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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.
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. Bridget Clausen refers to her seven grandchildren and three great-grandchildren as "the love of my life." She treasures each of them and is proud to have a great-granddaughter named after her.
At that time, Bridget was being treated for melanoma that had spread to several places in her body. The drug, now available under the brand name Keytruda, was approved by the Food and Drug Administration  in December 2015 as a first-line treatment for advanced melanoma. Bridget's journey to Mayo Clinic and the clinical trial that would be so important to her began in 2008 with a small, bothersome mole on one of her legs.
After reviewing and rejecting several treatment possibilities — and engaging in much discussion and thought — Bridget and her oncologist in Fargo, North Dakota, agreed she would seek care at Mayo Clinic. Although the clinical trial Bridget enrolled in was one of the first research studies to offer MK-3475, and she was among the first people to receive it, its roots stretched back more than a decade at Mayo Clinic. Being diagnosed with bile duct cancer that eventually necessitated a liver transplant wasn't enough to keep Steve Woodford down for long.
Back home, Steve was evaluated by a gastroenterologist and diagnosed with bile duct cancer, rather than hepatitis C, in February 2014. Steve's doctor recommended he contact Mayo Clinic in Jacksonville, Florida, to see if he could be evaluated and listed there, since the wait time for a donor liver might be shorter in the Southeast.
After a thorough evaluation by the transplant team at Mayo Clinic's Florida campus, Steve was placed on the liver transplant list in Florida. Less than two weeks after his wife's breast cancer surgery and after being listed for a donor liver for five months, Steve received his new liver on Jan. Four months after the transplant, Steve and Maria hitched up their fifth-wheel trailer and set out to visit the five states in the U.S. Now, a year after Maria's breast cancer surgery and Steve's liver transplant, both are doing well and have mostly resumed their active outdoors lifestyles. In December 2015, during one of her trips to Mayo Clinic, Bridget was pleased to have the opportunity to meet and spend time with Dr.
With the success of her treatment in mind — along with the knowledge that experimental drug MK-3475 has become FDA-approved Keytruda — in January 2016, Bridget decided to hold off on additional treatments. Bridget also is optimistic others may benefit from the progress made in melanoma treatment as a result of the clinical trial in which she participated.
Bill McWhite was vacationing along the Texas Gulf Coast — normally, a time to relax — when his body refused to let him unwind.
That incident was motivation for Bill — a pack-a-day smoker for 55 years — to quit smoking and to seek care with a lung specialist back home. The Mayo Clinic Lung Screening Program begins with a consult with a nurse practitioner to discuss risk factors and review the patient’s smoking history to determine whether he or she meets program criteria.
Depending on what the results show, patients may be advised to follow up in a year or to meet with a pulmonologist to discuss treatment options. Lung screenings are for patients 55 to 80 years of age who have smoked a pack of cigarettes per day for 30 years or two packs per day for 15 years. The Mayo Clinic Lung Screening Program stems from a national lung screening trial in which 53,000 patients — all current or former heavy smokers — underwent either a low-dose CT scan or standard chest X-ray every year for three years. About 150 patients have completed the lung screening in Eau Claire since the program began last year, with five of the scans identifying lung cancer. Most of us have known someone with cancer, either in our family or with a friend or an acquaintance.
Yadira Zepeda, a 67-year-old mother of four adult children, was first diagnosed with multiple myeloma in 1991 and was told by her physician in Miami that she probably had two to four months to live.
Yadira’s own battle with cancer took a back seat when in June 2008 her daughter Valeria was diagnosed with chronic myeloid leukemia after unexplained bruises began appearing on her legs and arms.
Today both Yadira and Valeria are living full lives one day at a time and continuing their treatment at Mayo Clinic. 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. 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.
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. The joy of a namesake is especially sweet, because when Bridget learned her granddaughter was pregnant, she wasn't sure she would be here to meet the baby. Interestingly, the foundation of the drug's development began in a Mayo Clinic lab more than 15 years ago. Although no evidence of melanoma was left after the surgery, there was a small area on her right kidney that concerned her doctors. She made the five-hour trip from her home in Nevis, Minnesota, to Rochester, where she met medical oncologist Roxana Dronca, M.D. For four years, she drove to Mayo Clinic every three weeks to receive an infusion of MK-3475. A South African native living in Utah, Steve is professional skydiving instructor, backpacker and canyon guide in Zion National Park.
