Wauseon Nonprofit Delivers Hyperbaric Treatment

Wauseon Nonprofit Delivers Hyperbaric Treatment

Article published Tuesday, March 20, 2012 by the Toledo Blade

WAUSEON — Northeast Ohio co-workers Laura Ramsey and Pam Haberkorn were trying gluten-free diets to help their autistic children when they learned of an alternative treatment showing promise in research: hyperbaric oxygen therapy.

In the summer of 2009, the teachers took their children to a private hyperbaric oxygen center in North Carolina to get the treatment, involving pure oxygen administered at higher than atmospheric pressure.

While in North Carolina, Katelyn Haberkorn, now 13, received two rounds of so-called dives and made remarkable progress, her mother said. Katelyn showed an interest in books for the first time and began talking more, making eye contact, and paying attention, Ms. Haberkorn said.

“When we learned about this, we had no idea what we were going to see,” said the mother of three from Medina. “She was bringing us books within a week, wanting us to read them.”

The two families since have found Sara’s Garden, a nonprofit center in Wauseon with two hyperbaric chambers, one with five seats and another with 10.

Such chambers have been used for decades, most commonly to heal wounds in diabetics and help divers with decompression sickness, but Sara’s Garden also treats patients with nonemergency ailments not covered by insurance and those who could not afford them elsewhere.

Each session costs $110 to $165 at the center staffed by five nurses and three chamber operators. A round typically involves 40 sessions, said Matthew Rychener, Sara’s Garden’s development director.

Sara’s Garden helps raise funds for treatments, and all patients must have a medical prescription and an X-ray, Mr. Rychener said.

Most hyperbaric clinics in Ohio and Michigan are associated with hospitals, although there are a few other independent facilities.

The Wauseon nonprofit organization got its start after Mr. Rychener’s sister Sara Burkholder died a few hours after her first child was delivered by emergency cesarean section a decade ago. Jackson Burkholder did not have enough oxygen during birth and was diagnosed with cerebral palsy, and his father, Jay, and other relatives researched treatments for him, Mr. Rychener said.

Hyperbaric oxygen treatment was an alternative Jackson’s family found was used in Europe for cerebral palsy, Mr. Rychener said. His nephew, he said, still has sessions at the center opened in 2005 that initially focused on treating children with cerebral palsy.

Cells receive more oxygen than normal during hyperbaric oxygen treatments, and blood vessels and nerves are built, Mr. Rychener said. One of his high school friends, Aron Sauder of Pettisville, did about 20 sessions to ease pain and speed the healing of his hands burned in a cooking fire in August.

“I was very happy with how it works,” said Mr. Sauder, 39, adding the area where skin was taken for grafting has healed.

So was Amanda Jarrett of Huntsville, Ala., a research analyst for a missile defense agency who grew up in Defiance. The 28-year-old was diagnosed with multiple sclerosis in July. After hyperbaric oxygen treatments helped alleviate many symptoms, she plans to return to Sara’s Garden periodically in hopes of slowing the autoimmune disease.

Mrs. Jarrett said she went on short-term disability and could not drive before getting hyperbaric oxygen treatments, which are used in the United Kingdom for multiple sclerosis. The numbness in her feet was so bad that the former ballet dancer could not point her toes, which she called heartbreaking, but she was able to resume driving after 20 sessions and now has about 5 percent numbness, she said.

“I felt like a 16-year-old who just got my license,” she recalled of being able to drive again. “Everything just continued to get better and better.”

Mrs. Jarrett, her husband, and another couple plan to start a nonprofit organization to raise money for patients who want hyperbaric oxygen therapy. They also plan to lobby the U.S. Food and Drug Administrative to approve usage for more conditions with the hopes that then more treatments would be covered by more insurance plans. An FDA spokesman did not return calls seeking comment.

Ms. Ramsey of North Ridgeville said her 8-year-old autistic son, Brendan Corrigan, looks forward to treatments because he feels better. So does Ms. Haberkorn’s autistic son, Kevin, 9, his mother said.

