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.

2013 “Drive Fore Hope” Charity Golf Scramble

2013 “Drive Fore Hope” Charity Golf Scramble

Sara’s Garden would like to invite you to participate in the 2013 “Drive Fore Hope” Charity Golf Scramble. We have put together a fun-filled day at Ironwood Golf Course in Wauseon, Ohio and hope to see you there!

Event Date:Friday, September 13, 2013
Event Location:Ironwood Golf Course, Wauseon, Ohio
Event Format:4-Player Team Scramble
Event Cost:$75 per Player ($300 per Team)
Dinner Only (Opt.):$20 per Person
Registration Deadline:September 1, 2013

If you would like to download a flyer for this year’s event to print, post and promote click on one of the links below:

  • “Drive Fore Hope” Partnership Opportunities – DOWNLOAD
  • “Drive Fore Hope” Promotional Flyer – DOWNLOAD

All proceeds from this event will benefit the 2013 Sara’s Garden capital campaign which is seeking to raise funds for the construction of an onsite Jackson’s House. This project is a 1-story, 12-bedroom facility for clients and families to stay during their treatment sessions at Sara’s Garden. Sara’s Garden is a recognized 501(c)(3) non-profit organization and is the only facility in the United States to offer Hyperbaric Oxygen Therapy, Conductive Education, Autism Intervention and Sensory Integration services.

Registration Includes:

  • Scramble format (4-player teams)
  • Green and cart fees
  • Range balls
  • Goodie bag
  • Contests and prizes
  • Awards for top teams
  • Lunch Buffet
Time
Schedule of Events
7:00 a.m.
Registration
Range Open
8:00 a.m.
Shotgun Scramble
1:00 p.m.
Lunch Buffet
2:00 p.m.
Awards
Corporate Partnership Opportunities:

“Healing” Partner Title Sponsor – $4,800

  • Includes two foursomes, event promotion, platinum title sponsor signage, company promotion table and program recognition.
  • This level of sponsorship will provide 40 hours of HBOT treatments or 137 hours of intervention services.

Gold Event Sponsor – $1,200

  • Includes one foursomes, gold event sponsor activity signage and program recognition.
  • This level of sponsorship will provide 10 hours of HBOT treatments or 34 hours of intervention services.

Silver Contest Sponsor – $720

  • Includes silver contest sponsor signage and program recognition.
  • This level of sponsorship will provide 6 hours of HBOT treatments or 20 hours of intervention services.

Bronze Meal Sponsor – $360

  • Includes bronze meal sponsor signage and program recognition.
  • This level of sponsorship will provide 3 hours of HBOT treatments or 10 hours of intervention services.

O2 Tee Sponsor – $110

  • Includes O2 tee sponsor signage and program recognition.
  • This level of sponsorship will provide 1 hour of HBOT treatments or 3 hours of intervention services.

For additional information regarding corporate partnership or team registration for the Sara’s Garden “Drive Fore Hope” Charity Golf Scramble please call 419.335.SARA.

Please join us for a great day of golf filled with fun, great food, auction items, skill contests and fabulous prizes. Take a day off work for a great cause and meet some of the amazing people you are golfing to help!

2013 Sara’s Garden Poker Run Photos

2013 Sara’s Garden Poker Run Photos

There are times that a thank you just seems far to inadequate. This is one of those times.

This past Saturday, June 29 we celebrated the 10th annual poker run to benefit Sara’s Garden. It is so hard to believe that this was the 10th year for the event. Harder to believe, is the continued support by so many amazing people and businesses!

Organizing a successful poker run can be very time consuming and tiring. However, seeing the expressions of joy on the faces of our clients who got to take rides around the parking lot on the motorcycles before the event made all that melt away and reaffirmed just how important events like this are.

Thank you so much to everyone who planned for, participated in, donated to and volunteered at this year’s Sara’s Garden poker run! We are truly grateful for (and humbled by) your faithful support.

Below are photos from the event. Click on a thumbnail to see a larger version. 

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.

NHA Now Enrolling for 2013/14 School Year

NHA Now Enrolling for 2013/14 School Year

New Horizons Academy at Sara’s Garden is presently accepting applications for new student enrollments for the 2013-2014 school year. Parents are encouraged to apply as early as possible as openings are limited.

New Horizons Academy enrolls children age 3 and up with problems that interfere with satisfactory functioning and progress in regular classroom programs or at home. This may include but is not limited to:

  • Attention Deficit Disorders
  • Intellectual disabilities
  • Developmental delays
  • Physical disabilities
  • Vision/hearing impaired
  • Seizure disorders
  • Speech & language disorders
  • Autism/PDD (Pervasive Developmental Disorders)

New Horizons Academy is a registered provider of the Autism and Jon Peterson Special Needs Scholarships and provides IEP-based services in accordance with the guidelines of the Ohio Department of Education. Families may enroll their children via these scholarships or through a partnership agreement with the student’s home school district.

For more information on New Horizons Academy, its eligibility guidelines and enrollment process, please contact Matt via e-mail or phone at 419.335.7272 ext. 201.

To learn more about New Horizons Academy at Sara’s Garden, its curriculum, educational plan and philosophy, please visit our website at http://www.NewHorizonsAcademy.org.

One size does not fit all. Parents deserve to choose the learning environment that suits their child’s unique educational needs. Fortunately, Ohio is one of the few states to offer such opportunities to its families.

