tag:blogger.com,1999:blog-50650280167526242682024-03-08T10:23:54.316-05:00They Tell Me I'm Dying But I've Decided They're WrongI've got at least five major diseases, all of which may kill me but none of which will kill me right away. It's like being slowly pecked to death by chickens. I want to leave a blog that tells people who I used to be and how I did what I wasn't supposed to do. And I want to tell who I am now.Susan Kemphttp://www.blogger.com/profile/17936512637067708280noreply@blogger.comBlogger40125tag:blogger.com,1999:blog-5065028016752624268.post-90266911857345955112011-06-01T04:53:00.006-04:002011-06-01T05:03:17.538-04:00If It's 3AM I Must Be wide-Awake and Listening to Lady GagaI get HBO On-Demand so can watch Lady Gaga's Madison Square Garden concert whenever I need background music to work by.<br />
I'm trying to face the reality of the staggering debt that I'm in. Like so many I thought since I had "good" health insurance I really had nothing to fear. I always paid my little $20 co-pays and thought I was good to go. But the co-pays resulting from 3 long term hospitalizations in 18 months coupled with the individual doctor bills I already had have added up to thousands of dollars. Throw in my husband's unpaid student loan, maxed out credit cards a $30,000 Small Business Administration start-up loan (don't even think about defaulting on these people) not to mention the 2 dear friends that invested serious cash in my business and I've got almost $75,000. There's an organization that may be able to help us but first I have to pull it ALL together. Looking at your financial picture, no matter how much or little you owe is a very scary thing. Between the money I invested to start up my small business (and was subsequently forced to close due to my stroke) and my medical bills I've never been so deeply in debt. Since I'm now on what is jokingly referred to as a "fixed-income" from disability and my pension) there'll be no more raises in my life time that I can count on to help me dig out of this hole.<br />
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My telephone is now being held hostage by collection agencies. They make robo- calls to me all day demanding payments. I've tried to make arrangements with them but paying $25 a month really doesn't' cut it when owe someone $2,500. So now I turn the ringer off and look at the ID listed to see if its someone I know or if the call is in my area code and from a doctor. When I worked and had a large salary I thought of people like me as "dead beats" that didn't honor their responsibilities. If you don't think the universe has a hell of a sense of humor talk to me about it sometime. To go from a six-figure salary to contemplating bankruptcy 4 years later is not nearly as funny as the movies would have you believe. I follow the recommendations you always read that say pay your mortgage and utilities, food, gas, etc. If there's anything left I try to send small payments to creditors.<br />
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Still, there is something about putting it all down on paper and facing it that's given me much more of a sense of relief than I expected. It's a relief to actually see the numbers rather than have them constantly rolling and rattling around inside my head. I've also decided this is a major step towards owning my own current situation, bad health, deep debt and all. I took myself from being a teenage welfare mother to being Assistant Commissioner of Welfare for my entire State. I can do this. Well I can do it at 4:30AM in the morning. The vampire in me fades a great deal in the daylight.Susan Kemphttp://www.blogger.com/profile/17936512637067708280noreply@blogger.com2tag:blogger.com,1999:blog-5065028016752624268.post-41558119029463561882011-05-30T04:40:00.002-04:002011-05-30T05:33:59.129-04:00Oprah's Last WordsLike so many people I watched Oprah's final show. Although I've enjoyed watching her over the years I never found it the life changing experience so many others testified to. Frankly I've gotten more inspiration and/or thought provoking from some of the lyrics in Lady Gaga's songs. But on her last show she talked about purpose - as in "we all have a purpose for being here." Now its not the first time I've heard that said but it is the first I stopped long enough to actually HEAR the meaning behind the words. My problem has always been how do you know your true purpose and what's the difference between hearing the workings of your own mind and actually hearing the truth of your own purpose for being here and no I'm not high. But watching my health take a nose dive over the past five years has left me alternately bitter, pissed-off, mad as hell and occasionally acquiesce. I'd think I'd caught a glimpse of my "purpose" but it would fade away just as quickly. I spent so many years climbing the ladder of achievement, so much energy and so much hope. Until the collapse of my small business I had never truly failed at anything in my adult life. I've had setbacks but never flat out failures. It took me more than a year to break out of my state of shock over it. It didn't matter that having a stroke in the middle of trying to get a business off the ground is pretty good excuse. My super type-A personality insists I relentlessly blame myself. <br />
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So I'm trying to figure out the reason for all that's happened in the last years and how it ultimately turns into a purpose. Each time I've been hospitalized I come to and a doctor says "You should be dead!" It's said with a tone that's incredulous, It's as if I do have a purpose and the universe won't let me go until I fulfill it. In the mean time it feels like I'm being pecked to death by chickens with each new hospitalization, each new diagnosis. I'm trying to figure out how to move from this stasis. <br />
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I fell again today. My husband sprinted over the bed and grabbed me preventing me from hitting the floor even harder. He never ceases to amaze me. When I was out in the world I had an intense dislike for people who whined or did the "poor me" dance. Now here I am doing the dance myself. I keep wondering exactly how I made the universe so angry. For those of you who have been hanging in there with me I'd like to think you've seen some movement forward from me. I'm working with a non-profit disability advocate group as a consumer advisor. Thank the Goddess for the Internet. It enables me to communicate with the outside world although I still can't leave the house. I'll be practicing getting in and out of my van this week. The first time I tried to climb into the driver's side I fell flat on my back because my legs wouldn't support the push off we all take for granted to get in a car. Walking up my inside steps and getting into the van are my two major goals for the next two weeks. Medicare will decide if I can continue having physical therapy and occupational therapy for another month soon but I've got to show progress. I think I do but the repeated falls to throw me backward. <br />
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And about the purpose thing - the caretakers tell me to slow down. Start the purpose search when I can walk without falling. Since I don't know when that may be its damn hard to be patient.Susan Kemphttp://www.blogger.com/profile/17936512637067708280noreply@blogger.com1tag:blogger.com,1999:blog-5065028016752624268.post-5234341266448823962011-04-24T04:23:00.000-04:002011-04-24T04:23:19.514-04:00The Black People's NodMany years ago I introduced a white friend to the black people's nod. After I explained it to him he saw it every where. Here's how it works. When I was a child I noticed that black people nodded their heads at one another as though they knew the person passing by them. I originally thought it was familiarity and something old people (read adults) did. I went through my teens and twenties occasionally seeing the nod but not often. It was the sixties and I was definitely not traveling in circles where people understood the nod let alone actually did it.<br />
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As I grew older the nod became more important to me, especially when I would find myself one of only a few black people at an event of some kind. The nod seemed to say to me "Don't worry. We're in this together. I'll watch out for you and you watch out for me." At least that's how I chose to interpret it. Throughout my adult years I've found myself nodding more and more often. I suspect it has something to do with getting older. It gives me a sense of calm and joy, especially when a younger person nods back at me. Though they may not even realize it but somewhere along the line a parent or grandparent introduced them to the nod, without explanation. They adopted it without even realizing it and so the tradition continues on.<br />