Meanwhile, Katelyn, who now has had more than 150 hyperbaric oxygen sessions, is a cheerleader and involved in a ski club, Ms. Haberkorn said. “It has been an amazing life change for our whole family,” she said.

Contact Julie M. McKinnon at: jmckinnon@theblade.com or 419-724-6087.

March 2012 Living Today

March 2012 Living Today

We are so grateful to Mike Nix and his entire staff at Front Porch Publishing for featuring our Hyperbaric Oxygen Therapy and Conductive Education services in their March issue of Living Today.

From the writers to the photographers… everyone at Front Porch was so much fun to work with.

To view the entire March 2012 issue of Living Today, click HERE.

If HBOT is so Good, Why Is It Not More Widely Accepted?

If HBOT is so Good, Why Is It Not More Widely Accepted?

Article published by Elmer M. Cranton, M.D.

Doctors are rarely taught about hyperbaric oxygen therapy (HBOT) in medical school and therefore most do not know about it. Only about 20 medical schools, less than 15 percent, have actual hyperbaric oxygen facilities, while perhaps another 20 have access to HBOT facilities. If physicians don’t know about a therapy, they obviously won’t prescribe it. If they don’t prescribe HBOT, there is no incentive for more hyperbaric treatment facilities to be established. Therefore, there exist very few hyperbaric chambers, compared with potential need and benefit that could otherwise be achieved—only about 400 chambers in the entire U.S.A. Many of those are dedicated to diving accidents (bends) and are not available for other medical conditions. And, many are located in hospitals that restrict HBOT to a small number of medical conditions reimbursed by Medicare.

Hyperbaric facilities are very expensive to establish and outfit. Because only a few of the many medical conditions that might be helped by HBOT are reimbursed by health care insurance, patients must commonly pay the cost out of their own pockets. Fees for HBOT can range from $150 per hour to almost $1,000 per hour. This denial of insurance reimbursement discourages the creation of new facilities and many patients cannot afford the cost of HBOT when refused medical insurance coverage. It is not uncommon to require 50 to 100 of the hour-long treatments for full benefit.

Advertisements and marketing claims for hyperbaric oxygen therapy is regulated like a drug by the government’s Food and Drug administration (FDA). It costs tens of millions of dollars to conduct medical research that meets FDA standards to allow claims for successful treatment of a specific illness. Medical insurance companies commonly take the position that if the FDA has not issued a formal approval, then the therapy is experimental and they refuse to pay. Because oxygen cannot be patented, profits on sales of oxygen are too small to pay for studies that meet FDA requirements.

Psychological defense mechanisms also come into play. If a doctor is not taught about HBOT in medical school (and most are not), and if a doctor therefore does not routinely use or prescribe HBOT for patients, then one of two things must be true in their minds: 1) either that doctor’s medical education was deficient and he or she is not providing the best of care for patients; or, 2) other doctors routinely using and prescribing HBOT for conditions that are not FDA-approved (off-label) must be “quacks” who exploit desperate patients. Which do you think their choice will be? It’s apparently difficult for many medical doctors to shed an attitude of God-like omniscience and admit that they simply do not know everything there is to know.

The medical profession is becoming polarized concerning HBOT. A large and powerful majority of medical doctors believe that HBOT should be restricted to treatment of those rare conditions with prior FDA approval. That majority now criticizes and even attacks the growing number of physicians who have become familiar with more than 30,000 published scientific papers the subject, and who advocate or use HBOT to treat patients with so-called off-label (non-FDA-approved) conditions. Opponents of such expanded utilization of HBOT should admit that they are remiss in their care of patients, they should open their minds, educate themselves further, and change their ways.

