Final Score: HBOT – 1, Antibiotics – 0

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

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

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.

HBOT Delivers a 1-2 Punch

HBOT Delivers a 1-2 Punch

Knee replacements are one of the most commonly performed elective, orthopedic operations. For the majority of patients, knee replacement surgery relieves pain and helps them to live fuller, more active lives. But for some, the opposite occurs.

No surgical procedure is without risks and a small percentage of patients undergoing knee replacement may develop an infection following the operation. Joint replacement infections may occur in the wound or deep around the artificial implants. An infection may develop during the hospital stay or after the return home. Joint replacement infections can even occur years after surgery. Unfortunately, that’s exactly what happened to Bill.

Bill had to have joint replacement surgery in 2006 due to a work related injury he had suffered on his left knee back in 1991. Over the years, his knee gradually deteriorated to the point that it finally had to be replaced. Bill’s surgery went according to plan. Following surgery Bill returned home to begin his recovery. Doctors continued to examine his knee annually to ensure that it was still functioning properly. Everything appeared to be going great.

In December 2011 Bill’s left knee began causing him a lot of pain. When he went in to see the doctor an x-ray showed that fluid was building up around his knee, which had to be drained off. His blood work and an MRI indicated the presence of an infection. By February, Bill was forced to stop working due to the excruciating pain in his knee.

Infections can be caused by a variety of bacteria and viruses that are usually kept in check by the immune system. However, because joint replacements are made of metal and plastic, it is difficult for the immune system to attack bacteria or viruses that make it to these implants. If bacteria or viruses gain access to the implants, they may multiply and cause an unrelenting infection. Despite antibiotics and preventative treatments, patients with infected joint replacements often require surgery in order to cure the infection. Because of the level of the infection and the amount of pain it was causing, the doctors decided on a plan to remove Bill’s artificial knee and implant another one.

However, in March, when doctors opened up Bill’s knee during surgery it was discovered that the replaced knee had worked itself loose. The doctor simply pulled it right out of the bone. A medical spacer was installed instead of a new knee replacement until they could clear up the infection. Bill began receiving antibiotics administered via a peripherally inserted central catheter (PICC or PIC line) to treat the infection. By the end of June, a filter had to be put in due to a blood clot that had formed in the left leg.

Bill had hoped for his new knee to be put in by July, but his blood work indicated that two new types of bacteria were now present. Because of these new infections, the original medical spacer was removed and a new spacer was put in. Bill received ongoing intravenous antibiotics but his blood work continued to show that the infection levels remained unchanged.

Bill was a 65-year-old man who loved working and staying busy. To his dismay, he was now confined to a wheelchair. When Bill arrived at Sara’s Garden to begin HBOT treatments, he had spent nearly six months without a knee. He was unable to bend his leg or bear any weight and was completely dependent on his wife to meet all of his needs.

Following Bill’s first week of HBOT treatments he returned to his doctors to have new blood work done. He was overjoyed to learn that his infection level had been cut in half. After his second week of treatments his infection level was once again cut in half. By the end of Bill’s third week of treatments, the infection level in his knee was virtually non-existent and his doctors were finally willing to allow him to have his knee replacement scheduled. Because Hyperbaric Oxygen Therapy is anti-viral, anti-bacterial and anti-fungal, it was able to do in less than a month what a constant supply of IV antibiotics had been unable to affect in months; eliminate Bill’s infection and get him back on the road to recovery.

By the end of September, Bill was able to finally undergo surgery to replace his knee and remove the spacer that he had lived with for almost seven months. After being released from the hospital, Bill continued to receive HBOT treatments to expedite his healing process and help him recover from his physical therapy sessions. Bill was very concerned about this pending recovery process. He knew how hard it had been for him to recover from knee surgery and undergo physical therapy following his first knee surgery. He feared this time was sure to be even more difficult for him due to the amount of time he had just spent confined to a wheelchair, unable to do anything physical in nature.

