Extremely Premature. Abundantly Blessed.

Fragile, tiny twins battling for their lives. After trying to get pregnant for over two years, it wasn’t supposed to be this way. There had been no complications. There had been no warnings. Yet somehow, that was the fate that Selah and Brynn were facing. These beautiful twins were born extremely premature after only 25 weeks’ gestation to first time parents, Ben and Kelsey, each weighing under 2 lbs.

Kelsey had experienced no issues during her pregnancy. She simply woke up one morning with contractions. After calling her doctor, Kelsey was instructed to head to the hospital to get checked out just to be safe. Doctors started running a myriad of tests but couldn’t determine why she was in labor. Even worse, they couldn’t find a way stop it. Five hours after arriving at the hospital, Selah started coming down the birth canal. Doctors immediately made the decision to deliver both girls through emergency cesarean. They feared that if they allowed Selah’s delivery to continue without intervention, the process would almost certainly kill her.

While this quick thinking saved the girls lives, their battle had only begun. Premature babies are not yet fully equipped to deal with life in our world. They are naturally behind in their development. They are forced to learn to do a lot of things on their own that should be done for them inside the womb. Additionally, their tiny bodies still have many underdeveloped systems such as the lungs, digestive system, immune system and skin. Babies do a lot of developing during the final trimester of pregnancy, and if they’re born early, they face a significant uphill battle.

Preterm birth is the leading cause of death among newborns. Those who survive are more likely to have lifelong health problems such as developmental delays, hearing loss, blindness, chronic lung disease, and cerebral palsy than full-term babies. About 25 percent of extremely premature infants (those born before 32 weeks’ gestation) suffer significant, long-term impairment of brain development. Ben and Kelsey were told Selah and Brynn had an 80% chance of surviving. The news was devastating, but Ben and Kelsey were optimistic as the girls appeared to do great the first 24 hours. There were no issues at all. That’s when their worlds were turned upside down.

The day after they were born, Selah and Brynn experienced pulmonary bleeds and struggled progressing. A few days later, it was discovered that both girls had an intraventricular hemorrhage (IVH), also known as a brain bleed. IVH of a newborn is bleeding into the fluid-filled areas (ventricles) inside the brain and occurs most often in babies that are born prematurely. Selah had a severe grade 4 bleed on the left side of her brain and a moderate grade 2 bleed on the right. Brynn had severe grade 4 bleeds on both sides. Because there is no way to stop bleeding associated with IVH, Ben and Kelsey were told that both girls would require surgery to place a tube (shunt) in their brains to drain fluid in hopes of relieving the pressure. Because of the severity of the bleeds, doctors told Ben and Kelsey that if they survived, both girls would never be able to eat or walk on their own and many other areas of their development would be significantly delayed.

Their initial brain scans following the bleeds showed a tremendous amount of damage. Seeing what little remained of their brains left a pit in Ben and Kelsey’s stomachs. Both girls had to undergo multiple brain and eye surgeries and have experienced health and development issues including hydrocephalus, pulmonary hemorrhages, respiratory distress, PDA, bowel issues and infections. In all, Selah and Brynn spent more than 4 months in the NICU before they were allowed to go home, connected to a host of tubes and leads to monitor everything from oxygen levels to sleep apnea.

Ben & Kelsey were determined to do whatever they could to give their girls the best chance to beat the odds stacked against them and provide a brighter future than doctors had predicted. As soon as they were released from the hospital, Selah and Brynn started receiving Hyperbaric Oxygen Therapy at Sara’s Garden. The family noticed changes immediately. From the moment treatments started, the sleep apnea monitors, which had been going off constantly, no longer registered any alerts or events. After just 2 days of treatments, Selah went from having eyes that bounced, floated, and disappeared below her eye lids, to looking around and trying to maintain a gaze. She is now able to track toys of all shapes and sizes about a foot away from her face and her eyes no longer float away or bounce!

Prior to Hyperbaric Oxygen Therapy, both girls were extremely far behind on their developmental charts. After two rounds of HBOT treatments, that is no longer the case. Brynn has now completely caught up to her adjusted age and Selah is making great strides. Both can now roll over and are gaining trunk and head control every day. Selah is gaining awareness and strength in her right side and beginning to use it considerably more. Brynn is crawling all over the place and can sit independently by herself.

To look at her scans, you would never know that Brynn had experienced severe grade 4 bleeds on both sides of her brain. In fact, Brynn’s next MRI following HBOT treatments showed that her brain had almost completely healed. The right side of Selah’s brain looks amazing as well. Her left side, while healing slower than the right side, has still improved dramatically. There has been so much healing and improvement in both girls’ brains that their neurosurgeons announced that no additional surgeries would be necessary. Ben and Kelsey were overjoyed when they were able to cancel the follow-up surgeries that had already been planned!

Thanks to Hyperbaric Oxygen Therapy services at Sara’s Garden, Selah & Brynn have begun shattering the limitations that were placed over them when they were born. Ben and Kelsey are certain that God has big plans for Selah and Brynn. They feel abundantly blessed to be able to witness their continued growth and watch how their stories unfold. No matter what you’ve been told, there is hope… for this and many other conditions. HBOT is treatment without drugs… without surgery… without pain.

Some Miracles Come in Pairs

Twins. Twins?! For Brittany, this revelation should have brought with it a sense of expectation and joy. Instead it was followed by an overwhelming sense of despair. Brittany was informed that while she was carrying twins, there were severe complications that would put her life, and the lives of her unborn children, at risk.

At her 10-week ultrasound, Brittany was diagnosed with Twin-to-Twin Transfusion Syndrome (TTTS), an exceedingly rare and potentially lethal condition that can occur in identical twins. Abnormal blood vessels in the shared placenta had caused their umbilical cords to fuse together. Because of these shared connections, one baby (Lukas) was getting an overabundance of nutrients while the other baby (Liam) was being deprived of what he needed to grow. Not only was this potentially fatal for the twins, but it put Brittany’s life in jeopardy as well. Doctors urged her to have an abortion. When she refused, Brittany was placed on immediate bed rest for the duration of her pregnancy.