The medical community eagerly accepts scientific research buttressing a therapy it already approves. Somewhat more reluctantly, it examines and debates entirely novel approaches. But what it really hates is reappraising a treatment once rejected—getting the egg off their collective faces. Medicine, after all, is made up of people—people trailing MDs after their names—who, like the rest of us, do not enjoy admitting error.

Someday when HBOT therapy is an established part of standard medical care, historians of twentieth century medicine will wonder how so much supportive research on its benefits could have been published by skillful medical researchers and even more scrupulously ignored by the guardians of our health. By that time, most of the individuals who attempted to keep HBOT on the fringe will probably not be alive to blush, sparing them extensive embarrassment.

The amount of positive research is certainly formidable. And some studies that purport to demonstrate that HBOT doesn’t work actually show the opposite. For example, a recent Canadian study of cerebral palsy showed significant benefit. Under political pressure from parents, the study was reluctantly designed and conducted by Canadian physicians who were inexperienced in the use of HBOT. Both the treatment and placebo groups were pressurized and both groups benefited. The published conclusion in that study mistakenly stated that HBOT did nothing. It’s easy for opponents to design flawed studies and interpret the results to support their biased positions.

In a sense, we’re attempting to set the record straight and to tell people—especially physicians—to become familiar with the published scientific evidence . Mainstream medical journals engage in unconscionable editorial censorship. They refuse to publish positive research studies on alternative therapies, and are quick to print editorial criticism and anecdotal letters to the editor that are biased against such treatments. They have also been quick to uncritically print flawed studies that erroneously allege to disprove a controversial therapy.

Elmer M. Cranton, M.D. retired in 2007 after 40 years of busy medical practice. For many years he was associated in practice with his son, John A. Cranton, ARNP. Dr. Cranton and his son, John, stressed evidence based medical therapies to enhance each patients’ inherent ability to heal, including primary care, family medicine, internal medicine, preventive medicine, nutrition, and healthy life-style. Additional specialties included EDTA chelation therapy, hyperbaric oxygen therapy (HBOT), clinical nutrition, geriatrics, chronic fatigue syndrome, fibromyalgia, preventive medicine, and cardiovascular disease.

‘Never’ Should be a 4 Letter Word

‘Never’ Should be a 4 Letter Word

Joshua was born at only 26 weeks. Doctors were unable to determine any cause for the premature delivery. Shortly after his birth, he experienced a Grade 4 intraventricular hemorrhage. This prolonged internal bleeding resulted in severe trauma and damage to his brain. According to the doctors, Joshua would never survive.

In what would mark the first in a long list of overcoming ‘nevers’ placed on him by others, Joshua lived. Due to issues with his biological parents’ home life, Joshua became a ward of the state, placing further uncertainty on his long term survival. Following Joshua’s successful fight to recover from his traumatic birth, the foster care system was told that he would be a vegetable for the rest of his life. They needed to understand that there were no positive expectations for Joshua’s life. Any prospective foster parents would need to realize the severity of his condition and come to terms with what his life most certainly would and would not be.

Joshua was given a list of ‘nevers’… things he could not, and would not ever accomplish. He would never walk. He would never talk. He would never eat on his own. He would never be able to take care of himself. He would need drugs to control his condition for the rest of his life. He would spend the rest of his life in a wheelchair. As he grew, no one would be able to take care of him on their own. He should be put in a home that would be equipped to meet his countless needs.

What a sad, limiting prediction for life. Thankfully, Joshua’s story doesn’t end with the ‘nevers’.

Joshua’s condition has since been diagnosed as Hemiplegia, a severe form of Cerebral Palsy. The damage to his brain caused him to have weakness and decreased control of the right side of his body as well as obvious developmental, physical and speech delays. Joshua has been in occupational, physical and speech therapy for most of his young life. At the age of 3, Joshua was adopted. By this time he was able to speak. While he had a limited vocabulary, he was able to accomplish one more thing that he had been told he would never do.

