Sherry Sobhy
This statue shows a child with epilepsy whose hand is being held by a helper (the mother or father) and who is being supported as it makes its first attempts at walking. The difference in size between the two people in the statue signalises on the one hand the sick child's need for help and protection, and on the other hand the active help and the safety which the helper provides.
I chose this sculpture as it emphasizes how each person who has epilepsy is in deep need for extra help and support. No matter how old the patient is, he/she will still want to feel safe and supported. They need the assurance that they are normal and can definitely live independently. They need to feel that they are accepted from the society around. As shown in that statue, parents, family, close friends are usually the first people who take this initiative in helping, supporting and assuring those patients with epilepsy that they are normal and that they are always accepted. During their week moments when they fall down, they will be looking around for those hands that will comfort them and help them get up and resume their lives normally.
Sherry, Great post. I really like the idea and how you interpreted this sculpture. As you mentioned it is really important that we offer help to those people with seizure or other neurological problems.
Simon Rasho
http://www.epilepsyhawaii.org/about-epilepsy/seizure-first-aid/
This picture from Epilepsy foundation shows a gentleman with tonic-clonic seizure or grand mal seizure and the importance of first aid. The first thing we need to do is to prevent injury by removing all sharp objects, glasses and cushion head. Also, loosen ties or anything around the neck that make breathing difficult. Then turn the patient gently onto one side to help with breathing. Stay with the person until the seizure ends and patient recover. Also, it is important to keep calm and reassure other people who are nearby and not to try stop patient’s movements. Be friendly and reassure the patient as consciousness returns and offer help if needed.
Both of these are excellent additions to the wiki. I believe with each post and reflection it becomes clear that the individual with epilepsy, or seizures will always on some level feel that they could lose control and Its hard to imagine how that must feel. Ruth Nemire