PI.07-JulAug95


Inspiration, news and knowledge from Polio Experience Network
No. 7: July – August, 1998

In This Issue:
“You Don’t Look Sick” (by Elinor Young and Alex Looms)
Just the FAQs (by Dave Graham)
“Will the Real Sharman Collins Please Stand Up?”
Copyright Information

“You Don’t Look Sick

A question at support group spawned this E-mail exchange.

Dear Alex,

At the last discussion meeting, you said something about how confusing it is for friends to see you in a scooter. You look as “normal” as they do! How, you wondered, do you convince them you’re for real? I’ve got an idea for you. An idea gleaned from my years with the Kimyal tribe of Irian Jaya, Indonesia.

The Kimyals live in the remote interior of the island, high in the rugged Snow Mountain range. Life for them is rugged, too. They live in small round thatch roof huts, grow sweet potatoes and raise pigs. In fact, pigs are money: a man needs them to buy wives, gardens and other necessities. Pigs spend the night in the women’s huts so someone can keep a fire going all night to keep this “savings account” from getting cold and sick. Kimyals consider sickness in humans as bad, but in pigs it’s a disaster.

I lived in a mountain-cabin, “Western-style” house, and no, no pigs lived with me! Even so, I fell prey to all the normal tropical diseases plus some. I got little sympathy from the Kimyals, though, and sometimes wondered why.

Toward the end of my years there, I had been having heart palpitations and bouts of tachycardia. No big deal, I thought. Then one morning my heart started racing 200-plus beats a minute and I couldn’t get it stopped. I knew this episode was different. Each beat was so violent that I could literally see my chest pound. My colleague was a nurse, but she was on another island for vacation. And weather was bad, so I couldn’t call a plane in to our single-engine size gravel airstrip to take me to medical help.

After 14 hours I talked to a missionary doctor by radio. He suggested the normal methods for getting my heart to stop racing. But neither his suggestions or any methods I had used in the past worked. At 18 hours I knew I was in danger; I was getting weak and wanting to give up.

I prayed one of those Peter-sinking-into-the-water “Lord help!” kind of prayers. I simply said, “I’m running out of time. Neither Dr. Ken’s suggestions nor my usual methods have worked. I’m going to lie down and try again. Please put into my mind what to do.” I did, and He did. I filled my lungs and used my chest muscles to press my heart against my ribs as hard as I could for as long as I could hold my breath. After I started breathing again, my heart stopped racing, but almost stopped altogether. It reluctantly, laboriously lumbered along for a minute or two, then settled into regular rhythm. And I began to hurt.

The pain was incredible. I knew my heart and chest muscles were bruised, and my heart was very tired. Consciously willing each leg toward the kitchen I cooked an “Impossible Quiche.” It was the weekend, so the gal who cooked for me during the week wouldn’t be coming. I knew I had to eat to give my body strength, but I also knew I did not have in me the ability to cook more than one thing. I lived on the quiche and powdered milk for three days while I laid back in my “big” chair and cried.

I cried because of the pain, because of the weakness, because of relief that I was alive, because I didn’t know why and because of fear. What did this mean? It wasn’t just my heart — my whole central nervous system felt like it was falling apart.

As they always did, my Kimyal friends frequently dropped in to visit or check up on me. I told them I was not well. Their response was a shrugged shoulder or a soft chuckle as if I’d told a joke. Finally, Sa’ale told me, “Sick! You don’t look sick! At least when we are sick we look like it. Our hair looks sick, our face looks sick, our skin looks sick — you don’t look sick!

He was right. The Kimyals make sure they look sick when they are. They smear their hair, faces and chests with pig grease and black ashes and, if they have one, put a dirty rag over their heads for good measure. Then they walk with a slouch and put on a long, long face. Everyone knows they are sick. No doubt about it.

As you can imagine, only ten months after that incident I had to leave Irian Jaya. My body had totally “crashed” with PPS. That was 1991. I went through a rapid decline which has now slowed way down. Friends who have been with me through this are so delighted about how well I am now. They’ll say, “It’s so good to see you looking so well!” They’re geniune. But every once in awhile I still see an old friend for the first time since PPS who, as I smile from my scooter, says, “My! You’re looking good!” Their confused expression and forced smile implies, “I thought you are supposed to be sick…”

We’re not sick, but how to prove we’re not joking? There’s only one answer. Bring our the pig grease and ashes. Find a dirty rag for good measure, and don’t forget to practice a long face.

Good luck Alex! Elinor

– – – – – –

Hey Elinor,

I think your story was wonderful. A great idea for all of us. In fact it really got me fired up! Although we were not planning any out-of-town trips for the Memorial Day holiday, we did have several local social outings planned.