Bill and his family were thrilled that he experienced the exact opposite this time around. Because of the HBOT treatments Bill continued to receive, the inflammation and swelling in Bill’s knee was reduced more quickly following surgery and physical therapy sessions. He was also able to gain greater flexibility and range of motion more quickly and experienced much less pain than in the past.

HBOT delivered a 1-2 punch for Bill in helping him overcome a debilitating infection and assisting in expediting his recovery process. Thanks to Hyperbaric Oxygen Therapy at Sara’s Garden, Bill was finally able to escape from his wheelchair and gain his independence 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.

Desperate for Relief

Desperate for Relief

Almost everyone has experienced a headache at one time in their life, but very few people have lived with a debilitating migraine that lasted over seven straight months.

Brianne had suffered from migraines off and on for over 14 years. She would typically experience burning, throbbing and stabbing pain that resulted in nausea and sensitivity to both light and sound. Despite undergoing countless tests, doctors could never determine what triggered Brianne’s migraines. Even worse, they were never able to find a medication to effectively control them. Brianne’s migraines would leave just as suddenly and mysteriously as they had arrived. That all changed on Mother’s Day in 2012 when a migraine struck violently and didn’t subside for over seven months.

Initially, Brianne’s family took her to the ER for shots in hopes of treating the migraine. Unfortunately, Brianne didn’t experience any relief so she went to see her family’s long time general practitioner who prescribed additional medications. When the pain still didn’t abate after several weeks her next stop was to meet with a neurologist where a CT scan showed no abnormalities. After several additional weeks and even stronger prescriptions, nothing had diminished the pain or eased the effects of the migraine. The neurologist told Brianne’s family that there was nothing more that he could do for her.

By now the non-stop migraine was entering week number nine. The family was referred to Michigan Head Pain and Neurological Institute (MHNI) which is one of the top clinics for head pain in the United States. After an all-day appointment that involved many tests and meetings with several different practitioners, Brianne was diagnosed with chronic migraine pain.

Brianne was admitted into MHNI, which has a 20-bed unit in Chelsea Hospital dedicated to only head pain patients. Each day of Brianne’s two week stay included rounds of IV medications, tests and procedures. Her brain was checked for tumors, lesions and any other abnormalities. She even had a test done on her heart to check for an abnormality that involves a tiny hole in the heart that can induce migraines. Nothing helped.

Months after Brianne’s migraine struck, her life was still on hold. Brianne had to wear darkly tinted lens indoors and a brimmed hat when outdoors. Earplugs would with any loud sounds when she is away from home. Due to the constant migraine pain she was experiencing, Brianne had to drop out of school and quit her part time job. Reading made her so nauseous that she was unable to study despite being on nine different medications. In addition to all the medications, Brianne tried chiropractic treatments, homeopathic remedies, acupuncture, and massage therapy.

Brianne had virtually no social interaction. The pain was so intense that she rarely participated in anything with her family. She slept all the time yet said that she was always tired and had no energy. She kept herself in constant darkness even when she was awake. Brianne and her family were desperate and on the verge of losing all hope for relief when they heard about Hyperbaric Oxygen Therapy (HBOT) at Sara’s Garden and learned that it had been successful in treating people who suffer from migraines.

When Brianne first came to Sara’s Garden she was extremely pale and was more than a little apprehensive. She and her family didn’t know what to expect. Her eyes were glazed over and she had a very difficult time conversing with the staff. The light from being out in public was causing her tremendous pain despite the fact that she wore dark sunglasses. Following her first treatment she begged her mom to let her go home to her dark room. Thankfully her mom didn’t acquiesce and Brianne continued to come back each day.

By the middle of her second week of treatments, Brianne had a 20 minute respite from her pain. This was the beginning of the light at the end of the tunnel! From that point on her pain began to recede. Because she had been living with this constant pain for so long she didn’t recognize the changes at first. She began using her hair dryer in the morning after showering. This was a tremendous milestone for her as noise and heat were typically unbearable. She then started to spend time with her family in the living room watching television with the sound loud enough for everyone to hear. Soon after, she was turning the radio on in the car on the way in for treatments.

