TIP: Click on subject to list as thread! ANSI
echo: fibrom
to: ALLAN QUIRK
from: ANN COOK
date: 1995-08-07 04:59:00
subject: Personal Polio 0

AQ>But sorry to hear about your father. Remember, it can take time to get
AQ>over. Others who have grieved during a prolonged downhill run to
AQ>death may get over it sooner. We each have our own time and
AQ>difficulties dealing with the grieving period. Friendss' understanding
AQ>can help.  I feel for you.
Hi Allan,
Things are a lot better now.
AQ>I gather from snooping on other echoes that you are from Shreveport
AQ>Florida?
Shreveport, La.
AQ> AC> Thanks for sharing your story...I hope some of the others will share
AQ>Glad it was of interest. I agree, that I find interesting and helpful to
AQ>hear about how other people manage their problems, because, generally,
AQ>the health industry seems to know so little about polio and pps and does
AQ>not yet have enough answers for us. I see the bbs as a means of
AQ>also providing Hints and tips amongst us.
I have got more of my information here on the boards. It was great, at
least we know the what and why. It makes understanding things a lot
better.
AQ> AC> We don't have a group here that meets that often. I wish we did..
AQ>That's not helpful. So many of our members have found it a help to be
AQ>able to work together sharing ideas. One common one, is that families
AQ>find it so hard to cope with a parent who used to be able to do so many
AQ>things, despite their disability, finding that they are now so out of
AQ>energy at times, that they find it difficult to find the energy to do
AQ>even the simplest things, that they would willingly do at other times.
I know that feeling well. I hid it from my family for a long time, but
now they can see it all to well. I have 6 grandchildren and that's makes
the no-energy visible all to fast.
AQ>Another point that has come out, is that some of the people who had
AQ>relatively minor disabilities - particularly ones they are able to cover
AQ>up most of their lives, find it most difficult with pps effects.
I get so aggravated because I lose a little more every day, it seems.
AQ> AC> I had Polio when I was 9 months old, in 1943. Some of the Drs. didn'
AQ> AC> Dallas Rehab. and was told that I had PPS. At least then I knew what
AQ> AC> happening to me and could deal with it...Us PPS'ers are a hearty lot
AQ> AC> don't give up easily.
AQ>What sort of problems were you having that sent you all the way to
AQ>Dallas?
None of the Drs. where I lived knew anything about PPS. Another woman in
Palestine that had had Polio told me about the Clinic.
AQ>What did they tell you to do about them?
They told me to rest 5 times a day and delegate some of my duties to
others and stop trying to do them myself. They also wanted me to wear a
brace on my right foot, but I refused. I told them when I started
falling, then I might.
AQ>get going in that 6-10pm sleepy period, and could feel myself pumping
AQ>willpower into my muscles so that I would get moving to get out of
AQ>the lounge chair.
I have the same problem, I will dose off too, but just for a few
minutes.
AQ>have an early night 9pm. The next day feels wonderful, but I always want
AQ>to do more and more
Did that last night, My son and his two kids, (4 and 16 months) were
here for two days and I was exhausted.
AQ> I am doing great, compared to a lot of the oth AQ> AC> I have to be
AQ>If you ever had breathing problems, you _may_ be more likely to have
AQ>sleep apnea (which can be tested - I don't know your costs). If it is
AQ>sleep apnea (stop breathing at night, wake up with headache, get tired
 * OLXWin 1.00a * Friends are like chocolate--good to have around anytime!
--- WILDMAIL!/WC v4.12 
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