Following Brittany’s 23-week ultrasound, doctors delivered more bad news regarding Liam. His arms were contracted, there were problems with his heart and he had Gastroschisis, a rare birth defect of the abdominal wall in which the baby’s intestines stick outside of their body. The news was devastating to Brittany. However, she never lost faith that Liam would be a fighter and could somehow overcome this.

Over the next few months, Brittany went into labor multiple times. Each time the doctors were able to stop it. However, at 31 weeks, they allowed the delivery to continue because there was concern that Lukas was receiving too much fluid and was in jeopardy of rupturing. Lukas was born not breathing with the umbilical cord wrapped around his neck and had to be resuscitated. Miraculously, despite being without oxygen during the delivery, Lukas did not suffer a traumatic brain injury or sustain any damage or negative repercussions from the TTTS. When Liam was born, he was immediately rushed into surgery in hopes of resolving his Gastroschisis.

Brittany spent the next three months in the NICU with both boys. Liam was ultimately diagnosed with Arthrogryposis Multiplex Congenita (AMC), a rare neuromuscular condition that causes many joints to be stiff and crooked at birth. Doctors told Brittany that Liam would never use his arms… that they would be completely useless. He would need to learn to do everything with his legs and feet. She was told that Liam would spend his entire life enduring painful therapies that would do nothing for him and give him little to no improvement in his arms.

While in the NICU, Liam was also diagnosed with a Patent Ductus Arteriosus (PDA), an unclosed hole in his aorta. Before birth, the two major arteries—the aorta and the pulmonary artery—are connected by a blood vessel called the ductus arteriosus. This vessel is an essential part of fetal blood circulation. After birth, this vessel is supposed to close as part of the normal changes occurring in the baby’s circulation. In some babies, however, it remains open allowing oxygen-rich blood from the aorta to mix with oxygen-poor blood from the pulmonary artery. This can put strain on the heart and increase blood pressure in the lung arteries.

When Liam was 4 months old doctors informed Brittany that he would need surgery to repair the hole in his heart. Liam’s lungs were not functioning properly because there was not enough oxygenated blood coming from his heart. That very night Brittany was up late watching television when she saw a commercial for Sara’s Garden that brought her to tears. Liam’s surgery was only a month away. Could this possibly help in time and prevent surgery? The next morning, she called her doctors back and told them she wanted Liam to receive Hyperbaric Oxygen Therapy and Conductive Education. Even though they told her that it was a complete waste of time and money, Brittany knew in her heart this was something she needed to do for Liam.

The first 4 months of Liam’s life were a struggle for survival. He was far behind in many developmental goals and milestones. He was also very lethargic and apathetic towards any activity. His arms and shoulders hung limp at his sides and did absolutely nothing. Soon after starting HBOT and CE, Liam’s personality finally began to emerge. He was no longer sleeping all the time. He began playing… and smiling. His joint flexion in arms began improving dramatically.

Following Liam’s initial round of HBOT, Brittany took him to the doctor for his scheduled well check in preparation for surgery. What was supposed to be a simple pre-surgical meeting turned into over 4 hours of testing. Specialist after specialist was called in to test and retest Liam. Something was different and no one believed what was being seen. By the time they left, the doctors had cancelled Liam’s surgery and ordered reductions in his oxygen and heart medicines. The cardiologist that had told Brittany that HBOT would be a waste of money and that surgery was his only hope was now speechless after the echo and ultrasound showed an amazing transformation: His heart was contracting normally, the murmur was virtually undetectable and the hole in heart was closing!

Liam is continuing to make progress and is beginning to meet his developmental goals and milestones. Doctors have said that Liam’s hands and fingers are now phenomenal. While his arms are still affected by his Arthrogryposis, Liam is now able to use them. He feeds himself. He grabs things off of tables. Most importantly to Brittany, he keeps pace with his brother and other kids that he plays with at church.

Thanks to Hyperbaric Oxygen Therapy and Conductive Education services at Sara’s Garden, Liam is a happy little boy who is defeating all of the odds that had been put against him. He is completely off all of his heart medications. Brittany knows that miracles do happen… and sometimes they come in pairs. She is confident that HBOT and CE have given Liam a chance at a much higher functioning life. No matter what you’ve been told, there is hope… and Sara’s Garden can help you find it.

The Empty Wheelchair

Most people spend the first week of a new year with great intensions of making healthy, life-changing goals and resolutions, and then worrying about how long it will be until they break them. For Mary, 2015 brought with it completely new and unexpected goals: survival and recovery.

Just after the first of the year, Mary suffered a series of severe strokes that left her fighting for her life. The result of the oxygen deprivation to Mary’s brain tissue had devastating consequences as she was no longer able to use her left arm or leg. When she was stabilized, Mary was transferred to a long-term care facility where she could receive intense therapy services in hopes of regaining her lost motor function.

Before Mary’s strokes, she enjoyed a very active, independent lifestyle both around her house and out in the community. She also was very conscious regarding her diet and physical health. For Mary, now being confined to a wheelchair was mentally and emotionally draining. Instead of healing and recovering from her strokes, Mary’s family watched her slip further and further away and feared that she might never reclaim her independence. They grew increasingly concerned that the medications she was now taking were having an adverse effect on Mary. Her cognitive abilities became obscured and she felt confused about almost everything. She sensed that she was literally losing her mind. Instead of rebuilding her motor skills, Mary began losing upper body trunk control and was no longer even able to even get out of bed on her own.

Most people have experienced a close relative or friend who has suffered a stroke that has left them crippled or unable to function by themselves, or without the ability to eat, understand or communicate. The end result of these severe strokes is often the same; patients with significant disabilities need round-the-clock advanced care. As in the case of Mary, the needs of the patient and family members after a stroke are enormous. Mary’s family knew that they needed to act fast or they ran the risk of watching her continue on this downward spiral into a complete loss of independence.