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I have seen so many customs and traditions among the new immigrants and often wish it were possible to just walk up to someone and ask "Why do you do that?" but in our present hypersensitive society such behavior is forbidden. I recently saw on TV that Hindu's were celebrating one of their holy days by making all kinds of sparkly doo-dads and then tossing them in the local river. Unfortunately the river was not the Ganges but water off Long Island Sound. The neighbors were furious when all that "trash" washed back up on shore. After some of the usual rhetoric there was a compromise in which the Hindu's gathered together on shore and cleaned up the water when the ceremony was over. I think some of their neighbors pitched in. A young man said it was time that the old and new found ways to coexist. Maybe all cultures have a nod of some sort. Maybe they'd share it with the rest of us.Susan Kemphttp://www.blogger.com/profile/17936512637067708280noreply@blogger.com0tag:blogger.com,1999:blog-5065028016752624268.post-19105886412456589182011-03-31T05:21:00.002-04:002011-04-09T14:59:10.724-04:00Hospital SchedulesIf you've ever spent any time in a hospital you'll understand when I say its really hard to break away from a hospital schedule. At 5am a nurse or aide magically appears at your bedside to give you your first mind boggling medications of the day, check to be sure your bed is dry and give you a light bed bath. Then, wrapped up like a baby in a swaddling blanket your covered up all warm and clean, lights out and back to sleep until breakfast time. At about 8am you're woken up for breakfast, after which you're expected, if capable, of sitting on the edge of your bed and washing yourself up.<br />
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The thing about this schedule is that it doesn't stop just because you leave the hospital or rehabilitation center. Your personal circadian rhythm keys right into it and viola - your wide away at 5am. I've been home from rehab for two weeks now and I still can't stop waking up at 5am. Its driving me nuts because I also have to lie down after lunch for that all important afternoon nap. Being home is tougher than I thought it would be. I've fallen twice now and because my husband wasn't home there was no one to help me get back up. Two hours lying naked on the kitchen floor is a truly humbling experience. I had to crawl to the front door to unlock it for the visiting nurse who fortunately decided to come early for her visit. She taught me how to <span style="background-color: yellow;">get to</span> the hallway steps and pull myself up just couple of steps high enough, swing round into a sitting position then grab onto the walker and pull myself up straight. Its all about the pivot. My goal is to be able to go all the way up the stairs (14 steps) by my birthday - May 13th so send out the prayers, light the candles and keep a good thought for me. <br />
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I'm working hard on focusing on can and not can't but for a negative soul like me it ain't easy. The good news is my son and a friend came over today and moved my dresser downstairs. Its great to stop dressing out of a clothes basket and finally have dresser drawers I can make messy instead.Susan Kemphttp://www.blogger.com/profile/17936512637067708280noreply@blogger.com0tag:blogger.com,1999:blog-5065028016752624268.post-68851271666955180282011-01-24T01:04:00.003-05:002011-01-24T01:11:53.588-05:00When the Doctor Says It's Time to Stop Fighting My IllnessesIt's a tough question to ask ones self - a tough question to face. Last week was hell. Mid-week I received 8 puncture bites from my dog. I came out of it black and blue and bruised half-way up my arm. I should have realized it would effect my lupus but I honestly didn't think about it. Over the next two days both hands swelled up and I was so tired I couldn't get out of bed. I knew my dog had its rabies shots so I wasn't worried about that. I was worried about the general dirtiness of a dogs mouth and the fact that I have very little left of an autoimmune system. Then the forgetfulness kicked in and I began missing medications and insulin. By Thursday night I couldn't get out of bed without help and my husband had to stay home from work to take care of me. My husband and I know the drill when it comes to lupus. We went back over the medications I missed, double checked my blood sugar listings and times I'd remembered to take my insulin. We caught everything up and by tonight (Saturday) I was able to get up and moving a bit. I finally kept a small amount of food inside.<br />
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Now what does this have to do with anything? Well this past August one of my way too many doctors said I was refusing to accept that my health was deteriorating and the many sicknesses were related to that deterioration. We had quite a fight actually and it later turned out I was yet again seriously ill but not due to deterioration. It was due to respiratory failure. Now I know the majority of my doctors have placed me on their "I can't fix her" list. If you've ever been on that list you know the one tell tale sign - the doctor says "I'll see you in six months." This basically translates to "I'll refill your scripts but I don't expect to see you again unless you're dying. Have a nice day." Apparently there are few things more frustrating to a doctor than a patient that just won't get well. Maybe it screws up their batting average or something.<br />
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Now on the one hand society tells us "Do not go gently into that good night. Rage, rage against the dying of the light" which I've been doing since the day I got my first diagnosis. But now that most of my doctors have placed me on their own personal "can't do nothin for her" list its become about my refusal to accept my own deterioration? Arghhh... How do you fight when your doctor doesn't think you should be fighting anymore? When is it time to give up?Susan Kemphttp://www.blogger.com/profile/17936512637067708280noreply@blogger.com3tag:blogger.com,1999:blog-5065028016752624268.post-84028727480062090022011-01-20T03:08:00.000-05:002011-01-20T03:08:15.001-05:00This Time My Dog Drew BloodIt's 2:30AM and I'm deeply confused. This afternoon when I tried to stop my Lhasa Apso Herman from running to front door when the doorbell was rung he turned on me and bite me in 8 places on my hands so badly blood was running down my fingers. My wrist has swelled up and turned black and blue. Now if you've been following my blog you know this is not the first time I've had this problem but never to this extent. I guess its been slowly building up as each time he's attacked me its worse. The dog trainer I've worked with before emailed me a "bite scale" to access the level of possible change. The scale goes up to 5 and Herman teeters on the edges of 3-4. That means its possible to change his biting behavior but it will require extensive work on my part. <br />
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Its so hard to hard to understand how the quiet ball of fluff snoring beside me on the bed savaged me the way he did earlier in the day. I try to keep the fact that he's an animal first in front of me at all times but he's also my companion. He sleeps beside me and goes wherever I go in the house. Now I can see that behaviors I thought were affection on his part were actually dominance. He must go up the stairs ahead of me always. Must eat when and what I eat, refuses to remain house broken. Whenever he's not permitted to do what he wants he begins with a low warning growl. If I ignore it and continue my behavior things escalate. The problem with today was there was no warning except to say "Let me go now or I'm going to bite you." <br />