He was told the cancer was inoperable and incurable. He was put on chemotherapy, underwent radiation therapy, and had a stent inserted in his bile duct, in an unsuccessful attempt to solve a drainage problem. Although Steve was placed on the waiting list in Utah for a liver transplant, the wait time in that region would be one to two years, and it was doubtful he'd survive long enough to get the organ he needed. He and his wife, Maria, packed up their RV and temporarily moved to Jacksonville to be near Mayo Clinic, where he continued treatment as he awaited a new liver. In fact, Steve attempted a world-record night skydive in Arizona over the 2015 Thanksgiving holiday, with 52 jumpers participating in the event.
After receiving 67 infusions and driving more than 37,000 miles in four years between Nevis and Rochester, she was ready for a break. Instead, the 69-year-old Hayward, Wisconsin, man experienced a flare up of his chronic obstructive pulmonary disease, also known as COPD, and found himself in the local hospital. The decision would ultimately lead his doctors to find that he had lung cancer, through a new screening program that identified the cancer at an early, treatable stage.
If the patient and nurse practitioner opt to proceed, a low-dose CT scan is scheduled to check for early signs of cancer.
The findings showed that patients who received the CT scans had a 20 percent lower risk of dying from lung cancer than those who received chest X-rays. But cancer can be particularly cruel when it seems to target a specific family over and over again. Not satisfied with what she heard and unwilling to give up after receiving that devastating news, at a friend’s recommendation she came to Mayo Clinic's Florida campus for the second opinion that has given her life and hope for the past 24 years.
Based on her mother’s experience, Valeria went to Mayo Clinic and began receiving targeted chemotherapy for her disease.
In a cruel twist of fate, she found a lump in her breast and was diagnosed with breast cancer in August 2008, resulting in a bilateral mastectomy, followed by chemotherapy. 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). 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.
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.
She decided to go to Mayo Clinic in Rochester, Minnesota, to see if doctors could offer any other options. It didn't appear to be related to the melanoma, and they were able to get rid of it with an ablation procedure. The work his research lab did to identify that molecule laid the foundation for the drug's eventual development. Almost 8,000 miles and four months later, they have now been in 49 States after visiting Michigan, Minnesota, Wisconsin, North Dakota and South Dakota. The idea is to detect cancer early, before symptoms present and when the disease is most curable. He had a positron emission tomography, or PET, scan that showed no spread of cancer outside the lung, so his doctors advised surgery, which Bill underwent in June 2015. According to the Centers for Disease Control and Prevention, about 157,000 people in the U.S. McWhite is exactly the person we’re trying to identify — somebody who had a very early stage lung cancer with potential to cure with surgery," Dr. For the Zepeda family of Miami, cancer has stricken a mother, her daughter, a number of other family members, and even the family dog. 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. 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. Getting sick unexpectedly during a backpacking trip to Belize two years ago seemed like just another challenge he had to overcome. Along the way, Steve had surgery at Mayo Clinic's Rochester campus for a bilateral hernia, which put him back three months in his plan to resume skydiving. In August 2013, she received a transplant with stem cells from her brother, who fortunately was a perfect match. In October of that same year, she also had part of her thyroid removed due to a benign lump that was found by her doctor. And the good news is that despite their family history of cancer, Yadira’s other three children and Valeria’s siblings are all healthy and remain cancer-free. 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. He did his first jump since his transplant in October 2015, instead of July as he'd planned. She continues to receive oral anti-leukemia targeted therapy every day for the foreseeable future. Knowing how dangerous melanoma can be, though, Bridget began regular appointments with an oncologist and a dermatologist. Maxwell will be deciding upon and after this illness passed we will take a look at producing these scripts into feature films or television productions. Maxwell is spending this time taking care of his wife, and not in production, he has plenty of time to read scripts. She has great conformation, exceptional movement and is the happiest dog I have ever owned. Thus, this is a wonderful time to have him take a look at your script.i»?A This page is set aside to give us an opportunity to keep our visitor abreast of what is going on with Maxima Vision Films and our film school. Her job as a therapy dog for an 83 yr old woman that had is stroke is one she takes very seriously. At the same time we encourage our visitor to write us anything they feel may be of interest in film and television to our community. Many of these articles are written by our own CEO who is serious about keeping our whole community up to date with any breaking news and events we may be involved with. We continually have Home Health therapists in daily and she greets each of them then quietly goes to her spot to watch everything that goes on. In the event you write to us a story we find the community may want to know about we will post here on this page. She accompanies me into the chicken coop and is great with the chickens as well as with her cat ( yes her cat that she found in a ditch).


