. Last fall Paige nominated the Mayo team for the Sarcoma Alliance 2015 Outstanding Care Award. Stewart Rosen was beyond anxious when he learned he had a tumor the size of a walnut by his right ear. Stewart noticed a change in his hearing in his right ear, and a friend had recommended he see an ENT (ear, nose and throat) specialist.
Acoustic neuromas are noncancerous, usually slow-growing tumors that develop on the main nerve leading from the inner ear to the brain.
Much to Stewart's surprise, his Mayo Clinic doctors told him they'd had a cancellation and could perform his surgery the next day.
Stewart continues to be checked to make sure his acoustic neuroma doesn't recur – a very slight possibility. Our daughter, Mallory, was born with several congenital defects known cloacal exstrophy (OEIS – omphalocele, bladder exstrophy, imperforate anus and spinal defects) found in 1 and 400,000 live births.
We instantly became patients of the Maternal Fetal Medicine team and were both closely monitored until birth. The defects identified at birth were more serious and complicated than originally predicted through prenatal monitoring. Our family has lived, witnessed and felt Mayo Clinic’s mission and values firsthand, and continue to experience it on a regular basis. Mallory has endured four major surgeries (largest surgery – six hours on day 2 of life, involving 3 specialists teaming up to complete reconstruction of bladder, pelvis and bowels), multiple MRIs, hundreds of procedures, and numerous appointments. Learn more about Mayo's Neonatal Intensive Care Unit and the Mayo Clinic Children's Center. These words from His Holiness the Dalai Lama resonated with Mayo Clinic staff and guests gathered to hear a special talk on "Compassion in Health Care" on Monday, Feb. His Holiness the Dalai Lama spent a good deal of time in his talk emphasizing the "sameness" of all human beings.
In a world of 7 billion people, the Dalai Lama says it is important to educate people that we are all human beings.


When we feel anger or irritation toward someone else, it is important to ask ourselves whether that person has been our "enemy from birth," according to the Dalai Lama. The Dalai Lama offered his advice for dealing with a patient who has received a difficult diagnosis. He also noted it was important to be honest with a person about a diagnosis, so that person can be prepared for the consequences.
Biased: While a person may have compassion and loving kindness, it may be limited to those that they are related to or only people they know.
Unbiased: Through awareness, 7 billion people can come to think of each other as brothers and sisters and to realize that their futures are interlinked. Even though she's just 24 years old, Megan has had a lifetime's worth of trials and tribulations. At the age of 21, just two months after Megan married her high school sweetheart, she was presented with another challenge.
Megan would require an extended course of chemotherapy to shrink the tumor before she could have surgery to remove it. Soon afterward, she was dealt another blow – one that must have been especially painful for someone who just completed cancer treatment. Everyone who signs up gets full access to our entire library, including our curated collections. Our Standard license allows you to use images for anything, except large print runs over 500,000+ or for merchandising.
Once you have downloaded your image, you have life-long rights to use it under the terms of the license purchased. Go west a few miles to the other side of Easton and you can see the house where Keller lived from 1939 until her death in 1968. Circa 1920, she was perhaps the second most recognizable Westerner on the planet behind only Charlie Chaplin – also a radical who, like Helen, used his brilliance to speak for the unrepresented. Her parents were of some means and she was thus spared institutionalization, the fate that befell thousands of blind and deaf working class children of the time. In a few months of incredibly intense work, Sullivan drew on teaching techniques she had barely just learned and helped Helen find herself. Medical experts were put in the awkward position of having to explain why so many of the great minds of the time had been so thoroughly upstaged by an undereducated woman driven primarily by a will of iron. It was mostly through her own experience, however, that she came to understand that health problems such as hers were often socio-economic in nature. She soon flew past the Socialists’ conservative electoralism, however, and joined the Industrial Workers of the World, then in its heyday and sinking deep roots among the working class. On one occasion, she insisted on marching with the unemployed in Sacramento despite threats of state violence. When she joined the vibrant women’s movement of the 1910’s that shook the country to its core, Keller allied herself with the radical wing of the movement. She was appalled that working class boys and primarily female non-combatants died by the millions so a select few who already had too much could accumulate still more.
