On a personal note, my husband has been diagnosed with ALS (Amyotrophic Lateral Sclerosis, also known as Lou Gehrig’s Disease) and demonstrates all the personality characteristics of the typical ALS patient, complete with “niceness” and the suppression of emotions.

He is reluctant to openly support my work, though, saying it is bogus and that I’m just playing with people’s feet. Of course, I know what he really feels; he’s often first to ask me to “play” with his feet! In so doing, he has let me know that he is being positively affected by treatments—whether he admits it or not.

His muscle atrophy has been considerably slow but is in constant progression.
He is still working, to his credit, and to that of his employer who is quite encouraging and wants to let him remain part of the contributing world for as long as he still desires to. I hope that what I have to offer him extends that time and continues to provide comfort and relief well into the future.

Those who suffer from ALS owe it to themselves to at least try these kinds of treatments. You deserve the attention and the relief too! There are practitioners throughout the world, and there is likely one near you. How about you give it a try? You have nothing to lose…

Sincerely,
Juliette Harrison
Cert. R.