FLORIDA  EAST  COAST  POST-POLIO  SUPPORT  GROUP   -   Vol. 14   #3

             12 Eclipse Trail  /  Ormond  Beach,  FL  32174  /  386  676-2435

        E-Mail:-  bgold@iag.net   --   Web Site:-  home.iag.net/~bgold/polio.htm

NOVEMBER/DECEMBER   2006

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WISHING  ALL OUR FRIENDS

A CORNOCOUPIA WITH THANKSGIVING GOODIES

A LIGHT-FILLED CHANUKAH

and the

MERRIEST OF CHRISTMASES!!

 

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MEETING  NOTICE

 

November 19th, 2006    Chris Wysocki of Hanger Orthotics will give a presen-

                              tation on orthotics for polios.

January 14th,  2007       NEW  YEAR’S  LUNCHEON –  Dr. Richard Tessler

                               of the Volusia Hand Clinic will talk on carpal tunnel syndrome.

                                       

March 18th, 2007

May 20th, 2007

September 16th, 2007

November 18th, 2007

January 20th, 2008

 

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CONTENTS


 

From Barbara                                      


Panama Canal Cruise                         

Improving Communication with

                                                                             Our Doctors                               

Doctor’s Appointment?                                

“Goodbye, Mom!”                               

Apples Pack More Punch                   

Mystery Ride                                        

Focus on Eyes                                  

Heart Health:  What You

                                                                             Need to Know                           

God is Watching                                 

Stroke Awareness Month               

I Got Polio When I Was….            

We Must Stop This Immediately   

 

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FROM BARBARA

 

          Just a quick update on the carpal tunnel surgery I had back in September.  It’s coming along, but slower than I thought it would.  The tips of all my fingers, with the exception of the pinky, are still somewhat numb.  The middle finger is still number than the others, but not as bad as when first operated on.  Hopefully, it will keep improving.

 

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The following article was sent to us by one of our California members.  Thanks, Betty.

 

PANANA CANAL CRUISE

By Betty VanGieson

 

We live in one of Del Webb's Sun City developments in Lincoln, CA (near Sacramento).  There were 81 residents going on a cruise May 13th to 18th, 2006, through the Panama Canal aboard the Coral Princess. Our buses arrived at our lodge to transport us to the Sacramento Airport.  The bus that had a lift had a great deal of difficulty getting the front piece of the lift to go down. After ten minutes of banging on it, I was able to board the bus and off we went to the airport.  We were not given our plane tickets until it was time to board the plane.  I had advised the group leader that I needed to be in the front part of the plane as my walking is limited.  My husband and I were seated in row 14 on our flight to Fort Worth, Texas.  There was adequate time to get to the gate for our flight to Ft. Lauderdale.  As we were about to board this leg of our flight we were handed our tickets. Whoops! This time it was row 38. With extreme effort I made it to my seat. I was the only handicapped person in our group. What happened to seating in the front part of the plane? Upon landing in Ft. Lauderdale, two buses were waiting to transport us to the Ft. Lauderdale Sheraton to spend the night. Neither bus had a lift.  I asked our group leader if either bus could be lowered or if not moved to the curb as the first step was very high.  I was informed by our group leader they could not be moved to the curb and neither bus could be lowered.  I struggled four times to try to get on the first bus using every muscle possible and with my husband trying to give me a boost without success.  The second bus looked a little lower.  On the second heroic try, I finally made it, but by then all my muscles were completely shot. After sitting down, the bus driver said he could have moved over to  the curb so the first step would not be so high.  A few choice thoughts about our "group leader" crossed my mind. First row 38 and then the buses could not move to the curb. When arriving at the hotel our bus driver pulled up to the curb so I didn't have any problems getting off. After getting to our room my husband and I had a long discussion. If I had to go through that again, I would suffer for days.  Against the protests of our "leader" that we would never be able to find our group, we took a taxi to the ship.  Our taxi pulled in behind the buses and we were with our group before everyone was able to get off the buses. Going though security was a breeze.  There was a quantity of manual chairs with people to push them at several places as we boarded.  We found our way to the Aloha Deck (Level 12) and found our room. This was our first cruise. After going through my limitations with our group leader she assured me that I didn't need a handicapped room.  I had taken my
Sporty Mini Travel scooter which is 22 1/4 inches wide. Just made it through the door with a half inch to spare on each side. I drove past the bed to a nice open area near the desk and TV to park and we went
out to sit on our deck.  When our room steward came in to check if everything was OK, he was extremely surprised at seeing a scooter sitting in the room. He went over everything with us and explained about the mandatory
4:15 evacuation drill.  He said my husband should go, but I should remain in our room as you had to go down the stairs as you would have to do if there was a real emergency.  He said if there was a real emergency he would personally come and assist me. My only difficulty was getting up from the chair on the deck.  As I have to use the arms of the chair to help me get up, the plastic chair on the deck would slide around.  He bought me a towel and put it under the front legs of the chair.  Problem solved!  There was a two inch step up to both the bathroom and the deck which was no problem as I could hold on to the door jams to get up and down.

     After two days at sea, we arrived in Aruba.  No problem getting off the ship.  We only took tours that were labeled handicapped accessible. My scooter went into the bins under the bus.  Since I could not negotiate the step up to the bus, the bus driver put his hands around my waist and when I was ready to step, he gave me a boost and up I went with no problem.

        We took a tour of the island. Aruba is beautiful, the sea ports are gorgeous, and the houses are painted in bright "south-western colors". Our tour bus driver stopped and picked a cashew from a tree. 
Something in the shape of a pear grows on the tree.  Later a single cashew grows from the "pear". The cashew gets all its nourishment from the "pear" not from the tree as it grows.  Along the way we saw lots of what looked like small children's play houses made of what looks like granite with steep roofs with lots of vases filled with flowers in them near the churches.  Our driver explained to us that although a few people are buried, most people are placed in these "houses" when they die.  They do not believe in cremation or embalming their dead and everyone is "buried" standing up.

The next day were at sea.  The following day we arrived at the first set of three locks at the Panama Canal. It took one hour and 45 minutes to go through these locks to raise our ship up to the level of Gatun Lake.