By the third week of treatments she ventured out shopping with no hat or sunglasses. By the end of the week she was stating that she was pain free and started driving for the first time on over six months! At the end of her treatments Brianne was pain free. She could drive, exercise and even do household chores. Over the past year, Brianne has had several migraines that she refers to as “normal people” migraines. These last only a few hours and have been traced to low blood sugar, fatigue or muscle strain in her neck. She combats this with frequent small meals, yoga, and the occasional nap.

Thanks to Hyperbaric Oxygen Therapy at Sara’s Garden, Brianne has her life back. Her family is convinced that without these treatments, none of this would have been possible. 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.

Wheeled In. Walked Out.

Wheeled In. Walked Out.

How many times have you been told not to take your health for granted? We all do though. When you’re a healthy 25 year old mother of three small children you rarely have time to stop and worry about how your life would be different if your health was suddenly taken from you. Yet that’s exactly what happened to Aubree.

On November 17, 2012, Aubree was a passenger in a car that was struck by a pickup truck that had run a red light. The impact from the accident took place on her side of the vehicle. Aubree suffered a Traumatic Brain Injury (TBI) and spent five weeks in the Surgical Trauma Intensive Care Unit (STICU). Doctors in the STICU were very guarded about giving the family too much hope for a promising outcome.

While in STICU, Aubree was kept sedated for approximately two and a half weeks. The most intensive part of her recovery involved an ICP drain/probe that saved her from needing a craniotomy in order to relieve the mounting pressure and swelling that had occurred on her brain. At the conclusion of the five weeks in the STICU, Aubree was transferred to a skilled nursing facility in order to prepare her for the intensive therapy she would need to undergo at an acute rehab center. Although Aubree had made great progress to this point, she still had a very long road ahead of her.

Upon arriving at the skilled nursing facility, Aubree was still in a minimally-conscious state. She was only able to move her body involuntarily, often rolling from side to side. She was not able to access her physical motor skills on command and could only sit up with assistance from an aide or family member. She was still on a feeding tube and was not yet able to speak or communicate. Other than family and a few close friends, no one appeared to hold out much hope for Aubree’s improvement.

Aubree’s family knew that they had to try every avenue available that could even remotely give her a greater chance at a full recovery. While they felt blessed that Aubree was still with them, they wanted to give her every opportunity they could for a bright and independent future and to help her return to her role as wife and mother. She had been a happy, fun-loving, and vibrant young woman who had many dreams and aspirations for her future. They wanted to provide that hope for her yet again.

As her family began researching alternative treatment options, they discovered Hyperbaric Oxygen Therapy and learned how it had been successful in treating TBI. Research showed that many military troops who have served in Iraq and Afghanistan are returning home with TBI and Post Traumatic Stress Disorder (PTSD). In the past few years there have been numerous Defense Department-led studies looking at the effects of HBOT on troops with TBI. HBOT is an effective and economical treatment for TBI and PTSD, without the very dangerous and negative side effects of antipsychotic medication.

Hyperbaric Oxygen Therapy has been shown to improve client’s fine and gross motor skills, speech, thinking (cognition), memory and physical healing. First Lady, Michelle Obama has even become involved in the White House’s Joining Forces Initiative. The program could play a significant role in recognizing HBOT as a premier therapy for brain injuries and PTSD. With the White House spearheading this initiative, it could mean that the tide is turning, and FDA’s non-approval of HBOT for the treatment of TBI or PTSD may be crumbling, as well as its refusal to use HBOT for TBI and PTSD because it’s considered “off-label,” while at the same time using antipsychotic drugs completely off-label for treatment of TBI and PTSD.