They began researching additional treatment and therapy options for Mary. What they discovered was that through the use of Hyperbaric Oxygen Therapy (HBOT), medical researchers have found a way to restore a significant amount of neurological function in brain tissue long thought to be permanently damaged by stroke, traumatic injury, and metabolic disorders.

The brain typically consumes 20 percent of the body’s oxygen, but that is only enough oxygen to operate five to ten percent of neurons at any one time. The regeneration process needed for healing following a traumatic brain injury requires much more energy. The significant increase in oxygen levels during Hyperbaric Oxygen Therapy supplies the necessary energy for rebuilding neuronal connections and stimulating inactive neurons to facilitate the healing process. This neuroplasticity allows the neurons (nerve cells) in the brain to compensate for injury and disease and to adjust their activities in response to new situations or to changes in their environment.

Additionally, when cells in the brain die, either from trauma or lack of oxygen, blood plasma leaks out into surrounding brain tissue causing swelling and reducing blood flow. These otherwise normal cells go dormant because they can’t function without the appropriate amount of oxygen. HBOT dramatically increases the amount of oxygen being carried in the blood plasma, making oxygen available to heal damaged capillary walls, preventing plasma leakage and reducing swelling. As the swelling decreases, blood flow can be restored to the dormant tissue (neovascularization) giving these cells the potential to function once again.

Research indicates that HBOT can lead to significant neurological improvements in post stroke patients even at chronic late stages. The neurological improvements observed in these late stages demonstrate that neuroplasticity can be achieved and activated by HBOT even years after a brain injury occurs.

In February, five weeks after Mary suffered her strokes, she started Hyperbaric Oxygen Therapy at Sara’s Garden. After the first hour of treatment she began lifting her left leg. Her daughter wept. A few days later, her family checked her out of the rehab center and took her home. The following week Mary regained the use of her legs enough that she began walking again. After three weeks she was able to shower on her own. During the fourth week of treatments, Mary was back to making bread and doing the dishes. As time went on, Mary continued to get even stronger. She was able to return to a schedule that was very close to her life before the strokes.

Thanks to Hyperbaric Oxygen Therapy at Sara’s Garden, Mary finally has her independence back. The wheelchair that served as a frustrating reminder that life was never going to be the same is now empty. It was hard work and her family pushed her, but they contend that it was the services she received at Sara’s Garden that ultimately gave Mary her life back. No matter what you’ve been told, there is hope… for this and many other conditions. HBOT is treatment without drugs… without surgery… without pain.

Life Beyond a Wheelchair… One Step at a Time

October 7, 2015
4:06 am
Success Stories: CE, Success Stories: HBOT

Who doesn’t enjoy a relaxing drive in the country on a beautiful, sunny day? Windows down… breeze blowing. Have you ever thought for one second that something as seemingly harmless as a receipt blowing in your face could alter the course of your life forever? That’s exactly what happened to Hannah.

On May 20, 2013, Hannah was driving down a country road on her way to a friend’s house. It was a warm day and the air conditioning in her car was broken so she had rolled her windows down to keep cool. A receipt from her back seat became suspended in the breeze and swirled around the car before startling Hannah by landing directly on her face.

As she reached up to brush the receipt away her car veered off the road striking a mailbox. As she regained control of the car she glanced back over her shoulder to see what she had hit. This reaction caused her to cross the centerline of the road and head straight towards the opposite ditch. In a panic, she over-corrected and lost control of the vehicle. Before she knew it, Hannah blacked out as the car was flipping over multiple times before coming to rest in a field. When she regained consciousness, Hannah realized that she could not move her legs and had no feeling from her waist down.

Hannah’s initial MRI just prior to surgery showed that she had suffered a complete spinal cord separation. Three weeks later, Hannah was tested and downgraded to a Level B incomplete spinal cord separation (T11-T12) in her lower back on the ASIA Impairment Scale. The only feeling that Hannah had below her waist was an intense burning and stinging sensation in her feet, thought to be from significant nerve damage sustained in the accident.

Hannah and her family were devastated when they learned the severity of the injury. Doctors told her that she only had a 0.1% chance of ever walking again. Hannah was determined to prove them wrong. After being released from the hospital, Hannah spent countless hours in physical therapy working towards being able to stand and take steps with leg braces. Before long, Hannah’s insurance wanted her discharged from therapy as it was felt she had reached her greatest level of attainable function. She wasn’t making enough noticeable gains. Therapists believed that Hannah was ready to live her life independently… in a wheelchair.

Hannah would not accept this limiting outlook for her future. Despite the fact that she was not yet walking, Hannah believed there was still considerable room for increased functionality and independence. Thankfully, Hannah and her family discovered Sara’s Garden. They learned how Hyperbaric Oxygen Therapy and Conductive Education have been extremely successful in treating people who suffered from serious accidents and injuries, in many cases improving the client’s fine and gross motor skills and physical healing.

Midway through Hyperbaric Oxygen Therapy treatments, Hannah started noticing feeling returning in her lower back and bladder. She also began experiencing significant relief from the burning nerve pain in her feet. She started having better results in her physical therapy sessions. Her therapists noted that she was using her legs more and was recording faster times in her exercises.

Immediately following HBOT, Hannah was evaluated for Conductive Education services. The conductors felt that Hannah could benefit from CE services, despite the fact that Conductive Education was not a widely accepted treatment modality for people with spinal cord injuries. Having just completed over 19 months in physical therapy, Hannah was skeptical about what CE would really be able to do for her but was encouraged by this new opportunity for increased independence.

Hannah began Conductive Education at Sara’s Garden on May 12, 2015, nearly two full years after her accident. It only took one week of Conductive Education to convince Hannah that this was what she had been looking for. Instead of spending her time working on accepting her fate and living independently in a wheelchair, Hannah felt challenged to push further by people who believed she could continue to progress beyond life in a wheelchair.