The Coral Princess had a clearance of two feet on each side of the ship and about seventeen feet in the front and back when we were in a lock .  Eight "mules" kept our ship straight in the lock.  A mule looks like a small train engine.  Each is attached to the ship with ropes.  The purpose of the "mules" is to keep the ship absolutely straight when going through the locks.  The slightest error one way or the other would damage the locks.  They are called mules because when the Panama Canal was first built they used real mules to guide the ship.  Each "mule" costs two million dollars. Each lock has their own set of mules. The ship uses its own power to go forward. Gatun Lake is beautiful.  There are lots of heavily forested small islands all over the lake. It is a very beautiful place with lots of birds.  We also saw some alligators. Later we went through a single lock and into a manmade lake.  The first hills we saw were heavily forested.  Later most of the hills were being terraced.  It seemed like we passed miles of areas being terraced. They have to continually dredge this area to remove the sediment that comes down from the surrounding hills.  Later we went through a set of two locks to enter the Pacific Ocean.  The Panama Canal is about 50 miles long.  The Coral Princess is one of the largest ships to go through the locks.  It costs the Coral Princess about $245,000 in fees to cross through the Panama Canal.

After another day at sea, we docked at Puntarenas, Costa Rica.  There was a long ramp with horizontal lines which I thought were friction strips to keep people from slipping.  A crew member said "Just drive down, lady" which I did only to discover they were a series of steps about an inch and a half high. (Massage central was needed from all that bumping.) Boarding the bus was easy using the same method as before.  Scooter in the bin under the bus and bus driver's hands around my waist to give me a boost. After a half hour ride, we arrived at a wonderful botanical garden and were given a special guide. After touring the garden, we took a tram ride over a beautiful virgin forest. As our bus was about to pull out, our guide came over and asked about my scooter.  He had been searching the internet for two years for something like that for his father who was paralyzed on one side. We gave him our e-mail address and have already sent information about scooters to "our friend, Carlos". This is a big purchase for them as we were told that workers earn $800 a month and professionals earn about $2,000 per month.  When back on the dock, a van with a lift arrived. There was a very large man in a big power chair and his wife.  They transferred him to a manual chair and it took four men to carry him up the ramp.  It then took five men using all their strength to carry his power chair up.

After another day at sea we docked at Huatulco, Mexico.  As my husband left to play golf, I waited until the stores near the dock opened.  The ramp there was wonderful and I whizzed down a very long dock.  All the stores have very high steps to get inside; so I just looked round.  There was a big banner "Rotary" under a couple of nearby trees. I assumed they were just handing out literature. Someone from the ship came by and said I should go over there to look as I would like it. There was an American woman and two men standing behind two tables under the banner.  She explained that the men were not Mexicans, but native Indians. The Indians were in dire straights and were not able to support their families. Last year a group of Rotarians had come down to teach them how to paint on rocks. Each group stays six months and then another group comes down for six months.  They paint the animals they see in nature using very small strokes. This year they were trying to teach them how to sell their rocks. The rocks are very beautiful and unique. The American lady said her husband had just been diagnosed with a very rare neurological disease which unfortunately will be terminal.  After much sole searching they decided to live life to the fullest while he could.  I spent a long time talking to her about my scooter. 

After another day at sea, our next port was Acapulco.  This time the "handicapped" ramp had big humps down the middle and a step up or down to get on and off the ramp. Not only that but there was an extremely loose rope strung along the sides between metal rings.  It was frightening as the rope was useless for stability as it swayed back and forth as you had to step over all those bumps in the center.  What were they thinking?

Another day at sea and then Cabo San Lucas. This time we took a tender. They took my husband and me down one level from everyone else, in a handicapped elevator. From there I could roll right on onto the dock. The sea was calm and I was able to take the step down to sit in a seat.  They then lifted pieces from near the opening top make a solid platform over the inside steps and loaded my scooter there.  On coming back there were two of us in scooters. I was loaded next to last, and
then they again formed the platform. The other person in the scooter was lifted on board sitting in her scooter and then they loaded my scooter. Upon arriving at the ship, my scooter was unloaded and then
they unloaded her in her scooter and unfolded the platform.   Some people sitting behind me started to push their way forward.  The crew told them in no uncertain terms that they had to wait.  We had two foot swells and the crew was fantastic in getting me off, including holding on to me until I was seated and had my power on.  They then let my husband off.  Everyone else was held until we were long gone.  Unless the seas are very rough, taking a tender is a breeze.  After another day at sea, we arrived in
San Francisco. Going through customs was a breeze.  Surprisingly they never even checked our carry on luggage. Two buses were waiting to bring us back home. The driver was on his cell phone for fifteen minutes getting instructions before he could get the lift to operate. As I finally got on the bus, someone asked what I would do if I got stuck half way up the lift.  I said I'd have them call the fire department.  Another person replied, "We have a retired fire chief on board the bus" at which time everyone chuckled. He said he's done lots of rescues during his career.  Many people learned some helpful information.
      Some things to think about when traveling. If you use power, take an extension cord as there are only two electrical outlets - one in the bathroom and one over the desk. Check if your chair
or scooter is small enough to be placed in the bins below a bus.  The bus driver will not take the seat off your scooter, etc. so have someone with you who can do this.  The bus driver will assist this person in lifting your equipment in and out of the bins under the bus.  You must be able to get up the steps on the bus, but the driver will give you a boost. All the drivers we encountered were very strong, however we only took trips that were labeled handicapped accessible.


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Reprinted with permission of author, Dr. Henry D. Holland, reprinted from PPRG of SE Wisconsin, June 2006, reprinted from Triad PPG Newsletter, The Seagull, April 2006.

 

Improving Communication

with Our Doctors

by Henry D. Holland, MD

 

Why am I qualified to offer these suggestions?  I have had the experience of being a patient many times in my life.

I have used a ventilator since I had a permanent tracheostomy in 1970.  This treatment resulted from the damage initially caused by polio in 1950.  I have an intensified interest in post-polio syndrome because I have experienced its effects since about 1990.

          I have been a physician since 1966, and my specialty is psychiatry.  I am currently a clini

cal professor at the School of Medicine of Virginia Commonwealth University (formerly the Medical College of Virginia), and each year I instruct second year medical students in the technique of interviewing patients.

 

          Most physicians follow the medical model, which is generally based on the scientific method.  The thorough physician would get a complete history from you and possibly members of your family, perform a physical examination, try to obtain copies of previous medical records from other medical sources, and would get laboratory and other objective tests.  Routine tests usually include a complete blood count, blood chemistries including electrolytes, liver enzymes, kidney screening tests, cholesterol, and others.  A chest X-ray and thyroid function studies might also be included.