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Anyway now I'm at the point of trying to change this behavior or have him put down. My hands are badly swollen and bruised and since the majority of the bites are on the palm of my left hand I can't close it. I cry every time I look at him which makes me feel really stupid. The Dog Whisperer says that dogs are initially a blank slate so any inappropriate behaviors that occur are the fault of the owner not the dog. That idea drives me nuts. So I'll see what the dog trainer wants me to do and take it from there. Meanwhile, he lies sleeping peacefully beside me and I'm sitting here so broke up I can't sleep. Isn't it ironic?Susan Kemphttp://www.blogger.com/profile/17936512637067708280noreply@blogger.com0tag:blogger.com,1999:blog-5065028016752624268.post-1814338325612043882011-01-18T05:45:00.000-05:002011-01-18T05:45:48.487-05:00The Grace of PeaceI marvel at the grace of peace. It comes to me rarely as I'm sure it does for most survivors of child abuse. The darker memories are what usually haunt me late at night/early in the morning. Memories of a drunken parent who'd rather lock me in a crate in the cold cellar than tuck me into bed on a cold winter's night. It's 4:30AM and I'm in my quilt room listening to Enya's music. It is as if the room has become something out of Narnia - a closet to step through into a completely changed room from the dark, depressing prison it was last year. It was a place of sorrow, sadness, pain, hopelessness and believed impeding death. A friend who had visited last yr. when I was so ill stopped by yesterday, sat down, smiled then said the entire vibe of the room had been replaced with joy. She explained the true concept of feng shui and that everything has energy. Where something sits, from a box to a chair and how its used often dictates how the energy disperses. If ever there was proof of this its my quilting room. Did I mention I just got access to the room across the hall as my own too? Rooms of Ones Own? I'm sure it's not what Virginia Woolf had in mind but since I don't have the money I'll take the space. <br />
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I finally gave away the treadmill that's been taking up the majority of space in the small bedroom my daughter occupied many childhood years ago. The treadmill had become an expensive clothes hanger combination resting place for the cats. The room itself had become that place every home has called "throw it in there and we'll sort it out later." Later never seemed to come and the room just kept filling up. Well in keeping with my motto "If I haven't used it in a year donate it or throw it away" I've been getting rid of things right and left. The amount of space that's opening up is positively astonishing. This tiny home I have hated for so long feels like a haven of peace and calm - no longer home crap home. Of course, since I swing from one extreme to another I now rarely want to leave my "safe" house. Its been 3 weeks since I last went out and then it was only for a doctor's appt. My therapist feels this may not be healthy. My friend says if I believe this is right for me at this time in my life then go with it. I think I'll go with my friend,s statement despite having to pay the therapist for her advice. It's 5:30AM now and the snow is coming down harder. This means I having a true and proper excuse for not leaving the house today. It's my husband's day off so we can curl up under the blankets and inhale the comfort of each others presence. Sleeping beside each other calms us and helps us feel safe. It is an abuse survivor thing for both of us, this need to feel safe in bed. It is a gift we give to each other.<br />
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Susan Kemphttp://www.blogger.com/profile/17936512637067708280noreply@blogger.com0tag:blogger.com,1999:blog-5065028016752624268.post-8029057927029061032011-01-17T19:13:00.000-05:002011-01-17T19:13:33.205-05:00It's My World and I'm Stuck In InLeaving the house has been a struggle for me since my stroke 4 years. The stroke left me with right-side weakness, verbal aphasia (using the wrong word when I speak- like saying door when I mean desk), and worse of all, the need to wear an adult diaper 24/7. I know I’m fortunate to be able to walk, with assistance, and still drive. Leaving the house from December through April is just too hard – between rain, cold, snow and the general miserablness of the weather and how it all affects my body. I have to carry the 10lb. battery for my scooter out to my van because it may freeze at night. It’s now been 3 weeks since I left the house for anything other than a doctor’s appointment. I start out each day with the intention to leave the house and run an errand, pick up something the house needs from Home Depot; the usual stuff able-bodied people do every day. I’m not agoraphobic. I just can’t bring myself to do everything it takes to leave the house because it’s like planning to go to war. I bought a large and I do mean large purple shoulder bag shortly after the stroke. I figure purple and red are “I don’t give a damn” strength colors. I pack it with 2 bottles of water, 2 diapers, cell phone, note pad, several pens, a very large and heavy daybook full of doctor's addresses, day notes, business cards and anything else you can think of including tissues, medical file folders, information about medications and any other miscellaneous things that will help me feel safe out in the world. It can take up to a half-hour just to pack the bag. Then it’s time to get “me” ready. My physical difficulties cause me to go very slowly so that usually takes me 2 hours to shower, lotion up and get dressed so basically it takes about 3 hours altogether to get myself out the door and do an errand that may only take 15 minutes to go and do something. Ultimately I decide why bother? Wouldn’t you? A friend said I needed to decide what MY beliefs are. She didn’t mean religious beliefs but personal beliefs about why I think I still have do things my old able-bodied way. Why do I think I have to leave the house on a daily basis? I’m working hard on this business of reinventing myself. I’ve made it to the thinking hard about it stage.Susan Kemphttp://www.blogger.com/profile/17936512637067708280noreply@blogger.com0tag:blogger.com,1999:blog-5065028016752624268.post-45297171154070376902011-01-08T23:08:00.000-05:002011-01-08T23:08:25.739-05:00A Room Of One's OwnI have lived with men my entire adult life, since the age of 17. I'm now 57. In that time, including raising two kids I have never had an entire room I could call my own. I recently saw, in a DIY magazine, how a woman could build a small shelf area in the kitchen for her laptop with equally small book shelves above it. I've had many spaces within rooms that I shared with LOTS of other people. This means that whatever was on my desk was considered open to be used by anyone. Clothes, makeup, books, papers, pens...it felt like the more important the thing was to me the more likely it would be taken without my permission. At one point my then husband made a beautiful little box just large enough to hold small things that mattered with a lock. The problem of space created many many screaming arguments in my home.<br />
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My children grew up and moved out. I divorced my starter husband and moved on to husband number two - who I've been happily married to for 13 years. Somewhere in my many rambling blogs I may have mentioned that after my last hospitalization I was forced to move our bed into the living room so I didn't have to walk up and down the stairs constantly. While I was in the hospital my wonderful son (its great when you finally reconcile with your adult children and they forgive all your parental mistakes.) I'm saying this somewhat with tongue in cheek. He, my daughter-in-law and a friends son moved everything from the bedroom into the living room. I put my sleeper sofa out in front of my house with a sign saying FREE and it was gone in 1 hour! At first I was really depressed. Only old really sick people slept in their living rooms. To be honest although I've lived in my house for over 25 years I've never liked it and at times have hated it. It has memories that make me want to run screaming into the night. I didn't put much energy into repairs, upgrades, whatever. I hated the house and I let the house know it. In retrospect I see now it totally reflected my depressed moods.<br />
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I never understood the whole feng shui thing. You put a chair down where it works best for you and that's that. But some massive kind of energy changed when we moved the bed into the living room. It started when I turned our former bedroom into a quilt studio. I've been a quilter since childhood, being sent every summer to an older woman who would teach me various sewing technique including quilting, crocheting, knitting and even something called tatting. I learned to stories of how quilts helped guide slaves to and through the underground railroad. I had shelves and shelves of fabric, fabric in boxes, fabric stashed in closets. Suddenly I could put it all in one place. My sewing table, my cutting table and ironing space, the 100+ quilt books, I was able to bring everything, every ruler and template together. I was able to raise the blinds all the way up which I could never do when it was a bedroom. Naked and open window don't work well together. I HAD A ROOM OF MY OWN!!! <a href="http://tinyurl.com/3ycaaj8">http://tinyurl.com/3ycaaj8</a> Virgina Woolf was right. OK so it took me a very long time to get here and I don't have the money she said should go with the room but I now have TWO rooms. The small room across the hall has always been the "throw it in there and we'll deal with it later" room. A massive treadmill took up most of the room. I used it as a clothes hanger. It worked fine I just never used it. Suddenly the cleaning woman asked if she could have it and my only price was she had to get someone to take it away. It was gone in three days and there was this wonderful small space across the hall from the quilt room. I was able to move all my paperwork, bills and everything else that I felt was negatively effecting the quilt space into the little room. I get the feng shui thing now. <br />
