Month: April 2015
Seniors traditionally are uncomfortable with change. They resent products and services disappearing and morphing into newer versions or eliminated altogether. For this group it also comes at a time when their synapses might not fire as quickly, memory is becoming harder to retain and even focus takes more effort. The Baby Boomers have been using technology for the last 30 years but did not grow up with it so learning curves are difficult the new improved is relentless. Many of us didn’t even have TV’s during our early elementary school years. Our learning curves involved how to work physical things like bicycles, swimming the breast stroke, skating, sports or creative arts.
Life moves onward so fast now. Like being on a really fast merry-go-round things past by in a blur but as it slows down periodically you begin to recognize the landscape and all of a sudden you notice things are missing since the last time you slowed down enough to notice. There are no pay phones, big blue mail boxes sitting on corners, VHS rental stores, paper maps or full service gas stations to mention a few and on their way out is land lines, CD’s, music stores, small bookstores, classified ads, cameras that use film, wrist watches, yellow pages and DVD players.
There are many I did not get around to mentioning that have already been phased out and much more in the process right now. However, there is an upside to this ever moving, ever changing, momentum of progress. New technology has and will continue to open doors of freedom for all ages. The ability to multi task well into the golden years is made possible by cell phones, web search options and wireless design. Being older or disabled is no longer confining because of the safety of cell phones to stay in contact. As they say “knowledge is power” and web research gives you unlimited power. Entertainment is enjoyed through internet TV which can stream movies as well as offer closed captioning, hearing enhancement and visual settings for low vision.
Social media sites enable seniors to keep in touch with family no matter how distant and web cam opens yet more doors. In my opinion the time spent over coming frustration and fear in order to learn new technology is well worth it. It will literally set you free to enjoy life independently and on your own terms. If you want to age in place be sure to put cutting edge technology in that place. http://www.independence4ever.org
1991 & on –
Life now is all about “bucking up” and getting on with our lives. My daughter and her sister came home two months after I did. She is in complete remission. I can walk with crutches now but can only use my thumbs because of the contractures. I taught myself to drive wearing leg braces and finally kicked my ex out. I am apprehensive on my own in my condition but I have faith I’ve done the right thing. The kids and I are all together again and that will get me through anything. I know someone is still by me from the other side as I can feel the presence at times and when I am conflicted over a decision or direction I want to go the knowledge is there. It is not a voice like it was in the coma rather it’s like intuition only more persistent.
I trusted it whatever it was and knew something was waiting for me to fulfill. During the next year I learned to walk with a cane and do most everything with my hands even though they were still in contractures. We all licked our wounds physically and emotionally and counted our blessings. I knew it was time to move toward my destiny but did not know where that was. My old plan to return to Phoenix didn’t feel right anymore. Then one evening sitting with the kids on the pier watching the crashing waves smash the shore it came to me. We had relatives who lived in Missouri. I had only drove through the town one time but I could not shake the feel of urgency. It was like a divine decree.
There was no way I could ignore this powerful pull. So, I sold the RV dirt cheap and everything in it. I bought new tires for my old 79 Ford pick-up, filled it with gas, three kids, two cats, clothes and one TV and headed north. I understood this was my destiny and I would make it. Within a week we rented our first house in six years. We had finally come full circle. Money was very scarce with just social security disability and a little child support but we were free, together and alive. It was good to be with family again. We had been through so much that the struggle to survive now was nothing comparatively.
But, surely this was not what I was pulled here for. One morning while enjoying a strong cup of coffee that powerful tugging returned. I knew I had to go find a job. My family thought I was crazy with all my complicated disabilities but I could not deny it. I was apprehensive of course. My only transferrable skills was my mind and my life experience. Everything else was braced up, atrophied or contracted. Nevertheless, I trusted this direction of my destiny. I was afraid the job search itself would do me in let alone a forty hour work week but by now I knew how to push through my egos fear.
My second interview was with an organization called Southwest Center for Independent Living. I was hired with a hand written resume in my hand but had no idea why or what they even did. It all soon fell in place as I learned they empowered people with disabilities to live their dreams by removing barriers physically, attritional and mental. All the lessons I had overcome, the struggles, the despair, the determination are now going to be played forward.
