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Knowing I will need to find another neurologist is causing me to be anxious. Seems silly. However, the year I spent wondering what was causing me to have a tremor especially when I was in church waiting for Mass to start seems funny. 11 years later I realize that was one of the precious times in my life when I had my children with me and they were still at home. Brightening up my day with their presence and all the associated activities. They are still with me but not physically as they like birds have lifted off and are doing what they were trained to do. Have their own lives. Why you are wondering am I changing ..it is because of my husband being now on medicare. Our hmo did not have this available for him. Reading the various postings about support groups, I find myself agreeing. I have just made contact with my local group in Winston-Salem. The one reason is because I plan to have them work with me on the political activism needed to help get the appropiations for the Parkinsons funding increase. AS you can tell I am approaching this as an accepted done deal. It is not in my mind I will not succeed. With the various levels of ability I know there will be some who will help, no matter the percentage of the group and that is success. Later this month, I will begin as I have a prior activity that needs attention. For those in North Carolina who would assist me. I ask them to contact me using my email address. I would like to outline my thoughts on what to do. I am planing to be in DC in June. And I would appreciate in put on a new neurologist for me as well. Thank you L&K S