Just prior to his 4th birthday, Joshua began taking Conductive Education classes at Sara’s Garden. He was still unable to walk without the assistance of another person, wheelchair, or walker. After spending six months in the CE program at Sara’s Garden, Joshua was walking and playing with his brothers and friends. Through much hard work he has been able to overcome more and more of the hurdles that were originally said to be impossible!

At 4½ years of age, Joshua began having seizures. According to the doctors, his test results showed that the seizures were coming from the area of his brain that had been most damaged at birth. After spending 3 long days in the hospital, his family was told that there was nothing more that could be done for Josh except to medicate him. Not wanting to accept this fate, Joshua began receiving Hyperbaric Oxygen Therapy treatments at Sara’s Garden.

His family noticed changes taking place in Joshua immediately. This shy, quiet little boy was emerging out of his shell. After completing a round of 40 HBOT treatments Joshua is seizure free. Additionally, his focus and awareness has improved, his vocabulary has expanded and the use of the right side of his body has increased.

Thanks to Conductive Education and Hyperbaric Oxygen Therapy at Sara’s Garden, Joshua has a much brighter future. The list of ‘nevers’ that he was given is gone. He has successfully checked off each and every limitation that was placed on him at birth.

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

We Put Athletes Back in Action

We Put Athletes Back in Action

Unfortunately, injuries are a common occurrence in sports. Sports injuries can be broadly classified as either traumatic or overuse injuries. These injuries range from bruises and muscle strains, to fractures and head injuries. Sara’s Garden has had great success in treating injured athletes.

Hyperbaric Oxygen Therapy is the ultimate natural therapy. It increases the amount of oxygen delivered to cells in order to stimulate the body’s natural healing processes, increase athletic stamina and endurance, speed up injury and surgery recovery and strengthen the immune system.

Below are just a few of the sports injury success stories that we’ve had here at Sara’s Garden:

  • 16 Year Old Male – Torn ACL A football player tore his ACL mid season. After undergoing surgery he was told that he would be out six months, effectively ending both his football and basketball seasons. After only 18 HBOT treatments, he was back to running and working out and did not have to miss the basketball season.
  • 17 Year Old Male – Stress Fracture A football player suffered a stress fracture to his foot in a preseason scrimmage. He was told that he would be out six weeks, almost his entire senior year. One week later, after only 6 HBOT treatments, he was back in action and did not miss a single game.
  • 14 Year Old Female – Hairline Fracture and Dislocation A soccer player fractured her clavicle and suffered a sternal dislocation during an intramural basketball game. She was told that she would be out one month and would miss the end of her soccer season. After only 1 week and 7 HBOT treatments she was cleared by her doctor and allowed to finish out her soccer season.
  • 17 Year Old Female – Stress Fracture A multisport athlete suffered a stress fracture to her shin during an off-season basketball camp. After sitting out while using crutches and a walking boot for over 7 weeks, she was released and began training for cross country. However, every time she ran she experienced pain and significant swelling in her leg. After only 6 HBOT treatments the pain and swelling disappeared and she was able to resume competing. She continued to undergo HBOT treatments periodically for the remainder of the season to recover from races quicker and boost her endurance.
  • 18 Year Old Male – Hip Flexor Injury A multisport athlete injured his hip flexor during baseball season at the end of his junior year. The injury did not improve and carried over into preseason workouts for his senior year of football. By the time of his first game he was barely able to run and did not know if he would be able to compete. After beginning HBOT treatments immediately following his first game he was able to continue playing and did not have to miss a single game while recovering from his injury. He went from not being able to run to being the first person down the field on kickoff coverage breaking the opponent’s wedge.
  • 18 Year Old Male – Dislocation A football player dislocated his shoulder near the end of his junior year causing him to miss the final 4 weeks of the season. He underwent surgery after the season was over to repair the damaged shoulder. The injury reappeared in warmups just prior to the first game of his senior year and caused him to have to miss the game. He began HBOT treatments following the first game and was able to continue playing the entire season without missing any additional games.
  • 17 Year Old Female – Severe Ankle Sprain A volleyball player suffered a severe sprain to both sides of her ankle after landing awkwardly following a block. She experienced tremendous swelling and bruising and was forced to use crutches as she was not able to put any weight on her foot. She was told that she would miss the remainder of the regular season as well as any tournament action. After only 4 HBOT treatments her swelling was reduced and she was able to begin putting weight back on her ankle. After a total of 10 treatments she was able to return to action and compete in her team’s post season tournament.