I have just retired after 22 years of empowering so many people with disabilities to see their potential and their self-worth, a career I never dreamed of pursuing. It was the most rewarding thing I’ve ever done in my life. I wondered what I’m to do now with all those years of working in the disability field and the intertwining of my life experiences. I had entertained the idea about blogging because I have always loved to write but knew nothing about blogs. About six months before I retired I got an email out of the blue from a blogging site so I looked into it. I created anyoneteachone.com and here I am. I’m still playing it forward and hope I can until I cross back over.
Never give up your dreams, never believe in prognosis and believe with all your heart the enormous power you own when you acknowledge you’re potential.
April – 1989
Recovery was slow and tormenting. It took almost two weeks to wean me off the ventilator that had pushed oxygen into my lungs for 91 days but my lungs were ready to take over now. They finally cut my medications back so I’m beginning to think more clearly and remember a few things before the illness. I have permanent systemic nerve damage and severe hand contractures, I may or may not walk again and I cannot raise my arms above my waist, I still try to make sense of what happened to me and why but I’m ready to push through whatever it takes to get my life back.
Soon as my ex entered the room I demanded he tell me where the children were and why I have not seen them. His shoulders slumped and he looked at the floor which immediately raised my anxiety level. He then explained our son was with him but the girls are in Arizona because my youngest daughter, 13 years old, was diagnosed with Hodgkin’s Non-Lymphoma stage 4 the week I went into a coma. A parent had to sign for treatments so her father came and took her and her sister back to Phoenix.
I stare at him in disbelief but I can tell it’s true. My mind is spinning and a silent primal scream comes from a place so deep in my Soul that I am trembling. Finally I find my voice, “CANCER? CANCER”? I thought my life was in chaos before but this is bedlam. “I have to talk to her, I plead. “No I have to go to her”, I yell. I’m thinking of three days ago when I sat up for the first time and only lasted a few minutes before passing out. I am beside myself with agony with the realization of the debilitating status of my body. This can’t be happening! We were all a healthy family just last summer. Its late evening so the nurses said they will help me call her in the morning and that helps to calm me a little.
I can’t sleep from overwhelming fear for my daughter. I shut my eyes when anyone comes in so they won’t give me any strong medication. I can’t wait until morning when I can hear her voice. But, sometime during the night they caught on I was faking and without my knowledge gave me a huge dose of valium through my IV. I was out for two days. Another two days of my life gone. I was beyond furious. The realization they could take complete control of me “for my own good” was a sickening reality and a horrifying one. The only other facility legally allowed to do that is incarceration.
I demanded they hold the phone for me to call my daughter. I felt better talking to her. She was finishing her chemo and radiation in a few months. I wanted to hold her, to rock her. She was so brave and so strong and without her mother. I promised soon as I got out of this hospital and she was finished with treatments she would come home. I called her every night.
Anger was my motivator and I used it to push myself to overcome each physical barrier that would qualify me for discharge. I was in constant fear they would drug me again “for my own good”. I tried to act the right way, say the right things, and not ask for pain medication. It was more stressful than the permanent disabilities I was left with. I lied about having home supports, going to an accessible house and a scheduled appointment with rehab in Pensacola. I was actually going home to an RV, no supports except for a 7year old son and an ex who I continually fought with. There was no way I was going to a 6 month rehab treatment as recommended. I knew by now this satellite hospital had no follow up staff to verify my story. I wanted to bring my daughters home as soon as possible and I no longer trusted the medical field to compromise with me or to honor my decisions.
By the beginning of May I was finally going home. The real struggle was just beginning.
Living inside a serious illness puts you, literally, into someone else’s hands. You lose a sense of autonomy and power. You are isolated, sealed into the private rooms of your own mind. You are in excruciating pain but it is hard for those outside the illness to understand, even those extensively trained for such work. Minutes have become the same as hours. There is no escape, no distraction, no peace.
I had some great nurses and I had a few who made me feel like I was just a patient with lots of needs they did not have time for. Those nurses came in handled me roughly, never made eye contact, completed their tasks and left without ever speaking. I could only move my eyes not yet able to speak. I was a prisoner without a crime.
