D

D was born a bit premature – following the failure basically of the umbilical cord – but wowed the doctors from the start with his fight and strength when he was in the NICU. But, as a result he was on all sorts of medicines in his first days of life and wasn’t able to immediately breast feed. As I had done for my first child, I refused the Hep shot in the hospital. At the time I thought this was progressive of me… oh how little did I know. D progressed marvelously in the hospital and eventually came home to us. We were delighted to begin our time together as a family after a rocky start for him. Shortly after D arrived home, he was due for his 2 month shots. Mother’s intuition struck me and I was very anxious about having D inoculated. He was already very constipated at 2 months, and suffering from severe reflux so I knew he was facing challenges already and the thought of vaccines scared me for the first time. But at the urging of my pediatrician, I consented and D received his DTap/Hib/Polio shot, and the Prevnar and Rota. Within 24 hours D spiked a fever and was very fussy though since the fever lingered for about a week the doctors said that it wasn’t related to his shots. But after these shots he stopped using his hands and turning his head. This pattern continued with the 4 month and 6 month shots. D ran a higher fever every time following vaccinations and was sick for a longer period of time. And each time he seemed to take longer to recover even after the fever had passed. His development literally regressed each time. But with babies, it is so hard to tell and I second guessed myself and allowed myself to think it was just fluke. Around 3 months D began occupational therapy and around 5 months D added in physical therapy to the OT. He was showing serious delays developmentally – both cognitively and physically – and he would have these moments where you would see a glimmer of a personality but for the most part he was a very sweet baby who was disconnected. All during this time (from 3 months of age onward) I was seeing a homeopath trying to heal D’s gut to get off medication for his acid reflux and strengthen his immune system and I was seeing a chiropractor regularly, sometimes as much as 2x a week to help support his growth and development. This is in addition to OT and PT. We made the decision to introduce a Special Instructor – another therapist that works on cognitive development just before D’s 1st birthday. D started to show some progress around 8 months, he rolled for the first time, and then he stood and we were so delighted with the progress. And then, his 1 year vaccines. D ran a 104 fever on and off for over 2 weeks. I was at the pediatrician almost every day. They simply could not figure out what was wrong and none of the doctors at the practice could agree on what was wrong; blood test after blood test yielded no result. And D became even more disconnected than ever. He stopped making eye contact. He became very agitated – it was a total change. D’s therapists each spoke to me individually, and gently, suggesting that something was really wrong, possibly neurological in nature. D was regressing in front of our eyes. A boy who had been about to take his first steps would barely crawl let alone stand. My chiropractor, in seeing such a change in D, suggested I reach out to Mary Coyle. I read as much as I could on line and made an appointment thinking – I will try anything. In our first appointment Mary seemed to understand what was causing D’s regression and offered real solutions to help. And I was optimistic until Mary told me D would be having daily bowel movements within 3 days. My heart sank at hearing this. D had been so constipated his entire life – maybe one bowel movement every 5 days. And we had seen so many specialists. I just knew she was over optimistic. Mary also told me that D would take his first steps within a week. There were many other small changes that Mary predicted that all sounded good but totally not plausible.

And then three days went by, and D had a bowel movement.

And then he did the next day too. And the day after that.

And then after five days he started laughing and smiling.

And then, six days after starting with Mary, D took his first steps.

And I realized, everything Mary predicted is happening. The changes were subtle but over the next few weeks my baby blossomed. He developed a personality, and he became a “normal” baby. Mary didn’t just give me back my child, because really, I had never had the opportunity to know my precious baby, Mary gave me the chance to get to know my child and his true self and personality. And now, while the road isn’t over for D, he is exceeding everyone’s expectations. At 16 months he is walking down the street pushing a baby stroller. He is pretending to stir and cook food at the play kitchen. He can throw a ball, do puzzles and play at the play ground. D has been given a life so rich and full of childhood moments, all in the last 3 months, and all because of Mary Coyle.

The same therapists that had approached me just months before were astounded by his progress. And shocked.

We just received our first positive and absolutely glowing written progress reports from D’s therapists – and basically, a child that was scoring so low on developmental tests he wasn’t even ranking on a percentile basis has done a complete 180 to where developmentally he is well above average for his age in all areas except speech – and we have Mary Coyle to thank.

