What’s Inside

 

 

· No Post Polio        Clinic?……...….P. 1

 

· One Member’s Story……...….P. 2

 

· Annual Conference Info, Registration Form……...…P. 3 & 4

 

· Bits ‘n Pieces, news you can use…..P. 6

 

 

When a Post-Polio Clinic is Not Easily Accessible

 

For many people, traveling to a post-polio clinic may not be feasible due to travel distance, financial costs, logistics, or other personal reasons.  That does not mean that you need to be left out in getting treatment for PPS.  In a presentation at the Ninth International Conference on Post-Polio Health, Dr. Carol Vandenakker outlined several steps you may try.  You may find the complete outlined steps at Post-Polio Health’s website www.post-polio.org.  The following is a summary of some of the outline and is not intended to be a complete listing of the steps/issues/treatments/conditions contained in the full presentation.

 

· Start with a good primary care physician-one you can trust and provide information about PPS that you have or will obtain from your PPS organization;

· Optimize good health through diagnosis and treatment of other conditions;

· Monitor aging changes and other health conditions;

· Control weight and maintain a healthy diet;

· Set up a controlled exercise routine;

· Manage stress through life changes, medication, meditation, rest, etc.;

· Have diagnostic testing and see specialists as symptoms dictate;

· Manage pain by its type and location;

· Post-polio muscle pain from overuse of weak muscles is acute; associated with cramps, twitching, crawling sensation; aggravated by activity, stress, cold; increases at end of day – TREATMENT – protect muscles, modify activity, pace yourself;

· Soft tissue pain from injury or inflammation, such as tendonitis, bursitis – TREATMENT –correct/adapt body mechanics, rest, ice, use NSAIDS, therapy;

· Joint pain from degenerative changes affects joints from normal or excessive use; for joint deformity in affected limbs; from mild degeneration – TREATMENT – bracing, assistive devices, therapy, medications;

· Spinal pain may be in spine or into extremities, with scoliosis increasing

 

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Text Box: The Post Polio Support Group of Maine is a private, non-profit 501 [c] (3) organization.  We offer the latest information on the late effects of polio to more than nine hundred polio survivors, their families, and health care providers throughout Northern New England and parts of Canada.  Support for our work comes from donations from the public, from Alpha One, and from a grant furnished by the Pine Tree Society.  For more information, contact us at:

The Post Polio Support Group of Maine
c/o 674 Hallowell-Litchfield Road
West Gardiner, Maine 04345
Phone: (207) 724-3784 
NOW ON THE WORLWIDE WEB:
http://www.ppsgm.org

The Post Polio

Support Group Of Maine

 

Summer 2006

PPSGMText Box:  Save the Date 
Saturday, September 30th 
2006 Annual Conference 
See Registration Info on page 3

Cont’d on back page

Polio Update

 Summer 2006