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As my mood improved it seemed the rooms got lighter, brighter. I usually hate people who say things like this. I consider them wimps who refuse to face the realities of life. Life is bleak and the universe is just waiting to slam you when you least expect it. So you can imagine how odd I find these warm, fuzzy feelings. Its just not me. Although it feels great I live in terror of these feelings just stopping when I adjust to all the anti-deps. So to protect myself I figure the best thing to do is to keep the basic darkness inside me going. This blog post started out talking about the gift of space. The bottom line is my husband said he only needs enough space to sit with his lap top and he really means it. Even after I dragged him all over the house demanding he tell me if this or that corner really mattered to him. We've been married 13 years so I figure I'm totally free to bring out the crazy now and then. He's helped me lug and lift boxes, tables, chairs to rearrange the rooms. Since neither of us have particularly good backs its been a slow undertaking but we've finally moved everything around to where we want it. Well to where "i" want it. I'm off to do a bit of quilting. After all its only 11pm. Thanks for reading.Susan Kemphttp://www.blogger.com/profile/17936512637067708280noreply@blogger.com0tag:blogger.com,1999:blog-5065028016752624268.post-88828386173460059712010-12-28T17:39:00.003-05:002010-12-28T17:42:29.814-05:00JUST MY OPINION<strong>Taken from my website "How to be Disabled In America" </strong><a href="http://www.skcllc.net/"><strong>http://www.skcllc.net/</strong></a><br />
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The blizzard of 2010 is all over the news with airports closed, roads blocked, streets flooded and electricity out. Whenever catastrophes like this happen my first thought is "What about the disabled?" I'm more fortunate than many in that I have a local man who comes over and shovels me out for a small charge. But I'm very aware that I'm left at his mercy. I pace from window to window while I wait for him to arrive, looking out to see if he's started yet. There's no getting to my van with all that snow in the waY. I start speaking to myself saying "When can I get out? When can I get out?" I run through my mind to be sure I've got enough supplies for a few days. No matter what the season I try to make sure I've got extra groceries and staples like paper towels and canned food in the house. I live in terror of being stuck in the house and running out of something I really need, like oxygen. I recently discovered a food delivery service called Peapod (http://www.peapod.com). I order my groceries online, pick the best delivery time and they show up at my door a day or two later. Again, I always order extra this or that so if I'm stuck because of weather or health, there are always some basics in the house. I think alot about people who don't have my options. How do they cope? Screaming might not help but it does relieve the tension. Just remember your neighbors might misunderstand. If you're reading this do you have any techniques or ideas that you use to cope with bad weather as a disabled person? Write to me at skemp@skcllc.net with the subject line "What About the Disabled?" and let me know. By the way, rain when you're wheel chair bound sucks.too.Susan Kemphttp://www.blogger.com/profile/17936512637067708280noreply@blogger.com0tag:blogger.com,1999:blog-5065028016752624268.post-59205951175107048902010-12-22T01:49:00.000-05:002010-12-22T01:49:33.259-05:00WE CAN'T ALL BE AS BRAVE AS ELIZABETH EDWARDS<span style="font-family: Arial, Helvetica, sans-serif;"><strong>WE CAN'T ALL BE AS BRAVE AS ELIZABETH EDWARDS</strong></span><br />
<span style="font-family: Arial;">From my webpage: <a href="http://www.skcllc.net/">http://www.skcllc.net/</a> - How to Be Disabled In America</span><br />
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<span style="font-family: Arial, Helvetica, sans-serif;">Edgy is one of those words like pornography. I don't know how to define it but I know it when I see it. It's my intention to make this website "edgy." I'm a cranky, pissed off disabled person. I don't consider becoming disabled to have been a life-enlightening moment. Frankly, I'd rather have the ability to walk freely back. When people tell me "I'm an inspiration because of how well I manage this change in my life" I want to tell then to stop by my house around 3AM and see how well I'm handling things then. There's a whole lot to be angry about (don't even get me started on the Americans with Disabilities Act) but to let you know that I'm not entirely dark and cranky (even though I'm an African-American) I wanted to share two of my favorite videos with you. Every day the local college track team runs past my house. Watching them run is like watching gazelles running across the savannah-heartbreakingly beautiful, all the more for knowing I'll never run like that again. When I told a friend how sad I was feeling she sent me a video called <a href="http://www.wherethehellismatt.com/">"Where the Hell Is Matt Dancing-2008."</a> Matt travels around the world getting various cultures to dance with him. It gets me smiling and crying at the same time. My other favorite video is also a dance one. I'm a sucker for people willing to make themselves look foolish in the name of having a good time and showing friends they love them. Its called <a href="http://www.youtube.com/watch?v=4-94JhLEiN0">"Wedding Dancers."</a> This is as bright and sunny as I get at 1AM on a Wednesday morning. As I write and send more information you'll probably find yourself wondering "what happened to that semi-happy disabled woman?" </span>Susan Kemphttp://www.blogger.com/profile/17936512637067708280noreply@blogger.com0tag:blogger.com,1999:blog-5065028016752624268.post-75321632202388902452010-12-13T03:38:00.000-05:002010-12-13T03:38:29.799-05:00GIMME THAT OLD TIME ACCIDENTAL SPEED-WAHOO!<span style="font-family: Arial, Helvetica, sans-serif;">I take something in the vicinity of 37 pills a day, half of which are pain killers. This many pain killers makes me positively narcoleptic unless my mind is fully engaged. In other words I can drive safely when I get home and sit for more than 10 minutes I fall dead asleep. I almost drowned in plate of mashed potatoes when I was in the hospital. So one of my doctors the newest drug for narcoleptics - Neurvigil. She checked me out on a low dosage and then upped it big time. I got the prescription filled, didn't pay attention to the time and popped one at noon. Now here I am at 3AM wide awake and CLEANING THE REFRIGERATOR!!! That's when you know you're over the edge. I took everything out and put it on the floor and washed all the shelves. The frig looks great and I've still got energy to burn. I'm actually thinking of vacuuming the living room.</span><br />
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<span style="font-family: Arial;">When I was in my twenties I worked way too many part time jobs, some at night. I used to buy speed from a woman I worked with. I would write her a CHECK and then on the memo line write "speed." Arghhh... Someone must have been watching over me because its a miracle I didn't get busted.</span><br />
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<span style="font-family: Arial;">Another story - in my twenties I bounced a check and then forgot about it. Months later a sheriff's deputy came to my apartment to arrest me for the check unless I covered it immediately. I was terrified with visions of being dragged off to jail so blurted out "Will you take a check?" He laughed so hard he had to step outside to catch his breath then gave me til the end of the week to get the cash. Believe it or not years later we became good friends when he ran for office. I helped him with his campaign . Each time we meet we say will you take a check?</span><br />
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<span style="font-family: Arial;">I love having this much energy. I rarely get out of bed before noon because the pills and the illnesses knock me out. I've learned to make appointments for after 2PM and do as much as I can on the Internet. If you've never heard of Peapod check it out. You order groceries on line and then deliver them to your house. Yet another great thing the Internet has done for the disabled.</span><br />