Edgar Hoover a close acquaintance even as the FBI was ruining the lives of many of her friends and associates. The young girl bursting with life is inseparable from the adult who stood arm in arm with the immigrant women who led the great Bread and Roses Strike. The Centre for Research on Globalization will not be responsible for any inaccurate or incorrect statement in this article. With renewed resolve, she consulted with specialists, reached out to friends, and sought referrals. This procedure corrects the curve of the spine by connecting two or more of the spinal vertebrae. Larson at Mayo Clinic, they discussed a variety of possibilities, including the VBT procedure. The surgeon attaches a cord to each of the screws and then pulls and secures the cord, so the vertebrae are cinched together on one side and splayed open on the other, correcting the curve.
Shriners Hospitals for Children and Mayo Clinic have a close relationship that dates back to Mayo Clinic's founders. At this time, though, it looks to be an encouraging step forward in the scoliosis treatment choices available to teens like Camden, who is happy she had the opportunity to give it a try. In fact, she says the heart transplant she received six years ago as a result of her condition has made her life even more fulfilling. While she had not had any symptoms of a heart problem since birth, the enlargement was significant enough that her physician at Mayo Clinic's Rochester campus suggested that a biopsy of her heart should be done right away. Over time, she became increasingly symptomatic as her heart failure worsened, and Minnesota winters were especially difficult. She is currently a medical librarian at Mayo Clinic's Florida campus, and she has been healthy and has led a fairly normal life in the six years since her transplant. She's had five craniotomies since 2001, and she has a scar from her right ear to the crown of her head as evidence.
Buckner says a genetic alteration in the tumor that was removed in Audra's last surgery showed a mutation that makes the tumor cells more vulnerable to a new drug combination. She explored the area with tours of Mayo Clinic's historical homes and buildings, a walking food and history tour, a trolley tour and concerts by the river. She was a healthy young woman, athletic, a former gymnast, and her initial chest X-ray showed what looked like pneumonia. Mayo Clinic transplants more organs than any center in the United States, and the Florida campus is one of the nation’s leading lung transplant centers.
During Reagan's lung transplant in 2004, he washed her remaining native airways with a chemotherapy solution to try to prevent any remaining cancer cells from inhabiting Raegan’s newly transplanted lung.
The next year, the lung allocation system changed, and the guidelines stated that outcomes for patients with Raegan’s disease were considered too uncertain to warrant transplant of a precious donor lung.
The center, now under construction, could make enough lungs available to enable transplants for people who currently don’t meet the waiting list criteria.
She had synovial cell sarcoma, a soft-tissue cancer that typically occurs near the joints in the arm, neck or leg in young patients. Despite the 250-mile distance between her home and Jacksonville, Paige chose to undergo the treatments at Mayo. According to the organization, the award is usually presented to one individual but Paige’s nomination moved the group so much that it honored everyone. And with the surgery he'd need to remove this tumor, Stewart knew that he'd lose hearing in his right ear. That doctor detected a major difference in hearing between Stewart's ears and ordered an MRI to rule out a brain tumor. After Mallory’s 20-week gestational ultrasound, we were referred to Mayo Clinic in Rochester, Minnesota, from Mayo Clinic Health System – Red Cedar in Menomonie. In the beginning, we wondered how these abnormalities were missed in the extensive prenatal monitoring. We are thankful for Mayo Clinic and know that its clinical practice, education and research saved Mallory’s life and continues to give us a bright outlook for the future.
She’ll have medical challenges throughout life, but with the gift of Mayo Clinic, she is well on her way to living a happy, healthy and “normal” life. We are thankful for strong dedication at all levels (Appointments, coordinators, social workers, HUCs, Housekeeping, CNAs, Child Life, nurses, NPs, flight crews, residents, fellows and consultants). The monk had spent five years as a hermit in the mountains with very little by way of physical comfort.
He advises people to then familiarize themselves with those positive emotions and train themselves to focus on those emotions. But a series of events, medical and otherwise, led her on a different path – an educational path that culminated with her sharing her surprising story at the Fiesta Bowl in Arizona on Jan. The chemotherapy cocktail was so powerful that Megan was cautioned not to kiss her new husband, as the side effects could be passed onto him. Doctors found Megan had a rare gene that causes Li-Fraumeni syndrome, which affects only about 400 people in the U.S. Still, Megan prefers to discuss the upside of her journey -- her supportive family, friends and Mayo caregivers who have encouraged her through her trials.