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.

What Happens When You’re Told There’s No Cure?

What Happens When You’re Told There’s No Cure?

When you’re 27 years old you feel like you have the rest of your life ahead of you. You never expect to hear that you have a life threatening condition. In July 2011, Amanda’s world was turned upside down when she discovered that the odd symptoms she had been experiencing for almost a year were the onset of Multiple Sclerosis (MS), a debilitating disease for which there is no known cure.

Multiple Sclerosis affects the ability of nerve cells in the brain and spinal cord to communicate with each other effectively. The body’s immune system attacks and damages its own nerves. When the nerves are damaged they can no longer effectively conduct signals. Almost any neurological symptom can appear with the disease, and often progresses to physical and cognitive disability. After experiencing a buzzing sensation in her tailbone for several months, Amanda woke up one morning numb from the middle of her waist down.

The next five months were tenuous and Amanda’s symptoms continued to progress. When she rubbed her feet together it felt as if there were spikes stabbing at her. Her back would go numb after taking a shower as the nerves became confused and sent improper signals to her brain. The numbness in her body made it difficult to sit at work all day. She would need to come home and lay on the couch on her stomach all night in order to remain comfortable. She began experiencing a sensation called binding, where her waist legs, feet and toes felt as if they had ropes and wires wrapped around them, constricting tighter and tighter.

By the time Amanda was finally diagnosed with MS, walking was difficult and she was no longer able to drive a car as she could not feel her feet on the pedals. She began the standard treatment for MS by receiving steroids in hopes of reducing her symptoms. The steroids made her feel weird and caused her mind to race. Unfortunately, after a long week in the hospital, her symptoms had not improved as well as had been hoped and she went home feeling worse than before treatments began. Amanda’s energy level began to drop and extreme fatigue became difficult to overcome. She could no longer work and had to go on short term disability.

Thankfully Amanda’s story doesn’t end there. She began researching additional treatment options and discovered Hyperbaric Oxygen Therapy (HBOT). Over the past two decades, international medical research has demonstrated that HBOT can play an extremely effective role in the treatment of Multiple Sclerosis. In many European countries, HBOT is now considered an integral part of the MS treatment program. In Britain alone, over 10,000 MS patients have received HBOT from the more-than 60 centers dedicated to treating Multiple Sclerosis.

Hyperbaric Oxygen Therapy should begin as soon as practical and preferably before irreversible lesions have become established. This does not mean that patients with long-term MS will not benefit; but it does mean that time is a factor. In a recent publication in the prestigious New England Journal of Medicine researchers demonstrated significant objective improvements in 70% of patients treated.

After completing a round of 40 HBOT treatments Amanda is beginning to feel like herself again. Feeling is returning to her legs and feet. She is walking independently and has started driving again. Her energy has increased dramatically and her family is amazed at the changes they have seen take place in her. She has returned to work and is ready to resume her normal life.

Thanks to Hyperbaric Oxygen Therapy at Sara’s Garden, Amanda has 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.

Hollywood Comedy Becomes Frightening Reality

Hollywood Comedy Becomes Frightening Reality

Sony Pictures’ 50 First Dates is a romantic comedy starring Adam Sandler and Drew Barrymore. Barrymore’s character, Lucy, has short term memory loss due to a brain injury she sustained in a car accident. She loses her memory every single night and can’t remember anything that has happened since her accident. It’s supposed to be a funny movie… but what would happen if this Hollywood comedy were to become your frightening reality?

