Part Three – Raising Families
On a farther side of the war conflict in 1960s, were the families of children who had been born with disabilities. It was standard practice to advise parents to institutionalize their children born with abnormalities from birth. They were seen as non-human and dealt with by locking them away in State medical facilities, unseen. In Chicago one family set about change that broadened the horizons for many more; for generations to come, by being of one to change their minds.
Kay and Marty McGee decided to take their baby girl home instead. They were one of many parents whose children had been born with Down Syndrome, then termed Mongolism. She outreached to other parents and professionals developing a support system. There were no programs or services in place; so the parents began programs in the basements of churches and other community buildings throughout the Chicago area. Together they developed educational programs for the medical communities and professional staff, with a clear message, children born with Downs are people too.
Out of the 60s era this Parent-to-Parent network, what was local to Chicago is now a nationwide coalition of an all volunteer staff of advocates for children born with disabilities. Their advocacy has, helped to stop the abuses and medical neglect so as children born with Downs, could be given life saving procedures at birth. They have been instrumental in the development of special needs programs throughout our nations school.
Children born with Downs Syndrome are no longer tucked away in a cold medical facility, or being taught their education in the basement of churches. These children are seen today as they are, vibrant human beings. Through the hard work and dedication of the parents, children born in the U. S. today with special needs can lead a more normal, happy and healthier life in our society. (more information at nads.org)
As a pioneering voice for change, these parents have been heard throughout our nation and into our laws and have become the organization we know today as NADS (National Association for Down Syndrome). People whose lives would have been left to whither, blossom today and this miraculous change was able to emerge through one voice determined to do right, by her child.
And as always, still gathering string …
Thank you for the information shared on downsyndrome, the continued Care for them, neglect and issues that aren’t seen from the human eyes most times. Very important information and many things must be changed to assure appropriate care of such individuals. There is hope though and we must press forward daily with that hope to reach many goals in Healing and overcoming in healthcare and medicine.
Thank you Jesse for reading and giving your feedback.
Very good information on children with downsyndrome and very thoroughly documented for the readers understanding. Healing is Highly possible for these children. Believe, stay dedicated and have patience when working together and reaching goals for their well being. Peace and great blessings be with you.