Sunday, April 3, 2022

April 3: Huge Baby Steps and an Indoor Beach

My independence is slowly but steadily growing. The biggest achievements of the week include taking a few teeny tiny baby steps using only a cane for support, getting outside and onto my front porch swing all by myself, and carrying a plate for a short distance while using only one hand on my walker! It is fascinating to me how these things can simultaneously be such huge achievements and show how low the bar is. I have realized what a powerhouse I was prior to surgery and I cannot quite contemplate how I will ever get back to the sheer magnitude of things I did in a day. I can sort of see that I will get back to being able to manage all of the home and kid stuff I did before. I’m back to making the kids’ school lunches every day and helping with breakfast preparations. I can sort of see that I will be back to teaching by the end of the month out of necessity (unless I really can’t), but just for Alexander Technique teaching or massage with vastly altered body mechanics. What I can’t see is how I will be able to get to my office with a huge bag of sheets and give a massage. Baby steps. I know. A week ago I couldn’t have imagined using a cane or carrying a plate. So I trust that I will get there, but it is ever humbling to be where I am now.

Sarah is in her school’s musical Peter Pan, Jr, for which the performances are April 22 and 23. She is a Lost Kid in the ensemble. While I may cringe when I hear the prayer recited school-wide at dismissal because it is all about how sinful and awful we are, I have to say that her school has always been wonderfully inclusive and loving. I love that Sarah and any other kid who needs extra help are welcomed to be in the musical and their main support teacher stays for all of the rehearsals. Sarah's rehearsal schedule is getting ever more intense. Last week she had rehearsal Tuesday-Friday for an hour after dismissal. Tomorrow her rehearsal will be twice as long. She will come home in time to get ready for her swim lesson. She has rehearsal every day this week and in theory I will be able to drive on Thursday and Friday to pick her up. I will do a short test drive Thursday morning so if that doesn’t work for me there is time to request assistance. Thank goodness for Grandpa being in town for such things and many other moments of help and support this past week. Also thank goodness for Anna helping with piano lessons and swim lessons and some dinners. Thank goodness for the mom of one of Sarah’s classmates who has been bringing Sarah home after so many rehearsals and will continue for most of this coming week. 

Amy’s week was good, but sometimes she has feelings in the evening because her days are so full that she doesn’t get much free time. And yet, whenever we discuss dropping any of her usual things then she doesn’t want to. I can definitely relate to that as I often have felt similarly with my own life and schedule choices. 

The weather has been predictably ridiculously March-ish. The day I went onto my porch it was 70 degrees and I was in a t-shirt. The next day it snowed. We are at our mountain house for the weekend and while the snow falls outside, the kids decided to play at the beach inside. Sarah had been looking at old photos and wanting a sandbox. Amy had the idea to bring out a sand-colored blanket and put it on the floor as a small beach sandbox. Carl brought up our bag of beach toys. The kids used puzzle-box lids to scoop pretend sand and build pretend castles. Then Amy spread out a gray blanket to be water and fashioned a snorkel mask for herself out of a cloth headband and a pencil. Later in the day they used pool noodles as reins as they rode sofa-arm horses. For another imaginative game, Amy sorted us all into Harry Potter houses. She used a witch hat to determine which house was appropriate for each beanie boo, doll, and actual person. Sarah and I were deemed a fit for Hufflepuff while  Carl and Amy were sorted into Ravenclaw. I love how anything can be anything with enough imagination. While our family might have been this way anyway, I feel like we also came to it because of our Sarah-Rise time where the premiss for the room was that of course any scenario could be achieved with a few props and some imagination. 

Sunday, March 27, 2022

March 27: Recovery Continues with a Special In-House PT

This has been quite a week. I am in much better shape than I was a week ago and yet I still feel like I am at the bottom of a large mountain. Each day I can do a little bit more around the house, such as making my coffee and breakfast, getting in and out of the shower independently (with a spotter for safety), folding and putting away laundry, getting down drying racks and hanging wet laundry, and washing a few dishes. I know this is all huge and exciting compared to just shuffling to and from the bathroom. But it is humbling to be able to do so little and have it raise my heart rate as if I was doing hard exercise. When I climb the stairs my heart is pounding at the top, and when I was helping with folding laundry I had to take two breaks to sit and rest. My Fitbit watch keeps track of how often my heart rate goes above my normal at-rest state. Pre-surgery my daily number for moments of an elevated heart-rate was maybe between 9 and 15. Yesterday I ended the day with 70 moments. I keep reminding myself that my body is working hard even when it looks like I’m at rest and even harder when I’m up and about. 