Aubree started Hyperbaric Oxygen Therapy at Sara’s Garden on January 9, 2013, nearly two months after the accident that changed her life so drastically. One week later, on January 15, Aubree started talking, bringing most of the staff to tears. As the month went on she began moving around more. She started getting out of the stretcher between treatments and walking up and down the hall with assistance. By January 30, Aubree was walking with no assistance at all. She was an inspiration to everyone around her and was actively encouraging other clients in their recovery.

Several of the EMTs who had been transporting Aubree to Sara’s Garden the first week did not see her again until her fourth and final week of treatments. They were shocked and elated at the progress she had made in that short time. The young woman that arrived for her first day of treatments on a stretcher walked out the door on her own 40 treatments later.

Thanks to Hyperbaric Oxygen Therapy at Sara’s Garden, Aubree once again has dreams and aspirations for a vibrant future. Most importantly, her family has their wife and mother back! Aubree plans on going back to school and finishing her nursing degree so that she can give back by taking care of others in need.

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.

Miracles For Makayla

Makayla was born a happy, healthy, little girl. Before, during and after birth there were no complications. Her family had no concerns or fears that Makayla’s life was to be anything but typical. However, when she was four months old, the unthinkable happened. Makayla started having seizures. Doctors ordered an MRI but couldn’t find an explanation for the seizures so she was simply put on medication in hopes of controlling the seizure activity.

One month later Makayla experienced a Grade 4 bilateral bleed that resulted in severe damage to her brain and caused her to slip into a coma. Doctors informed her family that Makayla would not survive the trauma of the brain bleed. They were told that even if, by some miracle, she was to recover, Makayla would live in a vegetative state for the rest of her life.

Thankfully, Makayla’s family got their miracle as she did come out of the coma. However, their elation was short lived as doctors informed them that Makayla would never be able to eat or breathe on her own. They went on to say that she would never be able to show emotion, speak, or even have the ability to make noise. Because of the extent of the brain damage they said that she would also be incapable of learning. She was later diagnosed with Cerebral Palsy, Intractable Epilepsy, Cortical Visual Impairment and Hydrocephalus.

The brain injury caused her to have weakness and decreased control of the left side of her body as well as severe developmental, physical, oral, vision and speech delays. Makayla endured countless scans, blood tests and genetic tests but doctors were never able to determine any cause for the brain bleed. They could not find any vascular malformation or sign of anything that might have triggered the bleed.

Since that time, doctors have tried over 10 different seizure medications in hopes of controlling Makayla’s seizures. Each medication caused her to be groggy and slowed her development. As a last resort, she was placed on a very strict Ketogenic diet to try and control seizures. Nothing worked.

Makayla’s seizures had become a daily part of her family’s lives. Her family would refrain from going out much or doing anything that could possibly overstimulate Makayla as over-stimulation seemed to lead to more seizures. On her best days, Makayla would have only 2-3 seizures a day, each lasting anywhere from 20 seconds to 4 minutes. On her worst days, Makayla would suffer a seizure every five minutes all day long. One week before Makayla and her mom left home to come to Sara’s Garden, Makayla had her longest seizure to date, a 30 minute seizure which resulted in another cerebral hemorrhage.

When Makayla’s family began researching HBOT and CE at Sara’s Garden they talked to all of her doctors and specialists in hopes of receiving positive feedback. Most didn’t know enough about either process to even offer an opinion. Unfortunately some were not on board and strongly discouraged them from doing HBOT. One specialist said that because Makayla’s seizures were uncontrolled by medication, doing HBOT could possibly make her seizures worse and more frequent. This was someone that they trusted and highly respected. Going against his advice was one of the hardest decisions they ever had to make. With a lot of prayer and faith, they decided to try.