These stories may be of any kind pertaining to the film and television industry, from casting calls our community may want to know about, to events in the area, to a new story ideas you come up with you think might make for a good film or television production. She passed her Herding Instinct testing at 5 months of age and now working on her Canine Good Citizen certification. I have owned and worked with many breeds of dogs and Arya is by far one of the most intelligent, willing and trainable. Randall Maxwell of Maxima Vision Films takes some of the backdrop of that particular White House, fictionalizes the story, orchestrates some look-a-likes and dramatizes a womana€™s lust for power who is willing to do whatever it takes to become the first lady president of the United States, including assassination, sex, love or war. I would totally recommend PATCHWORK SHEPHERDS and have friends now that have bought puppies from here as well and all of them are as wonderful as Arya. A He said, "she is really a love," and described her gentleness and cuddling even from the get-go. A She is very playful with her 'brothers' (two older choc labs), but is extremely responsive to me and is my 'watcher.' A No matter where I am, she is A watching over me.
A When we settle in the evening to watch a movie, she will quietly peruse the house, coming back to my side after she has checked everything out. A If she could, she would hop up on my lap and sit there, just as she did when she was a fuzz-ball pup! When three unlikely but well-intentioned groups of mighty people join forces to battle the demon, they face challenges within and without.
Their variegated backgrounds, including slavery, military, and commoners, must be overlooked if they are to stop Man Burnera€™s evil quest. The powerful and precious Atma stones must be kept secret if the world is to be saved.Will Man Burner be able to succeed on his quest to find the Atma stones? It was serendipity that brought you all the way over the mountains on Monday so we could get her!Also a couple of short videos if you're interested. This delay is expected to last a couple of months, postponing production of every film by a couple of months.The reason for this suspension is due largely to the fact of us not yet having our film school, which is attached to our production company at the point where our investment group had wanted it by summer of 2013. Another large factor is not finding a large enough pool of talent here locally who have enough professional film experience or training to allow us to completely cast four feature films per year, let alone finding enough professionally experienced crew.Thus, one of the things we are now awaiting is hiring a casting director in Hollywood to cast any remaining major speaking roles for each film we have been unable to cast thus far. I was just getting to the serious stage ofshopping for a black coated GSD to raise for my own pet and protection dogwhen my nephew T.J.
This is an all out effort to raise the bar in this region of professionally trained actors as well as crew. At this summer feature filmA  consortium; Whether you are an aspiring producer, director, script writer, editor, animator, actor, cinematographer, or just want to learn the ins and outs of the film making industry, you may begin as early as the summer of 2013 building your working resume by participation in our Summer Feature Film Consortium! BlackJack (Zoey x Drake 2009) is doing fine, being a good boy that loves to be around us (Right now he is under my desk sleeping at my feet).
Well, we have serious investors who share our same passions who are willing to put their money where their mouths are. Let us commit ourselves then together to perfecting our craft of film making and television production by committing to professional training and stop spending money with so-called agencies who are simply in business to sell schools and photos, but have no real connections to even consider making even a feature film. It is a very sad thing that so many have been lured into such scams and have been taken advantage of, but now it is time for change and a part of this change is a must, raising the bar of excellence.
It is now time for us to show our investors that we are willing to invest in our future so that very soon they will allow us the opportunity that all of us can make a very good living doing what each of us love doing and that we are extremely passionate about.A This film school has always been and will continue to be always a very specialA  part of our production company and our plans for the future as a means of keeping well trained professionals continuing to come on board with our production offices, from professionally trained actors to crew.
This keeps fresh ideas coming through the doors, but more importantly it allows us to always know we have the most highly skilled actors and crew that money can buy. Our investment group has always made the film school a stipulation on their investing in our feature films and will continue to do so.
We had many family gattering and other partys and he is always good around people in the house.
A One of the biggest concerns of our investment group is to keep from happening here what happened in Louisiana, where their film makers were at least diligent in getting their law makers to raise the incentives to entice major film production companies like Maxima to come into their state to produce films in their state.
They were able to do this by quoting statistics which prove, when major film production companies come into your state and begin producing motion pictures, they bring with them literally millions of dollars into the local economy.