My right thigh is almost back to its normal size, but continues to be achey at times. That makes sense given that even my various bruises from the IV attempts are still healing and those were minor compared to what happened to my leg. But what I don’t understand it why my leg aches so much more intensely at night when I am trying to sleep. Is it from overuse during the day? Or not enough use just prior to sleep? Or is it that I’m just more aware because I don’t have other things to distract me? All I know is that nights have been a struggle. I have tried the bed and the couch, with props of pillows in both locations. It hurts to stay still and it hurst to toss and turn, those actions being quite slow when they happen. My first few nights I woke miserably from dreams about pain. I don’t know if that was processing the past pain during surgery or the actual achiness of that moment. I think the couch is probably best for the moment, in part because then Carl can hopefully get some sleep. 

The PT regimen that I do is a 7 minute program on my phone. Sarah loves watching the little videos and kept asking what the PT was called. I finally said we could call him Brian. Then Sarah started helping me with the moves I can’t do independently. She has named herself PT Goodnight Moon House and she really is a great helper. She also likes to come over to my head when I am on the sofa and give me chin presses from behind my head and kisses on my nose. It is really sweet. 

Just to keep things extra interesting…. Amy got a big splinter in her foot last Sunday and Carl was unable to get It out. Since Amy really couldn’t walk comfortably, on Monday morning Carl took her to Urgent Care. Luckily the doctor got it out and Carl took Amy to school in time for a hike! Her teacher was going to let her sit out for the hike, but Amy felt up to it and insisted on participating. Then on Tuesday morning I got a call from Sarah’s teacher that she was throwing up and had a headache. My mom drove out to get her with me in the passenger seat. Sarah did need extra rest but then seemed quite well. So on Wednesday we sent her to school again. And again got a call that she was unwell and repeated our trip to retrieve her. This was perplexing given how well she seemed at home. Apparently she was feeling motion sick after her bus ride, which is unusual for her. Thursday we kept Sarah home all day and she seemed fine aside from one moment in the afternoon which was difficult to read. Sometimes when Sarah talks about ailments it is difficult to discern what tense we are actually in. Is she reporting on the moment or remembering the past or trying to get out of a future thing? On Friday Sarah went to school and stayed all day, although her teacher did have to help her at one moment to just drink water and breathe for a few minutes rather than spitting up phlegm. I feel like we do have a situation of too much phlegm too often but without Sarah’s usual seasonal allergy symptoms. So I don’t know if we need to change things or if she had a small bug. She sees her pediatrician tomorrow for a well-visit so hopefully the doctor will have some insight or wisdom. 

It was extremely helpful having my mom (aka Mom-Mom) here to help with kids, serving food, chores, and whatever I needed. We also had Anna helping with getting Sarah to piano and getting the kids to swimming on Monday. I felt nervous about my. mom leaving on Thursday because I wasn’t sure we were ready to not have full-time help. So we arranged for Sonia, her partner, and Grandpa to help out. I also realized that at this point I’m much more capable than before so I think I can be mostly independent at home on school days going forward as long as I don’t have to change floors and as long as I just eat standing at the counter. Or with minor help from Carl if he continues working from home. The kids can be my helpers when they are home, whether moving my walker up or downstairs or starting a load of laundry. 

One highlight I forgot to mention from last week… Sarah was sitting next to me while I talked to a friend on the phone. Sarah knew she was supposed to be quiet. And she mostly was. Until she whispered, “Mom, are you wearing underpants?”

Sarah also likes listening to people’s heads by putting her ear to their forehead. She did this with Carl, and when he asked what she heart inside his head she replied, “BOING!”

There was a month-long supply chain delay in getting the Girl Scout cookies for Amy to distribute to all who had purchased them from her. Sarah and Amy were an efficient team making piles and labeling them in our front room. Then last Sunday they went out with Carl to deliver the cookies around the neighborhood. Sarah pulled the wagon full of cookies. Amy knocked on each door and took care of taking payments. Then Sarah carried the cookies to the door. 