Joleen was an active, healthy, 30 year old mother of four, including a four month old baby. However, due to an incorrect combination of medications she received in a hospital emergency room she suffered hypoxia and her blood oxygen level plummeted to 23%. She turned blue and became unresponsive. Doctors rushed to revive her.

When she awoke it became apparent that she had suffered an injury to her brain due to a lack of oxygen. She had completely lost her short term memory. Every five minutes her brain would recycle and she would have no memory of where she was or why she was there. People were unfamiliar. She felt as if a fog had descended on her and she couldn’t find her way out. It was a hopeless, terrifying experience.

After four long, frustrating days she was released from the hospital. Her family was told there was nothing more that could be done for her. They would simply need to wait and see if her memory would ever come back.

Thankfully, Joleen’s husband, Juan, wasn’t in a waiting mood and he immediately began calling for help. Their family doctor told them about Hyperbaric Oxygen Therapy and advised them to take Joleen to Sara’s Garden as soon as possible. That’s all Juan needed to hear. That afternoon they were on their way to Wauseon for treatments.

When they arrived, Joleen was vacant, distant and totally unsure of her situation. She was scared, confused and could not engage anyone in conversation. Juan cried as he recounted their last five days. Joleen asked him why he was crying and if she had done anything wrong. Later she commented that she felt as if “None of the parts of my brain were touching each other.”

By the end of her first treatment she looked at her attending nurse and said she felt as if a fog was lifting off of her mind. She began remembering things. Juan was amazed at the change he was seeing take place in his wife right before his eyes as he watched and listened to her on the monitors.

Five days and eight treatments later, Joleen is a completely different person than she was when she first walked through our doors… physically, intellectually and emotionally. She is now alert and able to focus on her surroundings. She is able to carry on a conversation fluidly without pausing and struggling to consider every single answer or comment. She is able to smile… and laugh… and joke with people she comes in contact with.

Thanks to Hyperbaric Oxygen Therapy at Sara’s Garden, Joleen has her life back… and her family has their wife and mother back.

There is hope… for this and many other conditions. HBOT is treatment without drugs… without surgery… without pain.

You Don’t Know What You’ve Got Till It’s Gone

You Don’t Know What You’ve Got Till It’s Gone

As the saying goes, “You don’t know what you’ve got till it’s gone.” Steve lived an active lifestyle and enjoyed many different outdoor activities. He was an avid bicycle rider, loved working out and enjoyed shooting his bow at the local club. All that changed in 2008.

After dealing with uncontrolled Diabetes and the side effects from various prescription drugs for a number of years, Steve suffered neurological damage and collapsed. Doctors diagnosed him with Ataxia. Ataxia is described as a lack of order and consists of gross lack of coordination of muscle movement. For the next three years, Ataxia has caused a variety of neurological deficits for Steve such as impaired balance, lack of energy, poor coordination, nightly body tremors and memory deterioration.

Steve longed to be able to do all of the things that he had enjoyed for so many years. To his dismay, he was not able to any longer. He sold his bike, cancelled his membership to the club and began trying to cope with life without his physical activities and exercises.

Doctors placed Steve on a number of medications that were unsuccessful in treating him so he and his wife, Linda, began researching other forms of treatment. It was during this time that they discovered Hyperbaric Oxygen Therapy (HBOT) at Sara’s Garden.

When Steve first came to Sara’s Garden his movement was slow and deliberate and he needed the assistance of a cane in order to make it from his car to the building. His speech was slow and he looked to his wife to assist with many of the questions as he simply could not recall any of the answers. They requested treatments in the late morning and early afternoon as Steve could not get out of bed before 10:30 a.m. and took a long time to get ready.

After his first day of HBOT, Steve was out of bed and showered by 7:30 and began making coffee and reading the newspaper. A few treatments later Steve stated that, “It feels like a fog is lifting off of me.” He was able to think much clearer and his memory began to return.

