Physician, #HealThyself: Pt.lll Dr G, General Practioner/Family Doctor


I called Dr G a few days after Miss Cathy’s world wind of ‘white coat’ hopping (from ophthalmologist to neurologist to numerous test) to hear him say that no one had called him regarding her condition (quelle surprise!).

“This is the first I’m hearing of it, tell me what’s going on.”

So, I did.

Dr G is her primary care physician. He’s someone that she’s been seeing for well over 30 years. She is very comfortable with him and he with her; after all of these years they have a sort of shorthand when they get together.

I remember him from years ago when I used to visited mom from where I lived in New York and he still looks the same; old, wise and kind. Come to think of it…if he was ‘old’ then and now, thirty (plus) years later he’s ‘older’ still, the how old is it?

The mind reels.

Anyway, he’s one of the last of a dying breed of doctors that ‘might’ actually make a house call if you were in such a need.

Since I’ve been Miss Cathy’s caregiver he’s on time for our appointments (or damn near close to it) professional and compassionate. He always returns a telephone call and follows through with whatever he says he will do for you.

That’s pretty much the ‘gold standard” of a successful working relationship (in any profession) in my opinion-but when a doctor is part of the equation it’s even more important to know that you can count on them to do what they say they’ll do.

I’m not talking about a doctor becoming your bff and calling every time something funny happens on RuPaul’s DragRace (although lets face it-something funny is always happening on RuPaul’s DragRace).

But, even though we all know that doctors are busy and they have responsibilities WE as caregivers and patients are just as busy and we have a responsibility to our health (or the health of a loved one) and that needs to be respected and reciprocated.

And Dr G does all that.

A good doctor is like a the best waiter in a four star restaurant, you know they have other tables to serve besides yours but somehow they appear when you need them, listen to what you want, bring it to you and make you feel as if you’re the only table in the joint.

And that’s’ what I’m looking for from Miss Cathy’s’ ‘team’….I want to feel like we’re the only table in the joint.

Sometimes all you can do is #laugh


“Can you come here for a minute?”

I heard the familiar refrain come from the direction of Miss Cathy’s bedroom the other morning as I got out of bed to greet a new day.

“I can’t even put my damn bra on!” She said with disgust.

Well, at least she’s not trying to put her tee shirt on as pants I thought to myself as I wiped the last of sleep from my eyes.

And sure enough, as I walked the few feet into her room my newly wakened eyes saw that her bra was not only on backwards…it was inside out as well.

It’s been about a month now since her step downward; it started with a loss of vision, compounded by confusion over the ability to see and use everyday objects. And now the simplest of tasks (things she’s been doing her entire life) have become complicated.

Watching her struggle with her under garment, as if someone had made an over the shoulder Rubik’s cube instead of a brassiere, looking nothing like the iconic Horst P. Horst photo of a woman caught in the act of snapping her brassiere, so famously paid tribute to in Madonna’s “Vogue” music video, Miss Cathy seemed as emotionally twisted as her bra straps.

She’d managed to put one strap up over her shoulder but the other was lost under a fold of skin in her armpit, somehow the back was in the front, the whole thing was inside out and the closures were pressed down on her breasts with the cups hanging off her back, looking about as useful as tits on a bull.

“How in the world?” I started to say, then I had to laugh and so did she.

“Damn!” she said between chuckles as I gently unhooked the closures, releasing her ample bosom, taking the garment off her to reconceive it for its intended purpose.

“All these damn titties!” She said looking down at herself and talking as if she were divulging a secret her body was not aware of.

“I hate these fuckers!”

“Well” I said giggling, helping her to put her brassiere on correctly.

Nothing like seeing an old lady topless, especially your mom, first thing in the morning to let you know what kinda day you’re in for.

“Put you boobs away.”

“I wish I could cut ‘em off! I hated them even when I was a girl and they first started growing. I know men are suppose to like’m.” She said, arranging herself into her bra.
“I wonder what they’d think if they had them instead of balls and they had to lug’m around all the time.”

I helped her snap shut the last closure in the back the helped her with put on her top tehn said, “I’m sure if they had tits and no balls they’d think they were women.”