Yesterday Carl took the kids to brunch while I had brunch with a friend at home. Carl and the kids went to the library so Sarah could watch buses and play in the elevator, as she has been asking to do for quite some time. Then they all went to Sarah’s Anat Baniel lesson, which is a thing that only happens a few times a year. Sarah loves these lessons in part because she gets a great view of buses during her lesson. When they all came home the girls had a great time pretending to be going up and down in an elevator while jumping up and down in our kitchen.

There has been an abundance of love, generosity, food, and flowers coming this way. I so appreciate every bit of it. Our cat has mixed feelings. She really really wants to eat all of the flowers so on the one paw she loves that we have received them and on the other paw she is upset that she is foiled at every turn with the flowers being put out of her reach or behind glass cabinet doors. With one bunch of flowers, Carl thought we could keep them down low for a minute so I could enjoy them from the sofa. Our cat promptly walked over, licked her lips, hopped on the table and began to nibble. 

In other news, it is snowing steadily and even sticking because it has been so cold lately! Sarah's and Amy’s schools have both moved to optional masking, as has the massage school where I will hopefully (hip-willing) resume teaching in late April, and Carl’s work. We still all keep masks with us all the time just in case. Sarah also always needs one on the bus. Still, this all feels new and my face feels naked at the thought of teaching maskless.

I hope you are all well.

Sunday, March 20, 2022

March 20: Hip Surgery and Recovery

I am home and recovering from my hip surgery. In a nutshell it went well, but out of the nutshell there were lots of details that made the experience harder than it needed to be.

Carl and I left for the hospital at 4:45am Wednesday morning, and Sonia came to our house to take care of getting the kids to school. I insisted on walking from the car to the surgical check-in even though it felt like a long and awkward trek. I knew it would be the last time I did such perambulation so relatively easily for a while. I was quickly taken on my own to a freezing-cold changing room with a small shared bathroom attached. The bathroom was the most awkwardly and oddly shaped room, with locks for each door that were not at all clear or intuitive about how to successfully lock them. I think they were different for each door. The support bar to hold if you needed it encroached on your sitting space. The toilet paper was up above and behind my head, because that is totally what makes sense for a bathroom being used by someone about to undergo surgery for who knows what physical limitations. I managed, but wondered how others would if they were shorter or had more limited movement than I did. 

The nurse and her trainee came in to get me prepped for surgery. Noting how I was wrapped in a sheet on top of my gown she kept saying she would bring me a nice warm blanket. That did eventually happen, but I think it took 45 minutes. She also gave me deluxe mesh panties and a pad because - timing!- my period had just started. At least that meant they didn’t need to do a pregnancy test. But it did mean navigating that awkward bathroom again. A new person came to do some bloodwork and he was excellent. I didn’t feel any pain with the needle-stick. Then the original nurse tried to insert my IV port in my hand, noting that my veins were small but they needed a certain needle size to make the IV work. Her first attempt hurt but failed. She said she usually got it on the first try so if she didn’t then she wanted someone else to do the second attempt. I waited. The second person came in and tried a different vein, painfully but successfully. Still promises of a warm blanket to come but no actual blanket. 

Next were injections in between my psoas and quadratus lumborum (deep core muscles) to help me not feel anything in my upper thigh for a couple of days. Think of it like novocaine shots prior to dental work, except the target is much deeper. Those injections were not pleasant, but at least when they were done Carl was able to join me and I finally got the warm blanket. Then the surgeon came by to sign his initials on my right hip. The last thing prior to my being taken away was deciding what to do with my glasses. Carl was keeping most of my stuff, but my bag of clothing was going to a locker and it was suggested that my glasses stay with my clothing, as if maybe I could get them sooner that way. I really can’t see without my glasses. Not that I needed to, but having everything be blurry added to the surreal out-of-control feeling. 

I normally think that whatever life throws my way I could overcome with sheer force of will if I needed to. Surgery is always a humbling reminder that such a belief is a lie. I have no memory of the ride to the operating room. I vaguely remember the huge light fixtures. That’s it. The next thing I knew I was in the recovery room being told to stop moving my legs. Evidently my trying to move my legs so much was a sign that I was in a lot of pain. 