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<span style="font-family: Arial;">Which reminds me - I'm completely changing my website to provide disabled information from the perspective of someone that can't be Elizabeth Edwards. In other words we can't all keep a stiff upper lip and serve to reflect nothing but the positive in times of serious illness. I'm trying to get up the courage to write the piece but I thought out of respect I'd wait a week or two after her funeral. I'll let you know when the web page goes up.</span>Susan Kemphttp://www.blogger.com/profile/17936512637067708280noreply@blogger.com0tag:blogger.com,1999:blog-5065028016752624268.post-58813341484073633402010-11-25T10:40:00.002-05:002010-11-25T10:45:40.355-05:00It's Not What I Expected - November 25, 2010<div><span style="font-family: Arial, Helvetica, sans-serif;">I did not expect to have such a difficult time with the idea of feeling better. If you've spent most of your life dwelling in the dark places (you know who you are out there) then coming out into the light is a truly scary experience and that's where I am right now. I'm feeling genuinely good since the August hospitalization. That is to say great emotionally. My cadre of doctors continue to tell me I should be dead and I swear I'm not making that up. Some marvel that I'm alive and some seem genuinely confused. One of them gets so sad about the whole mess that I wind up comforting him by saying I'm actually feeling a little worse for the wear. No one should feel compelled to comfort their doctor but then again they're human too. I always question which type of doctor I would prefer - a House type personality or the general doctor personality - 15 second perfunctory visit, glance at the chart and scarcely remembering who you are or what meds they've prescribed. Oh yeah, did have my mammogram yesterday which is tantamount to smashing my breasts between two bricks and being told to hold my breath while doing so. Despite have to have several films because as the tech so kindly said "your breasts are wrinkly so it makes getting the picture difficult." </span></div><div></div><div><span style="font-family: Arial;">Anyway, saw a total of six doctors this week. Can you believe it? I've developed a nasty side effect and so far no one has been able to figure out how to fix it. Stop reading now if you gross out easily. It's called fecal incontinence which means I have no sensation of having a bowl movement. I wear an adult diaper 24/7 and live in constant fear that this will happen while I'm out in public with only the smell to alert me. Talk about your hidden illness. I KNOW there are other people out there with this problem (thank you Dr. Oz) but like me its just not something discussed in polite company. I've even had a couple of doctors grimace when I talk about it. For now one doctor has me off ALL carbonated drinks for the next two weeks as a test. He thinks that carbonation can be a major trigger for severe diarrhea. I'm open to trying anything. I finally got over the agoraphobia and now this. Whine whine whine. The thing is the concept of not being depressed is so new to me that this latest physical issue gives me permission to drop right back into old habits - hiding out and staying in bed. After all who wouldn't be depressed about crapping all over themself without warning. Yikes! Still I'm fighting and living on Imodium and being hopeful the doctor is right about carbonation. But consider this...if a doctor told you you were dying but still said you should give up the foods and drinks you really enjoy would you? You life is shortened anyway so why try? I wrestle with this one every day. </span><br />
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<span style="font-family: Arial;">I'm off to my son's and daughter-in-law for Thanksgiving dinner. He put himself through college as a cook and is fantastic at it. After so many years of making dinners it wonderful to have someone cook for me.</span></div>Susan Kemphttp://www.blogger.com/profile/17936512637067708280noreply@blogger.com0tag:blogger.com,1999:blog-5065028016752624268.post-77148141007660542722010-10-03T13:18:00.000-04:002010-10-03T14:20:15.904-04:00The Truth About RetirementA<span style="font-family:arial;"> long time <span id="SPELLING_ERROR_0" class="blsp-spelling-error">Facebook</span> friend wrote that her husband was about to retire. It took everything I had to not shout "Tell him not to do it!" Since I started working at the age of 14 retirement has been held out to me as the be all and end all of our lives. It would be a time when you could finally do the things you'd dreamed of. TV shows us retired people living in beautiful private communities, golfing, going on cruises or traveling around the world. These commercials of course, never mention you need money to do any of these things. </span><br /><br /><span style="font-family:arial;"></span><br /><br /><span style="font-family:arial;">I was raised by a child of the depression who often told me what life was like before social security. There were no fall backs like unemployment, welfare or social security. Families doubled and tripled up in tiny apartments. There were nights when there simply was no food and that was that. You couldn't say a bad word around my mother about Franklin Roosevelt, the father of social security I think. Between social security and a pension, she said, I would be set for life. When I vested my time with my State job I had no idea what it actually meant or why people were so happy for me. It was still a time of "set for life" jobs. Being a State employee was considered so powerful that you could walk into a car showroom and buy a car purely on the power of being a State employee. Those really were the good old days. </span><br /><br /><span style="font-family:Arial;"></span><br /><br /><span style="font-family:Arial;">I left my job as an appointee of Governor George <span id="SPELLING_ERROR_1" class="blsp-spelling-error">Pataki</span> (see blog history) courtesy of Eliot <span id="SPELLING_ERROR_2" class="blsp-spelling-error">Spitzer</span> sending me a letter saying I had two weeks to get out of my office. What goes around comes around doesn't it? Anyway I decided to start my own grants business but quickly learned that the old timers who said things like "At least you've got your health" weren't kidding. I had to close the business but what I learned quickly was how hard it is for a Type A personality to operate in a world that has little patience for retired people without titles. I still miss water cooler Mondays where you stand around and talk about what you did over the weekend. I actually miss meetings because what I didn't realize is they're a form of social networking too especially if you actually achieve something. I can honestly say I miss almost everything about work. OK on snowy winter days I'm delighted that I don't have to clear the snow off my car or drive on scary slippery streets. I've been retired for going on four years now and have been miserable every step of the way which maybe why my health has been so bad. But something shifted inside me in the last few months.</span><br /><span style="font-family:Arial;"></span><br /><span style="font-family:Arial;">No miracles but perhaps a quiet acceptance of change. My husband said he's looking forward to retiring one day <span id="SPELLING_ERROR_3" class="blsp-spelling-corrected">because</span> it will mean the end of doing things he doesn't want to do and his statement really clicked with me. Yes I'm aware that this could also mean the Prozac and <span id="SPELLING_ERROR_4" class="blsp-spelling-error">Wellbutrin</span> are finally working. I can only say something turned over inside me, something changed. Maybe its having to sleep in the <span id="SPELLING_ERROR_5" class="blsp-spelling-corrected">living room</span> (more about that in the next entry) or just finally <span id="SPELLING_ERROR_6" class="blsp-spelling-corrected">understanding</span> what <span id="SPELLING_ERROR_7" class="blsp-spelling-error">feng</span> <span id="SPELLING_ERROR_8" class="blsp-spelling-error">shui</span> means. Either way I can <span id="SPELLING_ERROR_9" class="blsp-spelling-corrected">honestly</span> say I think I feel better and if you've been following my blog you know this is an earth shattering statement for me. However my health still sucks so I continue to have something to complain about...<span id="SPELLING_ERROR_10" class="blsp-spelling-error">LOL</span>!