Hannah received Conductive Education 3-5 times per week for five months. At the time of her initial CE evaluation, Hannah was not able to maintain a free sitting position, achieve or maintain a standing position, or walk without Knee-Ankle-Foot Orthoses (KAFOs) and maximum physical help. Through Conductive Education services, Hannah’s leg strength has improved dramatically. She is now able to achieve and maintain a free sitting and standing position wearing only Ankle-Foot Orthoses (AFOs) and is currently working on walking with canes. When Hannah visits with her previous therapists they are shocked and amazed at how far she has come in only five months.

Generations ago, many people living with such severe paralysis may have been confined to wheelchairs or institutions, unable to perform even the simplest daily tasks like driving a car or getting dressed. Today, however, it is clear that people living with paralysis can live even healthier, more productive, and independent lives than was ever thought possible.

Thanks to Hyperbaric Oxygen Therapy and Conductive Education services at Sara’s Garden, Hannah now has more hope than ever before. Hope for a better quality of life. Hope for more independence and a better future. Like Hannah, no matter what you’ve been told, there is hope… and Sara’s Garden can help you find it.

Breaking the Chain of Pain

It was supposed to be a small surgery. Simple. In and out. In May of 2009 Kevin had what was supposed to be minor outpatient surgery to relieve pain in his left big toe brought about by years of arthritis. Unfortunately for Kevin, his healing process turned out to be anything but minor.

Following his surgery, Kevin began to experience an intense, burning pain in his left calf muscle. His doctor suggested that he get an ultrasound of his left leg. The ultrasound revealed that Kevin had a deep vein thrombosis (DVT) in his leg. He was immediately hospitalized for treatment. Over the next three years, Kevin was placed a variety of blood thinners to treat recurring blood clots in his left leg. In the spring of 2012 Kevin traveled to the Cleveland Clinic in hopes of determining why he kept having these painful blood clots and unexplained weight loss.

Specialists at the Cleveland Clinic were not able to determine why Kevin was experiencing this ongoing pain in his left leg. However, they assured him it was definitely not from blood clots. Kevin was referred to a pain management consultant who began treating his growing leg pain. He went through months of physical therapy, more than a dozen sympathetic nerve blocks, an implanted spinal cord stimulator and a radio frequency neurotomy to cauterize the nerves to his left leg. Sadly, none of these treatments gave Kevin any lasting relief. He continued to suffer from chronic, debilitating pain on a daily basis.

Doctors ultimately diagnosed Kevin with Reflex Sympathetic Dystrophy (RSD), also known as Complex Regional Pain Syndrome (CRPS). RSD is a rare disorder of the sympathetic nervous system that is characterized by one of the most severe levels of pain on the McGill Pain Index. This continuous and intense pain is out of proportion and beyond the severity of the original injury, and gets worse rather than better over time.

A good day for Kevin was when he simply had a burning sensation in his leg that felt like the most severe sunburn he had ever experienced. On his worst days it felt like someone had a piece of sandpaper and was constantly rubbing it up and down his leg. There were times that he couldn’t even put bed sheets on top of his legs because of the intense pain they caused. Kevin struggled to get a good night’s sleep as any movement during the night was extremely agonizing.

At work, Kevin depended on a motorized cart to get around the department store he managed. The fog of his every day pain made it difficult for him to remember anything, including client’s and staff member’s names. Every bit of energy or focus Kevin had was devoted to coping with the pain. There was little left for him to function. There were times that Kevin had to call someone to pick him up because he was in too much to even drive himself home.

Kevin’s situation became so dire that he started working with a psychologist in order to help him deal with the loss of normal, everyday life. He needed painkillers and sympathetic nerve blocks just to cope with the constant, intense pain. Ultimately, Kevin’s condition forced him to alter his career path. He had to take a step back and begin managing a much smaller store, considerably farther from home, just so that he could make it through the week.

Doctors had no answers for Kevin’s condition. They merely suggested increasing the dosages of his prescriptions. Sadly, the medications just left him feeling drowsy and lethargic… yet still in constant misery. Nothing was working to control the pain. Thankfully for Kevin, he had family members who personally experienced healing and relief from Hyperbaric Oxygen Therapy. They worked on him for over a year, encouraging him to look into HBOT because of the success they had with the treatments.

Five weeks before coming to Sara’s Garden, Kevin’s pain had become so unmanageable that he was no longer even able to work. All of his time was spent at home resting or at his various treatments. He had absolutely no energy and did not even feel well enough to perform simple household tasks. His family was at a loss, feeling that they were losing Kevin as he retreated farther into solitude and despair.

When Kevin finally arrived at Sara’s Garden for Hyperbaric Oxygen Therapy treatments he was guardedly optimistic that it would be able to provide him any long lasting relief. The mask of pain on Kevin’s face was very evident. Initially his pain would gradually subside while he was inside the chamber and then return shortly after finishing treatments. As Kevin progressed through his round of treatments, his relief became more and more sustained. A smile began appearing on Kevin’s face each day… before, during and after treatments.

Not only was Kevin getting better personally. He was also connecting with all of the other people he was receiving treatment with, his new chamber family. For the first time in years, Kevin began experiencing an overwhelming and emotional sense of hope. This was also a very emotional time for his family. They commented on more than one occasion that they felt they were finally getting their dad back.

Thanks to Hyperbaric Oxygen Therapy at Sara’s Garden, Kevin has his life back. He states that without a doubt HBOT has saved his life. Kevin has been able to reduce his pain medications and is in the process of eliminating them altogether. He has shared countless hugs and tears with family, friends and co-workers who are thrilled to finally have the old Kevin back again. No matter what you’ve been told, there is hope… for this and many other conditions. HBOT is treatment without drugs… without surgery… without pain.