          I think it is essential and extremely important to have a doctor who will listen to you.  As a patient I think it is equally important for you to present your history of polio and post-polio syndrome symptoms in a concise manner and as objectively as possible.  I recommend that you answer the physician’s questions in a similar manner.  If your doctor seems hurried, that is a distinct disadvantage for both you and him/her.  It is a good idea to write some notes so you remember to tell the doctor about the onset of symptoms, when the symptoms seemed to progress, and what you have done that seemed to increase the symptoms or decrease the symptoms.

          Most physicians will formulate a possible or differential diagnosis based on the history and the physical exam even before the objective test results are known.  In some cases, treatment may be started at that time.  After the results of the objective tests are known, often the diagnosis can be made.

          The diagnosis of post-polio syndrome is one of exclusion.  The usual symptoms – weakness, fatigue, and pain – are very similar to other conditions.  Therefore, your physician must exclude these other possible disorders as an explanation for your symptoms.  The most important initial factor is to make sure that your physician knows of the history of polio in your life.

          My initial diagnosis in 1991 was a self-diagnosis.  A neurologist and a pulmonary doctor did not think that I had post-polio syndrome, but I am not sure that they knew much about it.  Fortunately my primary care (internal medicine) doctor was willing to listen to what I had to say.  He was also willing to read the articles that I brought him.  Admittedly, I had an advantage because, as a physician, my opinions and observations were not immediately dismissed.

          As a patient, you can become frustrated early on in the diagnostic process.  Hopefully your physician will be honest and not defensive and will admit if he/she knows little about the disorder.  This is likely a good sign that the physician is willing to learn.  If you can afford it, give your doctor either Managing Post-Polio Syndrome (1998) by Lauro Halstead, MD (www.nrhrehab.org)  or Post-Polio Syn-drome:  A Guide for Polio Survivors and Their Families (2000) by Julie Silver, MD, now in paperback (www.polioclinic.org.)   A gesture of this type can be mutually beneficial, but I would not recommend presenting any literature with a know-it-all attitude or to a doctor with a similar attitude.  A little humility is good for both the doctor and the patient.

          I often hear that polio is not taught anymore in medical schools.  I think that this is an inaccurate perception.  Infectious diseases, including polio, are taught in accredited medical schools despite the possibility that an American physician may never see an actual case.

          I have never seen a case of leprosy, bubonic plague, elephantiasis, or yellow fever.  However, I studied and was quizzed on all of these diseases.

          Post-Polio Syndrome is probably taught less because this disorder is a “syndrome.”  A syndrome is a group of symptoms that collectively indicate or characterize a disease, a psychological disorder, or another abnormal condition.  The causes of some syndromes are known and others are not known.  When the cause of a syndrome is not clearly known, the teaching emphasis would be on recognition.  As treatment may vary or change, a precise treatment plan may be suggested but with reservation.  This is the case with post-polio syndrome.  For example, how much exercise is enough or how much exercise is too much?  The treatment of post-polio syndrome is more individualized and less empirical than known disease processes.

          The average physician may never have a case of post-polio syndrome cross his/her office threshold.  If a case does, that physician may focus on other causes before considering the diagnosis, assuming that he/she knows about post-polio syndrome and assuming you told him/her your polio history.

          Communicate honestly about the severity of your symptoms.  Many polio survivors minimize the severity and dysfunction of their symptoms.  Don’t hesitate to tell your story with complete disclosure of how bad you are feeling or hurting.  It is important for you to communicate with clarity and emphasis about what has changed and what you are experiencing.  You could simply complain of fatigue, pain, and weakness, but if you explain how the fatigue, etc., is limiting, then your doctor will begin to understand.  For example, if you report that walking up a flight of steps is no longer possible without resting or extreme effort, you are more objective in your description than simply reporting fatigue. You, as a polio survivor, understand what you are experiencing.  If the doctor has a genuine ability to emphathize, he/she may also be able to understand.  However, the doctor may worry about missing something that is more treatable than post-polio syndrome, such as a malignancy, multiple sclerosis and other CNS diseases, HIV, or any other disease that might present with a complaint of fatigue, pain, or weakness.

          The successful doctor/patient relationship depends in part on a feeling of comfort between the two personalities involved.  The patient wants help with a problem and trusts the doctor to use his/her expertise in solving the problem.  The doctor’s goal is to diagnose correctly the patient’s problem and initiate the appropriate treatment promptly.

          This process will be more rewarding if the doctor and the patient have mutual respect, are not competitive, and both are capable of listening with attention and interest.  IF a doctor does not seem interested, finding another doctor would be wise.  If the doctor admits unfamiliarity with post-polio syndrome and is not interested in learning more, then that doctor should refer you to a colleague who is both more knowledgeable and more interested.

          The best outcome is to find a doctor who knows about post-polio syndrome or is willing to learn, is a good listener, is not obviously hurried, respects all of his/her patients, and takes a genuine interest in you as a patient with a problem and as a person.  You will know when you have found a doctor with whom you can relate.

 

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FECPPSG Editor’s Note:-  After Dr. Holland’s article (above), I felt this was most apropos.  It appeared in the Daytona Beach News Journal “Medical Guide  issue of June 25, 2006.

 

Doctor’s Appointment?

Be Prepared

By Lynda Shrager

New York Times News Service

 

Have you ever left your doctor’s appointment and realized you forgot to mention a symptom, ask a question or say you didn’t fully understand the instructions?  If we are lucky, we get about 15 minutes of actual face time with our doctor, and remembering everything that needs to be discussed is difficult.  Therefore, being well prepared for an appointment makes the office visit more productive and increases the potential for a more effective outcome.  Use these tips to prepare for your doctor’s visit.

 

DETERMINE YOUR GOALS

·        Is this a well visit or preventive checkup?

·        Are you looking for a diagnosis, a name for what you have?

·        Do you want to establish a treatment plan, either a modification of what you’re already doing or a new one?

·        Do you want to discuss the prognosis:  What will happen to you, what will the future likely bring?

·        Are you looking for reassurance, help with feelings, fatigue or depression?

 

GATHER YOUR MEDICAL INFORMATION

·        Prepare a detailed medical history of your own health and that of your immediate blood relatives.

·        Create a list of current medications – prescription, over-the-counter, natural and herbal – with dose and frequency.

·        If the doctor orders tests to be completed prior to your appointment, call ahead to ensure the office has the results.  If you need to bring the actual X-rays, MRIs or other films to your appointment, determine where they are and make plans to pick them up in advance.