Meanwhile, Carl was waiting in the surgical waiting area with the pager they had given him so he could be reached when I was out of surgery. Evidently they tried paging him three times and then called his cell phone so the doctor could talk to him. The pager had died. I don’t understand why they didn’t just use their voice to call his name, but perhaps that is an old-fashioned mode of communicating. Anyway, the surgeon told Carl that the surgery was a bit more involved than usual because of the angle of my femur neck (more vertical than usual) and that I had lost a lot of blood. They had a way of collecting what blood I lost and putting it back into me so I didn’t need a transfusion. However, note to self for if I have to have the left hip done in the future, I will donate my own blood for my own use if needed. I’m O negative which means I’m the universal donor, but it means I can only receive other O negative blood. 

I was in the large, blurry recovery room for maybe 4 hours without Carl. I was in and out of sleep. I still had no glasses. They were waiting for a bed to open up of me to go to a hospital room to continue my recovery. They brought me some food, which was so bad I wondered how hard they worked to make it that bad. Clearly I have been spoiled by all of our trips to the Children’s Hospital which has food so good I would consider getting it as take-out. Bad food was still food though, so that was appreciated. The PT came to help me switch to a hospital bed. Since I felt lightheaded standing momentarily it was determined that I should stay the night at the hospital. That was disappointing even if it really was the right answer. Carl was eventually brought to me in the large recovery room, but had not been given my clothing and glasses as we had expected. Since it was finally time to move to a room we decided to wait for him to go find my stuff. 

From my hospital room, Carl went to ask about my bag of clothing and glasses. While he was doing that, someone arrived with the bag. I felt stressed about how Carl would be fruitlessly searching and I had no way to reach him because he had my phone. Luckily all was sorted out and he returned in short order. And I could finally see! Just in time for the nurse on duty to check my incisions, which were glued from the inside and thus not covered, aside from a drainage port. As soon as I saw the incisions I burst into tears. If this was minimally invasive I hate to imagine what maximally invasive scars would look like. The nurse commented, “Oh, you’re crying… like a baby.” As Carl noted, that was when Jenny Bear emerged. I vouched for myself loud and clear that crying was a good thing and that I had just been through surgery. I mean!!! Her tone hadn’t been unkind, and she regrouped and brought me tissues and took good care of me overall, but it was not the greatest way to begin our nurse-patient relationship. 

When I asked the nurse how it would work when I had to pee, she said I would just get up and do so. Ummm.. ??? I felt like I  couldn’t move at all. Eventually this was put to the test and the nurse brought a commode next to my bed. An aide was brought in to assist me. A young male aide. Oh good. I know it shouldn’t matter, but that felt like an added challenge to any shreds of my modesty that might have remained. After helping me move he did leave the room, but the regular nurse was still there and then the surgeon’s nurse came in and was talking to me while I was peeing! While I was feeling increasingly lightheaded and nauseous as if I was going to pass out. I have no idea what she said. Why couldn’t she have waited five minutes?! She left. I was helped back into bed, each step of which was excruciatingly painful and impossible. Then the surgeon came in and talked to me while I was nearly falling asleep. Luckily Carl was there to actually listen because I have no idea what was said. 

We made arrangements for Sonia to take over childcare from Anna, who had covered the afternoon and early evening. Carl brought dinner from Five Guys for us and then went home to be with the kids, who were quite disappointed that I wasn’t coming home as expected. He came back to the hospital as soon as the kids were on their way to school on Thursday. Wednesday night I was mostly miserable and so glad to be in the hospital. Every time I had to pee was excruciating and so hard. Imagine those dreams where you are trying to move and your body doesn’t respond to your commands. The aide or nurse would always step out to give me privacy. While, yes, I had wanted that from the surgeon’s nurse, in this case it was frustrating. They would tell me to press the button to summon them when I was done. I only needed a minute! Then I ended up waiting bare-butted and freezing while it seemed an eternity until they returned. I gradually learned that my shivering was due to muscle exertion more than cold, but that didn’t make it less shiverful.