In Louisiana, they experienced tremendous success in enticing these companies into their state.A Unfortunately, these companies came by the droves, however, once there they found there was not enough professionally trained talent already there to produce the number of films they wanted to produce, causing them to have to hire the bulk of their needed talent out of state. Because these incentives are based on hiring local talent, these companies when they were forced to hire outside of state talent, they lost their incentives. Louisiana has since worked diligently trying to get professional instructors in their public schools and universities to train up a workforce of professionally trained film and television professionals to salvage what they can of the professional production companies who have remained and tried working with them.A At Maxima Vision Films, we have experienced the same thing in this region as far as finding sufficient professionally trained talent to do here what we had planned to do in this region.
When I speak of this region, I am speaking of the region of Tennessee, Arkansas, Oklahoma and Louisiana. We have two investment groups, one of which has already committed to funding four feature films or television productions per year over the next five years here in this region with Maxima. We want to shoot films that matter, films which can help to shape our culture positively as opposed to negatively. These films will be marketed directly to the Christian community, which when one considers 70% of the USA population are professed Christian, this is an enormous market. When my kid gets around to it she will send you pictures, sorry Ia€™m not the computer savvy one. We are certain if we can keep our production cost down under a million dollars the odds are in our favor of at least breaking even if not making a few dollars, especially considering telling stories that matter. If we can keep our films under $500,000 the odds go up even further, and we know one film in 6-7 will make a substantial return. Our main goal though is telling stories that matter, that might help shape our culture positively, and we can all make a decent living while doing what we are all passionate about doing. A To accomplish all of this though, we are going to have to raise the bar here in this Texas region as far as talent goes. We are diligently seeking those individuals who have a real passion for film making and television productions, who are driven by this passion to do whatever it takes to one day be able to make a living in a industry that chances are very bleak in anyone getting to a point of making a living.
Thank you again for Morgan, she is a gem, here is her 9 week picture (the ear did come down). However, one thing is for certain, to have any chance at all, the more one is willing to do in the industry, whether it be sweeping the floors, taking coffee to the director, or being the lead role, or simply investment of time, energy, and money to keep perfecting their craft, all tends to lead to work, which gives us more exposure, that in turn leads to more work, etc, etc, etca€¦ A The point is this; we have investors, which is something, if not the one and only thing which keeps most from doing what they truly want to do in this industry! These investors are seeking individuals like yourself who are like minded, those who have a real passion for film making and television productions, but who are also just as passionate about telling stores that matter. However, the real key is finding these like minded individuals who take this business very serious, as serious as our investors take it, those who are willing to invest into their own future, so as to help them to perfect their individual craft so that they are the very best they can become, so that as a collaborative art form we are able as a group of individuals creating a quality product. After he began his own recovery, he helped set up centers to help other addicts."I abandoned my old life to serve the Lord Jesus Christ," he said. One twin struggles with an addition to prescription drugs, while the other battles doctors whose prescription anti-psychotics are driving her sister to madness and death.a€?One is what I call a€?preachya€™ and more for the church community and affirming faith,a€? Maxwell said. With the first type of film we will focus on films which are considered preachy and on the nose which will be marketed directly to the Christian community. The second types of films we will focus on are those designed to reach the un-churched with a message of hope for a hurting world, a film with at least a redemptive message. This investment group is especially interested in getting involved with projects where the project owner has some sort of invested interest in the project themselves or have some avenue to put together a split funded project somehow, thus splitting the risk as well.A A Thus, this investment group funded many trips around the country for Dr. Maxwell to travel and meet with other investment individuals, companies and groups who had expressed interest in partnerships with the films we were already in pre-production stage which were our films a€?Rachela€™s Gracea€? and a€?Sister Surrendereda€?, both of which had an estimated production budget of around $300,000. We had felt with partnering with others who could double the production budget we could add at least some actors with much experience as well as other talents. Unfortunately, at this point, though we met many such investment groups who had expressed interest in split funding our film projects, most simply had projects themselves who they wanted our investment group to invest in their film projects and did not show us even any interest what so ever in split funding our film projects after our investment group paid travel and lodging expenses for Dr Maxwell to meet with these people.
I think he will excell, and it will be good for the boys to learn how to deal with him (other than play). A With this being said, this has been a very expensive summer for our investment group in trying to put together split funded film projects. We purchased Pruett (black collar male from Zoey x Doc August '08 litter) and were so thrilled with him that we had to get another!