2013 Sara’s Garden Poker Run

2013 Sara’s Garden Poker Run

Get ready to ride! The 10th Annual Poker Run to benefit Sara’s Garden is right around the corner! It’s so hard to believe this is our 10th year for the event!

Event Date:Saturday, June 29, 2013
Sign In:8:30 a.m. – 10:00 a.m.  Ride begins at 10:00 a.m.
Event Location:The Hope Center at Sara’s Garden220 Lawrence Ave., Wauseon, OH  43567
Rider Cost:$20 per Rider
Passenger Cost:$15 per Passenger (Optional)

Just like last year, we plan on having a photographer out on the course taking action shots of each one of the bikes as they pass by. We hope to provide everyone with a free high resolution action shot of themselves out on the poker run… so slow down and be sure to strike a pose!

If you would like to download a brochure or flyer for this year’s event to print, post and promote click on one of the links below:

  • Poker Run Promotional Flyer – DOWNLOAD

All proceeds from this event will benefit the 2013 Sara’s Garden capital campaign which is seeking to raise funds for the construction of an onsite Jackson’s House. This project is a 1-story, 8-12-bedroom facility for clients and families to stay during their treatment sessions at Sara’s Garden.

Registration Includes:

  • Poker Run entry
  • Coffee & doughnuts
  • Water for the road
  • High res action photograph
  • Lunch buffet
  • Prizes for top hands
  • $20-rider, $15-passenger (Optional)
Time
Schedule of Events
8:30 a.m.
Registration
Detailing Station Opens
Kid Ride-a-Longs
10:00 a.m.
First Bikes Out
Photo Shoot
12:00 p.m.
Lunch Buffet
1:00 p.m.
Awards
Partnership Opportunities:

“Healing” Title Partner – $4,800

  • Includes eight rider or passenger entries, event promotion, title partner signage, company promotion table, lunch presentation speech and program recognition.
  • This level of partnership will provide 40 hours of HBOT treatments or 137 hours of intervention services.

“Help” Event Partner – $1,200

  • Includes four rider or passenger entries, event partner signage and program recognition.
  • This level of partnership will provide 10 hours of HBOT treatments or 34 hours of intervention services.

“Hope” Contest Partner – $720

  • Includes contest partner signage and program recognition.
  • This level of partnership will provide 6 hours of HBOT treatments or 20 hours of intervention services.

“Inspiration” Meal Partner – $360

  • Includes meal partner signage and program recognition.
  • This level of partnership will provide 3 hours of HBOT treatments or 10 hours of intervention services.

“O2” Stop Partner – $110

  • Includes O2 stop sponsor signage and program recognition.
  • This level of partnership will provide 1 hour of HBOT treatments or 3 hours of intervention services.

For additional information regarding corporate partnership or participation in the 10th Annual Sara’s Garden Poker Run please call 419.335.SARA.

Please join us a great day of riding filled with fun, great food, auction items and fabulous prizes. Come spend the day on the open road for a great cause and meet some of the amazing people you are riding to help!

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.

New Horizons Academy at Sara’s Garden

New Horizons Academy at Sara’s Garden

New Horizons Academy at Sara’s Garden offers a holistic, all-encompassing educational path for children who have special learning needs and are preschool through grade twelve. Our mission is to provide the highest quality of educational programming available and empower children with disabilities to recognize and optimize their full potential.

New Horizons does not solely focus on any one area of development; rather, each developmental domain (social, emotional, communicative, physical, and cognitive) is developed simultaneously throughout the school day. Great importance is placed on setting high goals and expectations and providing students with the appropriate assistance required for them to achieve their individual goals. Providing an academic curriculum that is challenging is of utmost importance, while simultaneously discovering and exploring the ways our students are best able to access that curriculum.

At New Horizons, Conductive Education methodology is utilized for students who have neuromotor disabilities such as cerebral palsy, spina bifida, and traumatic brain injury. Use of this educational system ensures that our students are able to learn to be as independent as possible. Sensory integration is used for children who are on the autism spectrum and for any other children who would benefit from it. This assists them in their learning process and provides them with tools and strategies as they are learning to be as independent as possible.

Please visit the website at New Horizons Academy to learn more about about this exciting new educational endeavour.

2013 Harley-Davidson Street Glide Raffle

2013 Harley-Davidson Street Glide Raffle

On June 22, 2013 the Delta Eagle Riders will be raffling off a 2013 Harley-Davidson Street Glide from Napoleon Harley-Davidson. Tickets are $50.00 and include dinner the evening of the event. A percentage of the proceeds from the raffle will go to support Relay for Life and Sara’s Garden.

Event Date: Saturday, June 22, 2013
Time: 5:00 p.m.
Location: Fraternal Order of Eagles, Delta, Ohio
Ticket Cost: $50.00 (Includes dinner and chance to win prizes)
Prize List:
1st Prize: Motorcycle or $15,000.00 Cash
2nd Prize:  $1,500.00 VISA Prepaid Card
3rd Prize:  $1,000.00 VISA Prepaid Card
4th Prize:  $500.00 Cash
5th Prize: $250.00 Cash
6th Prize:  $100.00 Cash
Rules & Notes: Must be 18 years of age to win Need not be present to win Winner is responsible for taxes and fees associated with prizes

Tickets may be purchased at the Sara’s Garden main office via cash, check or credit card. For additional information regarding the 2013 Harley-Davidson Street Glide Raffle please call 419.335.7272.

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.