At one point I was in so much pain I couldn’t sleep but I was scared to ask for oxycodine. I had the nurse come in. This was my nighttime nurse and was different from the first one. She didn’t bat an eye about my crying and just helped me by reassuring me that it was ok to take pain medication so soon after surgery. I slept a bit more, until it was time to check my vitals and my IV beeped. It was 4:30. My nurse said that at 5:30 she would be transferring me to a chair, so I opted to just stay awake. Luckily, after that first time when I thought I would pass out, the other times were slightly better each time. So moving to the chair was ok. Then a super-confident-radiating-mansplaining- energy cardiologist came in to tell me that I was prone to vasovagal responses. That means that when I get scared or upset to enough of a degree I can nearly or fully pass out. Yes. I don’t need a fancy name to tell me that. Nor do I need a label to make it seem more dire or serious than I think it is. For goodness sake! It was just after surgery!! Meeting that person did reaffirm how little I have to deal with that kind of toxic overconfidence in my usual life. 

The surgeon and his nurse came to check on me at 6:30, probably before he went into surgery with other people. I’m glad they checked on me, but wish the timing could have been later so Carl would have been back.

I know this probably sounds like a lot of negative details. It was hard. Super hard. But overall everyone was kind and helpful, and I am safely at home now. Sonia, my mom, and Carl have been taking care of things around the house while helping me move to and from the bathroom with a walker. I can now even get in and out of bed or the sofa by myself. I have to have help to do PT three times a day because there are some moves that my muscles just can’t do, even though they strain and burn at the attempt. My leg is slowly going back to it’s normal size. The kids help bring my walker or other requested items, and Sarah once tried to help push my walker along. 

Yesterday Sarah witnessed my PT attempts and tears at how hard all of this feels sometimes. She then got quite upset and sad for a couple of hours. I will try to shield the kids more from my upsets with this because I think it is hard enough to have me so unavailable to help them like normal and so helpless on my own. Later in the day Sarah did my PT with me and both of us were in better emotional shape.  She likes to give me chin presses and kisses while I am on the sofa, which is very sweet. 

Each day I get a bit more capable. Yesterday I even managed a shower. But everything is hard and a trip to the bathroom or up or down the stairs is exhausting. Nighttimes are harder than daytimes, perhaps because I’m expecting myself to sleep peacefully but am more aware of aches and pains. So while I know each day is monumentally better than the previous one, this still feels daunting and like I have a long road ahead of me.

I’m no longer needing the oxycodine and will dispose of it responsibly once I’m really sure I’m done with it. I’m still taking Tylenol and baby aspirin and using an ice pack. 

I hear my heartbeat in my right ear often, but usually after some effort. I hope that sensation will go away.

Friday was my shared birthday with Amy. She had a great day. I did not. But Carl collected wonderful input from people about their memories of me or reasons why they love me. That was a really wonderful present that he gave me the night I was in the hospital. I kept not being able to see the words as they blurred with my tears of feeling so seen and appreciated. So a huge thank you to any of you who contributed. 

Last night we watched Turning Red, which is a wonderful Disney cartoon movie about becoming a teenager and how parents and teens have their relationships change. We all loved it. Sarah likes to pretend she is turning into a giant red panda. Amy likes to pretend she turns into a fluffy black kitten. 

Thank you all for your well-wishes, prayers, and support during this time. It all means a lot and really does help.

Sunday, March 13, 2022

March 13: In-Person Parties and Missing Shoes

This weekend Amy had her first in-person birthday party since 2019 (her actual bday is yet to come). Two years ago we had to cancel her party because everything was just shutting down for Covid. We kept the party small with just 7 kids, two of whom were our own. Sarah didn’t actually participate in much of it. She helped Carl get the pizza and joined everyone for the food. Then she and I went up to my room to snuggle and nap, which was fine by me. Amy and her friends had a riotously good time and were extremely loud and energetic. They played hide and seek, played a cat murder mystery game, and made cat puppets. This was all inside (masked) because it was cold and snowy outside. Amy had been looking forward to this party intensely for weeks so was understandably a little sad when it was over. We have assured her that this is just the start of more indoor playdates, and that she can even have the same people all together again. (Although we wouldn’t mind if it was warm enough to be outside!)

For Amy’s weekend homework, it has worked well the past two weekends to have her do her work near me. We set a timer and both of us do something that isn’t our favorite thing to do. I usually clean something or put away laundry. Then we set a timer for doing something fun together. Yesterday I didn’t have the timer going and I was reading a book for fun, but it still felt nice to be together and I could nudge her along with the math in between our times of talking. 

