Guest guest Posted December 6, 2008 Report Posted December 6, 2008 > > As I was reading literature from Gift of Life Speakers Training, I thought some of these ideas would be good for pulmonary fibrosis. > > Here's a list of places to present, if you can't speak, bring family or friends with you who can speak for you. Bring literature with you to hand out. Make a poster for display. > > Religious institutions–churches, synagogues, men's clubs, women's clubs, sisterhoods > Educational institutions–schools, colleges, health classes, individual classes, PTAs > Civic Organizations–Rotary, Lion's Club, > Health Fairs–set up a table with literature > Social Groups– Social Club meetings/ breakfast, luncheon, dinner meetings > Senior Centers > Community Centers > Libraries > > Hospitals and Medical Centers– " in-service training " – there are a lot of doctors, nurses and other medical personnel who don't know much about pulmonary fibrosis, perhaps meeting someone with the disease will make a difference in their training and/or practice > > Support groups– since rehab groups seem to have mostly COPD members, maybe those of us with pulmonary fibrosis can present or bring in literature > > Messages on telephone answering machine– if it's a wrong number, the person might hang up and say " What in the world is Pulmonary Fibrosis? " > > Local television talk show > Local radio talk show where people call in > Reunions–high school or college > AARP meetings > Local newspaper writers, editors > Local sporting events, including little league, set up a display table with literature > Shopping centers, malls, department stores, supermarkets–set up display tables with literature > > Maybe your grandchildren, children, nieces or nephews could do a research paper on pulmonary fibrosis to present to the class; talk to the teacher or principal about doing a poster contest for pulmonary fibrosis > > Create a bumper sticker– I wonder if blank bumper stickers can be purchased at an office supply store, or craft store such as Staples, 's, AC , Joanne Fabrics > > Do it yourself t-shirts for yourselves, family and friends > > My vision of a poster is a large butterfly with details about the disease in each wing, either words or pictures [include a picture or drawing of someone with a " hose in his/her nose " ] or a dragon without its fire > > Sources for literature: Pulmonary Fibrosis Foundation [acorn], Coalition for Pulmonary Fibrosis [butterfly], internet > > The idea is that if we start publicizing on a small scale, maybe it will grow and be recognized on a larger scale. > > Some people have managed to get published in local Newspapers [Peggy and someone in Arizona]. > > Tell your personal story with the disease, keep it short and to the point. Present the facts. > Limit the negatives. Give some statistics. Tell the audience where they can get more information. > > You need to contact the appropriate people for permission to do this. > > Sometimes I have the ideas, I need to motivate myself to act on them. > > Pink Joyce IPF 3/06 Pennsylvania >pink Joyce, those are great ideas. You can get the brochures from the organizations listed above. KathyS54/dx10-04/tx. Quote
Guest guest Posted December 15, 2008 Report Posted December 15, 2008 great suggestions thanks for all your input; patti ipf 06,raynauds, scleroderma, pulm hypertension Quote
Guest guest Posted December 15, 2008 Report Posted December 15, 2008 great suggestions thanks for all your input; patti ipf 06,raynauds, scleroderma, pulm hypertension Quote
Guest guest Posted December 15, 2008 Report Posted December 15, 2008 great suggestions thanks for all your input; patti ipf 06,raynauds, scleroderma, pulm hypertension Quote
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