Makayla’s first HBOT treatment was April 23rd, 2012. Her very last seizure was hours before going into the chamber. A week later, Makayla looked at her mother and held her gaze for over 20 seconds, something she had never done before. Since completing HBOT and CE at Sara’s Garden, Makayla has made huge improvements. Because her brain is no longer constantly seizing, it has time to do what it’s supposed to do: learn and develop. Her vision has improved and she is able to focus more easily. The muscle tone in her neck and core has improved. Prior to coming to Sara’s Garden, Makayla only used her left arm and leg about 20% of the time. She now is using them over 85% of the time. She can hold things in her left hand as well as transfer a toy from one hand to the other or hold her hands together. She has also been experimenting with making many new noises and sounds. She now enjoys activities that would once have overstimulated her and caused more seizures.

Makayla was not expected to live. Yet three years later, she continues to thrive and progress further than all the doctors ever thought possible! Thanks to Hyperbaric Oxygen Therapy and Conductive Education at Sara’s Garden, Makayla’s family experienced yet another miracle. She once had the muscle tone of a wet noodle and would spend most of her day coping with the ravaging effects of seizures. She can now hold her head up, sit independently with the assistance of arm splints, walk with assistance, and most importantly… Makayla has been seizure-free since the day she started treatments. Miracles never cease.

No matter what you’ve been told, there is hope… and Sara’s Garden can help you find it.

An Angel Spreads His Wings

Solange has always referred to her son Jose as her angel. He was born a healthy, happy baby. However, when Jose was just 18 months old he contracted a virus that led to a multi-organ system failure. He was first diagnosed with Hemolytic Uremic Syndrome and required dialysis, blood products and respiratory assistance.

As time went on Jose began to improve physically but his cognitive abilities seemed uncertain and he still required intensive care. Further complications ensued when Jose began convulsing during a meal. He aspirated milk into his lungs causing him to suffer a stroke. From this moment on, Jose did not develop as he should either physically or cognitively. Jose’s official diagnosis was Cerebral Palsy but he exhibited strong Autistic tendencies and traits.

By the time Jose was eight years old, he was still unable to stand or take steps independently. He crawled everywhere he needed to go. His mother had to walk behind him, holding him around the chest in order to provide the balance and support he needed to take steps. She also had to feed him at every meal as he was unable to grasp utensils or his glass by himself. He had very minimal verbalizations and was not able to follow even simple requests. He displayed almost no emotion and would not notice or acknowledge anyone entering or leaving the room.

Jose’s family was told that he would never walk independently. They were told he would not have the strength or coordination to pedal a bicycle and he would never be able to communicate beyond a few unintelligible syllables. He would spend the rest of his life in a wheelchair and need constant care and supervision.

Thanks to a loving and supportive community, Jose’s family was able to travel to Sara’s Garden from New York City in June 2012 so he could receive Hyperbaric Oxygen Therapy and Autism Intervention services. By the end of his initial month of treatments Jose was starting to do things on his own. He started to initiate standing and began taking steps with minimal assistance. At meals he began holding his own drink and started using the utensils to feed himself.

His family was so thrilled at the progress Jose made that first month that they made plans to return again a month later in August. Throughout his second month of treatments Jose continued to make physical and cognitive advancements. He improved with following requests and began expressing personal choices when he needed something. He started showing more emotion and began recognizing when others would come around him. For the first time in his entire life he pedaled a tricycle all by himself and began taking his first independent steps!

Solange has said that she feels like she is living a miracle after being told for years all of the things that Jose would never be able to do. Upon returning home to New York, Jose’s mom took him back to his school to show them his progress. They were amazed at what they saw and commented that they had never before seen a child improve as fast as Jose had. Instead of being confined to a wheelchair the entire day, Jose is now in a more advanced classroom with higher functioning peers. Teachers and friends alike are now trying to keep up with Jose and his newfound freedom!

Jose continues to make gains. He is showing much more interest in the world around him. He is now able to focus on activities at home and school. Instead of eating every meal at Jose’s side, Solange is able to sit across from him and enjoy their meal together. For the first time they are able to have family movie nights as Jose is now able to watch the movie and focus on what is taking place. It brings them so much joy to hear him laugh when he sees or hears something funny. He is no longer a little boy who is constantly told all of the things he will never do.