She has a passion for educating others about the gene that has changed her life — and she wants to be there for young adults or children who are going through the same thing. If at any time you're unsatisfied with your experience with us, you can cancel your subscription. Beginning in 1887, Keller’s teacher, Anne Sullivan, helped her make tremendous progress with her ability to communicate, and Keller went on to college, graduating in 1904. If you don’t know the house’s location, however, you’ll never find it, for there is no stone or plaque marking the spot even though Keller lived there longer than anywhere else. As a young girl, Keller developed a homemade sign language that she used to communicate with those close to her. Orphaned at a young age, she had lived for many years in a Massachusetts institution alongside mentally ill adults who often preyed on the children in their midst. And the self she helped Helen find contained one of the greatest hearts and minds of that or any time.


Had she acquiesced and remained polite, virginal and respectable, Keller could have become part of the high society scene.
She indicted industrialism and capitalism as the main causes of disease, blindness and deafness included.
The IWW “points out that the trade unions as presently organized are an obstacle to unity among the masses, and that this lack of solidarity plays into the hands of their economic masters,” Keller wrote after becoming a member. She became an impassioned advocate of, among many other causes, easily accessible birth control. She lectured tirelessly against the carnage and, when dissent became virtually illegal after the US entered the war, she stood strong and true behind the thousands who were locked up for demanding peace. Unbeknownst to her, Hoover had also for decades amassed a thick dossier on activities of hers that he considered subversive. Her books were translated into many languages and she championed the rights of the deaf and blind into her eighties. Although she lived in relative comfort, Keller refused to turn away from the ugliness of class society, choosing instead to do what she could to eradicate it. The Center of Research on Globalization grants permission to cross-post original Global Research articles on community internet sites as long as the text & title are not modified. However, she began to lose strength in her early 30s and went to the doctor with her father, Paul. But as she watched another member of her family struggle with symptoms she recognized in herself, her own condition became harder to ignore.
While eating dinner, Vivian would often have to lie down for half an hour before returning to her meal because she would become so tired and lightheaded. Finally, she received a precise diagnosis — apical hypertrophic cardiomyopathy, a disease in which the heart muscle becomes abnormally thick.
Schaff immediately to discuss the possibility of the procedure she had been told did not exist — an apical myectomy. Not only will this generous gift benefit Mayo Clinic patients, but patients throughout the world, including East Asia, where the Tsai family calls home. So when doctors told her, at age 13, that she had to wear a brace for 22 hours a day to combat scoliosis, and surgery to fuse her spine was likely in her future, Camden was devastated. And her mother, Teresa Christopherson, wasn't ready to accept that a brace and fusion surgery were her daughter's only choices. She was fitted for a brace, but due to the severity of her condition, her doctors were concerned it wouldn't be enough to correct the problem.
Metal screws and rods typically are used to hold the vertebrae together, so they can heal into one solid unit. In 2015, Shriners Hospitals joined the Mayo Clinic Care Network, a national network of organizations committed to better serving patients and their families through physician collaboration. She was diagnosed with hypertrophic cardiomyopathy, a disease in which the heart muscle becomes abnormally thick.
Tara went into ventricular fibrillation and was taken to the hospital where an automated external defibrillator, or AED, was used to restore her normal heart rhythm.
Audra is the first person at Mayo Clinic with anaplastic PXA to be treated with proton beam therapy. She also took advantage of classes offered at the Mayo Clinic Cancer Education Center, including tai chi, Reiki, nutrition, meditation and stress management.
Mayo Clinic is collaborating with United Therapeutics, which has developed technology to sustain and rejuvenate donor lungs, making previously marginal lungs suitable for transplantation and extending the time lungs remain viable. After an exploratory surgery in 2001, doctors told her she had a neuroma, an area of increased sensitivity and pain that often develops after physical trauma to a nerve.