</span><br /><br /><br /><span style="font-family:Arial;"></span><br /><br /><span style="font-family:Arial;"></span><br /><br /><span style="font-family:Arial;"></span><br /><br /><span style="font-family:Arial;"></span><br /><br /><span style="font-family:Arial;"></span><br /><br /><span style="font-family:Arial;"></span><br /><br /><span style="font-family:Arial;"></span>Susan Kemphttp://www.blogger.com/profile/17936512637067708280noreply@blogger.com0tag:blogger.com,1999:blog-5065028016752624268.post-46733250195201877782010-09-19T07:46:00.000-04:002010-09-22T05:33:34.699-04:00Up Again at 2amI've been writing inside my head so much I decided it was time to pull things out and put them on paper. I'm just out of the hospital again after a two and half week stay. Each time this happens I'm hopeful that the shock and humiliation of it all will result in my changing what I believe are some unhealthy behaviors. It almost never does although after the 2007 intubation I finally stopped smoking. I'd been a smoker since the age of 14 so believe me it was no small feat. However, I'd wound up on oxygen 24/7 and frankly couldn't figure out how to use a lighter around oxygen. I had visions of people diving out windows every time they saw me try to light up. So I locked the image of the intubation tube down my throat and thought constantly of the movie Alien. I kept waiting for something to come out of my stomach. I'd tried everything including Chantix but nothing worked. But visualizing that tube down my throat was more horrifying than anything I could possible think of related to smoking. I've been a non-smoker for 3 years now and there's not a day I don't miss it.<br />Working seriously on self-change is exhausting!<br /><br /><br />This time I went to the coronary care unit because they thought my heart was going to stop. And still I come out of these events able to talk and think and function. The doctors always say they're amazed but my husband tells them "If you're surprised she's alive then you don't know my wife." I think he's afraid I'll come back and haunt him if he pulls the plug. Still I took the realization that my bed would have to be moved to living room very hard. I'm adjusting and the house actually looks larger. We put our beautiful sofa bed out on the curb with a free for the taking sign. It was gone within an hour. Slowly but surely I'm working on this healing thing.Susan Kemphttp://www.blogger.com/profile/17936512637067708280noreply@blogger.com0tag:blogger.com,1999:blog-5065028016752624268.post-16264601126808267422010-04-13T22:24:00.001-04:002010-04-13T22:28:47.715-04:00Still Alive<span style="font-family:arial;">Just a quick note to say I'm still alive. Just finished my income taxes and am staggered at the amount I spent on medications and medical bills in 2009 - almost $10,000 and that's with "good" health insurance. Never thought I'd agree with a Democrat but Obama's right - the medical system is out of control. Thank you for the kind supportive emails. I'm hanging in there. The Prozac is really starting to work. I volunteered to worth with a local disability advocates group. The irony has not escaped my notice. As my therapist said - the years will go by whether I decide to do something or not.</span>Susan Kemphttp://www.blogger.com/profile/17936512637067708280noreply@blogger.com2tag:blogger.com,1999:blog-5065028016752624268.post-6347202849772141782010-03-31T19:58:00.000-04:002010-03-31T21:11:35.708-04:00A Different Point of View On Race<span style="font-family:arial;">I have strong opinions about race. I'm allowed since I'm black. I remember my mother being absolutely appalled when we kids (I was a teenager in the sixties) started called ourselves black. She said when she was a teenager she was delighted when whites finally started calling blacks Negroes. It was a tremendous step up from nigger. She was born in 1910. I was born in 1953. Martin Luther King had not gone to the mountain top yet so things were still pretty ugly in the early 60's. I spent most of my time being called white girl and being told I talked like a white person. But at home my mother insisted I speak proper English. She bought a set of Encyclopedia (which back then was the equivalent of buying a used car) and demanded I read them from cover to cover. I think this was to compensate for her brutal abuse but that's another story. </span><br /><span style="font-family:Arial;"></span><br /><span style="font-family:Arial;">All of this training led to my dropping out of high school. You see I went to the guidance counselor when I was in high school and said I wanted to go to the Philadelphia School of Music to learn how to be an orchestra conductor. She gently said that my people generally went to the local training school to learn how to be top notch cleaners, janitors and maybe if I worked real hard - a nurses aide. I dropped out the next day and ran away from home. Long story short, I came back a year later pregnant. Anyway I spent most of my adult life overcoming many of the really dumb mistakes I made in my teens. I went from being a high school dropout to graduating from Vassar in my late thirties. I gave the commencement address at the local community college I graduated from, an experience I highly recommend. It was phenomenal! I went from being a teenage welfare mother to being appointed Assistant Welfare Commissioner for my state. And then everything came to a halt. I've been frozen like this for the past three years. You know how the old ones would say "Well at least you've got your health." I always thought that was such a ridiculously weird thing to say but I totally get it now. My brain is as much on fire with ideas as it was in my 30's and 40's. Writing, books, articles, editorials, thoughts, thoughts, thoughts. The difference is my bad health has left me frozen, frightened, afraid I'll be hurt by someone if I say the wrong thing. So this is my first attempt to break out of that icy encasement. </span><br /><span style="font-family:Arial;"></span><br /><span style="font-family:Arial;">For 25+ years I worked in the grants/non-profit field. Too often I saw organizations given breaks because they were minority operated and the white folks funding them didn't want to risk being called racist. I saw an article the other day about ACORN closing and that's what set me to thinking. Everyone knew it was poorly managed long before the stupid setup they got caught in. But why didn't anyone say something? I can't tell you how many times I've seen gross <span id="SPELLING_ERROR_0" class="blsp-spelling-error">mis</span><span id="SPELLING_ERROR_1" class="blsp-spelling-corrected">management</span> that no one would address. At one point in my career I was hired because I was black and willing to take on the organizations that needed a serious house cleaning. To me the federal regulations were not grey, they were black and white and strict. They did not have wiggle room. Looking back there were times I should have allowed a little wiggle rather than shut an organization down. But I was so afraid of getting it wrong that the Federal regulations became a bible to me. Still I did a great deal of teaching about how to manage grants and I'm proud of that. Any organization that came under my tutelage was expected to adhere to the regulations governing their particular grant. I think one of the biggest mistakes and changes is that back in the day when a federal or state grant was given the organization was expected to spend 3 to 5 days in that state's capital being trained or in Washington if it was a <span id="SPELLING_ERROR_2" class="blsp-spelling-corrected">federal</span> <span id="SPELLING_ERROR_3" class="blsp-spelling-corrected">grant</span>. As time passed this changed from face to face training to <span id="SPELLING_ERROR_4" class="blsp-spelling-corrected">conferences</span> <span id="SPELLING_ERROR_5" class="blsp-spelling-corrected">calls</span> to online training to being sent a 300 page manual with the "suggestion" the grantee review it. To be given a <span id="SPELLING_ERROR_6" class="blsp-spelling-corrected">quarter</span> million dollar grant with little to no training is a setup for failure. To move from that to fear of saying there are mistakes is an even greater setup for <span id="SPELLING_ERROR_7" class="blsp-spelling-corrected">failure</span>. </span><br /><span style="font-family:Arial;"></span><br /><span style="font-family:Arial;">So this is me, stepping out of the ice cave to say its way past time to stop <span id="SPELLING_ERROR_8" class="blsp-spelling-corrected">expecting</span> to be <span id="SPELLING_ERROR_9" class="blsp-spelling-corrected">given</span> breaks based purely on being on the side of the angels or because of race when you screw up. It may be a part of the overall scheme of things but the days of it being the predominate reason for looking the other way when serious mistakes are being made should be <span id="SPELLING_ERROR_10" class="blsp-spelling-corrected">over</span>. Deep breath.....whew.