….more laughter.

The other #”F” word: Pt lll


Back in 2010 when it was discovered that Miss Cathy had first stage Dementia with an Alzheimer’s diagnosis, I asked Dr Alemayehu, her neurologist what to expect.

He said something to the effect that “each patient is different and their mental faculties diminish differently at varying rates, some deteriorate rapidly while others can remain relatedly stable for years ”. What I remember most clearly was that he sounded about as matter of fact and dry as if he were talking about actuarial tables.

He couldn’t and wouldn’t give me a timetable for progression of the disease (and rightly so). The control freak and planner in me would just have to sit tight.

As my mother used to say, “You can’t set your clock by crazy”.

It was going to be a game of ‘hurry up and wait” (for what who knew and how much care she’d need was a question mark). There’s not much one can do to prepare except avail oneself of books, support groups, websites, et al so that’s what I’ve been doing.

Then, that day not long ago, the clock chimed ‘Koo-coo” and the alarm bells in my head went off, time to put all that ‘book learnin’ and research’ to use.

The slide downward had begun again and it was obvious that the doctor was right; her disease was just on holiday….much like I was.

It’s not like I thought there was a “sell-by” date on Miss Cathy’s sanity but I couldn’t help but be surprised when the time came and things started to change.

I found that I’d started to live day to day much like the characters in the movie “Groundhog Day”, on a calendar that doesn’t change and if/when it does its only toward a future grounded in the past.

I’ve also realized that caregiving is a marathon and not a sprint.

Unlike a disease where you can have a nice hospital stay where friends and family can come visit to feel better about themselves (in-patient treatment for Alzheimer’s is few and far in between-and are usually the result of a fall or some other by-product of the disease) or get an operation for a cure (there isn’t one) or take a pill to put your illness in remission (it doesn’t exist).

So, it’s not about the ‘quick fix’ because there isn’t one, buying a helium “get well soon” balloon is well intended but not what’s needed to tend to your loved one’s well being.

It’s about living close (or in close proximity) and day to day care, teaching the same things over and over, aiding and guiding your loved one through simple tasks that they’ve performed thousands of times before but now are as foreign to them as you will one day become.

It’s also about being available 24/7 for comforting and empathizing, explaining the same questions and correcting the same mistakes again and again, day after day, after day.

So, Miss Cathy and I are joined, hand in hand, walking through the valley of the shadow of decline.

For her, the loved one, the one with Alzheimer’s, her “F” word may be “Forgetting” and, for me, the caregiver, the one that has chosen this journey my “F” word may be “Frustrating”.

But, at the end of a long day, when your loved one is tucked away, and there is peace and quiet in the home, one might just think of the other “F” word……“Faith”…….faith in the knowledge that tomorrow is a new day, and with your loved one, a new chance wipe the slate clean and to start again.

Postscript: Since this posting Miss Cathy has undergone an MRI (which was non conclusive) and is scheduled or an MRA and a Diabetic Retinopathy while her ‘team’ continues to find an answer for her sudden loss of vision.

#Flareups


It’s been months since my last communiqué and for that I am sorry.

Simply put there hasn’t been much to post; other than the occasional “flare up” of “Alz” life seemed to have fallen into a predictable, non eventful pattern.

I had a respite from the disease but, life being “life” and “Alz’” being “Alzheimer’s” things were bound to change.

So, I am back, sharing the little things and the not so little things that have happened and that are happening now.

I haven’t been posting but I have been writing so some of what I’ll be sharing has already past so it’s out of time but not out of context.

It is odd and peculiar to this disease (and particularly cruel, I think) that weeks, even months can go by without incident then all of a sudden, as if someone turned “off” a switch, things that were routine and known are all at once foreign and unfamiliar.

Miss Cathy has gone from an occasional state of confusion to living in a place where simple acts; putting her shoes on the correct foot, disarming the security system and operating the television remote have become almost daily challenges.

Things that she’s done for years are now a struggle of some kind, I’ve watched as she seems to approach her routines with trepidation.

