My 8 year old grandson was diagnosed with Duchenne Muscular Dystrophy (DMD). He slowly deteriorated (it had
been coming on for a few years but we've never had any experience with Muscular Dystrophy (MD) and didn't recognize
the signs). Then suddenly the progression of the disease accelerated. He had problems walking, falling down often;
raising himself off the floor became a challenge. He is unable to climb stairs, having to crawl up the stairs.
After crawling up the stairs a couple of times he would be exhausted and I would have to carry him up and down the
stairs. His energy level was low, tiring very easily. His arm and leg muscles caused him pain and cramped often
during the day, even when he was lying in bed. His breathing was labored after physical exertion. He had been
experiencing abdominal pains for over a year and they had been getting increasingly worse to where the school nurse
calls for him to be picked up, missing many days of school. He would wake up with abdominal pain, have it just
before eating, during meal times, be unable to finish his meals and have pain after meals. He is also a finicky
eater and generally is a poor eater. He has night sweats, nightmares and night terrors. He is generally a happy
child but with the progression of DMD he often became very angry, lashing out frequently at his parents. All these
are symptoms of DMD.
I had just received my first order of ormus when my grandchildren came over the following day to spend the night.
The following morning I gave my grandson 1 full tsp. of ormus. An hour or so later I fed him breakfast, then lunch
and later dinner. He did not experience any abdominal pain throughout the entire day. His energy level was high,
playing and running around the house with his sister, being very active. He was able to go upstairs quite a few
times, not walking but crawling and walk down the stairs slowly by himself hanging onto the banister. He did not
experience any leg cramps that day and did not fall once due to weak muscles. He did trip once over a toy they had
left on the floor. His appetite was good that day and continued to increase over time to where it amazed us.
Imagine, such a marked improvement with just a 1 tsp. dose of ormus!
It has been 4 weeks now since he has been on ormus. He still has problems with bladder control, getting up off the
floor and occasional minor abdominal pain when he eats the wrong foods or overeats. He still falls, his leg muscles
giving out when he over exhausts himself; and/or it could be because my daughter has not been giving him 1 full
tsp. each dosage in order to stretch the ormus. But he hasn't been experiencing muscle cramps in his arms and legs
(it used to take 2 people, one massaging his legs and another his arms in order to give him some relief), his
energy level is much higher than before and he can walk without his legs giving out from under him though he still
has to pace himself, which is hard for an exuberant 8 year old. He seems to breath easier now after physical
exertion.
His night sweats, nightmares and night terrors are lessened. He still has them but instead of screaming when he
wakes up during the middle of the night, wakes up with a start. There are fewer nightmares and overall, concerning
these, he is greatly improved. He no longer lashes out in anger and frustration. He is much more in control of his
anger and has mellowed, being much more laid back.
Duchenne's is the fastest progressing MD. Generally by the age of 8 years they are in a wheel chair half of the
time and wearing leg splints. By the time they are 9 years of age they are most likely in a wheelchair full time.
After that, the other muscles are worse too and they are using an apparatus to help them breathe. They rarely live
beyond 22 or 23 years of age. Life expectancy is generally up to their late teens. This is why there was such an
urgency on my part to try alternative treatments and to catch it early enough so there is possibility of a reversal
and hopefully, a full recovery and healing of the disease (Edgar Cayce's readings say a reversal is possible when
treatment is started in the early stage of the disease. That is with the use of his wet cell appliance.).
We currently have him on several types of ormus, many food/nutritional supplements and a few anthroposophical
herbal/homeopathic prescriptions. The ormus was the first of these packages to arrive, so it was given to him
first. I am so happy he was with me when he received the first dose so I was able to see for myself the huge
difference it made towards my grandson's well being. My daughter works many evenings and long hours on weekends and
would not have seen the difference the ormus made.
Thank you so much for spending time with me on the phone, for all your help and disseminating the ormus
information.
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