Sarah’s newest love is pretending to be the bear who sings “One Shoe Blues” in Sandra Boynton’s Blue Moo book. She most enjoys wearing one sneaker while looking at the page in the book while the song plays in the background. One evening after dinner, both kids had a ball pretending to be the bear.  Sarah had one sneaker and kept brandishing her one shod limb in front of me. Amy put on headphones and then asked us where her headphones were. Then she put on one leg of her snow pants, one flipflop, a mask on one ear, and pushed a walking duck toy while holding an empty pizza box, asking us where all of the items were. You see, in the song, the bear is lamenting his inability to find one of his shoes, and then at the end realizes that he was wearing it all along.

Amy drew a clock while looking at a school-timer clock but not looking at her paper. She doesn’t think much of her achievement because to her it doesn’t look like a very accurate depiction of a clock. Meanwhile, many grownups feel a deep resonance between her work and their experience of time. 

This is the last update prior to my hip replacement on Wednesday. I’m less scared than I have been at some moments, but it also continues to feel surreal. Any good thoughts and prayers are most welcome. I have no idea how soon I will feel up to doing anything beyond the bare minimum. Possibly right away or possibly it will be a while. This is all to say, if I don’t send out an update next Sunday, don’t worry. But I hope I’m feeling good enough to do so. Also, if you live nearby and want to receive the link to the Mealtrain that Sonia created for me, just let me know.

Sunday, March 6, 2022

March 6: Corrections and Mouse Poop

I must issue a correction for one item in my last update. Sarah didn’t cut the carrots by herself. Carl did that part. However, this week Sarah did cut zucchini with Carl supervising. 

Speaking of corrections, we needed to correct the radon situation of our mountain house. Ideal radon levels are below 4. When we tested our levels in late autumn they were over 200! Yikes. So we had a company come test again and then do some things to fix the situation. Now we monitor the levels continuously and things are mostly good, but not quite steady. We came to the mountain house this weekend for the first time since Thanksgiving. Aside from mouse poop and shredded linens deemed mouse-nest material, all is well and it is wonderful to be here again. I did, however, throw away a pillowcase, two dishrags, a dish towel, and some cloth napkins that had been shredded beyond acceptability. I also found mouse poop and seed hulls in the pocket of my bathrobe! We don’t keep any food where a mouse could get to it, but they bring in seeds that they find outside. So far we have only used live traps when we are here, but I admit that this latest poop-a-palooza has me wondering if we need stronger measures.

When we arrived at the mountain house I reminded the kids that the water might splurk and sploosh out of the faucets at first since it had been turned off for so long. They did an energetic interpretive dance of the water splashing and splurting.

Carl and Amy had a wonderful time skiing yesterday, while Sarah and I stayed snuggly at the house. Sarah’s new favorite song is “Love Shack” by the B-52s so we listened to that many times. Good thing I love the song too. We also drew some musical notes and Sarah drew a staff with notes above her rendition of a penguin. She recently rediscovered a love of Personal Penguin by Sandra Boynton, complete with musical notes scattered over the cover. Sarah’s penguin is a large smiley face with stick legs and earnest round feet. 

Sarah continues to enjoy talking about the hitch in my get-along and how I have run out of padding in my get-along. I continue to limp around physically and swing all around emotionally. When I walk almost normally and don’t hurt, then I think I have been making it all up and I don’t really need surgery. Other times I am hurting a lot and or incapable of walking normally and then I know I need the surgery, but I’m scared and sad about it. Realizing that I am like a car with a flat tire and that even if I am not in pain I just need a new tire to be structurally sound has helped me accept the need for intervention without feeling guilty or like I have failed in someway. 

Love and earnest penguins to you.

Sunday, February 27, 2022

February 27: H.p .... H/p.... New Hip

 H.p . . . H/p . . . New Hip.

After an x-ray and meeting with my new orthopedic surgeon, it is abundantly clear that I am in need of a new right hip. In my ball and socket hip joints, what is supposed to be round has some flat areas and corners. What is supposed to have space, on the right has none. My surgery is scheduled for March 16, shortly before my 45th birthday. So I guess a new hip is my birthday present. It is hard to remember what it is actually like to walk normally. People have assured me that hip replacements are easier than knee replacements, and that I’ll be walking the day of the out-patient surgery. I have also been reminded that just because they say “you’ll be doing stairs right away” that doesn’t mean it will be easy or fun to do them! That may be a monumental task. They say that some people are back to work in two weeks if they have a desk job. I don’t know what to expect given that my job requires me to be up on my legs. I know there is no way to really know what my experience will be except to go through it. 