The Battle Began When the Tours Were Over

Called the “Signature Wound” of the war, Traumatic Brain Injury (TBI) caused by explosions has become one of the most prevalent combat wounds suffered by soldiers serving in Iraq and Afghanistan. While severe TBI can leave a person incapacitated, even a mild TBI (mTBI), often known as a concussion, can lead to debilitating symptoms including headaches, balance control, hearing problems, lack of self-control, mood changes, ringing in the ears, problems sleeping and memory loss.

Situations in Afghanistan and Iraq, where troops are likely to face multiple deployments and repeated ambushes by roadside bombs or improvised explosive devices (IEDs), are especially conducive to suffering a TBI or mild TBI. Additionally, according to recent studies, traumatic brain injuries sustained during deployments appear to increase the risk of troops experiencing Post-Traumatic Stress Disorder (PTSD). Unfortunately, for many soldiers returning home from service, the battle begins when the tours are over.

Jeremy was deployed to Iraq in 2003 and was stationed at the Abu Ghraib Prison / Central Detention on the western edge of Baghdad. His unit was heavily attacked with mortars five nights a week on a consistent basis while he was stationed there. During that period, he and many other members of his unit began to experience migraine headaches, nausea and dizziness from the exposures as well as the hazardous environment around them.

Following that initial tour of duty, Jeremy deployed to Iraq for a second tour at the end of 2004, this time stationed in Tikrit. His unit immediately began providing convoy security to transport equipment, material and personnel all across the country. They ran over 200 missions and were exposed to numerous ambushes, RPG attacks and IED explosions. The constant headaches, loss of sleep, hearing and vision problems only worsened and increased in severity and frequency.

Sadly, stories like Jeremy’s are far too common for soldiers returning from service. Just how many troops are affected is difficult to know. Sections of the government have released numbers ranging from 50,000 (Department of Defense) to 115,000 (the Pentagon), while the Brain Injury Association of America estimates the number at 360,000 and RAND corporation has suggested it could be as high as 400,000.

Unfortunately, it may be impossible to arrive at an exact number. Many soldiers are reluctant to be diagnosed for TBI. Many service members have said they refused to seek treatment for psychological illnesses because they were afraid that their unit leaders would treat them differently or cause their peers to lose confidence in their abilities. Others feared that admitting they suffered from a TBI would harm their future careers after they got out of the service. Because many are unwilling to ask for help, they resort to alternatives to cope with the disorder, such as alcohol abuse, physical violence and even suicide.

According to Stop Soldier Suicide, every single day over 22 veterans and active duty soldiers take their own lives. Burdened with the stigma associated with mental health issues and the military “shame” surrounding TBI and PTSD, they instead turn to suicide as their only option to relieve their suffering.

Thankfully, that’s not how Jeremy’s story ended. He recognized that the issues he was facing were very serious and it caused him to seek out help. He discovered Hyperbaric Oxygen Therapy (HBOT) and Sara’s Garden through Stop Soldier Suicide and the Wounded Warrior Project. The Veterans of Foreign Wars Ohio Charities learned of Jeremy’s story and stepped in to help fund his needed round of HBOT treatments.

Jeremy was excited to try a different form of treatment. All of the prescription drugs he had been taking were completely ineffective. Years after his discharge from the service, he was still unable to function and perform normally. For years he had been living a life with constant headaches, from minor to completely debilitating. As excited as Jeremy was to begin HBOT, he was equally as skeptical. He had serious doubts that sitting in a chamber breathing oxygen could help rescue him from this life of nonstop pain.

Jeremy was amazed at the immediate relief he began experiencing from the treatments as his headaches began to subside. After only one week in the chamber Jeremy was seeing recognizable improvements in a number of areas as his energy level and appetite were both increasing. The pain in his shoulder and lower back began to subside and he began sleeping 3-4 hours per night, which he had not been able to do in over 10 years.

By the end of his round of treatments, Jeremy was migraine free! In fact, he had not experienced a severe migraine from the moment he started treatments. His sleep patterns continued to improve to the point where he was now experiencing 5-6 hours of uninterrupted and restful sleep every night. The pain in his shoulder and lower back had improved to the point that he was able to begin working out and exercising again and allowed him to begin spending more time playing with his kids. Most importantly, Jeremy was able to reduce, and in some cases, eliminate his need for pain medications.

Thanks to Hyperbaric Oxygen Therapy at Sara’s Garden, Jeremy rejoices that his life has been restored. He has stated that he is forever grateful to compassionate and caring staff at Sara’s Garden. He firmly believes that every soldier could benefit from HBOT and is passionate that it should be easily accessible and available to veterans returning home from service. No matter what you’ve been told, there is hope… for this and many other conditions. HBOT is treatment without drugs… without surgery… without pain.

Final Score: HBOT – 1, Antibiotics – 0

Hearing the words “Your cancer has returned.” can be very alarming. Finding out that the only recommended course of action is the removal of your entire colon is downright terrifying.

In 2008, a routine colonoscopy revealed a large tumor in Matt’s ascending colon. During surgery to remove the tumor it was discovered that it had breeched the wall of the colon and was sticking to the small intestine. The surgeon was able to successfully perform resections of both the colon and small intestine, removing over a foot of each.

Following six months of chemotherapy, Matt was placed on a preventative checkup program consisting of quarterly blood work and annual CT scans and colonoscopies. For five years, reports came back successful and life went on as usual. In early 2014, Matt’s oncologist noted that his cancer markers appeared to be going up after reviewing his latest blood work. A CT scan was ordered and showed thickening in the walls of the cecum.

A followup colonoscopy found that a small tumor the size of a dime had started to form in his ascending colon. Knowing Matt’s family history with cancer, his doctor recommended that he see a colorectal specialist. After reviewing the medical history of Matt and his family, the specialist was convinced that Matt had Lynch syndrome.

Lynch syndrome is an inherited, genetic condition that gives a person an increased lifetime risk of developing colorectal cancer and other related cancers. Several genes have been identified that are linked to Lynch syndrome. They include MLH1, MSH2, MSH6, PMS2, and EPCAM. These genes are involved in the repair of mistakes that occur when DNA is copied in preparation for cell division (a process called DNA replication). Mutations in any of these genes prevent the proper repair of DNA replication mistakes. As the abnormal cells continue to divide, the accumulated mistakes can lead to uncontrolled cell growth and possibly cancer.