 

LIST ALL YOUR SYMPTOMS

·        Keep a diary of when symptoms start, what triggers them, how often they occur, how long they last and what seems to alleviate them.

·        What do they feel like or look like (if appropriate)?  For example:  achy, burning, stabbing, dull, stiff, tingly, sore, annoying, crushing, red, swollen, oozing (you get the picture).

·        How severe is the pain?  Use a scale of 1 to 10, with 1 being barely a problem and 10 feeling as if you need to go to the hospital.

Determine what referrals or pre-authorizations you may need from your health insurer.

 

CREATE A LIST OF CONTACT INFORMATION

·        Include name and phone numbers for emergency contacts.

·        List all other doctors who treat you and why, plus their phone and fax numbers, and office address.

·        Include pharmacy name, phone and fax.

 

LIST SPECIFIC AND DIRECT QUESTIONS

·        What kind of diagnostic tests do I need?

·        What exactly is my disease or condition?

·        What are my options for treatment?

 

HAVE A PLAN FOR DOCUMENTING WHAT YOU LEARN – LEAVE A SPACE AFTER YOUR QUESTIONS TO JOT DOWN NOTES:

·        Bring an advocate to take notes, so you can focus on what is being said.

·        If an advocate is not available, ask permission to tape record the doctor’s responses (especially if this is a second opinion or specialist).

 

EMPOWER YOURSELF

·        Do research so you have a better understanding of some medical terms the doctor might use.  If you are having hip pain, prepare by learning a little bit about the hip joint.

 

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The following is an e-mail sent to me by one of our members, Gary Fredericks of Horsehead, NY

“Goodbye, Mom!”

A guy shopping in a supermarket noticed a little old lady following him around. If he stopped, she stopped. Furthermore she kept staring at him.

She finally overtook him at the checkout, and she turned to him and said, "I hope I haven't made you feel ill at ease; it's just that you look so much like my late son." He answered, "That's okay."

"I know it's silly, but if you'd call out "Good bye, Mom" as I leave the store, it would make me feel so happy." She then went through the checkout, and as she was on her way out of the store, the man called out, "Goodbye, Mother." The little old lady waved and smiled back at him. Pleased that he had brought a little sunshine into someone's day, he went to pay for his groceries.

"That comes to $121.85," said the clerk. "How come so much... I only bought 5 items. "The clerk replied, "Yeah, but your Mother said you'd pay for her things, too."

Motto: Do not trust all little Old Ladies

FECPPSG Editor’s Note:-  Gee, wish I had thought of that….

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Reprinted from USA Weekend, October 1, 2006, EatSmart by Jean Carper

 

Apples pack more punch

 

An apple a day also may keep away memory loss, asthma, cancer, diabetes, heart disease, stroke and tooth loss.  Crisp, new details:

  Cancer.  An Italian study showed that eating at least an apple a day cut risk of cancer of the mouth and pharynx by 21%; esophagus, 25%; colon, 20%; breast, 18%; ovaries, 15%; prostate, 9%.

   Asthma.  Apples are rich in an antioxidant called apigenin that, in animal tests in Japan, suppressed responses leading to asthma and allergies.  Apigenin also is found in beans, broccoli, celery, cherries, grapes, onions and parsley.

   Diabetes.  Harvard investigators found that women who ate an apple a day were 28% less likely to develop type 2 diabetes than women who ate none.

    Heart.  Eating apples may help stifle blood clots and plaque in arteries, which lead to heart disease.  Example:  Eating two more apples or 1 ½ cups of 100% apple juice a day slowed changes in bad LDL cholesterol that contribute to artery-clogging plaque, says University of Califor- nia-Davis research.  And European studies suggest less fatal heart disease and 40% fewer strokes in apple eaters.

    Teeth.  Harvard epidemiologists say men who stopped eating apples were more apt to lose their teeth.

 

TIPS:- 

    Eat the skin – it can have 6 times more antioxidants than the flesh.

     Red Delicious is tops in antioxidants.

 

Contact Jean Carper at stopagingnow.com.  Scientific sources are at usaweekend.com

 FECPPSG Editor’s Note:-  Guess I have to start eating more apples and I really prefer Granny Smith apples to Red Delicious….

 

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MYSTERY  RIDE

By Barbara Goldstein

 

Many of you have said that you like when I tell you about my “adventures” so, here’s another one.

Several of my friends and I belong to a social group called “Friendship Force.”  It is a worldwide organization.  One of the benefits (and why we joined) is that they plan one or two day trips within reasonable rates. 

Well, middle of October we went on a MYSTERY TRAIN RIDE.  Of course this meant that we wouldn’t know where we were going until we got there.  Actually, when we got on the bus, the “tour” leader handed out a sheet basically telling us what we would be doing and going on each day, EXCEPT where the actual Mystery Train would be taking us.

          I’ll start with getting me and my scooter onto the bus.  The new charter buses seem to have very little or no trouble getting the scooter into the luggage compartment.  I have an Electric Mobility Rascal and the front tiller is able to be brought down to the level of the seat and the backrest can be brought forward too.  This makes it extremely easy for the bus driver to get the scooter into the bus.  I had more trouble getting into the bus then my scooter did.  The first step was slightly higher than I could raise my good leg to get on – however, with a little bit of help from the tour leader I was able to do it.  Whenever I go on one of these buses (and I’ve gone on several trips) they reserve a front row seat for me so that I don’t have to walk too far into the bus.  This is appreciated by me as these front seats also have extra leg room, which we usually need.

Of course we made several stops the first day and I had to get off (and back on) the bus several times.  The bus driver made sure that he took the scooter out for me and set it up as soon as he was able to once we reached our destination(s).

The first day’s long drive (from Daytona Beach to Ft Myers) ended when we reached the Hampton Inn.  We did stop for lunch on the way.  The tour leader had made sure that there would be a handicap room available for me and my able-bodied friend.  The Hampton Inns are usually very good with their handicap facilities.  The only problems with this particular one was:  1.  they had a king size bed in the room.  I get very frustrated with this because, as we all know, not all of us travel with spouses or significant others, and we don’t really want to sleep with our travel companions.  2.  the bathtub was so high that my able-bodied friend had a problem with getting in and out of it.  Oh, the tub had plenty of grab bars, but the height of the tub made it impossible for me to get into it.  Many of the Hampton Inns have walk-in showers, this one didn’t. 

That night we went on the Mystery Train ride and it was absolutely fantastic.  My scooter was able to get onto the train but I had to get off it and walk into the actual dining car which was only a two-step walk.  