With our large family, rags are easy to come up with — the kids can turn any item of clothing into rags with amazing speed. Rags were not a problem! Black ash had me a bit confused. My bride, Ann, accused me of being too obsessive. Heck, ashes come in colors from off white to charcoal. After considerable fretting, I chose ash from the barbecue. Besides, we were going to more than one place so I could adjust for that just-right “sick” look. But pig grease!!!! Now that was a tough one! Living “out in the sticks” like we do here in North Idaho, I figured it would be easy. Well it wasn’t.

Apparentrly we live in a more depressed neighborhood than I thought — nobody owned any pigs. We may have to move and get a pig of our own. Although, I’m not sure how much energy I’d have to exert to squeeze out the pig grease. Just in the nick of time I thought, “4H — finally pig grease!!”

I applied a liberal coat of everything — could one look too sick?? I even gave my scooter a dash of ash for effect. Well, as I’m sure you can imagine, everywhere I went people said, “YOU’RE SICK!!!” I guess that was the effect we’re looking for. But from their tone of voice I’m still a bit confused about what kind of sick they meant.

I must admit that, although fatigued, after a shower I “felt better.”

Bye for now, hugs, Alex

Just The FAQs

Frequently Asked Questions about Post-Polio Syndrome
by Dave Graham

#1 How do I know I have Post-Polio Syndrome?

The diagnosis is one of exclusion. Other conditions that have similar symptoms must be ruled out. These include Fibromyalgia, M.S., Myasthenia Gravis, ALS (Lou Gehrig’s Disease), Parkinson’s, tumor, etc. Having Post-Polio Syndrome does not rule out the possibility of also having another disease though. A physiatrist or neurologist familiar with PPS can perform appropriate diagnostic tests.

#2 My regular doctor doesn’t have a clue about PPS…. who do I see?

The library of Polio Outreach of Spokane is a wonderful resource. In it you will find a list of local specialists. The Easter Seals Society also publishes such a list.

#3 Am I going to die from PPS?

Everyone’s going to die someday, but not from Post-Polio Syndrome.

#4 What About Social Security and disability insurance companies?

Again, the support group is the place to go for this information. Many people can offer their experiences and the library has some great articles on the topic.

#5 What changes can I expect?

As you experience decreased strength, energy, and function, and a higher level of pain, you can expect to have to make some lifestyle changes. You may also confront some of the other common PPS symptoms (twitching, “tired brain,” etc.) However, just as the severity of symptoms varies, so also the number and magnitude of lifestyle changes differs from person to person. The Polio Outreach library can give you more specifics. Dr. Mavis J. Matheson, MD, says, “The way we see ourselves may interfere with our ability to change. One approach to the whole issue of activity is to be kind, positive, and gentle to ourselves.”

Will the Real Sharman Collins Please Stand Up?

by Sharman Collins

Dealing with post-polio syndrome forces me to reexamine my definition of who I am. The quality of my day used to depend on how manny “tasks” I had accomplished. It was a “good” day if the house was clean, a gourmet dinner was on the table, and there were cookies in the cupboard. I also expected to be able to ride my bike at least 20 miles daily and liift weights for an hour three times a week. Plus, my grand piano waited for me every day between 4:00 and 5:00. And, in the evening, I would “watch” TV with my family while I busily knitted sweaters and sewed my own clothing. I loved being involved with the activities of my athletic husband and four sons. My identity revolved around what I could do and how well I could do it.

Self-esteem. Quality of life. Buzzwords of the 90’s. What happened to my self-esteem and quality of life when all these “accomplishments” and “activities” were ripped from my life by post-polio? My yardstick by which I measured my “worth” was broken to pieces.

Wave after wave of agonizing “giving-up” of loved hobbies, sports, and activities left me feeling empty and barren. Eventually, I found new avenues of expression and productivity. Not based so much on doing, but on being. My faith that the Lord’s plan is to use me in some way to exhibit his strength even in my weakness keeps me reaching out to grasp what life offers.

Having post-polio, I don’t know what new physical problems I am going to have to cope with next. Losing the ability to ride a bike or to ski is a loss. But, losing the ability to walk, sit-up, stay alert, and breathe sufficiently on one’s own are catastrophic occurrences that demand total dependence on the Lord’s control and will. I can trust that He is in charge and, in some way, He will use my life to serve His purposes. I can still be productive. But, it is His definition of productive, not society’s and not always mine. The Lord knows who the real me is, even when I don’t.

“But blessed is the man who trusts in the Lord, whose confidence is in him, He will be like a tree planted by the water that sends our its roots by the stream. It does not fear when heat comes; its leaves are always green. It has no worries in a year of drought and never fails to bear fruit.” (Jeremiah 17:7-8)

P.E.N. & ink,
Providing experience based advice and emotional support for Polio survivors. Mailing address. 
…………….508 Shoreline Dr.
…………….Liberty Lake, WA 99019

Copyright © Polio Experience Network (P.E.N. & ink), 1995. May be reprinted in other newsletters as long as proper credit is given. Please send a complimentary copy of the publication to P.E.N. at the address above.
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