I cannot emphasize enough how much I wanted someone to look at me, to touch me, to remind me I was still part of the human race. Even after endless painful turning of my body that had wasted to skin and skeleton, I longed for physical touch. Tears rolled down the side of my face as I tried to remember the last time someone caressed me. It was long, long ago before I was ever sick before I lost my first love.
All my life my Mother had fought for me, had kept me safe. At even the hint of harm she threw open her wings of courage and fought. But, she was not here and for the first time in my life I was starkly vulnerable and way too debilitated to fight for myself. I needed to know there was someone who would fight for my life. I became more afraid that no one might care than I did of dying.
I thought of my children and where they could be. Why haven’t they come to see me? I needed to look at them, to hear their voices. I became angry locked in this body. The more I thought of my children the more infuriated I became. I felt a rush of power come over me, a fury that pushed me over some invisible barrier and busted through the wall of helplessness.
And then, this vehicle that had failed me, that the doctors said had no hope of recovering from the severe damage the sickness had ravaged on it, began to heal itself. My vitals started to stabilize; my heart began to beat stronger and with balanced rhythm. My kidneys began to function and my ability to push breath began triggering the ventilator alarm forcing them to start weaning me off of it. I was visibly awake and aware. I was back, I knew it, and at that moment my cup runneth over with the desire to live again and I was going to fight with every cell in my body.
It is now the day before the deadline to remove me from life support. My body is in the same critical condition. The doctor has told my ex to go ahead and make funeral arrangements. They have done all they can do. But life has a way of flexing its muscles just when you think there’s no hope. I am about to be reborn and enter a life full of purpose. However, before that can happen struggle and determination like I’ve never known before will have to be conquered. It will stretch my mental and physical endurance to the breaking point. It is a destiny I had never even considered and a 360 degree turn of where I was going before.
Dr Recall – end of March 1989
The doctor just left a meeting with the hospital ethics committee and met with my ex to confirm the decision to take me off life support was really what he wanted. The other option would be to try and move me regardless of risk to a facility appropriate for long term critical care. The doctor stated he felt I would not make the trip before I coded but wanted to put it as an option. My ex stood by his decision. I think he was afraid I would linger there the rest of my life.
My Spirit – end of March 1989
I realize, beyond doubt, I have to go back. I must answer my destiny whatever it is. The resistance is pulsing within me viewing that pitiful body. What could I possibly give to humanity now? All the questions, all the ambiguity and perplexity would not be answered on this side. I had to live it.
My Spirit – evening before the date with death
Focusing back in the body was seamless but painful beyond belief. I have made a commitment to follow my destiny so whatever it takes I must do. Memories from my life started to flow back into me like a tsunami. Where are my children? What happened to me? Where am I? How long was I asleep? I cannot talk or move. The nurse notices my eyes are open and I hear her calling for the doctor. The ventilator alarm is screeching because I am breathing, although shallow, and trigging it because the breath I take replaces the machines. It thinks I am not breathing. Medical staff rush in to take vitals and re-evaluate my condition. No one expected my recovery and they are in amazement.
I am still critical but this is the first sign of improvement in three months and it is only the beginning.
Nothing is improving my condition including time. It’s the third month of the coma and I remain unresponsive. When patients show no improvement they are usually transferred to a nursing home or rehab but there are no nursing homes around that can deal with such an unstable situation. There is a rehab in Pensacola but I am too fragile to transport. The financial office is voicing their discontent because it is costing a lot of money to keep me alive. They are pressuring my doctor to re-evaluate the justification of continuing life support with apparently no hope of recovery. He is in a precarious situation so he lets the decision rest with my ex-husband who he thinks is my legal husband. My life literally lies in the hands of the man I was trying to flee from.
My daughters have been flown back to their father in Arizona as my youngest daughter at 13 yrs. has just been diagnosed with Hodgkin’s Lymphoma stage 4 while I am in a coma. My son remains with his dad here in Destin who I must give credit has stayed with me instead of fleeing with our son. My relatives are unaware of how critical I am and live across the United States so are not available. I am basically alone now.