At first she made the usual excuses; food being burned (“The meat cooked too fast”) or not being able to operate the telephone (“Something is wrong with this phone, I need to call the telephone company”) and the remote (“I can’t see these numbers, they seem to be moving or something”) to a realization that it could possibly be something else, something more (“There’s something not right with my brain”)….and I agree.

Enough has happened that it’s time to get her ‘team’ (general practitioner, neurologist and even her ophthalmologist) back on board to check her out. Maybe she just needs new glasses, her diabetes could be a factor or her meds need to be adjusted-or a combination of all the above.

No matter, it’s time to send a flare up to signal that the “Alz” has awaken from it’s slumber and it’s time to do battle; time to re-engage, re-learn and chart a new course of action.

I hope to get back to posting regularly and that you will continue to follow me on this journey-

Thank you

The UPS man (should) always rings twice


I came back to Miss Cathy’s the other day after running errands to see a notice that UPS had tried to deliver a package. As I pulled the “ups-it” off the door I saw that the “No answer” box had been checked. I had been expecting the package (a pair of cargo shorts from Macys online-nothing work related or that couldn’t keep but “I wants wat I wants”). I was as disappointed as a kid on Christmas morning that gets socks instead of an Xbox.

My options for re-delivery were to reschedule (and wait) or pick the package up myself-not exactly Sophie’s choice but still….

I was pissed because I knew mom had been home when the UPS man came so there was no reason that the package shouldn’t have been there waiting for me. I sulked into my room-childish I know but hey, apparently there’s not much going on right now in my life if a delivery from Macys is what makes my day.

I realized I was being silly and was prepared to let the whole thing drop until later that day when Miss Cathy said something that annoyed me (quelle suprize) so (petty Mr. Pettington that I am) I brought up UPS. Without missing a beat she sidestepped any responsibility for the missed delivery like Wonder Woman deflecting bullets with her magic bracelets.

“I didn’t hear anybody knock,” she said dismissively, ”You know they just tap, tap, tap on the door anyway.”

Funny, I thought to myself, it’s awfully curious that she couldn’t hear the UPS man knocking on the door in the middle of the day when old eagle ears could hear me parking my car, walking up the steps and pulling out my keys when I come home late at night (and she’d been fast asleep).

I found it interesting that she was pleading Helen Keller when the last time this happened she had a completely different rationale. Back then she’d taken the position that she wouldn’t go near the door if she weren’t expecting someone. I tried to tell her that a robber or murderer wouldn’t be so polite as to knock so chances are whoever was on
the other side was harmless-or a Jehovah’s Witness.

Besides, the door is made of solid steel with a New York worthy Medeco lock so she was well protected as long as she didn’t open it.

I was annoyed about the whole thing but it’s not like I kicked the cat (and before you forward this post to the ASPCA I’m just joking and a) we don’t have a cat and 2) I’m still grieving the death of my 18 year best friend, Missy the cat.

I went about my day and later decided to call UPS to negotiate how/when/where I could pick up my package without having to wait another day (heaven for fend I deny the world the sight of my skinny calves).

Soon after I got off my cell Miss Cathy came to my door. “I have something I need to talk to you about” she said (Never a good opener where she’s concerned-right up there with the infamous relationship killer “We need to talk”).

“You know this wouldn’t have happened if you would have bought that doorbell like I asked you, too.”

So, now it was MY fault-touché, the best defensive is a strong offense (no matter how offensive).

“I can get it myself if it’s too much for you to do,” she said, meaning the doorbell-not the package. “I’ve asked you time and time again and you just ignored me and I know you heard me” Clearly, she was on a roll, “And I didn’t appreciate when you said, “you don’t need one-no one comes to visit you anyway”.

Why….I was stunned. First of all I didn’t know what had set her off since I wasn’t…even…talking…to…her and “bee” I don’t remember saying anything as catty (or mean) as “no one comes to visit you anyway” (not out loud at least…I mean, it did sound like something I would say).

Honestly, I don’t remember if I said it or not but that wasn’t the point. She went off and I went to my happy place. I agreed to buy a new doorbell “soon” and got the hell out as soon as was politely possible.

