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bluerollersppssupport · BlueRoller's PPS Support - Post Polio Syndrome (PPS) Support
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Reply | Forward Message #17 of 522 |
Re: Looking for information

I had polio in 52 at age 13 months. Wore a leg
brace all my life, but walked swam, rode a bike,did a
35 mile walkathon at age 15, water-skied, Carried
music equipment as a mobile DJ, went to the gym etc.
Worked to jobs, 6- 7 days per week and up to 16 or more
hours in a day mostly on my feet. I was diagnosed with
PPS in 1990,and as was my style fought back with a
vengence ( no wheelchair for me!) <br>I went back to the
Gym, pool and took electrical stimulation with physio,
kept up all my activities, increased my walking, 2
miles/day and continued working 12- 16 hours a day 6 days a
week. DON'T DO IT. Each year I got weaker, gradually
and un-noticebly for the most part. A few more
stumbles and falls here and there, occasional overwhelming
tiredness which I did not relate to the PPS. <br>Last year
I went to VEGAS, walked everywhere and came home to
unbelievable fatigue. For a month I could barely get up many
days. I could't think straight and could not do my job
which by now only involved sitting. I couldn't
concentrate to study at night and could not do the lightest
yard work. <br>As I was sitting at home unable to go
to work I used the internet and found a lot of info
on PPS and the pieces started to fall into place. I
wasn't crazy and what the Dr. had warned 10 years
earlier was only the tip of the iceberg. Fortunately I
found groups like PRYS and this one where info is
shared and I could start to understand the changes that
were taking place in my body over the years of
overuse. <br>If you are more active than the average
polio, I believe you will fall harder. As Dr. Bruno
says, every muscle in your body was affected but the
ones with 60% fibres remaining, seem normal, FOR A
TIME. <br>Don't kid yourself, I use an electric scooter
today and can barely walk around the house. My arms
ache ,my back aches etc.I am tired most of the time
and my doctor says I won't work much longer. CUT BACK
NOW. Once the nerves die, they are gone FOREVER,
OVERUSE MAKES IT WORSE. <br>Cheers keep well and pace
yourself, please <br>Your friend in pain (peacefully at
last b/c I understand the source) <br>WES




Sun Apr 8, 2001 12:46 am

wesleyhazlitt
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Message #17 of 522 |
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i'm in the proses of closing my restaurant down been doing it for 5 years now but to day was bad my legs stopped and droped no phone and no one around set ...
djcinc_1999
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Mar 14, 2001
4:35 am

I had polio in 52 at age 13 months. Wore a leg brace all my life, but walked swam, rode a bike,did a 35 mile walkathon at age 15, water-skied, Carried music...
wesleyhazlitt
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Apr 8, 2001
12:46 am

hi same with me love hiking,biking, and all outdoor things but really have slowed down now. i dont like it either but i try when i feel good still working tho...
djcinc_1999
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Apr 15, 2001
11:08 pm

You all sound like my husband...he was 18 months old when he got polio (in 54)...he, like most polio victims, is an over-achiever. He played in a band in high ...
catnap49721
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Jun 17, 2001
1:59 am

How has life been during the three months since your post about the restaurant? I'm so sorry you had to go through it by yourself. Like you said, we know ...
catnap49721
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Jun 17, 2001
2:10 am

Hellooooo....I check this site everyday and don't find any new messages...is anybody here? Does anybody use the chat line? I had a doctor appt. today at 4:00 ...
catnap49721
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Jun 21, 2001
1:06 am

Hi catnap,<br>reviewed your messages today, and thought I would rrespond. I contacted polio in '52, I was 22 months old. Of the 3 strains, I ended up with ...
OrigDruid
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Jun 21, 2001
5:09 pm

Hey, Druid (interesting name)--thanks for responding...as with all pps people we meet, so sorry you are having to go through all this, too. Also for your ...
catnap49721
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Jun 21, 2001
8:42 pm

I am a 51 year old female with pps. Would enjoy speaking with someone.<br><br>:)...
ashia51
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Jul 17, 2001
10:19 pm

I am 53 and had polio when i was 5. Was in a brace from my neck to my feet for several years and following several surgeries wound up with 3 separate braces....
kneenab2002
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Oct 30, 2001
12:11 am

I've sent one message just a couple of days ago. It doesn't seem as tho anyone else is using the club. I would like to get to know more of you. I'll tell you...
kneenab2002
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Nov 3, 2001
3:40 am

I can't remember if I have introduced myself before or not...imagine that will ya! I am 49 and was diagnosed with PPS in 1987, quite work in 2000, and am now ...
treevines.geo
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Nov 17, 2001
6:34 am

Hi! Haven't seen much action on this club, but would like to get to know others in the club. My name in Nina and I live in Arkansas. I was diagnosed with PPS...
kneenab2002
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Dec 23, 2001
9:40 pm

Hi Nina,<br>I have requested your permission to add you to my yahoo friends list.<br><br>Look forward chatting with you real soon.<br>Becky...
myridin2001
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Dec 24, 2001
1:47 am

New member here in so. oc/ca... Hoping to meet other PPSer both here.. and in person, should you like.<br>Please view my profile.. and if i seem like someone...
gentleman_pps
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Jan 16, 2002
4:50 am

Hello.... ?...
gentleman_pps
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Feb 2, 2002
5:21 pm
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