Lucas

Lucas

Before:

After:

“Prior to Mary Coyle and the introduction of homotoxicology, my son was on 12 prescribed medications and was labeled in his medical chart as “failure to thrive”.  Although he was in a better place on the medications than he was previous to them, we felt like we were holding him together with a band aid.  If any medication was missed or removed, he would immediately be in intense gut pain and regression would occur.  We had decided that it was time to look at a treatment plan that would allow his body to heal itself naturally and we are so thankful we did! 

Our son has been on Mary’s protocol for 6 months and the biggest development we have seen is that he is now down to 2 medications and not only is he maintaining, but he is thriving!!  We are excited to say that we will be pulling the final two prescribed medications in the next month or so.  A dream finally realized!! He has already gained about 15 pounds, has color in his face, no more dark circles under his eyes, and has begun (at 8 years old) to finally lose his baby teeth and get new teeth! It is vividly apparent to us and everyone around us that he is not only healthy, but has been able to make huge strides cognitively and socially through our Son-Rise program because of his body’s ability to thrive and heal itself through homotoxicology…no doubt effecting his brain development in many positive ways.  On our blog sonrisewithlucas.com, you can most definitely see the difference in the past year cognitively and physically.  Mary is amazing and has been so wonderfully supportive, encouraging and compassionate!  I wish we would’ve done this sooner!”

Michael

Michael

Michael
Tonight Michael played Walter Hobbs in his school’s rendition of Elf. So darn proud of him! Surrounded by kindness and respect from his peers and teachers, he memorized and flawlessly delivered 81 lines along with a few solo singing parts. He was so confident and animated, I found myself wondering if it was all a dream. When he wasn’t speaking at almost 4 years old , we would have never imagined this degree of success.

Cheers,
Maria

Sebastian & Benjamin

It’s been 10 months since we started Homotoxicology with Mary Coyle and it has been a blessing in our lives. We have been doing a biomedical protocol to treat the Autism of my older son, Sebastian (6), and since we incorporated homotoxicology our son has progressed 10 times more than he did during the last 4 years. It’s been progress, progress, progress, with no regressions at all. My son is coming back to us. He is putting words together, he is singing complete songs, he is smiling all the time. He has KISSED us for the first time in 6 years! He is so affectionate now! He is playful, he is eating 100+ foods! He is growing and gaining weight. His skin is more clear. His nails and hair are growing like crazy. (His nails didn’t grow for years). He is answering basic questions, he can follow directions, he is requesting on what to play with him. We haven’t seen a serious tantrum in months. His sensory issues are gone, now he plays with sand, rice and even Playdough!
His thinking is blowing us away! WE cannot be more thankful
We also started doing the same protocol with our youngest son Benjamin (3) since he was also diagnosed with Autism the month we started with Sebastian. When we started the Detoxosode Protocol, that very same day, he said his very first words! Since then, 10 months later, his vocabulary keeps growing, Sometimes he  needs to be prompt but he is doing fantastic! He is playing super appropriate for his age and doing pretend playing with Little People. Now he loves the water, he makes requests of what he wants. He loves watching his favorites shows and he interacts and responds to questions asked by TV characters.
His BCBA Supervisor, told us that she has never seen in her ABA Clinic in 10 years a kid that progressed that fast in such a short time.

Mary Coyle: You have been a blessing to my family! We cannot wait for what’s about to come!

 

Sean

Our son Sean was on anti-fungal medications from age three to seven years of age. In addition to the numerous anti-fungals, he was also on, at one time or another, anti-inflammatory medications, such as 6MP. I was able to get him off all of his medications. His lab test showed no yeast and low oxidative stress for the first time within eight months of beginning homotoxicology.

Sincerely,
Jennifer

 

Sara

“Sara’s teachers and friends are amazed with the changes in Sara.  Right now she is attending a full day typical class with a shadow, but by looking at her class no one can make out who is the child with the 1:1 aid.  Sara’s detoxification is still going on and with each protocol we are seeing further improvements  Thank you for your dedication, patience and love.  Sara could not have progressed so much without your help.” 

Parents