My trip to the UPS customer center was like being at the DMV; the line was long and the workers at the counter were surly and lethargic. An hour later I had my fashion in hand and headed back knowing that I was going to be getting several more deliveries in the days ahead (what can I say…online shopping is my new addiction).

The next day I put a post-it of my own on the door that read, “UPS: Please Knock loud and Knock twice, Elderly inside, Thank you”

Home


“When I think of home I think of a place where there’s love all around me. I wish I was home, I wish I was back there”…but there is no there, there.

All Dorothy had to do was click her heels in the movie or on the Broadway stage and there she went, back over the rainbow safe and sound to a familiar place.

Great sentiment and a wonderful feeling I’m sure but I haven’t felt at home for some time now. I left my life to join Miss Cathy in hers in her home some time ago but it’s never felt like “home” to me.

I told an ex of mine once that “home” is wherever your mother is-not the address or the physical place. But now, as Alzheimer’s has started to claim even a fraction of my mother’s mind she’s less “mother” and more “patient”.

Alzheimer’s has turned what used to be a safe place into a battleground; full of land mines that have to be avoided less they blow up into harsh words and tension.

These days I find that it’s easier to isolate myself in my little bedroom to avoid conflict. So, I inhabit the different areas of the room or “zones” as I call them as I move through my day, always having an ear out for when the coast is clear to go to the kitchen or use the balcony.

I don’t think I’ve sat in the living room in months, and if I have it’s just for the few moments it takes to relay some information to Miss Cathy or to listen to a request of hers.

Things have gone downhill since my last post which is the reason I haven’t been writing. It’s gotten too real to relay. I found that (unlike before) it wasn’t therapeutic or helpful to write about what’s going on because it was too painful emotionally to relive it on paper (on online as the case may be).

So, I don’t feel like I have a home and with no home you have no foundation and with no foundation you have no support and without support you’re all alone and that is a lonely place to be, “especially in a crowd” as Marilyn Monroe says in Gentlemen prefer Blondes.

But, what I have learned even in the face of no home, no foundation and no support is that I have “me” and that’s a pretty good start. I think of me as being a brick, and my “will to continue” my mortar so with brick(s) and mortar I can start to construct my own foundation, my own support and ultimately my own home.

Or maybe…just maybe, because I’ve always had me- like Dorothy I was (am) home already.

As time goes by


I’ve been remiss in writing for the past month. The reasons being unexpected work (which is good) and a monetary self-consciousness (which is bad) about what I’ve been blogging and posting these last eighteen months or so.

I’d been blogging more or less as I’ve kept my journal for decades now; un-self conscious and un-varnished, pretty much the truth of my experience (as I see it, of course), without thought (not much anyway) of tone, ramifications or implications.

Funny how with a little time and distance you can look at something and suddenly see it in a completely different light (kinda like putting on that swim-suit that you got on sale in the off season and now that it’ll soon be summer you put it for the first time and wonder-what was I thinking?).

I made the mistake of re-reading some of my old posts and felt suddenly naked and very exposed (except for that swim-suit of course;) Well, I won’t be doing that again (reading that is-not writing). I’m not going to start editing myself or over thinking what I write-I mean, what would be the point if I did that? No, I’ll just continue to move forward in print and leave the looking back to others.

Since my last post I’ve taken Miss Cathy to her neurologist and to her primary care physician for her regularly scheduled check-ups. They both gave her glowing reports. She did better on the neurologists’ memory and cognitive skill’s tests than she’s ever done before and other than gaining a little weight, her health is better than ever, too.

Dr Aleymayehu, her neurologist explained (once again when she asked about her medication) that the Aricept she’s taking is not a “cure” but it “delays” the Alzheimer’s patient from progressing in the disease. Since she was diagnosed so early moms’ pretty much frozen in time with most of her wits about her so Miss Cathy is one of the lucky ones.

Sure, she still has some confusion, she still has anger issues and some days she gets overwhelmed when there are too many things going on. But, lets face it; those things are all manageable considering what others who are further along in the disease are experiencing

With her doing so much better I can understand why she keeps asking the doctor about the Aricept and what it’s suppose to be doing to help her. We know (well, I know) that Alzheimer’s is a progressive disease and it has no specific timeline of deterioration so it’s possible that Miss Cathy could be the way she is now for years to come. So, it’ all wonderful news but “what’s a caregiver to do?”