Genetic testing confirmed that Matt did indeed have Lynch syndrome due to a mutation of the MSH2 gene. According to the specialist, the recommended protocol for someone with Lynch syndrome is to remove the entire colon at the first sign of colon cancer and that Matt’s colon should never have been re-sectioned and left in before.

Surgery to remove Matt’s colon was performed in May 2014. After spending a week in the hospital, Matt returned home to continue his recovery. Unfortunately, the recovery did not go as planned. He began experiencing constant fever, severe dehydration and a complete loss of appetite. Less than a week after returning home, Matt was standing at his bathroom counter brushing his teeth when he felt his feet getting wet. Looking down, he saw fluid pouring out of the incision in his abdomen. Doctors instructed him to put a dressing on the incision to try and stem the flow of fluid. Days passed, and the incision continued to discharge fluid. Matt’s dressings had to be changed multiple times throughout the day as the fluid would soak through and spill out onto his clothes. The more he moved, the worse it got. Before long, more holes had opened up in Matt’s abdomen and his incision was dangerously close to tearing completely open.

Matt was finally readmitted to the hospital as surgeons and infectious disease specialists scrambled for answers. Matt went through countless tests and received many different antibiotics in hopes of determining what was causing this infection and buildup of fluid.

After a week in the hospital, the infection was still present and the fluid was still coming out of the open wounds in the incision. However, since Matt’s temperature had come down and he was once again able to eat food, he was released from the hospital to continue his recovery at home. Matt was sent home with a wound vac attached to his abdomen and a PICC line inserted in his arm. He was to continue receiving daily IV antibiotics in hopes of fighting this infection.

Unfortunately, the infection did not go away. His weekly blood work showed that the infection levels remained unchanged throughout the course of the summer. Matt had no energy. After attempting to work only partial days, Matt would return home and fall asleep, often unable to even spend time playing with his son. Doctors again changed the antibiotics to no avail. There was a growing conflict between the surgeon and the infectious disease doctor as to what the correct course of action should be.

In August, Matt asked his infectious disease doctor if Hyperbaric Oxygen Therapy would benefit him in treating his infection. She responded emphatically that, no, it would not help. She said that the infection was far too shallow and that HBOT would not do anything to affect it.

After dealing with this problem for over 2 ½ months Matt and his family had enough. On Monday, August 11th, Matt had his usual blood draw to determine his current infection levels. He started Hyperbaric Oxygen Treatments the very next day. Every week for the next three weeks, Matt’s blood work showed that his infection levels cut in half each and every time. By the end of his third week of treatments all of the pertinent markers in Matt’s infection levels were back in their normal ranges.

Matt’s doctors were astonished at how quickly Matt’s infection levels had come down and that the open wounds had stopped hemorrhaging fluid. Matt was able to discontinue the use of the wound vac and have his PICC line removed. He no longer needed the daily IV antibiotics or wound dressings. Matt continued to receive HBOT treatments over the next three weeks to aide in the healing and closing of the holes that the infectious fluid had opened in his incision.

In just three short weeks, HBOT had done what an entire summer of antibiotics couldn’t. HBOT was able to overcome the infection that had controlled Matt’s life and assisted in expediting his healing process. Thanks to Hyperbaric Oxygen Therapy at Sara’s Garden, Matt once again had his life back, and family had their husband and father back. He now had the energy and absence of pain that allows him to enjoy spending time playing with his son! No matter what you’ve been told, there is hope… for this and many other conditions. HBOT is treatment without drugs… without surgery… without pain.

White to Gray: The Hyperbaric Way

The nursery is decorated. The tiny clothes are washed and folded. The hospital bag is packed. Becoming a parent is simultaneously one of the most beautiful and scariest moments that we may encounter in our lives. Many parents understand the joys of having a child as something they wouldn’t trade for all the riches in the world.

Denny and Charli were eager to begin the next chapter of their lives with their new son. From the moment they received the news that they were expecting, they couldn’t wait to hold their new bundle of joy. They were thrilled when Kye was born on January 23, 2014, a beautiful, healthy baby boy. Unfortunately, that joy soon turned to terror when, shortly after his birth, Kye began to exhibit signs of seizures.

Doctors used a cooling blanket on Kye in hopes of decreasing the amount of cerebral edema, or swelling, around his brain. This cold blanket reduced Kye’s core temperature from 98 degrees to 91 degrees over a period of 72 hours, triggering a protective hypothermia in hopes of preventing further brain damage.

During this time, Kye continued to suffer additional seizures and stopped breathing numerous times. Once the cooling process was complete, Kye’s body was warmed back to normal temperature. Doctors then performed an MRI and an EEG to get a better picture of what was going on inside his little head. After reviewing Kye’s first MRI, Denny and Charli were given the terrifying news that virtually his entire brain was damaged and consisted only of white brain matter. Doctors could find no evidence of any gray brain matter.

The primary function of gray matter is to carry sensory information that comes from grey matter cells and sensory organs. This information is then passed to the areas of the brain that process sensory information. Intelligence and skill are often attributed to this brain matter, largely because it covers so much of the brain. Unlike white matter, gray matter is crucial in the development of muscle control, cognition (such as how things are seen and heard or the formation of memories) as well as speech and emotions. The fact that Kye’s brain did not possess any gray matter did not bode well for any potential development.

When Kye was released from the hospital, he was placed on two seizure medications as he continued to experience subclinical seizures every day. His parents were given a very uncertain and disheartening prognosis for what Kye’s future and quality of life was going to be.