DR Recall – March 1989
My body remains in limbo. The life support equipment is sustaining my life. I cannot live without it. The doctor must make a time line as to how long to continue treatment with no improvement and give to the financial department who are now insisting there has to be an end to the money being spent on this expensive care. The dilemma he sees is that I have brain activity but nothing else. He confers with my ex-husband who breaks down and states I never wanted to be kept alive on machines and gives his permission to pull the plug by next week if there’s no improvement. This mercy killing has now been put in place. Time is running out.
My Spirit – March 1989
I touch the colors in sequence like I’m instructed and the melody fills my Soul then I am back but not in my body. I watch the nurses caring for me. The body is in agony which I can feel. The nerve endings are hyperextended and even a breeze as the nurse walks by is excruciating. My body is on fire from a raging fever and the muscles ache from not being used. As the nurses attempt to reposition me my back feels as though it will snap in two. My hands are curled into contractures. Nothing is functioning on its own. I do not understand why I came back and I do not want to stay. There is too much devastation here.
I turn away and I am back in beauty and peace. This is where I want to remain. But I am conflicted in my decision because I have a feeling I am not done with this life. I have not finished. It is so ethereal sitting here in front of the magnificent alabaster buildings. I ask in the stillness of the mist why I am unsettled and I hear it say, because you have not given all the gifts you intended to share this lifetime. What are they? I ask. You will discover them it says if you return. But, I don’t want to still. I am aware the body cannot last much longer and then I will not have a choice. The voice speaks again and tells me if I choose to return there will be guardians to watch over me and guide but I am also welcome to stay here. “I am afraid”, I say “that the body is not fighting. It seems to have lost its will to live, its strength and determination.” “That’s because it does not possess those things within its vessel, you are carrying those things within you and unless your Spirit returns your vessel will fail to thrive. Every single Soul has that choice.”
I lie motionless like I have for the last month and will continue for the next two. Several times they tried to make plans to transfer me to the larger and the better equipped Humana in Fort Walton Beach but every movement of my body triggers the alarms that monitor my heart. So I remain in the small satellite meant for minor illnesses and procedures. Other patients that are considered complicated are quickly transferred to the big Humana. Everyone is stepping up to the plate to take care of my rapidly deteriorating body that is determined to die. But, I remain unaware as my sojourn spurs me on to mystical realms I’ve never even imagined.
DR Recall – February 1988
My heart is in extreme danger. It is in congestive failure, it is double its size and it is infected. A heart transplant is considered and I’m put on a waiting list but only if I recover enough to withstand it. My lungs are still not able to function on their own. My kidneys have ceased to give output and I am on dialysis. I am on the strongest kidney medication available. I have a feeding tube, a surgically inserted vent tube and four IV’s flowing blood, electrolytes, pain medication and nutrients to my failing body. Every day there are new complications on top of the existing ones. The doctor has already spent many all-night sessions expecting me to code at any moment like I have twice before.
My Spirit – February 1988
Colors, beautiful bright colors that I must chose correctly. The colors represent tones. I’m spinning and I feel lost but the Voice directs me. “Watch”, he says, “You know this you have just forgotten”. He touches a color one at a time in some sort of sequence and a familiar melody comes forth. The tones are connected to a color each color producing a tone. The spinning increases speed and the whirl creates a circle. We don’t go to a place rather the place comes to us. It is strangely recognizable with alabaster buildings that look more like holograms than solid structures. The beauty is luminous but unpretentious at the same time.
I want to touch them but the Voice says, “no need for they are a creation of your Spirit, there is no solid here nor time, or past or present or future there is only now.” “You can be any age, go anywhere, experience any sequence of events you desire.” I try this concept out by thinking of an immense ballroom with white marble floors with thousands of tiny azure stars imbedded. I create a rendezvous with a handsome partner and we glide on the dance floor to an orchestra. I am over whelmed with happiness and love. “The language here he says is “feeling” not thinking, there is no need for ego.”