The following morning, after breakfast, we once more got onto the bus and went to the Edison-Ford Museum in Ft Myers.  I was very pleased to find that it was almost 100% accessible, especially the rest-rooms.  After enjoying the tour, we left there and headed to our final destination – the Hard Rock Casino in Tampa.

I had been to the Hard Rock Casino in Miami and had been very disappointed with it as my scooter was not able to move around the actual casino.  Here, however, there was more than ample room between the slot machines to maneuver the scooter.  Their restaurant (Green Room) was also most accessible (and a delicious lunch was had), the restrooms too were no problem.  The only difficulty I had was that I left them a donation – I had been hoping that they would let me take home a donation from them instead of me leaving them one.

Our bus ride back to Daytona went smoothly and I’m looking forward to doing many more of these one or two-day trips.  My next “excursion” is my cruise right after Thanksgiving and I will, of course, tell you all about it in the January/February newsletter.

                  

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Reprinted from USA Weekend, April 28-30, 2006, HealthSmart by Dr. Tedd Mitchell

 

Focus on eyes

Here’s why even small changes

affect your quality of sight.

 

          Within the same week, my 15-year-old daughter was fitted for glasses, and my father underwent surgery for cataracts.  Although their specific problems are quite different, the interventions both had will distinctly improve the quality of their lives.  Those of us with normal eyesight may have a hard time relating, but we all know the eyes are wonderful and complex organs.  In fact, a significant portion of our brain function is required just to interpret the information our eyes provide.

          Even small changes in our eyes can affect how we see.  Although there are many causes of vision problems, the most common one is a change in refraction, or the way light enters the eye.  As light enters the eye through a round, smooth cornea, it is bent, or refracted, and sent through the clear lens and toward the back of the eye (the retina).  The bent light rays focus directly on the retina, which pro-cesses and sends information to the brain, where it is interpreted as sight.  If not properly bent, the light rays focus either in front of or behind the retina.  As a result, the retina’s ability to process information is compromised, and the brain interprets a blurred image.

          Optometrists and ophthalmologists use glasses to correct these refractive problems.  When properly prescribed, eyeglasses make up for the error in refraction from the cornea to give us clear vision.  Fortunately, recent surgical advances have made altering the structure of the eye (such as the cornea and the lens) possible to correct refraction problems, reducing or even eliminating the need for glasses.

 

3 Major Types of

Refraction Problems

 

     Nearsightedness.  “Myopia” occurs when the focal point of the refractive images fall in front of the retina instead of directly on it.  Those with myopia can see objects that are near clearly; distant objects are blurred.

     Farsigntedness.  Hyperopia” occurs when the focal point of the images falls behind the retina.  People with hyperopia see distant objects clearly, but near objects are blurred.

     Astigmatism.  This condition occurs if the cornea’s shape is irregular, causing light rays to scatter through the lens toward the retina.  Consequently, light focuses on several focal points in the eye instead of one.  Astigmatism often occurs along with either farsightedness or nearsightedness.  People with astigmatism have difficulty seeing fine detail close-up or at a distance.  Correction requires glasses that bend light rays at various angles over the misshapen cornea.

 

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 Reprinted from Elder Update, May/June 2006, Health and Wellness

 

Heart Health:

What You Need to Know

        

         Although heart disease is sometimes thought of as a “man’s disease, it is the leasing cause of death for both women and men in the United States, with women comprising 51 percent of the total heart disease deaths.

         While heart disease is the number one killer of women, only 13 percent of women in a 2003 survey by the Centers for Disease Control were aware that this is their greatest health problem.  Here, the term “heart disease” refers to the broadest category of “diseases of the heart,” which includes acute rheumatic fever, chronic rheumatic heart disease, hypertensive heart disease, coronary heart disease, pulmonary heart disease, congestive heart failure, and any other heart condition or disease.

         Studies among people with heart disease have shown that lowering high blood cholesterol and high blood pressure can reduce the risk of dying of heart disease, having a nonfatal heart attack, and needing bypass surgery or angioplasty.

         Studies among people without heart disease have shown that lowering high blood cholesterol and high blood pressure can reduce the risk of developing heart disease.

 

Facts About Women and Heart Disease

         Heart disease is often perceived as an “older woman’s disease,” and it is the leading cause of death among women age 65 and older.  However, heart disease is the third leading cause of death among women age 25-44 years of age and the second leading cause of death among women aged 45-64 years.  Additionally, in 2002, death rates for heart disease were higher among black women than among white women.

         There is a range of risk for heart disease depending on family and personal health history and the treatment recommendations from a physician will depend on a woman’s level of risk.  Regardless of the risk level, these life style modifications are recommended for all women:

·        Cigarette smoking cessation

·        30 minutes physical activity most days

·        Heart healthy diet with weight maintenance / reduction.

·        Evaluation and treatment of depression

 

Facts About Heart Failure

   Heart failure is a condition where the heart cannot pump enough blood and oxygen to meet the needs of other body organs.  Heart failure does not mean that the heart has stopped, but that it cannot pump blood the way that it should.

  Heart failure is a serious condition.  There is no cure for heart failure at this time.  Once diagnosed, medicines are needed for the rest of the person’s life.

   The risk of death within five years of being diagnosed with heart failure is more than 50 percent.  About 80 percent of men and 70 percent of women with heart failure under the age of 65 die within eight years.

   People with heart failure are at increased risk for sudden cardiac death.

Source:  Center for Disease Control

 

Women Experience Different Symptoms from Men

          Heart attack symptoms in women are often more subtle than those experienced by men.  Women are more likely to experience the following symptoms during heart attacks:

·        Fatigue

·        Anxiety

·        Sleep disturbance

·        Stomach complaints

 

Unfortunately, these symptoms are not generally associated with an AMI (acute myocardial infarction).  Even members of the medical profession sometimes fail to link these symptoms with heart problems.  It is not unusual for a woman’s heart attack to be dismissed as anxiety.

Although considered a classic heart attack symptom, chest pain is not commonly experienced by women.  Results from a survey of 515 women published in the American Heart Association’s journal Circulation, revealed some interesting statistics:  more than 70 percent of women experienced no chest pain prior to the attack, and as many as 43 percent of women reported no chest pain symptoms during the attack.

Further, women who do experience chest pain may describe the pain as “sharp,” rather than “crushing.”  This description does not match the popular (and traditional medical) perception of heart attack symptoms, and may be misdiagnosed.

