Originally Posted by Evon

Thank you both Lindylanka and Chicory for your input. Its always good to hear from people who have had to deal with the same type of problems. I will take your ideas to my MDS on my next visit. At times I am willing to try anything to relieve the painful cramping. I don't come across too many PWP who have dystonia so I thought I would check out this forum, everyone here is very helpful.