From the moment they heard the news of his first MRI, Denny and Charli both agreed that they would do anything in their power to provide their son with the best possible outcome and chance for a bright future. They began to research Hyperbaric Oxygen Therapy and learned of its successes in treating children with traumatic brain injuries who suffer from seizures. Unfortunately, they were warned against doing HBOT treatments with Kye and told that it was a complete waste of time.

When Kye first arrived at Sara’s Garden for treatments, he had not yet achieved any of his development milestones. He wasn’t looking around or tracking movement. He wasn’t making facial expressions or clasping his hands around objects. All indications were that Kye wasn’t responding to outside stimuli and was neurologically blind.

Early on in Kye’s treatments, his parents and family began noticing changes taking place. He was becoming aware of things going on around him. He began responding to touch and tracking movement. His motor functions improved as well as he began crossing midline and reaching for and grasping his bottle. One particular evening, Charli received a telephone call. When she went to answer her cell phone she noticed that the glow of the screen had caught Kye’s attention and he began following the movement of the phone. She was so excited as Kye had never before done anything like this.

Kye is now hitting all of his development milestones. According to Kye’s parents, his Occupational and Physical Therapists have been nothing but thrilled with the progress he has made. Miraculously, Kye’s last EEG came back completely normal! In fact, tests now show that his brain does indeed consist of gray brain matter everywhere it is supposed to be. Seeing Kye make such amazing progress has been very exciting to Denny and Charli. They are so thankful that Kye’s development is turning out much differently than what they were originally told.

Kye is actually progressing so well now that doctors have a hard time distinguishing the difference between Kye and a “typical” baby. Denny and Charli believe they owe so much of Kye’s progress to the Hyperbaric Oxygen Therapy treatments that Kye received at Sara’s Garden.

For Denny and Charli, it’s been a long year filled with uncertainty and apprehension. Thanks to Hyperbaric Oxygen Therapy at Sara’s Garden, Denny and Charli no longer fear what Kye’s quality of life will be and have renewed dreams for his future. No matter what you’ve been told, there is hope… for this and many other conditions. HBOT is treatment without drugs… without surgery… without pain.

Saved from Surgery

Eight-year-old girls are supposed to spend their time enjoying games, watching TV, reading books and playing with their friends; not worrying about seizures, sinus headaches and bone-eating infections. Unfortunately for Rachel, her life’s journey over the past six months has been much different than most kids her age.

In December 2013, mere days before Christmas, Rachel wasn’t feeling well. She was taken to the doctor and diagnosed with the flu and an ear infection. A few days later, Rachel’s mom called the doctor because she had become so sick that she wasn’t able to keep her meds down. Her prescriptions were changed but it didn’t help. Rachel became so sick that she couldn’t even go to her grandma’s house for Christmas.

On December 27th Rachel went back to the doctor where she was diagnosed with Acute Sinusitis. This condition causes the cavities around the nasal passages to become inflamed and swollen. This interferes with drainage and causes mucus to build up. Acute Sinusitis can be caused by the common cold, allergies, bacterial and fungal infections.

Two nights later, Rachel’s family was sitting around the table playing board games. All of a sudden, Rachel’s speech became slurred and no one could make out what she was saying. She then began to stare into space and not talk. It took 20 minutes before they finally were able to get her to respond. Rachel had trouble sleeping that night so her mom held her in a recliner chair downstairs. A few hours later she suddenly threw up, became unresponsive and started convulsing.

Rachel was rushed to the emergency room as she continued to seize. Her right eye, cheek and arm were twitching and jerking and saliva was starting to run out of the side of her mouth. Her seizure lasted over 2 hours. Rachel was transferred to Peyton Manning Children’s Hospital in Indianapolis. They learned that there was fluid on her brain and an infection between her skull and brain called an Epidural Abscess. Within twelve hours Rachel was having surgery to clean out all of her sinus cavities in hopes that the infection would begin to subside. Rachel spent the next week in the hospital to see if the antibiotics were having an affect on the infection.

Doctors tried several antibiotics. Nothing seemed to work. On March 20, 2014, Rachel had a second surgery to clean out her sinus cavities once again. An MRI uncovered an infection in the front follicle bone that had started eating part of her bone. Doctors tried several additional antibiotics with no success. The family was told that if they didn’t see significant change on the next MRI on April 29th, Rachel would need to have a major surgery to remove her front follicle bone and replace it with a cement-like bone with a metal plate on top for protection. Rachel’s family immediately began praying for healing so that this surgery would not be necessary.

Their answer to prayer came when someone they attend church with asked if they had ever heard of Hyperbaric Oxygen Therapy and encouraged them to call Sara’s Garden for more information.

Rachel arrived at Sara’s Garden five days before the impending April 29th MRI. After receiving five treatments, Rachel’s family noticed that she was no longer complaining about experiencing the painful sinus headaches that she had been dealing with over the past few months. Encouraged by this revelation, the family returned to Indianapolis for Rachel’s next round of testing. The results showed a slight improvement in the infection level. Their doctor encouraged them to continue receiving HBOT and suggested they postpone the surgery. She and her family returned to Sara’s Garden with renewed hope that they would be able to fight this infection with HBOT and keep Rachel from needing to undergo a major surgery.

After Rachel’s 29th treatment, the family headed back to Peyton Manning Children’s Hospital for yet another CT Scan. When they met to learn the results of the test later that day, the infectious disease doctor just kept repeating over and over again how shocked and amazed she was. Rachel’s front follicle bone was completely healed. There was no longer any trace of an infection anywhere. The doctor had read the report over three times before meeting with the family to be sure she hadn’t read it wrong and commented that she would have had a hard time believing the results if it hadn’t been read by her most trusted radiologist.

They were overjoyed to learn that major surgery would not be needed. However, because of all of the damage to Rachel’s sinuses, there was still a chance that Rachel would have to undergo another surgery to clean out the sinus cavities again. The doctor encouraged them to continue on with HBOT and see what would happen.