My mom was already planning to come out for the double birthday celebration for Amy and me. As one friend said, we could also call this a Joint Birthday! Now my mom will extend her stay to help with my initial recovery. In addition to this wonderful help, when you are preparing for hip replacement surgery and being rather out of commission for at least a couple of weeks, I highly recommend having a professional event planner as your sister-in-law. Sonia came over yesterday to meet with Carl and me for a couple of hours, talking through all of the different ways to support me and our family through my recovery. Everything from meals to meeting Sarah’s bus to helping the kids with homework will be covered. As when Sonia was my full-time Sarah-Rise helper, I feel like she is already two steps ahead of thinking about what is needed and how to support everyone. What I especially appreciate is her insistence that Carl not be the one to manage all of the cooking, cleaning, and laundry on top of his increased role as an emotional support person for the girls and me. 

Emotionally I’m all over the place. I’m impatient to have a new hip. I’m scared of the surgery and pain and recovery. I’m daunted by the list of things to organize before the surgery. I’m uncertain how much longer I should keep working before the surgery, mainly because my discomfort seems to be increasing daily. I’m relieved that help is in sight. I’m crying hard at least once a day because of how difficult all of this is in so many different ways. I feel less independent by the moment, relying on Carl’s arm or walls as I make my way around. I miss going for walks. I miss doing anything without first evaluating whether or not it is a good idea. I feel old. I wonder how this can be happening to me. This is not something that happens to me. This is for other people, thank you very much. I’m glad my doctor has done this ten thousand times. I’m worried because I successfully weaned off of my cluster headache medication a few weeks ago, before my hip fell apart. Can my head actually survive these new stresses and not begin a new cluster of headaches? 

Now, on to some other news and positive things. The kids are finishing up a Triple Birthday Extravaganza sleepover with Anna. It is to celebrate the birthdays of Sarah, Anna, and Amy since it is roughly in between all of them. Carl and I had a date night, going out to dinner and then attending a showing of Return of the Jedi with live music played by the Pittsburgh Symphony Orchestra. It was wonderful, and it was hard because of my hip. But overall I’m still glad we did it.

Sarah likes to call me Hitchie because of my hip, and she still likes being called Hedgie, the baby hedgehog. So we are Hitchie and Hedgie. She also likes to scratch my hitch or press on my hitch, meaning she presses on my thigh sort of near my hip. 

Sarah checks in with us many times daily with “I’m a good listener? I do not need a nickel chart?” While sometimes I am tired of answering, I can see that she needs the reassurance. And truthfully the answer is yes. She is a very good listener, especially lately. She is ending her technology turns easily most of the time and is being increasingly helpful around the house. Last weekend when she was Carl’s sous chef for the Hello Fresh meal they made together, she took care of the carrots from start to finish all by herself. She peeled them, chopped them, put them on a cookie sheet with oil, put them in the oven, and took them out of the over. One hundred percent by herself. 

Sarah also did a Peppa the Pig jigsaw puzzle with 24 pieces completely on her own without anyone else even in the room or coaching at all!! Until a few months ago this had seemed like a skill that would elude her possibly for her entire life. With her increased cooking prowess, her independent unloading of the dishwasher yesterday, and her new puzzle ability, I begin to see that maybe she can eventually live semi-independently. This is always what we hoped and half-way expected, but it is comforting to log more evidence of it really being possible. 

Sarah likes to be various babies with new names of babies being born often. This week Baby Getting It was born. I was confused so she clarified, “More feeling, keep trying, you are getting it!” This is a reference to a Mo-Willems book called Elephants Cannot Dance. I laughed long and loud. I love how Sarah can turn any word or concept into a baby. There are no limits.

Sarah got a musical note umbrella and she loves playing with it inside.

Last weekend we went to see an art exhibit that included some of Anna’s work. We were surprised and delighted to discover that it was also Amy’s debut in the professional art world! One of Anna’s pieces of art included a sock on which Amy had drawn a cat face and written “Beatrix.” 