Additionally, in the days before the attack, 95 percent of women surveyed reported unusual symptoms; the most common being fatigue, anxiety, and sleep disturbances.  This list presents some of the common symptoms experienced by women both prior to and during a heart attack.  These symptoms are important to consider in addition to chest pain, since in some women they may be the only symptoms present.

 

Symptoms Before an Attack

Fatigue (71 percent)

Sleep disturbances (48 percent)

Shortness of breath (42 percent)

Indigestion (39 percent)

Anxiety (35 percent)

 

Symptoms During an Attack

Shortness of breath (58 percent)

Weakness (55 percent)

Fatigue (43 percent)

“Cold sweat” (39 percent)

Dizziness (39 percent)

Source:  NCERx

FECPPSG Editor’s Note:-  I, for one, was not aware of many of the symptoms of a heart attack.  Hope none of us experience any of them for a long time to come.

 

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Time for another “funny” – here’s another one from Gary Fredericks –

 

God is Watching


         
Children were lined up in the cafeteria of a Catholic school for lunch. At the head of the table was a large pile of apples. The nun made a note, "Take only one, God is watching."

 

          At the other end of the table was a large pile of chocolate chip cookies. Moving through the line a boy wrote another note to leave by the cookies, "Take all you want, God is watching the apples."

 

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Here’s another article reprinted from the same issue of Elder Update, May/June 2006, Health and Wellness

 

Elder Affairs Recognizes MAY

As National Stroke Awareness Month

 

          Stroke is the third leading cause of death in the United States and a leading cause of serious, long-term disability in adults.  About 600,000 new strokes are reported in the U.S. each year.  The good news is that treatments are available that can greatly reduce the damage caused by a stroke.  However, you need to recognize the symptoms of a stroke and get to a hospital quickly.  Getting treatment within 60 minutes can prevent disability.

 

What is a stroke?

          A stroke, sometimes called a “brain attack,” occurs when blood flow to the brain is interrupted.  When a stroke occurs, brain cells in the immediate area begin to die because they stop getting the oxygen and nutrients they need to function.

 

What causes a stroke?

There are two major kinds of stroke:

        The first, called an ischemic stroke, is caused by a blood clot that blocks or plugs a blood vessel or artery in the brain.  About 80 percent of all strokes are ischemic.

        The second, known as a hemorrhagic stroke, is caused by a blood vessel in the brain that breaks and bleeds into the brain.  About 20 percent of strokes are hemorrhagic.

 

What disabilities can result

from a stroke?

          Although stroke is a disease of the brain, it can affect the entire body.  The effects of a stroke range from mild to severe and can include paralysis, problems with thinking, problems with speaking and emotional problems.  Patients may also experience pain or numbness after a stroke.

 

What are the symptoms of a stroke?

          Because stroke injures the brain, you may not realize that you are having a stroke.  To a bystander, someone having a stroke may just look unaware or confused.  Stroke victims have the best chance if someone around them recognizes the symptoms and acts quickly.

          The symptoms of stroke are distinct because they happen quickly:

      Sudden numbness or weakness of the face, arm, or leg (especially on one side of the body).

      Sudden confusion trouble speaking or understanding speech.

      Sudden trouble seeing in one or both eyes.

      Sudden trouble walking, dizziness, loss of balance or coordination.

      Sudden severe headache with no known cause.

 

Women Experience Different

Symptoms from Men

          Women may report unique stroke symptoms, including the sudden onset of the following:

·        Face and limb pain

·        Hiccups

·        Nausea

·        General weakness

·        Chest pain

·        Shortness of breath

·        Palpitations

 

Act in Time

Stroke is a medical emergency.  Every minute counts when someone is having a stroke.  The longer blood flow is cut off to the brain, the greater the damage.  Immediate treatment can save people’s lives and enhance their chances for successful recovery.

 

Why is there a need to act fast?

          Ischemic strokes, the most common type of strokes, can be treated with a drug called t-PA that dissolves blood clots obstructing blood flow to the brain.  The window of opportunity to start treating stroke patients is three hours, but to be evaluated and receive treatment, patients need to get to the hospital within 60 minutes.

 

What is the benefit of treatment?

          A five-year study by the National Institute of Neurological Disorders and Stroke (NINDS) found that some stroke patients who received t-PA within three hours of the start of stroke symptoms were at least 30 percent more likely to recover with little or no disability after three months.

 

What can I do to prevent a stroke?   

         The best treatment for stroke is prevention.  There are several risk factors that increase your chances of having a stroke:

·        High blood pressure

·        Heart disease

·        Smoking

·        Diabetes

·        High cholesterol

 

If you smoke – quit.  If you have high blood pressure, heart disease, diabetes, or high cholesterol, getting them under control – and keeping them under control – will greatly reduce your chances of having a stroke.

Source:  National Institute of Neurological Disorders and Stroke

FECPPSG Editor’s Note:-  This should have gone into our May/June issue, but – better late than not at all.

 

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Reprinted from The Post-Polio Experience with the express permission of the author, Margaret E.
Backman, Ph.D. Published by iUniverse, Inc., website (www.iUniverse.com).
 No further reprints allowed without obtaining the permission of Dr. Backman (mebackman@aol.com).

 

DEVELOPMENTAL STAGES:

“I GOT POLIO WHEN

I WAS…”

 

          One of the first things polio survivors tell me is how old they were when they got polio – be it 10 months, 10 years, or whatever.  Instinctively polio survivors know that age of onset is a very significant factor in:

·        how they experienced the illness.

·        how their families experienced the illness

and

·        how they coped with life afterwards.

With this in mind, let us take a look at the childhood stages of development.  In so doing we may better understand how the child perceived the polio experience, and how this would influence his or her personality and later adjustments to life.

 

CHILDREN’S REACTION TO ILLNESS

 

Infancy and Early Childhood

          When polio occurred at the preverbal stage of development, the little patients did not have the vocabulary to help them express their feelings and needs.  Because infants were not able to commun-icate and had no outlet for their feelings, except perhaps crying, early experiences remained in the unconscious.  The lack of verbal labels attached to their emotions meant that painful and frightening events associated with medical procedures, physical restraints, and ventilators, were not consciously remembered later on.

          The underlying feelings, however, could still surface at a later date, triggered by something that stirred the memory.  But without the verbal cues, the person can become bewildered by the emerging feelings that seem to come from nowhere.  In later years, many of those who had polio in infancy or early childhood may experience isolated symptoms, such as free-floating anxiety or shortness of breath in stressful situations.  Without psycho-therapy to help them make the verbal connections, they may not realize why they are experiencing these feelings and may find themselves in a state of panic, thinking that something is wrong with them mentally.