A few weeks later we welcomed Daphne (hot pink collar female from Anna x Doc August '08 litter) into our lives. He quickly learns new commands and we are currently practicing, "seek", where we will tell him to "sit and stay" and then we go hide his ball and tell him to "seek" and he finds it. She loves to play in the snow!!She has been doing really well in the house, she is a very quick learner. I know the "puppy stage" lasts for awhile, but if it continues to go as smoothly as it has been going, it will definitely be a breeze. She loves to play fetch and she is really good at it, which is surprising to me for her age. She is such a sweet puppy, she is always trying to make friends with all the animals she meets, most which unfortunately haven't been too fond of her. Miah is starting to be a little friendly, not much, but like I said, Tymber is a persistant little pup and I believe that eventually they will be pals. We will be taking her on her second fishing trip tomorrow, which is always very exciting for us.
She loves playing with any kind of plants and grass- we are hoping she grows out of that stage for our landscape's sake! Anywho, I just wanted to let you know what a great pup she is and how much Tyler and myself enjoy having her. He is everythingA I could have ever hoped for in a German Shepherd and I am really happy that I got him. Several people in our training class have commented on his lovely conformation as he trots across the room while playing with the other pups.
He's a great dog!A Anyway, hope all is well in your part of the world and that you are enjoying the holiday season. Although I had some concerns on how Gracie would react, from the first walk that we did on the way home from Patchwork, she has been wonderful. Already they play together, with Gracie laying down so that she is on Argus' level, letting him crawl all over her. He already knows his name, figured out how to negotiate the step up the deck, and how to run from me when he picks up something I don't want him to have. He follows us around from room to room and always sleeps next to us when we are in the room. I do have a crate and have used it but not very much, mostly I just watch him and when I catch that certain look I just take him out and tell him to go potty.
When I was in shop he would play under my bench and when he was tired he would sleep under my stool.
He and Gracie had a good time exploring and finding just about every kind of poop there is out there. Everyone that meets her is in awe of not only her beauty and structure, but even more so of her super sweet and willing disposition.A  I cannot say enough about her. She is very gentle, smart, intelligent, super athletic, and just wants to please and love everyone.A  She loves to crawl into our laps and pretend she is a tiny lap dog. A His big brother Jackson and he are the best of buds, they have really bonded into something special!
A Also, wea€™d like to thank you for letting us come out and see him when he was a puppy, and for giving us little updates on how he was doing when he was just a lila€™ guy.A  (10lbs when we picked him up to take him home seems little compared to the size he is now!
After working for a vet for more then 10 years my husband had to really talk me into getting a GSD. She has gone though a basic and advanced off leash obediance class and this comming year brings more fun with tracking and agility classes signed up. We are now thinking of getting her a little brother and look forward to coming out to visit and meet more parents.
He is adapting quickly to his new home on Orcas Island, WA A and after 3 days already knows his new name. We have had him for two days now and he has already learned his name, learned how to come when called, walks great on a leash, has learned the command "gentle" for when he takes things with his mouth, is completely potty trained and sleeps all night long in his crate with no problems.
We have never seen such a loving, well behaved, intelligent puppy before and we feel so lucky that he is now a part of our family. John and I were so pleased to see the safety measures that you take prior to letting anyone be near or handle any of the puppies. Because of your loving care for your dogs we now have two of the greatest puppies that anyone could ever ask for in life!
I am grateful for the time that we were able to spend with the puppies getting to know each and every one of them. You are wonderful about keeping everyone informed through your website just as you did while we were waiting to be able to take the Sebastian and Kasia home. We were also very impressed that you were so willing to let us come visit and you even encouraged us to do so. We thoroughly appreciate that you allowed us to be a part of the puppies lives even before they were in their new home.
Through your attentive behavior to each and every one of your puppies we new the silly things they did, what they liked to play with all the way down to their little itchy spot that they liked to have scratched. Because of all your love and attention we have two beautiful, healthy puppies that we will get to love for years to come.A A Thank you so much for our beautiful puppies! A  I got hopeful when I found your pages, with your dog Penny, who reminded me so much of our Isis, who was a beautiful, athletic,and loving black and red blanket pattern longcoat. You DID say on your page that your goal was to find the right dog for people, right down to the color.
The way you described the parents of different litters, and later the pups themselves, was exactly right.A  Patiently, you discussed all the little characteristics of each pup in a way that just about made up for our never being able to actually see the pups in person or hold them in our arms.
Pashi learned every trick all of my other dogs know in one 10 minute session at age 11 weeks, and never forgot them.A  She and Itta (9 weeks) both sit at the door automatically now, better than any of our other dogs who have been working on it for ages.



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