She made a five-hour roundtrip five days a week for five weeks. “It was hard but I wanted to maintain a sense of normalcy for my family and I trusted this team … doctors who care, show compassion, and genuinely took time to know me as a patient,” she says. But Stewart, an accountant by day and violinist by night, worried that removing the tumor, an acoustic neuroma, might affect his ability to play music.
It was explained that Mallory’s condition of OEIS is so rare that the Maternal Fetal Medicine team did not know to even look for that type of defect. Almost every person on Mallory’s team was unfamiliar with her condition of OEIS, but no one ever feared the unknown. From the day she was born, Mayo Clinic has given us hope and realistic solutions to her “never seen before” problems.
When you read about her on paper, you expect to notice great physical abnormalities, but to the untrained eye, she is a happy, healthy, thriving toddler.
He says he is impressed with Megan’s resiliency and ability to understand what her treatment program would require.
Curtis were invited to watch the game from a suite at the stadium in Glendale, Arizona, and a brief video of her story was shown on the big screen. Treatment options and educational opportunities were few, however, and her quality of life was minimal. Staff were abusive and apathetic and the facility was little more than a holding cell which few left alive. While advocating for better treatment, Keller insisted that the greatest emphasis be placed on poverty and unsafe working and living conditions as the root of illness.
Echoing not the Suffragettes so much as Emma Goldman, she dared to suggest there might be more to female sexuality than reproduction. Although it would’ve surprised no one had Keller been called before a Congressional committee or two, Hoover apparently thought better of subjecting an internationally acclaimed seventy-year old woman who could neither see nor hear to a grilling about her political activities. She lived to see the elimination of many of the dangerous conditions she worked against as well as the implementation of important teaching techniques that she advocated. Amidst the darkness and ugliness that surround us, perhaps the best lesson to draw from her life is that we continue to collectively attempt to do likewise.
Nishimura explained that she had an undiagnosed apical aneurysm, which had been present in her body for at least two years, putting her in extremely high risk for blood clots. The finding was surprising, because a year earlier, an exam showed no signs of spine problems. Because this is a new procedure that hasn't been in use long, though, Teresa wasn't ready to commit to it without doing some additional research. Together, the team conducted the procedure through five small incisions on Camden's right side. The thickened heart muscle can make it harder for the heart to pump blood throughout the body to vital organs.
Unfortunately, her heart failure was progressing rapidly, and in June 2009, she received a ventricular assist device. She also has had three regimens of chemotherapy through the years and six weeks of radiation therapy at Mayo Clinic in 2007. Murray and Perdikis followed, reconstructing her leg with tissue and muscle grafts from her calf. Today Paige has a 14” scar but complete use of her left leg. Express concern and let the person feel that the person is really taking care of them seriously.
Despite the love of her devoted but heartbroken mother, Kate Adams Keller, Helen lived much like an untamed animal.
Although she did for much of her life live, in part, off the largesse of several capitalists, she refused to allow herself to be run up anyone’s flagpole to wave as a testament to the good intentions of the well-to-do. We can imagine some of her  benefactors getting into the wind as a result (the men anyway) and more leaving her side when she came out against World War 1 and in support of the Russian Revolution. We get a sense of the fire that burned within both she and Sullivan in The Miracle Worker, which beautifully depicts the beginning of their relationship. Guided by images from a tiny camera inserted through her back and using a technique called intraoperative low-dose CT computer navigation, the surgeons inserted the screws and cord into Camden's spine without needing a large incision or causing any significant muscle damage. Eventually, she had an implantable cardioverter defibrillator implanted to provide an immediate treatment for any future episode. The device allowed Tara to recover and be healthy enough to be put on the heart transplant list. Among the other horrors, she watched in agony as her younger brother slowly died of neglect despite her best efforts to protect him.
Both the play and the 1962 film adaptation unflinchingly present the many obstacles both faced, including the period of Sullivan’s institutionalization. Thereafter, she burned with a determination to ensure that other children would not share his fate. All these years later, the climactic scene at the water pump when Keller’s life changed forever remains incredibly powerful.
Our memory cards on our phones and cameras are both overloaded and everyday has become such a fun new adventure. I'm head over heels for him, what an amazing dog (my dad tried to take him home with him, and my boss - who does not like dogs - got on the floor any played with him for about 45 minutes).



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