          In the days before the polio vaccines, it was not the custom to have parents visit on a regular basis, let along sleep overnight in the hospital room.  In fact the little patients were often in quarantine, with very limited contact with familiar faces, if at all.

          There is some thought that children can tolerate short separations from their mothers or primary caretakers up to 9 months of age.  But the impact of these separations is not well understood.

 

Preschool:  1 – 3 years

          During the first two years of life, children are still very dependent upon their parents and cannot understand why the parents are not able to make their pain and discomfort go away.  Young children may blame their parents for causing their disease.

          The initial emotional reaction is anger, often expressed as demanding and clinging behavior. If the caretakers (parents and/or nurses and doctors) do not understand the reason for this behavior and react harshly, the child can feel rejected and withdraw in despair.

 

          Separation anxiety.  Children with polio also could not understand why their parents did not save them from the doctors and the hospitals and convalescent homes.  And of course they did not understand why their parents were not there with them, protecting them and taking care of them.

          Separation from parents at this early age can have a severe effect on later emotional development, resulting in separation anxiety and dependency.  The children feel that the absent parents have abandoned them.  Anxiety and depression set in as the little patients begin to fear that they can no longer depend upon their parents, or that they may never see their parents again.

          In today’s thinking, a parent or a supportive other should be included as much as possible in the medical visits and hospitalizations, particularly after about 9 months.  But this was not always done in years past.  Fear of separation from the primary caretakers (usually the mother) peaks at about age 3 and gradually declines after that to age 6 or 7, when youngsters can better understand what is going on – not to say that they don’t miss their parents, but that they can tolerate such separation better.

 

          Lack of trust.  Some children who had polio were not informed about the hospitalization, only to find themselves suddenly taken away from their parents and put in a strange environment, where they may have been physically restrained, stuck with needles, put in an iron lung, or had other unpleasant treatment.

          Their language was not yet developed to the point that one could readily communicate with these young children.  So when older, many had trace memories and disturbing feelings related to these early experiences that they could not understand.

          To stop the young patients from crying, adults often fell back on “white lies,” such as telling them that they would be going home sooner than actually was to be the case.  This set the stage for distrust of authority, which can last into adulthood.  Trust is important and adults should not promise anything they cannot deliver, but they often did.  It is in these young years that the basis of trust and mistrust is laid down.

          Today children are given better preparation when going to see a doctor or when going to the hospital.  In keeping with their age, they are told what to expect as a way of alleviating anxiety, and parents are included as supportive figures more than in the past.

 

          Lack of mobility. In addition, children between 1 and 3 years of age are very active.  They do not accept physical restraint easily.  Lack of mobility, plus the restrictions of hospitalization, can be particularly hard on them.

 

          Shame and doubt.  Early childhood is the period where children struggle with issues of shame and doubt, and develop their sense of autonomy.  Toilet training, which normally takes place during this stage, plays a significant role in the developmental struggle.  The child with polio may have had problems with toilet training as a result of the illness, but the involvement of others besides the mother cannot be overlooked.

          Whether those in the medical facilities were patient and helpful enough in encouraging these children cannot always be known.  But this is the period where the children learn about control and begin to form a self-image and pride.  If they were called bad or punished for lack of control or cooperation during this time, their personality development may have been negatively affected.  Some of these early traumas can be overcome later, but an accumulation of these negative effects can take its toll.

 

Ages 3 – 6 Years

 

          Theoretically, since children, three and older, have more mature verbal and cognitive functioning, their patterns of psychological adjustments to illness would be more complex, as contrasted to the isolated symptoms infants develop.  Later in life, these psychological reactions might appear as unresolved issues of dependency, submission, and helplessness.

          After age 3, children have more awareness of themselves and their environment, including more awareness of their body parts and functions.  This also leaves them vulnerable to fears of physical assault.  During these years, they also begin to communicate more coherently, but with language comes the development of fearful fantasies.  Understanding of reality is not well developed – Even seeing another child needing assistance for breathing, for example, can be terrifying.  They may falsely interpret this as a punishment the other child is getting for being bad.

          An interaction of psychological development and early hospital experiences is illustrated by the reactions of Jim, who still becomes quite anxious even when going to the doctor.

Jim was almost six years old when he was hospitalized.  It was the first time he had been separated from his mother.  He said he found the hospital very institutional, cold, unattractive and fright-ening.  He actually shuddered when telling me.  Jim remembers not liking the nurses.  He said he particularly hated the thermometer.  When asked if it was a rectal thermometer, he replied, “Yes, and I felt violated and exposed.”

On the same theme, he said that he also hated the hospital gown – that he felt “naked underneath, vulnerable.  People could see your body.  It was the same with the thermometer.  I was always a very private person,” he would explain.

Jim also remembers when he was wheeled into the operating room, screaming and crying.  “I felt like I would never come back.  I wasn’t afraid of dying,” he explained.  “I didn’t know where I was going, and I was afraid I would be separated from my parents, particularly my mother.”

 

Jim’s experience illustrates his early fears of separation, as well as his feelings of vulnerability.  Jim’s extreme modesty and concerns about his body are typical for a child of that age; in his case, however, these feelings stayed with him into adulthood.

Children 3 to 6 years of age are beset by fantasies and often fear mutilation of their bodies.  Polio was certainly an assault on the body – the body image and the body integrity.  Since physicians and nurses usually did not speak directly to the children, overhearing conversations amongst adults – who spoke in front of them as though they were not there – added to the terrifying fantasies and contributed to feelings of depersonalization.  Perhaps this is familiar to you.

When adult patients, who have experienced such traumatic events as children face medical care again in life, they may become extremely anxious.  Physicians may not understand the underlying cause of the patients’ anxieties and may become impatient with the constant questioning or misinterpret the patients’ behaviors.

(The rest of this chapter will be in the January/February 2007 newsletter.)

FECPPSG Editor’s Note:-  Would love to hear from any of you as to how this may have or may not have applied to you.  In my case, I contracted polio at 10 months of age and don’t remember anything of my early childhood.  I only know what my mother told me.

 

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I’ve been wanting to reprint this for the longest time – don’t remember who e-mailed it to me but know that I’ve received it several times.

 

 

We Must Stop

This Immediately!

 

THIS KIND OF STUFF HAS GOT TO STOP IN OUR COUNTRY !