I think of a question that I have been afraid to ask because I think I know the answer. I ask if I am dead. The Voice says,” absolutely not as we are eternal beings, death is a concept of earth society created out of fear of the unknown.” Why am I here then I wonder. He says, “Because you are placing your focus here, when your desire is to return you will focus back into the physical, it’s as simple as that.” So now I wonder what my intentions were. I want to stay but something is pushing me forward. I have not yet learned all I need to know. Can I visit my body and come back? I ask. “You have always been able to do that,” he explains. I’m not sure why I need to do this but the desire is over powering even though I know I will not stay there.
“I can’t breathe!” is the last thing I remember saying on January 1, 1989. My left lung had collapsed and my heart was beginning to starve for oxygen. Somehow my ex-husband got me to the pickup and drove to the emergency room at the small Humana satellite hospital near the campground. My eyes try to open in the sterile room I’m in but they won’t comply. I am spinning from vertigo and they are trying to put something down my throat. It feels like a tube and it hurts. I am in and out of consciousness but I am aware that I am totally in the control of other people. The rest of this story is a chronological history of what was happening outside my body (DR Recall) and what my Spirit (Me) was experiencing on the inside.
DR Recall – January 1, 1988
My left lung had collapsed and my heart was in tachycardia. They attempted to use a scope to see if I was bleeding internally but had to abort until I was stabilized. They put me in a trauma room to observe me. After an hour I opened my eyes in a stare and began talking in what seemed to be another language but no one recognized what it could be. I spoke like this for approximately 5 to 10 minutes then in English said, “I am going now and won’t be back.” At that moment I went into cardiac arrest and was rushed to intensive care and put on life support systems including a ventilator because I was no longer breathing on my own. Extensive blood and toxicology tests were ordered.
My Spirit – January 1, 1988
I was in no pain whatsoever. A film of green the color of sea foam floated down and covered my body. I could not feel it but rather sensed it. If Nirvana was a color it would be this. I felt I was in a kind of holding pattern. I had no desire to leave this place. I had no fear. I was alone but not alone. Like a baby being rocked by a loving mother I was content and I was safe.
DR Recall – Mid January
Toxicology and blood work gave no indicators that would cause the life threatening symptoms. The doctors are stumped as to how to proceed. I had lost huge amounts of blood by throwing up while unconscious so extra blood is being given, the heart remains a huge problem as it is inflamed and twice the normal size. The kidneys have shut down and dialysis has been started. The lung is being drained but both lungs are unresponsive. I evidently tried to pull the vent tube out and all my IV’s by thrashing about. An ICU nurse on each shift has been assigned to me alone. I am monitored 24 hours a day because my condition is so unstable.
My Spirit– Mid January
I’m traveling to a beautiful lush green environment with soft rolling hills and cottages lined along the road. There is light shining out and I can hear people laughing and talking. I cannot see myself but I am aware I exist. I cross a small bridge and walk into the first cottage. I do not feel like a visitor. I feel like I belong. It’s like I’ve always been there. I recognize my relatives that have passed many years ago. Someone from behind me is saying these are your people who you have shared your life with. It feels like home but I don’t know why. I enter the next cottage with more happy people and recognize them also. Some were childhood neighbors, friends, teachers and some just people I met once a long time ago. The voice explains that these are people who made an impact on my journey. It makes no difference the duration of the encounter he explains, only the significance of the influence on your soul. I want to stay here but feel a momentum pulling me away. I know I have died but it has no connotation to it. There is no sadness, no regret only acceptance. So I trust where I am being taken.
I’m struggling now to find out what is wrong with me. The chronic pain is peeling off the layers of my strength and determination. Things are deteriorating in my body in other places besides my stomach. I am no longer hiding my discomfort but I am trying to hide my fear. I know now my dream of leaving will have to be postponed until I’m better. I’m still thinking this is just a bad case of something and I will get better. Losing control of my body is causing me to lose control of my life. I’m swinging between despair and determination as the realization I am helpless covers me like a dark shadow. These are the last entries I found before I will slip into a coma. I will tell that story too from the doctor’s recollections and from mine which was a voyage to another realm.