Lately I feel I have less purpose here. The first year was all about getting her acclimated to her (and my) new life and for some time she really seemed to struggle with the “day to day” and needed a lot of hands on care. And I was good at helping with that.

Don’t get me wrong, I’m not saying I want (or need her to be sick) it’s just that my days had purpose when she needed me and every day seemed to be a re-affirmation of my decision to leave my life to come join hers.

As time has gone by she’s more independent (compared to where she was after her fall in January of 2010) and has more days where she’s cleared headed and functioning like she had before her diagnosis (albeit slower than before).

She needs me less and I (feel anyway) like I’ve gone from caregiver to reluctant roommate. Or like I’m trapped in some vortex where it’s ten years ago and I’m on a visit home to see my mom but the visit never ends.

I hate to be a “Debbie downer” but I have to ask, “why am I still here?”

MIss Cathy goes country


I don’t know when it started exactly. When I first moved in with Miss Cathy she would talk about how she’d occasionally watch a music video on CMT (Country music television) and I thought little of it.

Then I noticed that her days started to have a different soundtrack; instead of the usual sounds floating through the apartment of courtroom show gavels, one of the Cartwright’s’ needing “Pa” to help them out of a jam “down on the Ponderosa” or the applause of the game shows I would hear the soft twang of a guitar and warble of love lost from some unknown baritone.

I on the other hand seemed to be listening to the sounds of my own discontent. All I could hear were thoughts of how hard it is being here and questioning how much longer I can keep this commitment to care for Miss Cathy.

Believe me, I’m sick of the sound of my own belly aching and crying “whoa is me” but I don’t know….. I think I thought things would have gotten easier by now or…..different somehow-anything but the constant frustration, anger and ill at ease that I feel.

But, I constantly remind myself that this isn’t about me and it’s still early in the disease. This is the easy part where she’s more or less still herself so how can I possibly be thinking of bailing now? These are Halcyon days compared to what’s ahead.

So, I sit with my discontent, sharing coffee with it in the morning knowing it will leave me at some point during the day and freeing me to feel-sometimes joy, sometimes satisfaction in knowing that I’m doing the right thing but there’s never peace.

Mom on the other hand seems to have adjusted pretty well. Sure, the last tow years have been a big change for her too after living alone for almost ten years after pop died, but she’s always said she likes having family around. I’ve spent most of my life living alone, as if I were hatched and not part of any clan.

I can say that it is satisfying to know that she’s happy (or as happy as one can be with Alzheimer’s) I know that she likes having her son around-and I am “that” and I am “here”. Even though I keep to myself and lord knows we don’t talk very much she’s got Garth, Brooks, Dunn and Lady Antebellum to keep her company. It’s pretty much all country-all the time, she watches country music videos for hours at a time as she sits on the couch where she spends her days.

I drove her over to Tony’s for the Super Bowl last Sunday and on the drive we’d pretty much exhausted all conversation ten minutes into the hour plus drive leaving just the radio to fill the silence. But then I happened to switch from the classical station that I prefer to the country channel and through the rearview mirror I could see Miss Cathy light up like a Christmas tree.

Her mood was infectious and soon I was listening and humming along to the few songs or riffs that I recognized. We started talking between sets and before you know it we’d arrived at my brother’s place. I can’t remember having spent such a good time in her company for a long while.

Soon after we were inside the spell was broken, the old dynamics came back into play in my brother’s family room so I withdraw as Miss Cathy launched into a story that we’d all heard before but I could safely leave Tony and Suemi to be her audience as I once again turned to the sound of my own inner dialogue.

I wonder, like Miss Cathy’s new found interest in country music if this is just a phase or if I’m the last to know that this is it-life changes and suddenly you find yourself in Nashville and not in a New York state of mind.

F-bombs


Miss Cathy is no stranger to how shall I say ……”salty language”. Let’s face it, she can make a truck driver blush but since her diagnosis she’s even made me wince and I’m about as vulgar as they come (I guess the foul-mouthed apple didn’t fall very far from that tree).