</span><br /><span style="font-family:Arial;"></span><br /><span style="font-family:Arial;"></span><br /><span style="font-family:Arial;"></span><br /><span style="font-family:Arial;"></span><br /><span style="font-family:Arial;"></span><br /><span style="font-family:Arial;"></span><br /><span style="font-family:Arial;"></span>Susan Kemphttp://www.blogger.com/profile/17936512637067708280noreply@blogger.com0tag:blogger.com,1999:blog-5065028016752624268.post-58182836488997019702010-03-23T17:49:00.000-04:002010-03-23T18:28:16.432-04:00I Made It Through the Winter<span style="font-family:arial;">WAHOO! I made it through the winter. Believe me when someone tells you you may only have six months to live, living a year is a very big deal. I saw the pulmonologist who was shocked at how well I was. I'm working with one lung but that's much better than they initially expected. You have to be below 50% lung capacity to even be considered for a transplant. I feel like I spent the entire winter trying to climb out of a deep well and now I've finally got my fingers on the edge and may be able to actually pull myself out soon. First, all jokes aside, let's hear it for Prozac. It has literally been a life saver for me. It ain't easy when you're feeling suicidal and there are two, count 'em two high bridges within walking distance of your house. So to avoid the bridges I spent most of my time curled up in my bed watching DVDs including the complete seasons of Sex and the City. I've even got parts of conversations memorized. I know more about the characters personalities than the actors do. lt always amazes me how easy it is to lose muscle mass when you stay in bed for even a brief period of time. Of course my wonderful devoted husband took his usual extraordinary care of me. Things got so bad that at one point he had to feed me. All I could eat was applesauce because of an infected throat. A long time ago a therapist told me "Never underestimate the importance of just being able to get out of bed in the morning." I totally didn't get it back then but I sure do now. The first thing I did (after I took a much needed shower)was call a good friend who works at a non-profit and say "I need somebody to help." I'll be volunteering for two hours a week helping...wait for it...the disabled. Since I've been fighting the label of disabled for ten years I find this particularly ironic. Don't tell me the God's don't have a sense of humour. I know that helping others for those two hours is going to be really tough physically but I've got to get outside of myself, if you know what I mean. I've got to be reminded that there are others who need help, who are in worse shape than me. So maybe I can help them by just talking.</span><br /><span style="font-family:Arial;"></span><br /><span style="font-family:Arial;">You remember my promise to myself to get financially straight by the end of the year? Well I paid off a major credit card this month. I'm trying to not look at my debt as a whole. Its too overwhelming. So I started with the lowest credit card and am working my way up the list. </span><span style="font-family:arial;">I don't care what the economic pundits say, there ain't no jobs out there! My husband has been searching for nine months now and so far had only had three interviews. So many people showed up that it's almost not worth the effort. But he keeps trying and I'm deeply grateful for all he does. He went to a job fair in February and there were close to 3,000 people there.</span><br /><span style="font-family:Arial;"></span><br /><span style="font-family:Arial;">Many thanks for the kind and supportive emails telling me to hang in. Things like that really matter when you're down. It keeps you going. I've spent three years trying to pull myself together for this journey. I think the journey's about to begin.</span>Susan Kemphttp://www.blogger.com/profile/17936512637067708280noreply@blogger.com0tag:blogger.com,1999:blog-5065028016752624268.post-69829080348394789662010-02-19T22:53:00.000-05:002010-02-19T22:54:42.033-05:00My AbsencePlease pardon my absence on line. Sometimes my illness get the the better of me. I’m able to sit up now at the computer for brief periods of time and expect to be back to myself in another week or so. This time it was a severely infected throat, which the lupus wouldn’t let heal followed by the temporary loss of the use of my right hand. You can’t make this stuff up. Hope all’s well with you and yours. SusanSusan Kemphttp://www.blogger.com/profile/17936512637067708280noreply@blogger.com0tag:blogger.com,1999:blog-5065028016752624268.post-22102089355731206772010-02-05T22:07:00.000-05:002010-02-05T22:32:27.600-05:00This Astonishes Me<span style="font-family:arial;">I realized today that I have absolutely no reason to get out of bed. If it wasn't for Herman needing to go outside and then be fed twice a day I doubt I'd get out of bed at all. It's astonishing! I was go go go for so many years - college college work work work and suddenly it all came to a grinding halt and here I am am. </span><span style="font-family:arial;">Standing still. </span><br /><span style="font-family:arial;"></span><br /><span style="font-family:arial;">I went to check my email and there were 3 requests for grant searches. Since I don't believe in coincidences I've got to believe that the universe is speaking to me...rather loudly. It seems to be yelling GET UP!</span>Susan Kemphttp://www.blogger.com/profile/17936512637067708280noreply@blogger.com0tag:blogger.com,1999:blog-5065028016752624268.post-25625114284828497712010-01-08T23:36:00.000-05:002010-01-08T23:48:25.093-05:00Herman and I Are Down for the CountThey say that sleeping for long periods of time is an example of being depressed. Well I can't drag myself out of bed before 1PM most days. It doesn't bother my dog Herman at all because he's adopted my schedule and sleeps as long as I do. The thing is that it's his sleeping so long that <span id="SPELLING_ERROR_0" class="blsp-spelling-error">bother's</span> me. A dog shouldn't sleep so long. Even if he's just out on the backyard run he shouldn't sleep so long but he wants to be where I am and I'm in bed. I haven't left the house in a week, sometimes two weeks if I don't have a doctor's appointment. Someone asked me what terrible thing would happen if I left the house and I said someone might recognize me and ask what I'm <span id="SPELLING_ERROR_1" class="blsp-spelling-error">doing</span> these days or ask how I am. I couldn't <span id="SPELLING_ERROR_2" class="blsp-spelling-corrected">bear</span> saying I'm doing <span id="SPELLING_ERROR_3" class="blsp-spelling-corrected">absolutely</span> nothing. I can think of things I could or <span id="SPELLING_ERROR_4" class="blsp-spelling-corrected">should</span> do but I'm not. It takes too damn much energy to even get dressed. In part I'm on a new anti-<span id="SPELLING_ERROR_5" class="blsp-spelling-corrected">depressant</span> which makes me sleepy but I'm supposed to reach a <span id="SPELLING_ERROR_6" class="blsp-spelling-corrected">point</span> of adjustment. I sound so self-pitying I don't think I could stand to read this if someone else was writing it. But even if it was 1pm I did get up and a therapist once said never under estimate <span id="SPELLING_ERROR_7" class="blsp-spelling-error">the</span> importance of just getting up. So I did manage to face another day. I'm hoping that I'm getting better bit by bit and just can't see it.Susan Kemphttp://www.blogger.com/profile/17936512637067708280noreply@blogger.com0tag:blogger.com,1999:blog-5065028016752624268.post-45126873602115175842010-01-01T23:10:00.000-05:002010-01-01T23:15:44.325-05:00A Quick NoteJust wanted to say Happy New Year to you all. You already know my resolution (to be in a better place at the end of 2010) and I'm wishing you all luck with whatever resolutions you may have made for this new year. Just watching the 11pm news, so much violence, so much death. It definitely makes you sit up and take a longer look at yourself. Somehow your life isn't quite so bad in the face of what many are struggling with. It's humbling.Susan Kemphttp://www.blogger.com/profile/17936512637067708280noreply@blogger.com0tag:blogger.com,1999:blog-5065028016752624268.post-29987367243750383312009-12-31T18:13:00.000-05:002009-12-31T18:45:15.695-05:00Where I Want to Be In One Year<span style="font-family:arial;">It's New Years Eve 2009 and I'm miserable. I have more bills than money, my health sucks and my husband can't find a job in the field he studied for. I am absolutely determined to change all this in the coming year. Now understand I don't mean I'm going to win the lottery or my husband will magically find a job. What I mean is I'm going to find a way to be satisfied with where I'm at. Remember I was told I was dying and had about 6 months to a year to live. The doctor ultimately admitted, although he had no explanation for it my lungs were better than he expected and I was functioning at 50%. He expected