Journal entry – November 1988
It’s almost Thanksgiving and I’m still living with this awful pain in my stomach. I’ve missed my first day of work today but will drag myself in tomorrow. I feel weak and unable to chase down the waiting orders as fast as I did before. My old black waitress shoes from Walmart feel like I’m wearing concrete blocks. I quit using the huge food trays because I can’t seem to lift them stacked with earthenware platters laden with food. Of course this means I have to make many trips back to the kitchen instead of just one. I am falling behind here at home with chores. The girls are helping by doing the laundry and getting their little brother ready for school. I’m disgusted with myself for getting sick.
Journal entry – December – 1988
I missed two days of work in a row. The boss is concerned and insisted I go to her doctor or my hours would have to be cut drastically. So I went today and he took lab work but nothing stood out as a problem. It was $155 that I was guarding in my travel money but I needed those hours at work. He said I needed extensive tests that they could do in the hospital. That is impossible of course with no insurance and needing to be here for the children. I am consumed with fatigue tonight and my muscles quiver like Jello to keep me upright.
Journal entry – December next morning
I woke this morning still exhausted and when I put my feet on the floor I could not feel them. They were numb and tingling. I rubbed them, elevated them but nothing works. Whatever has invaded my body is advancing every day. I am now truly scared. I want so badly to get through Christmas as it is a favorite holiday for us. I tried to get dressed but I am so feeble it’s impossible. I have no fever so must not have an infection I’m thinking. My body is literally shutting down. Reluctantly I asked the kids to call me in sick to work.
Journal entry – Christmas 1988
I made it until Christmas but did not really enjoy it. My travel money has dwindled down so when I recover I will have to start over, Maybe we can shoot for Spring Break. I never returned to Western Sizzlin because of my condition. I tried to work a few hours in the KOA store because I thought sitting on a stool would not be hard physically but as I stumbled home I fell and the kids had to help me up. My life is closing in on me. I’m depressed and terror stricken that I will never get better. My legs as well as my feet are numb now. My hands and fingers feel like they are asleep and my skin is hypersensitive. I can’t sleep, I can’t eat and I feel like I’m dragging around an extra 200 pounds. I’m trying not to cry but foreboding envelops me.
The beginning of the crisis has begun only I’m still not aware how my life is beginning to slip slide away. October will be the last full month of work for me. Like seeing the red engine light come on the car dash board you are not immediately alarmed but concern is in the back of your mind. If you don’t hear unusual noises or see smoke you continue to drive and check it out later maybe on payday. That’s how I handled this approaching illness. I had no medical insurance but knew when I got to Phoenix a good job would provide it and I would get the stomach problem fixed for good. I could see the finish line and attempted to drag my body to it.
Journal entry – Early October 1988
The truck broke down last week and no money for the part it needs. I refuse to dig into my secret travel money so will have to take it out of tips. Since I now have to take a cab to and from work I try to work double shifts. The cab is $15 each way so it doesn’t make since to just make a little over cab fare. I should have enough by end of the week for the part to fix it. It’s been frustrating to get a cab every night then at least every other night have him wait at a grocery store so I can buy a few necessities to keep the kids fed. On those nights the meter runs me an additional $7 as he waits. My usual abundant energy is waning from the extra work and stress. I can’t finish a shift without eight to ten Excedrin and a pot of coffee anymore and my stomach remains a fire pit. I feel I’m running out of steam. I know I’ve worked my body way beyond its normal limits for a long time but it’s not too much longer now. I have $900 saved.
Journal entry – middle October 1988
Truck is fixed so no more taxi thank goodness. I bent over in stomach pain today at work. Seems I can’t keep anything down. The boss insisted I go to emergency room so I promised I would right after work. $75.00 later they said I probably have an ulcer and sent me home with a diet sheet and Maalox. The only time the pain is halfway tolerable is if I don’t eat. I don’t understand why I’m not getting better and every day it’s harder to push through this agony. Maybe it’s just a bug, maybe it will pass in a few more days. I’ve always been healthy surly I will overcome.
The stars are out tonight and there’s a soft breeze. It’s not like the night sky in Arizona where the stars seem so close and the brilliance takes your breath away but it is a different beauty. The pain is a constant reminder that I probably won’t be able to work double shifts or weeks with no day off and that slices through my ego like a paper cut. Only six more weeks and things will be very different.