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Manifestations of a rare genetic condition in baby Sydney, including growth issues and a gap between the length of each leg, miraculously turn around as she heals herself while participating in The AIM Program.
Tags: Genetic disorder; Turner's Syndrome;
I wanted to share Sydney's improvement with Turner's Syndrome since she has been on The AIM Program. There are so many changes in her that are positive, but most markedly her physical growth and personality.
Sydney was one year and 4 months old when she and the rest of our family began our participating in The AIM Program due to my worries about her short stature (she was barely registering on the growth chart). We were facing growth drugs at some point, and I was hoping to minimize that possibility or eliminate it if possible. She is now 36" tall at 2 years and 7 months old and is in the 50-55th percentile for height. She grew 7.5 inches in a little over a year, just a phenomenal growth rate and of course an enormous relief to me and my husband. During one 6-month period during her first year of self-healing guided by The AIM Program, she grew 4 inches. We were obsessively measuring her and always did three measurements (since she is a wiggly toddler) and then we averaged the three each time.
Also, Sydney's right leg was a full inch longer than the left when we had it x-rayed at Children's Hospital on 10/30/07. This causes quite a limp, as you can imagine. I have not had her x-rayed a second time yet, but when we measure her by hand, this gap seems to be closing up. She seems to be about 1/2 inch off rather than the original 1 inch, but we will have to get x-rays to confirm. I'll keep you posted.
The other worry I had about Sydney everyone laughed about. She was absolutely the most perfect, agreeable child in the world. That's great if your child doesn't have Turner's, but to me, her passivity and constantly delightful mood was potentially a danger sign. Even when she got shots at the Dr.'s office, she would cry for 10 seconds and reappear with a smile as if nothing had happened. To me it seemed that she wasn't fully engaged on some level. You'll be pleased to hear that she is now incredibly disagreeable and pretty much says NO to everything. I just want her to have a voice and to be able to express herself as a normal toddler, so this is music to my ears (very grating music, admittedly).
I believe Sydney is a healthy, normal toddler and will go on to continue growing naturally. Her re-check on The AIM Program confirmed that she does not have the Mosaic Turner's Syndrome subtle energy frequency any longer. This is not something we can really confirm medically, because they would have to test chromosomes in cells from many different parts of her body, including her brain, which is obviously too invasive. I personally don't care about any medical confirmation. We're very grateful for the self-healing that is taking place.
Thanks again for your personal care to our situation and for connecting us to AIM.
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