me to be much lower than that. People from everywhere sent me prayers and I did a fair amount of praying myself. Something changed me inside. Despite all that I've been miserable all day. I wait all month for my pension check and its gone before I get it. So I'm determined that in 2010 I'm going to get a handle on my money and figure out where its running off to. I'm going to adhere to a strict budget and give myself an allowance. I'm going to face the large amount of money that my medical bills take each month. Facing this means facing the illnesses the medicine takes care of and that's a tough one. Telling myself repeatedly that I'm better off than many doesn't work. I suspect it doesn't work for most people struggling through tough times. But I'm going to figure out how to get through this and will write about it here. As I've said before, I'm going to figure out who retired Susan is and that includes figuring out who Susan In Control is. I've been wrapped about this big rock for the past 3 years and its been rolling me instead of me rolling it. </span><br /><span style="font-family:Arial;"></span><br /><span style="font-family:Arial;">Now don't get me wrong. There aren't going to be magic changes. I figure if at some point the Prozac starts working that's going to help alot. A big part of all this is that I've never failed at anything in my entire adult life. I've had set backs but failure is simply not a part of my thinking. I have to find a way to move beyond the failure of my business and move on to the original dream...the dream that drove me to work all night and go to college all day. It never went away. I just assumed it was too late to pursue it. Instead I got in touch with my college professor and asked a hard question. Is it too late for a 56 year old woman to become a published writer. He looked at me as if I lost my mind and said "Of Course Not!" So I'm going take his response and try to write just a little each day on the novel that's been rolling around inside my head for years. Cross your fingers for me that at the end of 2010 instead of frustration I'll have a completed novel.</span>Susan Kemphttp://www.blogger.com/profile/17936512637067708280noreply@blogger.com0tag:blogger.com,1999:blog-5065028016752624268.post-20192046843271868472009-12-26T17:41:00.000-05:002009-12-26T18:21:03.929-05:00Did You Know Its Possible to Dislocate Your Foot?<span style="font-family:arial;">Well I went to the foot doctor and it turns out my foot's dislocated. My toes separated from my foot! Who knew? I didn't even know that was possible. The doctor says he's going to put a caste on the foot but didn't go into alot of details because first he has to cure the blister. All of this is scary stuff. The blister is on the toe bone and its been getting larger. Once we fix the blister (because I'll be damned if I'll lose my foot over a blister) then we'll cast the foot. Stay tuned for how he'll put the foot back together. I'm having some pretty horrifying images in my head like snapping it all back together again. Yikes!</span><br /><span style="font-family:arial;"></span><br /><span style="font-family:arial;">I'm fighting the depression hard. Some days it wins and some days I win. You can tell when I win because I manage to write in my blog. I can only hope you're not sick of my bitching and whining. Hang in there with me. I WILL overcome this. Have you ever considered how much of what you do focuses around work? If you rarely left the house how often would you wash up, dress up, put on makeup, all the things that are a part preparing for work each day? We think of not having to do those things on the weekend as a relief. And getting a vacation break as a great time to not have to do those things. I greatly miss the work world and all the social things that go with it. I'm trying to figure out what you do when you don't have the work world. I'm genuinely baffled by this. My New Years resolution is to leave the house more often. I'm becoming way too comfortable with staying home and I think I'm bordering on agoraphobia which is definitely not the direction I want to go in.</span><br /><span style="font-family:arial;"></span><br /><span style="font-family:arial;">Hang in there with me folks. I'm still searching for answers. If I can figure out the things that are blocking me (health issues, inertia) I can overcome all the other things. </span>Susan Kemphttp://www.blogger.com/profile/17936512637067708280noreply@blogger.com0tag:blogger.com,1999:blog-5065028016752624268.post-30665321910636526342009-12-20T14:01:00.000-05:002009-12-20T15:10:34.422-05:00Finding Time to Write<span style="font-family:arial;">It's surprising how motivating it can be knowing people are actually reading what I write. I've switched around to writing first thing and then facing everything else I have to deal within the day. Rather than think of my writing as a self-pitying tirade I know (from the comments) that there are other's out there dealing with chronic illnesses so on I go. I've got a theory about some people who appear mentally ill and walk around talking to themselves and won't talk to others. I think they're in pain. Imagine having lupus or fibromyalgia or rheumatoid arthritis and being unable to get the medical care or medicine that would help with that excruciating pain? The cold you're living in only makes it worse. Who would you trust to tell about the problem? It maybe a catch-22. The colder it gets the worse the problem. </span><br /><span style="font-family:arial;"></span><br /><span style="font-family:arial;">I hate dealing with money. There never seems to be enough no matter how I try to slice up the month. Being on a fixed income from disability and pension check means there's nothing coming in in the future, no raise, no bonus, this is it. Since I'm only 56 its a long time to deal with one income. I know I'm luckier than so many since my pension and disability are based on the final income I received from NYS while working as an appointee. And I have my husbands income which I know will improve once the economy improves. But for this moment its not enough and I want to scream. Its my job to make the money thing work. He goes out the door each night and making the budget work is my job. I spent 8 HOURS going over bills and budgets and goddess knows what else and I still couldn't get it right. Where do people get their magic money at Christmas time? Do they max out their credit cards? Do they pick a bill they just don't pay? We don't even celebrate Christmas time anymore. The children are grown so its just a simple gift for one another. No tree because the cats would climb it and who knows what Herman would do to it. What baffles me even more are people who go shopping after Christmas. I'm talking about ordinary people. Where does that money come from? Do they wait to buy all their gifts? I know I think way too much about money and I don't know how to stop it. When you've had money and then you don't have money it can be positively painful. To go from a six figure salary to just being able to pay your bills messes with your head. I find myself looking at the tv and thinking "I bet Katie Couric takes a town car home. I bet Whoppi Goldberg doesn't worry about bills." Now Whoopi is one of my favorite movie stars and I know she came up through tough times. There are people you just have to give their props to. They deserve everything they get because they worked hard for it. Still its easy to get lost in the jealousy and hard to fight.</span><br /><span style="font-family:Arial;"></span><br /><span style="font-family:Arial;">When my children were small I tried to give them these amazing Christmases which would practically bankrupt me. When Christmas was over I was usually left with a stack of bad checks and the fear of being arrested. I look back on that time and wonder what the hell got into me. I wanted to give them something better than I had which I guess everybody has tried to do. This morning I saw Sting talking about the exact same thing. His memories of how his childhood Christmases didn't match his expectations and how we don't recognize the reality of that. I have alot of respect for him saying that. Sometimes we only see these movie and rock stars as they are right now and not how they got here from there.</span><br /><span style="font-family:Arial;"></span><br /><span style="font-family:Arial;">Tomorrow is foot doctor day. Since my toes went right and my foot went left the primary doctor says that's what happens to people with rheumatoid arthritis and there's nothing that can be done. I hope she's wrong. Even an orthotic for my sneaker would stop me from constantly falling over. Cross your fingers for me.</span><br /><span style="font-family:Arial;"></span><br /><span style="font-family:Arial;"></span>Susan Kemphttp://www.blogger.com/profile/17936512637067708280noreply@blogger.com0