Before coming to Sara’s Garden Jose depended on his mother for everything. That is no longer the case. Every day he becomes less and less dependent on her and for some that could be a scary thought. Thanks to Hyperbaric Oxygen Therapy and Autism Intervention services at Sara’s Garden, Jose is learning what it is like to be an independent young man. Solange wouldn’t have it any other way.

No matter what you’ve been told, there is hope… and Sara’s Garden can help you find it.

What If Nobody Knows What’s Wrong?

What If Nobody Knows What’s Wrong?

Taylor became ill at the end of her sophomore year in high school when she was fifteen and a half years old. Over the course of the next year she would suffer from intense fevers, rashes all over her body and debilitating pain in her head, joints and neck.

In May 2005 Taylor was hospitalized while countless doctors and specialists attempted to diagnose her condition. Unfortunately, no one could give her an answer as to what was wrong with her. She was treated for a variety of conditions but nothing seemed to provide any relief. Taylor limped through the next year seeing specialist after specialist, making emergency room visits and missing school. She had to quit all of her activities and things she loved the most… dance, horseback riding and running.

By the following spring Taylor was so weak and wracked with fever and pain that she was hospitalized once again. For over a month a team of neurologists experimented, drugged and tested her for everything imaginable but were still unable to determine the cause of her suffering. In June 2006 Taylor was given a spinal tap which indicated a serious, deep tissue infection. Based on all of their clinical findings, doctors diagnosed Taylor with Lyme disease. Left untreated, Lyme disease can progress to more serious symptoms involving the heart and central nervous system which can be debilitating, difficult to treat and even fatal.

Lyme disease is the most common tick-borne disease in the Northern Hemisphere and is transmitted to humans by the bite of infected ticks. The disease is named after the town of Lyme, Connecticut, where a number of cases were first identified. It has long been speculated that Lyme disease was created and accidentally spread from a US biological warfare laboratory at Plum Island, just off the coast of Connecticut, by Nazi scientists recruited by the US for post-war purposes. These scientists had specialized in using ticks and mosquitoes to spread diseases in Nazi Germany during World War II.

Lyme disease is incredibly hard to diagnose due to the fact that its signs and symptoms mimic those of numerous other diseases. The flu-like symptoms which often accompany the onset of Lyme disease can easily be mistaken for viral infections, such as influenza or infectious mononucleosis. Other symptoms of Lyme disease such as joint pain can be mistaken for types of arthritis. The clinical diagnosis of Lyme disease is most often based on the patient’s personal history, as well as recent admittance of exposure to possible tick-infested areas.

For the next two years, Taylor underwent every imaginable Lyme disease treatment available. Nothing helped. By the end of 2008 Taylor was incredibly weak and had virtually no energy to do anything. She could not work and was forced to drop out of college. It was during this time Taylor’s family discovered Hyperbaric Oxygen Therapy (HBOT). This treatment was instrumental in turning her health and life around.

After much research Taylor’s family contacted Sara’s Garden in Wauseon, Ohio regarding possible treatment options. While receiving HBOT at Sara’s Garden, Taylor finally turned a corner in her recovery. The pain that she had lived with for so long was was diminishing with each treatment and her energy had returned. She was now able to complete college, started a job at a hospital as a phlebotomist, got married and began a whole new life.

In January 2012, Taylor and her husband became concerned when she skipped a menstrual cycle and started hot flashing severely. Five different doctors diagnosed Taylor with premature ovarian failure and told her she would never be able to get pregnant and have children without an egg donor. She was devastated. Her dreams of starting her own family were now suddenly taken away.

