PPS ClinicIf you are experiencing any post-polio symptoms such as unaccustomed fatigue - either rapid muscle tiring or a feeling of total body exhaustion; new weakness in muscles, both those originally affected and those seemingly unaffected; pain in muscles and/or joints; sleep problems; breathing or swallowing problems or decreased ability to tolerate cold temperatures and your primary care physician cannot find any other cause, you may want to be evaluated by a Post-Polio Specialist. We, in central Virginia, are fortunate to have a Post-Polio Clinic at Sheltering Arms Hospital, 2805 West Broad St., Richmond. The Director of the PPS Clinic is Dr. Albert Jones. Information can be given by calling: 804-764-1001. Support the CVPPSGThe Central Virginia Post- Polio Support Group is a non-profit organization that relies on donations from its membership and the community to continue its work. All contributions are tax deductible to the extent provided by law. We appreciate your help. Donations should be made out to the Central Virginia Post-Polio Support Group (CVPPSG) and mailed to: Linda VanAken, 14606 Talleywood Ct., Chester, VA 23831 |
October 4th Meeting2:00 pm at Children's Hospital, 2924 Brook Road, Richmond Our speaker will be Joe Thomas, Environmental Health and Safety Manager with Tompkins Builders. Joe will conduct a group session intended to focus on the future of our Support Group. He will use a managerial gaming technique where all persons have input to problems – all persons have input to solutions. This two hour session is a spin off of the nominal group technique, as taught at the National Fire Academy, Emmittsburg, Maryland. First, using 3x5 cards, and no talking, each person will identify what they think are problems, challenges and roadblocks with CVPPSG. Using round robin systems, every member will state the problem and it is written on a flip chart for the group to see and ponder. Then the same technique is used for the solutions. In the end, values are assigned and the group votes and assigns priorities. Some items will not survive and others will have more weight than when first identified. The end result is a plan for CVPPSG to move forward. The idea is to get feedback from all members and not to allow the more vocal ones to take control of the meeting. The end result is a group plan…not the loudest talking plan! We encourage ALL members to attend and participate in this exercise, as many support groups around the country are finding it hard to carry on due to “burn-out”, aging membership and lack of interest. November 8th MeetingPLEASE NOTE: This is the second Saturday in November due to the Teddy Bear Run at Children’s Hospital on Nov. 3rd 2:00 pm at Children's Hospital, 2924 Brook Road, Richmond Our speaker will be Debbie Barbuto, who will address: Sweet Dreams and Nightmares: A Journey into Understanding our Dreams Why do we dream? What is their purpose? Why do you keep having repeat dreams? Ever have a flying dream? What about the dream you recently had about your friend from elementary school? Debbie is a professional speaker and workshop facilitator who has been working with dreams for over 20 years. Come join Debbie and your friends and journey into the dream world layer by layer. You may be surprised at what you learn….or maybe you dreamed about this before. Debbie has a M.S., Gerontology/Adult Education, VCU and is owner of Successful Aging Consulting Service. Mid-Month LunchesThursday, October 16th, we will meet at Manakin Grill at 11:30 Thursday, Nov. 13th, we will meet at Dolce Vita Italian Restaurant at 11:30 Call Bev Lordi at 569-4232 by the Monday before each lunch date with your reservation.
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Our Support Group
The Central Virginia Post Polio Support Group was organized in 1986. Our group meets regularly to offer support, provide meaningful education and encourage advocacy for those survivors of polio who are now experiencing Post Polio Syndrome (PPS) and the medical community. Our members strive to help others in seeking an appropriate diagnosis, finding effective treatments, and assisting with necessary life style changes despite the increase of limitations caused by PPS. Spouses, family and friends of those with PPS are equal members and partners in our group. In addition to expert speakers and the sharing of knowledge, we often enjoy social events among our many activities. Our group attempts to be a supportive and caring community to anyone affected by the pain, weakness, fatigue and grief of PPS.