By the end of his first week of treatments, Steve began walking without the use of his cane. His gait became much more confident and he began walking with much more purpose. When he needed to bend over to tie his shoes or towel off after showering, he no longer had to hold onto something to maintain his balance. The nightly tremors that they lived with for so long went away and Steve began sleeping through the night.

After three weeks of treatments Steve now has plans to start getting back into all of the activities he loved so much. Since beginning his HBOT treatments his blood sugar levels have never spiraled out of control and he has been able to reduce the medications he has been taking. He feels great and now has the confidence in his body’s abilities to resume his active lifestyle.

Thanks to Hyperbaric Oxygen Therapy at Sara’s Garden, Steve now has his life back… and his family has their husband, father and grandfather back.

There is hope… for this and many other conditions. HBOT is treatment without drugs… without surgery… without pain.

Hard Work Pays Off for William

Hard Work Pays Off for William

William Denver Burton was born not breathing and, as a result, suffered hypoxia – a lack of oxygen to the brain. His family went through two life flights, with many scary times following. After six months, it became obvious to William’s mother Angie that he was not developing as a normal baby should. That was when the typical treatment approach began – physical and occupational therapy one or two times a week.

William began individual Conductive Education sessions around ten months of age. At that time, William presented with severe hypotonia, or extremely low muscle tone. He was unable to nod or shake his head, roll over continuously, ambulate in any way, achieve a sitting position, or participate in the process of standing up. William had little to no social skills, could not or would not pick up food and bring it to his mouth, did not vocalize, and had chewing problems.

Around approximately 12 months old, William began attending a more intensive group CE program. With the help of his parents and caregiver, William began to learn the crucial skills required to meet the milestones of rolling over, sitting up, and moving around more independently.

William has continued in the group CE program over the past two years and has achieved so much, including sitting up from lying; maintaining a hands-and-knees kneeling position; standing up from a seated position with his walker; and walking just about everywhere independently with the use of his walker.

The achievements are not just limited to physical skills however. He no longer has chewing problems and picks up and brings food to his mouth willingly. After eating, William opens the container of baby wipes independently, pulls one out, closes the container, and cleans his face independently.

His verbalizations are becoming more clear, and his vocabulary has expanded to approximately 25 easily understandable words and names of friends, teachers, and caregivers. His mother is amazed at how dramatically his verbalization has increased since beginning Conductive Education.

William is now incredibly social. He enjoys interacting with peers, he waves and smiles appropriately, and enjoys a good joke.

Currently William is learning to walk with tripod canes. It began slowly, as every individual part of the process must be learned. When William first began using the canes, he needed physical help to keep his balance to stand with the canes, move a cane forward, and take a step. After a few months, William now requires only verbal help to remind him what he needs to do. He can stand safely for several minutes on his own with the canes and he can move the canes forward on his own.

At three and a half years old, William is now able to attend preschool full-time. “The results are just phenomenal,” William’s mother has commented, “It’s just amazing how independent he has become since he’s started Conductive Education. William is such a hard worker. We are very proud of all of the accomplishments he has made.”

Thanks to Conductive Education at Sara’s Garden, Will has a much brighter future. No matter what you’ve been told, there is hope… and Conductive Education can help you find it.

Sara’s Garden Chosen For 2011 “Making A Difference Awards”!

Sara’s Garden Chosen For 2011 “Making A Difference Awards”!

We’re excited to announce that the Northwest State Community College Foundation has chosen us as one of its recipients of the 2011 Making a Difference Awards!

The Making a Difference Awards are presented annually to those who have displayed an ongoing dedication and commitment towards contributing to bettering the quality of life in the communities around Northwest Ohio.

The 2011 recipients to be recognized:

  • Individual: Dean Spangler
  • Business: Farmers & Merchants State Bank
  • Organization: Sara’s Garden

It’s a true honor for us to be mentioned along with such great individuals and businesses.