While waiting to see a reproductive endocrinologist Taylor again contacted Sara’s Garden. Given Taylor’s medical history of Lyme disease it was suggested that HBOT could assist in eradicating any remaining active Lyme bacteria present and that the treatments could also help rejuvenate hormone levels and functionality. Taylor again began receiving Hyperbaric Oxygen Therapy. Soon after, Taylor went to her appointment with the reproductive specialist. He couldn’t explain it, but Taylor’s uterus and ovaries were now very healthy and she was deemed fertile. Several months later Taylor was overjoyed to learn that she was now pregnant and she had not needed any drugs or medical assistance in order to conceive!

Thanks to Hyperbaric Oxygen Therapy at Sara’s Garden, Taylor’s life has been changed forever. Her health, her life and her dreams of starting a family have been restored. 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.

Concussion puts NHL Dreams on Ice

Concussion puts NHL Dreams on Ice

There can be no denying that hockey is Canada’s national game. It is on television and radio all day… every day. Virtually every young Canadian dreams of playing in the National Hockey League when they grow up. Stratford, Ontario’s Joey Hishon was no exception. In June 2010 those dreams were on their way to becoming a reality as Joey was selected by the Colorado Avalanche in the first round of the NHL Entry Draft. As he donned the Avalanche jersey and stood there on the stage of the Staples Center in Los Angeles, California, it began to sink in that all of the hard work and late night skates had finally paid off.

Joey went on to play his final season of Canadian junior ice hockey. He led the Owen Sound Attack in scoring with 87 points (37 goals, 50 assists) averaging an impressive 1.74 points per game. He was instrumental in guiding the Attack to the J. Ross Robertson Cup as the 2010-11 Ontario Hockey League Champions.

Everything was going according to plan. Joey was to compete in one final Memorial Cup tournament before heading to Colorado for training camp to fulfill his dreams of playing in the NHL. The Memorial Cup is awarded annually to the Canadian Hockey League champion. It is a four-team tournament between a host team and the champions of the Ontario Hockey League, Quebec Major Junior Hockey League and Western Hockey League and is the pinnacle of junior hockey success.

On May 21, 2011 Joey’s dreams of playing in the NHL were in danger of being put on ice as he sustained a violent, illegal elbow to his head in his team’s first game of the Memorial Cup. Blood dripped from his face as he lay on the ice before being helped off by staff and teammates. Joey was diagnosed with a concussion and was forced to sit out the remainder of the tournament. Little did he know that this was just the beginning of a long break from the game he loved.

Nearly four months after he was knocked out of the Memorial Cup, Joey was still not able to take part in on-ice activities at Colorado’s fall training camp. Daily headaches kept him from participating in any physical activity. As more time went by, headaches continued to provide an ongoing reminder of the injury he had received to his brain. Even on days when he would not have a headache, Joey felt like his mind was clouded, as if he were walking around in a constant fog. Any physical exertion would cause him to experience painful pressure in his head.

Doctors refused to clear Joey for play until all of his headaches and concussion symptoms had subsided. The only remedy that they would prescribe to him was rest. Before he knew it, four more months had passed and half the season was lost as his condition did not improve. Then a friend told Joey about Hyperbaric Oxygen Therapy and explained how it had helped him overcome a similar injury. Unfortunately, Joey was asked not to pursue treatments and told that while there was evidence HBOT would aid in post-concussion recovery, there was no proof that it would help in the relief from headaches.

Joey was forced to continue waiting. Three more months passed and the entire 2011-12 season was lost. He could wait no longer. Joey arrived at Sara’s Garden a mere 14 days shy of the one year anniversary of his concussion. As he progressed through his round of treatments he became hopeful as the frequency of his headaches began diminishing. He started working out in his hotel’s gym and noticed that he was not experiencing the pressure in his head as he had in the past.

After completing a round of 40 HBOT treatments, Joey is now on the path to recovery and working towards becoming an NHL player like he has always dreamed of. Thanks to Hyperbaric Oxygen Therapy at Sara’s Garden, Joey is back on the ice and his dream of a career in the NHL is no longer on hold.

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.