The National Scoliosis Foundation was started in 1976 and has served as a beacon of light for scoliosis patients and their families by rejecting, rather than accepting the darkness of hopelessness. The non-profit organization, originally created by Mrs. Laura Gowen, grew out of a rejection of the status quo and a realization that scoliosis doesn’t have to define a person, or their lifetime. She realized that a person is more than just the summation of their pieces and parts; especially if some of those parts happen to form a cobb angle.
It is because of these heroic beginnings that it brings so much concern to see the NSF’s chief mouthpiece, the online public forum, degrade into the negative environment that it is today. Opinions, non-main stream ideas, alternative treatment experiences, and even published research that doesn’t fit into the narrow perspective of a few out-spoken forum members/moderators routinely come under attack (often on a personal level) and are subject to “got-ya” style political ambushes.
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Pfister in the Literature
Impressive. So, when it is said that there is nothing in the literature to support the use of exercise in the treatment of scoliosis - I guess this piece from the Milwaukee Medical Journal 1897 (pg...
mamamax 09-03-2010 10:53 AM