Upon completing 40 HBOT treatments, Rachel’s family met with the neurosurgeon one last time. When the family was ready to leave, he commented to the student doctor who was shadowing him, “We tried everything on this little girl and nothing helped until they went and did Hyperbaric Oxygen Therapy! That saved them so much heartache and a major surgery! I can’t tell you how thrilled I am for them!” Additionally, Rachel’s Ear, Nose, Throat Specialist (ENT) was so pleased with the results of Rachel’s treatments that he said it would not be necessary to undergo the surgery to clear out her sinus cavities.

The past six, long months had been extremely hard on Rachel’s family. At times it seemed like they had more questions than answers. It was so painful seeing Rachel suffer from the effects of this ravaging infection. Rachel’s family knows that their faith and the continuous prayers from countless supporters helped carry them through this difficult time.

HBOT was able to do what months of antibiotics couldn’t in fighting a serious, bone-eating infection. Thanks to Hyperbaric Oxygen Therapy at Sara’s Garden, Rachel was saved from having to undergo multiple surgeries and was finally able to experience healing. No matter what you’ve been told, there is hope… for this and many other conditions. HBOT is treatment without drugs… without surgery… without pain.

Turtle Comes Out of His Shell

April 18, 2014
4:04 am
Success Stories, Success Stories: ABA, Success Stories: NHA

Education and friendship can play a huge role in the life of any child, but they may be even more vital for a child with Autism.

Autistic children differ in the way they perceive things and respond to the world around them. They often have great difficulty making sense of the world as other children see it. Too often, children with Autism are not the preferred partners of typical children. In the worst of cases, they may be bullied because they look, act or sound different than their typical peers. Children with Autism require caring, individualized attention from teachers and intervention specialists. They may also need extra help interpreting friendships, non-verbal communication, using school equipment, paying attention in class or controlling their behaviors.

For Glen (Turtle as his mother affectionately calls him), the first two weeks of school at New Horizons Academy at Sara’s Garden were extremely rough. It represented yet another change in his life. He had struggled in his previous school placements, often acting out and exhibiting behaviors that made it nearly impossible for teachers to control and teach him or peers to get to know and befriend him.

For weeks, Glen’s mother would literally pry him from the car each morning and carry him into the school. Glen would be hitting, screaming, kicking and biting her the entire way into the building. Each morning, the NHA staff would immediately take Glen into the multi-sensory room when he arrived and spend time with him, helping to calm him down and get him ready for the school day ahead. Many times, he would need to be restrained so he would not hurt himself. His sole focus was on his mother. He desperately wanted to stay with her, fearing that she was leaving him at school forever. However, after spending time in the multi-sensory room Glen would calm down and eventually go to his classroom with his peers.

When Glen started school at NHA, we were told that he had Selective Mutism (SM), an anxiety disorder in which a person who is normally capable of speech does not speak in specific situations or to specific people. We learned that Glen had been teased because of his speech impediment at previous schools and had therefore stopped speaking in public. He lacked self-confidence and was terrified to try new things. Glen had no friends. In fact, according to Glen’s mom, he had never had friends before in his life because other children were afraid of him due to his negative behaviors.

While each morning was difficult for Glen those first weeks, the staff began to notice significant changes.

Every morning, Glen’s outbursts became less severe and shorter in duration. Then, during the third week of school an amazing event took place. Glen came rushing into school, not waiting for his mother to bring him! He appeared to be very excited. Our school administrator, Mr. Burkholder, asked his mother what brought about the change. She stated that she had taken him to Wal-Mart to purchase a special toy… not for himself, but for the new friend that he had made at New Horizons Academy. He could not wait to come to school to give his new friend this toy. This began a new pattern. Glen loves coming to school each day and no longer has negative behaviors.

What has developed from this one friendship is a young boy who quickly began developing self-confidence and trust. He began to excel in his academics and the teachers watched him blossom into a special leader. He continually wants more academic challenges. The teachers realized that despite what was written in all of the reports they had received on Glen, he had so much ability and potential. It was not long into the first grading period that Glen had already mastered the goals that had been written on his IEP.

Now, six months later, he has become his classroom’s “Chatty Cathy”. He loves interacting with his classmates and completing his classwork. Learning how to do simple addition has just clicked in Glen’s brain. It was like watching a light bulb come on. He picked up the concept and is exceeding his yearly goal. Now he wants to do his math work first. Reading continues to be difficult for Glen due to his speech impediment, but that doesn’t stop him from trying. He reads with his classmates at his ability level and is always willing to attempt reading new words, which includes weekly spelling words. He has also shown significant improvement when writing letters with the proper formation and always turns in his homework. Once Glen is assigned a task or classroom chore he doesn’t stop. He is the one student that can be given a task and you know it will get done with no supervision. He takes on the responsibility of teaching his classmates how to complete a task or chore with pride.

Glen is now able to receive individualized and differentiated educational instruction. Combined with NHA’s diversity of intervention tools such as Conductive Education, Autism Intervention and Sensory Integration, delivered by a specialized staff that is able to give Glen the necessary focused attention, he continues to excel. He now has many friends. He loves to come to school and you can see him walking around NHA with a smile on his face. When you look at Glen now, as compared to September 2013, you will find a boy full of self-confidence, pride, and happiness.

New Horizons Academy provided Glen with a safe, nurturing environment where he could feel accepted and loved. Once the behaviors were overcome, the teachers no longer have to address bad behaviors, and can focus on his education. Thanks to New Horizons Academy at Sara’s Garden, Turtle has come out of his shell. Glen’s mom gets to see her son’s emerging potential and has renewed dreams for his future.

No matter what you have been told, there is hope. Hope for a child to emerge into the responsible adults we as parents pray for. There is hope for those who were told they would not learn, or walk, or talk. That hope, is rekindled through the work that is happening at New Horizons Academy. The loving, caring and true compassion that is shown to each and every student, no matter how difficult their condition, disability, or behavior might be, is where the success story starts. Come join us and you’ll see what is possible for a child who has been labeled as “different”. New Horizons Academy at Sara’s Garden… Where kids come first!