Have you noticed that Stairs are getting steeper. Groceries are heavier. And, everything is farther away.  Yesterday I walked to the corner and I was dumbfounded to discover how long our street had become!


And, you know, people are less considerate now, especially the young ones.  They speak in whispers all the time!  If you ask them to speak up they just keep repeating themselves, endlessly mouthing the same silent message until they're red in the face! What do they think I am, a lip reader?


I also think they are much younger than I was at the same age.  On the other hand, people my own age are so much older than I am.  I ran into an old friend the other day and he has aged so much that he didn't even recognize me.


I got to thinking about the poor fellow while I was combing my hair this morning, and in doing so, I glanced at my own reflection.... Well, REALLY NOW – even mirrors are not made the way they used to be!


Another thing, everyone drives so fast these days!  You're risking life and limb if you happen to pull onto the freeway in front of them. All I can say is, their brakes must wear out awfully fast, the way I see them screech and swerve in my rear view mirror.

Clothing manufacturers are less civilized these days.  Why else would they suddenly start labeling size 16 shirts as 18 1/2 or 19?  Do they think no one notices that these things no longer fit around the waist, hips, thighs, and chest?


The people who make bathroom scales are pulling the same prank, but in reverse.  Do they think I actually "believe" the number I see on that dial?  HA!  I would never let myself weigh that much! Just who do these people think they're fooling?


I'd like to call up someone in authority to report what's going on -- but the telephone company is in on the conspiracy too: they've printed the phone books in such small type that no one could ever find a number in here!


All I can do is pass along this warning: We are under attack! Unless something drastic happens, pretty soon everyone will have to suffer these awful indignities.


PLEASE PASS THIS ON TO EVERYONE YOU KNOW AS SOON AS

POSSIBLE SO WE CAN GET THIS CONSPIRACY STOPPED!



PS: I am sending this to you in a larger font size, because something has caused my computer's fonts to be smaller than they once were.

FECPPSG Editor’s Note:-  I don’t know about you, but these things are happening to me every day!!!  (Also, every newsletter send to you [or put on-line] is in a larger font).

 

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UPCOMING CONFERENCE

 

April 9 – 11, 2007 at the Radisson Hotel Downtown in Miami, FL.

More information in January/February 2007 newsletter.

Hold those dates!!!!

 

 

~*~*~*~*~*~*~*~*~*~*~*~*~*~*~*~*~*~*~

 

FLORIDA  EAST  COAST  POST-POLIO  SUPPORT  GROUP

12  Eclipse  Trail  /  Ormond  BeachFL  32174

 386-676-2435  /  e-mail  address:  bgold@iag.net

RESERVATION FORM/MEETING NOTICE

 

DATE:                Sunday, November 19th, 2006

TIME:                 1:00 – 4:00 PM

PLACE:              Red Lobster Restaurant

                             International Speedway Boulevard

                             Right off I-95 – Exit 261– Daytona Beach, FL

                             (head EAST for about 1/4 mile)

 

 

PROGRAM:-     GUEST SPEAKER:-  Chris Wysocki, an orthotist with

Hanger Prothetics & Orthotics in Daytona Beach will

give a presentation on bracing for polios.

                                                                       

Cost of the Luncheon is $10.00 all inclusive.   As usual we will have a choice of several different menu items.

 

Please send in your reservation tear sheet and check

no later than November 16th, 2006

 

Any questions call Barbara at 386-676-2435.

 

=================================================================

 

R E S E R V A T I O N   F O R M

November 19th, 2006 Luncheon Meeting

  

Name:- _______________________________  Phone No.:- _________________

 

Number of People Coming:- _________ Number in Wheelchair(s):-  ___________

 

Amount of Check Enclosed:-  ________________  @ $10.00 per person

 

Make check payable to and mail same to:

FLORIDA EAST COAST POST-POLIO SUPPORT GROUP

12 Eclipse Trail  --  Ormond Beach, FL  32174

11/2006

 

~*~*~*~*~*~*~*~*~*~*~*~*~*~*~*~*~*~*~

 

DUES FOR 2006:-  Please take a look at your mailing label  -  on it you’ll see the month and year we received your 2005 dues, i.e., 01/2005 means it was received in January 2005, so your 2006 dues was due in January 2006. If your mailing label has the year first and then the month, i.e., 2005/01 it means that you indicated to us in January 2005 that you wanted to receive the newsletter but paid no dues.  That’s OK as we still believe that anyone who wants information should receive it – but we do need you to return the tear sheet with either the “Dues” box checked or the “Keep me on the Mailing List” box checked.

          Your dues covers the supplies we need to send out the information packets to all inquiring about Post-Polio Syndrome, any other correspondence we do, and postage for publicity and for the out-of-country (25) newsletters that we send out.  We’re fortunate in that the “Free Matter for the Blind and Physically Handicapped” status takes care of the postage for the over 450 newsletters sent out within the United States.  We network with approximately 60 other support groups throughout the United States, Canada, Australia and New Zealand – some 40 of these reciprocate by sending us their newsletters.  We receive as many dues checks from our out-of-state members as we do from our Florida members.  So, please check your mailing label and return the tear sheet if your date is due.  We really need your support now more than ever.  Just to keep you advised, in addition to the previously mentioned countries, our newsletter goes to England, France, Germany, Israel, Panama, Portugal, Lebanon, South Africa, Sweden, Taiwan and Wales.

***********

WHEN YOU MOVE  PLEASE be sure to send us your new address.  Sometimes the post-office will return the newsletter to us with a “forwarding period expired” notice on the front with your new address but most of the time they are just returned to us with “address unknown” on it.  SO, if you want to continue receiving the newsletter it is UP TO YOU to make sure we have your new address.

 

=========================================================

 

2006 DUES/MAILING LIST

 

____ Dues Enclosed                                                            ____ Keep me on mailing list

 

If sending dues, please make Check ($5.00) Payable to and Mail to:-

 

FLORIDA  EAST  COAST  POST-POLIO  SUPPORT  GROUP

12  Eclipse Trail,  Ormond  Beach,  FL  32174-4936

 

NAME:- __________________________________________________________

 

ADDRESS:- _______________________________________________________

 

E-MAIL ADDRESS:-__________________________ FAX #:- _______________

 

TELEPHONE NO:- Home _______________________ Office ________________

 

Date of Birth:-_________________   Wedding  Anniversary:- ________________

 

Name and Date of Birth of Spouse:-_____________________________________

 

Support Group I belong to:- ____________________________________________

11/2006