Last week with the redecorating and remodeling half way finished I was excited that when the ice maker for the new refrigerator was delivered that would at least signal the end of things to do in the kitchen for a while.

All of the new stainless steel appliances; stove, over the counter microwave and refrigerator came from the same big-box, discount electronic store and for the most part I was happy with the purchases.

On the day the ice maker was delivered I was surprised to see two guys at the door and not one and I was further puzzled that one of them didn’t just hand me the package and leave. The one holding the box said that they were here to “install” the ice maker so I proceeded to let them in.

Like everyone who now visits I asked them to please take their shoes off in the foyer before coming any further into the apartment. To my surprise they balked, one saying that we were their first stop of the day (as if that immunes them from bringing outside dirt inside) and that the installation wouldn’t take long. Since I wasn’t expecting them to install the ice maker (I hadn’t paid for that service-just the ice maker) I decided to not look a gift horse in the mouth and allowed them in (for some reason only the one who spoke came in and the other went back outside).

Unfortunately 45 minutes later the installer tells me that he was given the wrong ice maker at the warehouse for our refrigerator and another would have to be ordered.
I looked over at Miss Cathy on the couch after letting him out and she was fuming-not about the mistaken ice maker but about the fact that the guy didn’t take off his shoes.

I was on the phone with the store making arrangements for the correct item to be shipped and I made a point to complain about the installer’s objection to my request. When mom heard me mention the incident I could hear her in the background saying, “Let me talk to them.”

I ignored her, finishing up the conversation in my room and then I came back into the living room to tell her that I had handled it.

This seemed to calm Miss Cathy a bit but she was still worked up. “Well good”, she said, “that’s good that you know how to talk to people and get things done because I was ready to tell that fucker off and the people on the phone, too.”

“I don’t know who the fuck he thought he was saying he wasn’t going to take his shoes off, this is my house-not his!” “Makes me hot, I want to get that fucker fired!”

Alrighty then I thought, after stepping out the way of the last of the f-bombs and sitting next to her on the couch. Her reaction was kinda over the top but that’s par for the course lately so I just listened. She didn’t go on much longer and seemed appeased when I told her that the store apologized for the installer’s behavior and they were going to refund my money for the ice maker and ship and install the correct one for free.

That made her happy, crisis averted. The f-bombs are tucked away for another day, ready to drop at the next battlefield whether real or imagined.

Design on a Dime in time for New Years: Part I


While I was in Kansas City visiting Chad on my (long over-due) quarterly break early in November I had a brainstorm for a Christmas gift for Miss Cathy. I got the idea to makeover her condo (a la one of the design shows on HGTV). Think “Design on a Dime” and not “Divine Design”. For one thing I’m not blond or Canadian like Candice Olsen (y’know) host of the big budget “Divine Design” and I certainly don’t have the $30 to $50 thousand dollar budgets that she spends on her gorgeous transformations.

I’d done some redecorating, a sofa here, a microwave there, what I mostly did when I moved in was alot of purging and deep cleaning that (to her defense) she simply can’t do anymore.

No, what I had in mind (and about as much money for) was something more along the lines of “Design on a Dime” the show where the challenge is to use a modest budget (usually around $3000.00) and a lot of creativity to achieve their goal.

I’ve been living with Miss Cathy for about a year and half now and the best I can say about her décor and decorating is that it’s dated-lost somewhere in the 80’s. Unfortunately it’s not the high glam or kitsch one thinks of on (now classic) TV shows like “Dynasty”, “Dallas” or even “Who’s the Boss?”- it’s more like “who was the decorator?”

Not to knock my mom or her taste (well, I am actually), we all like what we like-but does hers have to be soooo tacky and tasteless?

Quite frankly, it was depressing to wake up everyday and walk out of my little, dull white walled room with old beige caret down a hall of powder blue “faux” shag carpet (it may have been shag at one time, I’m not sure, whatever it “was” it is now a soiled, matted mess) and continue into the living/dining room covered in the same hue. There’s textured beige wallpaper (some peeling a bit around the edges-looking as if it’s given up and just wants to lay down after holding trying for decades to be tasteful and failing) and there’s the heavy “Mediterranean” furniture that was made of some material not known to man but other than wood (and heavier than a Sequoia) and not found in any province of Italy that I’ve ever seen.

