Bob Newhart and Mo Collins dramatize an interaction between a patient and a healthcare provider. There’s a lot of ongoing discussion about methods to use to improve communications between patients and professionals. Newhart, reprising his famous psychologist role, illustrates a method many patients feel is all too common.
Zach Sobiech passed away May 20, 2013. Our hearts and prayers are with his family and friends. We are forever touched by his story. Thank you for sharing your life and music with us, Zach. You are dearly missed and loved.
Published on May 3, 2013
Zach Sobiech is a 17 year old diagnosed with osteosarcoma, a rare form of bone cancer. With only months to live, Zach turned to music to say goodbye. Zach turned 18 years old today (May 3rd, 2013) and continues his fight against cancer with a smile that can change the world. Happy Birthday Zach! You are in all of our prayers!
Zach’s song, ‘Clouds’ is available on iTunes and other online music stores and that proceeds benefit the Zach Sobiech Research Fund of Children’s Cancer Research Fund http://www.childrenscancer.org/zach
SoulPancake presents, in collaboration with Wayfarer Entertainment: Director/Producer: Justin Baldoni Producer: Ahmed Kolacek Producer: Sam Baldoni Associate Producer: Fouad Elgohari Editor: Olly Riley-Smith Special Thanks to Dirty Robber DP: Kieran Murphy Cam Op: Sam Rosenthal Grip/Gaffer: Erik Christensen Sound Recordist: Jordon Justice Composer: Jamey Heath Colorist: Kurt Nishimura Mixed by: Jamey Heath VFX: Abdullah Nabil Cam Op: Kraig Adams Cam Op/DIT: Emerson Boergadine
Songs: Flowers in her hair – The Lumineers Clouds – A Firm Handshake For My Grace – Original song from Zach Sobiech Sandcastles – A Firm [...] continue the story
Published on May 7, 2013
“The only true defeat is giving into bitterness. No matter how our cancer journey ends, we can all be victorious.” – Mike, Valleys: Episode 6. In the finale of the Valleys webseries, Amy talks about the most important thing that gets her through treatments and Annie shares what she has learned about being the best supporter to someone with cancer.
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I was diagnosed in 2003 after 88 days in the hospital, the physician said he was treating me for ulcerative colitis but thought it was crohn’s so I signed for exploratory surgery. He said we would take a section of my colon or do an biopsy..let’s try a look, then. I awoke with an ileostomy, and had 5 more sugeries (not the pig intestine transplant that I’d hoped for or the stem cell transplant suggested) but I no longer have an exit, so this is not reversible.
I’m on Cimzia injections, still deal daily with pain but am grateful for every day that I live well. He’s now considering TPN for the rest of my life and I’m only 48? Seems drastic, but I met a man on a mission trip in Lufkin, Texas, last summer (while building wheelchair ramps with United Methodist ARMY youth volunteers…he’s in his 70’s and watched his grandchildren grow up for the past 14 years. I can do this, if I have to!
I hope to be an inspiration to others, I’m a psychologist and getting my doctorate in Autism Spectrum disorders to work toward my future…however, long or short that may be. My mantra is…I can [...] continue the story
At 21 weeks gestation, we were informed that our daughter, Annie, had a genetic condition associated with profound disabilities. Thus began the most difficult but, ultimately, most enriching journey of our lives.
We realized it was highly likely that Annie would require life-saving interventions in her infancy. From the outset, we wrestled with an agonizing, moral question: Would these interventions and the preservation of her life be in the best interests of our daughter and our family?
To make an informed decision, we began to research. We discovered children who were certainly very impaired, and we were afraid. However, as our knowledge increased, and we met more families with children deemed to be ‘severely disabled’, our fears were alleviated.
Shortly after Annie’s diagnosis, I attended the funeral of a young man with severe cerebral palsy, who had never walked or talked. The midweek service was filled beyond capacity. After the service, I spoke to his teacher. Tears fell freely from her face as she told me that her student had ‘changed her life’. How could that be?
Children with Annie’s condition seldom live into their teens, yet we have observed that when their child dies, the families are absolutely [...] continue the story
I was diagnosed with type 1 diabetes on November 12, 2010 at 20 years old. I knew absolutely nothing about diabetes when I was diagnosed and looking back at the past 3 years amazes me at how far I have come. I’ve had some rough patches especially with the medical professionals in diabetes ‘care’ units. My first experience with a nurse who was supposed to help me was very unpleasant and I had to file a complaint with the hospital. I left her room crying because of the hurtful words she said to me. I had a crap endocrinologist who couldn’t even look me in the eye. I learned about insulin pumps through a friend and asked him about it. He laughed and said its a stupid device don’t do that and waste your time. I was so shocked because I had never heard a doctor speak like that. I decided there and then that I was done with him, the nurse and multiple injections. The only good thing he ever did was to refer me to my present diabetes team.
This team deserves a shout out. I have a wonderful, understanding endo, a great nurse, and amazing dietician. I also [...] continue the story
By Jennifer Hicks
After 34 years living in my body, I became an expert. That is, an expert in myself. And I discovered, after all that time, that I am not ordinary.
I have Bipolar Disorder. But that’s not what makes me different. I am unique because of how I have learned to manage my Bipolar Disorder. Yes, I need medication and psychotherapy, but there’s more to my wellness plan. I use Nia – a fitness practice which not only offers me physical fitness, but also a lifestyle, and now a profession.
Looking at me, you’d never know I have a mental health issue. Spend a little bit of time with me and you still likely wouldn’t guess. Ask my family or friends about its impact on my life, and they probably wouldn’t be able to pinpoint anything “abnormal”. In fact, people would actually describe me as engaged, ambitious and driven. Looking at me from the outside, this mental illness thing appears to be rather invisible in my life.
Still, appearances, as they say, are deceiving. I do swing between abnormally elevated and depressed moods.
It’s difficult for folks to appreciate the considerable amount of energy I use every single day to level out my moods. [...] continue the story
I have Cystic Fibrosis, CF. Its a rare diagnosis that forces me to live like a top athlete in order to stay fit and free from injuries. Home treatments take approximately two hours every day, all year round. I must always be careful not to get ill and healthcare is a lifelong partner. – Sonia Hager, 9 years old. Published on Apr 22, 2013
Published on May 1, 2013
“If you bottle that grief up… after a while you just pop.” Amy, Valleys: Episode 5. Amy struggles with this conflict as she tries to find release from tormenting anger and guilt.
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Published on Apr 24, 2013 “I know I can’t control everything, but I can’t completely let go either.” Amy, Valleys: Episode 4 — “Letting Go” Amy talks about her biggest fear and Annie shares her feelings honestly with Amy. Both of them take steps to begin letting go.
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