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Kirk had vestibular challenges, seizures, severe dizziness, sound and crowds was overwhelming. Nine years of seizure disorders.
He wore eye covers because anything that moved would induce seizure or vestibular challenges.
Still doing fine after thirteen years. His MD said if it wasn't for the steel plate in his head, he wouldn't know he had a TBI.
... and he got his drivers license back.
Over 16 years treated at a major U.S. University for RSD. Lots of pain medication, morphine for over 16 years including having an implant. Her implant was turned off a week into the program and she has not had RSD affects since.
This video was taken three months after the program. It has now been three years and still no pain and RSD free.
Adrenals working fine.
Izaiah was run over by a drunk teenage driver at the age of 18 months. He was in the hospital almost 300 days. He had 7 surgeries, blind and paralyzed. He was sent home to hospice.
We were contacted to work on his case after he was released from the hospital. His vision returned after 2 weeks and movement in his arms and legs at 5 weeks.
The family has been featured on the Doctor Phil show two times regarding his accident.
John lost his ability to walk and speak following a stroke. He was unable to dress himself and had other stroke related issues.
Read report updates from his wife and emails from his therapist.
Enjoy watching John as he walks through his home and through Farmers Market and enjoying time with his wife in the swimming pool.
Above all, listen to him telling his wife he loves her!
Read and watch this strong man and his wife keep their sights on recovery. We magnify what we focus on. From walking again to some of his first words.
Tori was referred to us at the age of 15 1/2.
She was working with a Cerebral Palsy institute in Pennsylvania.
I loved Tori's attitude. She came for her solution and got it!
Watch her video as she tells how she got movement back in her arm and was able to get out of the wheelchair.
Pay close attention to what her Ceberal Palsy institute wrote in her file - It's all in her video. Also, pay attention to that UN-paralyzed left arm.
It has been over 10 years since she was paralyzed.
Way to go, Tori!
Gabby was involved in a traffic accident as paramedics rushed her to the hospital.
The oncoming car did not see or hear the ambulance's siren; the ambulance did not see the car.
The impact put Gabby in what would be a seven-year coma.
Gabby's left collarbone and left hip were broken, and she lost her ability to speak or track with her eyes. Now, panic attacks and spasms were a major part of her life
.
There is nothing stronger than a mother's love. When the world drops on you, a mother's love runs deep.
Her mother saw us on Telemundo news and started calling the station and the charity representing the child on Telemundo, and we made contact.
Mariam was determined to find her solution. Click on the link below to meet Gabby, her mother, Mariam, and her physical therapist, Eric.
Finally, Mariam and Gabby were able to return to their home in Ecuador.
How do you reach for a solution when you are in a coma? This family did it with their heart, prayers, and much family love.
When this gentleman was referred to us, he could stand for only a few seconds before feeling like passing out.
His speech was very challenged as his wife had to interpret his words.
The family's support, determination, and love during his therapy gave him the determination to work with Jerry and me in reaching his solution.
He is now communicating with accurate words and minimal hesitation in his words. He told us his life was normal except for his inability to drive.
Notice the shape of his brain's midline and the angle of the skull while he was in the halo.
Self-esteem and confidence can be brutal on a person with Learning Disorders, from Autism to ADHD.
Riana's school teacher told me how she would evacuate the classroom as she would be screaming and throwing objects (staplers, erasers, etc.).
I knew Riana's father, a television chef, through our meetings with the National Football League Charities. We would frequently discuss the family's challenges in tolerating their child's loud, emotional, acting out behavior of a child with Aspbergers.
One day he asked me if I would see her. I did.
One day he asked me if I would see her. I did.
About two weeks later, I received a call from her school teacher asking, "What did you do to this child? !" She told me she had not had to evacuate the class in two weeks. She attended our next training session.
Riana was always good academically; her challenge was emotional behavior. Riana attended high school at High Tech High, a school with high admission requirements.
Listen to Riana's un-rehearsed interview. I was impressed with her confidence and poise.
Watch the video of her interview. No script. No one told her what to say. Her words and thoughts were her own. I loved her poise, cognitive clarity, and her choice of words. Everyone in the room, including her school teacher, brother, and parents, were excited.
Several months after Riana was on her own, I went to dinner with the family. I seriously tried to see if I could get her to return to her previous behavior. It didn't happen; she maintained perfect behavior! I was so proud of her and still am proud of her.
Click the link below to hear Riana tell her story.
Link to Top Gun's Video.
He tells the story of how we helped his visual range, OCD and PTSD.
Watch the video. He tells the story much better than we could write it !
Life can be difficult and exhausting for a family with an OCD child.
OCD affects the entire family, often causing excess anxiety, stress, and depression for other family members. People suffering from OCD can feel just as down.
They are aware of their rituals and compulsions; they are aware of the irrational behavior but feel unable to control it.
Her son's grades suffered severely.
He couldn't walk upstairs to his bedroom without waiting at the bottom for several minutes, thinking about the challenges of his trip. There were many other challenges, such as getting him ready for school and family outings on time. But the one that I was most concerned with was his graduating high school.
Listen to the video of his mother describing the changes within only one week.
Yes, he graduated high school, went on to college, stayed in a dorm by himself, and took care of himself - on time. His grades were good in college, and he developed a social life.
The teen's doctor, school, and friends noticed the drastic change.
Link to the video as his mother tells the story.
Venice was one of our Certified Clinicians who lived without the sense of smell for over 20 years.
She asked me one day if I could work with her on her loss of the sense of smell.
Watch her video as she explains how rapidly she gets her sense of smell back.
I remember Valerie and I took her to lunch during her visit after she got her sense of smell back. We stepped inside the restaurant, and she took a deep breath and excitedly, Wow, it is so good to smell and taste food again. She made my day!
Her Solution came quite rapidly!
The Abby Story As Told By Her Parents.
Abby went 18 minutes without oxygen. Doctors decided to turn off her life support. They called the family in to say their goodbyes ... but Abby kept breathing, and her heart kept beating.
When I first saw Abby, I could hold her up with my hands under her arms, and she would only dangle. She was like a rag doll.
I will never forget that night. I placed her on a blanket on the floor and turned on a protocol for her first protocol.
I went back behind my desk, stood, and started talking about that beautiful raven-haired baby lying on the mat in front of the desk.
This little lady who couldn't move a muscle suddenly raised her head and moved her ear in the direction of my voice.
Listen to this wonderful family as they tell their story. Their positive attitude is only the beginning.
Their focus on their solution and went for it!
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