Every surface is covered with knick knacks, bric a brac, chotchkes, keepsakes from a lifetime (and remember she’s seventy-three) of collecting (more like hoarding but I promised myself in the new year I’d be kind (er).

And did I mention the stuffed animals (again)? They sit on every surface either along with or instead of a chotchke. There were over one hundred in the living/dining room alone when I first moved in here and I bagged up over half and put them in the storage room but the few that remain seem to have multiplied somehow and they’ve taken over all the seating again…….but I digress, back to my “desire to design”.

Suffice to say, it was definitely time for change and seemed the perfect Christmas gift for Miss Cathy (and trust-for me, too).

Now that the idea was born I just needed to put a budget and a plan together. Upon hearing my idea Chad immediately volunteered to fly out and help but ultimately that didn’t work out but I really appreciated his gesture. I hadn’t thought about help until Chad then I thought,”Fuck, if Chad was going to fly out to help what about Tony?” so I not so much asked but called and enlisted the support of my brother, (but I soon learned in a later conversation that he would be laid up in early January through February recuperating after surgery on his Achilles tendon so he was going to be useless to me-other than financially) So, the bulk of the execution of the plan would still fall to me.

In keeping with the TV theme I thought it would be great if I could somehow get Miss Cathy to leave for a week in say, February and that would give me time enough to re-paint and re-carpet the entire condo and replace/upgrade one or two major appliances in the kitchen. So, the germ of the seed of the idea to re-decorate was born in the Midwest and I came back East eager to put my plan in action.

Early in December I started to research costs and materials, trying to stick with my (arbitrary) budget of $2000.00. I soon realized the challenge was going to not only be trying to blast Miss Cathy out of her home for a week but also trying to stretch my dollars to accomplish all that I wanted.

I got three estimates for wall-to-wall carpet. I learned that I needed about 1000 sq feet of carpet and in order to get any of the “deals” I’d negotiated the carpet needed to be installed sooner than later (throwing my schedule of a February makeover out the window and making me re-think the order in which I got things done). Originally I wanted to paint first, make a mess without having to worry about the floor then laying the carpet last). But, with no guarantee that the prices would be honored into the New Year I decided to re-vamp my “plans” and just go with the flow and let “bargains” and “deals” dictate the schedule.

I negotiated (to me) the bargain of a lifetime for the carpet (little did I know what was ahead), I was having the entire condo re-carpeted, the installers would be responsible for removal of the old carpet AND “moving” the furniture as they worked to install (there is usually an “extra” fee (per item of furniture left on the floor during the install) charged for furniture moving which can be very steep. The other estimates I got ranged from $2,200.00 to $2,800.00 (without furniture moving).

“Mike’s Carpet” (a local company that ran an ad in the “PennySaver” believe it or not) agreed to do the work for $1,500.00 cash. Granted, this isn’t the finest quality wool or Berber carpet but it’s new, it’s clean and with just me and Miss Cathy toddling around on it-how much wear and tear could it possibly get. The best thing is that it’s all the same color, “Raw oyster” (a light beige) instead of the crazy quilt of colors on the floor now-living/dining room/halls-powder blue, my room –dirty beige and Miss Cathy’s room….wait for it-blood red.

With the carpet scheduled to be installed on Wednesday the 21st, I asked Miss Cathy if she could arrange to go over to her girlfriends house for the day-sort of a septuagenarians’ “play date”. I told her I had a surprise that needed her out of the condo and to my “surprise” she said “sure”, called her girlfriend and agreed to be gone from 8 am that day till 5 pm.

With her onboard, and without any questions from her I was feeling good. It wasn’t going to be the complete “reveal” that I’d envisioned when I first came up with idea but I’d resigned myself to the notion that a series of mini “reveals” could be just as effective-fingers crossed, it was all about to begin….

Next week: Design on a Dime in time for New Years: Part II