Amy’s morning preparations went more smoothly this week, with her making more Mom choices instead of Dad choices. That is how Carl talks about things with her because I tend to make choices to do what is required before I do anything extra, whereas Carl and Amy often prefer to do the opposite order and sometimes get burned by it. Amy still has big feelings around homework sometimes and I can’t say that I blame her. It is tough to have to do homework in the free hour or two she has after school before some of her other activities such as swimming or Girl Scouts. Some of the homework makes me want to go to sleep or do anything else first because it is annoying or dull. I don’t want to write complete sentences to give two examples of each vocabulary word on her list! Who wants to do such a thing?! I’m glad she is the one that has to do it instead of me, but I wish she didn’t have to do it either. I know this is a small thing, but sometimes it feels like homework takes over her home life. 

Any of these struggles seems inconsequential and not even worth airing given the situation in Ukraine. My heart breaks for everyone there. I think of the kids trying to do their vocabulary and math homework where such things now may be truly impossible, but would feel like a simple heaven compared to war. I think of the people awaiting hip replacements, trying to get their family to safety as they hobble about and wonder when life can go back to the simple details of pursuing a more comfortable gait. I feel helpless, though I have donated to organizations doing what they can. Still, the Russian invasion of Ukraine is the real heartbreak of the week.

Lots of love to all of you. 

Sunday, February 20, 2022

February 20: A Hitch in my Get-Along

I have a Hitch in my Get-Along. That is the unofficial diagnosis for my hip issue. Sarah finds it hilarious, and the words often morph into her telling me that I have a glitch. Yes, yes I do. I have a hitch and a glitch, and unfortunately, resting doesn’t seem to have improved things. I don’t think resting made anything worse. I think my hip is just in worse shape than it was, so what was manageable for years is no longer manageable. I limp or walk slightly awkwardly at almost all times and if I’m lucky then I don’t have too many moments of severe pain where I can’t hold my weight on my right leg. I did get a chiropractic adjustment yesterday because my top cervical vertebrae, known as the atlas because it holds up the world of the head, was quite out of alignment. That adjustment did not fix my hip, nor did I fully expect that it would. On Thursday I will meet with an orthopedic surgeon and find out if I need more scans or a shot of something or surgery of some sort. As my 45th birthday looms, contemplating a possible hip replacement really doesn’t help me feel young and spry.

My hip pain and not being able to reliably do what I usually do in life has been emotionally challenging to say the least. I feel worn out physically and emotionally. I’m enjoying my work much less than usual and tears are flowing more often too. I am reducing how many clients I see per week, but that means that when people want to schedule I’m already looking at April. 

Despite being told by the bus company that Sarah’s regular driver would be back this past Monday, he was not. The bus company was evidently the most surprised by this revelation, scrambling to come up with a substitute on Monday morning when Sarah normally would have already been picked up. After that stressful morning, the bus company did in fact supply subs in a timely-enough manner. Now we have been assured that Sarah’s regular driver will be back on Thursday. 

Getting out the door on time with Amy has also been a challenge, even though she has a flexible window of departure since she walks. Because of my hip, Carl was walking with her to the main intersection where we always want to make sure there is a crossing guard. She walks the rest of the way on her own, so could do the whole walk independently but that isn’t how we have done it so far. Anyway, Carl has a morning bus to catch so needs Amy to be ready by a certain time on the dot. This goal proved elusive, with all parties frustrated. 

Enough with grumps and frustrations…. Last Sunday we had a wonderful visit from N, one of our Sarah-Rise volunteers from the past. N. was with our Sarah-Rise program for the four main years that we did it full time. I realized recently that we met him almost 10 years ago. That boggles my mind. How can so much time have passed? And yet, of course it did. Anyway, it warmed my heart to have him here again. We reminisced about the time when he and Sarah pretended that he was a snail shopping for a new shell, while she assisted him in trying on different options. For this visit, Carl, N, and the girls played the Goodnight Moon game with much laughter and hilarity. Everyone except me attempted to sit criss-cross, some of them hamming it up to tip over. Amy turned herself into a veritable pretzel, as she so often does with her toes up by her ears. It felt so rejuvenating to have company in a way that felt so normal but has been anything but normal for the past two years. 

There has been much silliness from all parties living in this house. Amy and I donned exaggerated serious faces to tackle some of her math homework. Then she and Carl made all sorts of faces while taking selfies, and Sarah played with a paper bag on her head while helping Carl make dinner yesterday. 

I hope you are well and that if you have a hitch in your get-along you also have some serious silliness to alleviate some of the sadness.