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Category Archives: crying

Calgon take me away

Preface: This blog is about me and my experience/feelings with regards to medications. It is not a judgement on or valuation of what anyone else does/feels with regards to their anxiety, depression, pain, insomnia, allergies…etc.


Monday morning I went to physical therapy for my shoulder. I’ve been going for close on to six weeks I think, but only once a week because they are so booked they can’t usually fit me in twice a week. This past Monday, I actually cried during the appointment because the pain was a) so bad and b) so frustrating. For the first three weeks or so, I was doing my exercises religiously at home. Then the therapist started adding in more and more exercises–without giving them to me in written or picture form–and I got overwhelmed and lost. I still try to do stuff daily, but it’s not everything I should be doing. Even so, I’m continuing to progress with my flexibility, but the pain continues. And I guess because the therapist is trying to push my range, the pain is…bad.

I am extremely sensitive to medications, and have been for most of my adult life. I don’t even take OTC pain killers like ibuprofin or acetaminophen or tylenol because they either screw up my stomach or they don’t work. I will take anti-biotics when prescribed, but I hate the experience and it’s mentally very challenging for me.

So last night I was in the shower and thinking about how much my shoulder still hurt, how sore it was, and I was under the hot spray of water and thinking…if I only took pain killers this would be a lot easier. And I knew…I KNEW part of the reason I don’t take pain killers or cold medication or antihistamines or sleeping pills or any other medication is that I would cause a bigger issue for myself. It’s NO LIE that I have medication sensitivities…I very much do have them. But maybe if I searched hard enough I could find things that work for me. I don’t do this…and here’s why.

About fifteen years ago I had a bad cold…a sore throat that was horrendously painful. I started using these OTC throat drops that had some kind of liquid medication in the middle. It was probably Haul’s brand, probably cherry flavored. I used them constantly in the beginning and they seemed to help. Then my throat started getting better but I literally got addicted to them and was continuing to suck on them like they were candy. I had to use them. I was addicted and I had to have one in my mouth almost all the time. It was vaguely terrifying when I finally realized what was happening (maybe like 3-4 weeks later). I quit them cold turkey and made Hub take the bag to work with him to throw away. I knew if they were in the trash in my house, I would dig them out and eat them. I don’t buy those kind of lozenges anymore, though in the last two or three years I have started buying honey-drops for sore throats.

I don’t do drugs and I don’t drink any alcohol and I don’t smoke. I never did any of those things. I feel like if I did or if I started using something like pain killers or anti-anxiety medication or sleeping pills, I would be using them constantly and for the wrong reason. I’d be in less pain, I’d probably have less anxiety, I might sleep more, but I’d also be zoned out and not living. I would just figure out the best way to shut myself off from everything and everyone in life by doping myself up on OTC or prescription medication. I would be gone, in every sense of the word. I’m not sure I’ve ever admitted this fear to anyone out loud, but in my heart I know that I’d use the medications to hide away. I’m not sure I’d be doing anything illegal or overdosing on the meds–or even overusing in any significant way–but I’d be using them in a way that would excuse me from life.

I feel like my anxiety over medications keeps me safe from all of this. Yes, I DID use some pain medication after my first surgery, but it was only a day or so (and so regimented!) and then I used tylenol. And then after a day or so I used nothing. The second surgery I didn’t use pain meds because I didn’t like the way they made me feel the first time, so I used tylenol as needed and I suffered through. I suffer through pain on a daily basis because I’m afraid of who I would become if I muted all the pain in my life…physical and mental.

Before I first got sick in 2001 (at 29yo), I’m not sure I ever really needed medications. Sure, I probably took cold meds on and off over the years, and never gave it another thought. Yes I did use Advil every month for cramps (which is how I ended up with stomach issues!) and probably occasionally for headaches. But after I got sick, everything changed, including who I really was. Who I really am.

The physical therapist said that I could go back to my Ortho doctor and ask to get a steroid injection to help with the pain as we continue with rehab, but I declined. I hate the pain I live with daily, and I hate the pain that reduces me to tears during PT, but the pain reminds me that I’m alive. I’m alive and I’m experiencing life.

This all sounds very fucked up. I guess I’m not surprised at that revelation.

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2190 days

Six years.

It’s been six years since Hub and I had to let our Sweet Pea go to the Rainbow Bridge. I post about her every year, usually before the anniversary of our loss, but this year I didn’t. I’m writing this today, ON the day, 6 hours after we let her go. Today, as it happened on the first year anniversary, I am alone at home. Hub has been out since early this morning and will not be home until late tonight. I have not and will not bring up the anniversary to him…he deals in his own way and I deal in mine.

I was re-reading what I’ve written in the past on this day, and I cried. I cried for the pain of losing her, I cried for the pain of loss, I cried because it hurt me how much she was hurting in the last weeks. We never had a final, concrete prognosis of what would have happened if we had made her try to hold on…would it have been days, weeks, months? It didn’t matter in the end, because there was too much pain in her for us to even consider prolonging her life. There was no way…

In all I’ve written, this is what I would want to say again and again. I just don’t want to find new words this year.

In 2011, she started slowing down. Not surprising to us, because based on what we knew we adopted her, she would have been going on 12 years old. That’s old-age for a large dog. Then, in late July of that year, she developed a cough. It scared me. We took her to our vet, but he found no reason for the cough…but found an auto-immune disease that would explain her increased and pretty marked lethargy. And as the tests continued–along with medications–the news got worse. And so did Sweet Pea. She became unable to walk the stairs to our bedroom, so Hub began sleeping on the couch in the family room to be near her. She started having trouble walking down the three deck stairs to the yard, so Hub began helping her out to the front yard down only two concrete steps (one step out the door, then the concrete porch and one step off the porch) to do her business. Then she began having trouble getting up…and the medications made her pant heavily…and they made her painful. And every day, I died a little inside. Not only because we knew this was serious–likely fatal–but because she was suffering. Even though it was only a little at that point, there was no uphill from there. I prayed she would give up. I prayed G-d would take her in her sleep–though she only dozed during the day, she was restless at night. I prayed that we would get some kind of report saying there was no hope and that it was time. I got none of it. The tests were inconclusive, but experience from our vet said there was likely nothing we could do except extend her life a few weeks or a few months…maybe. But in the end, she was not going to last long…and it was not going to be an easy time for her. And letting her hang on and die “naturally”…our vet said it would be painful for her. Like drowning, or being unable to breathe…struggling, gasping. It was three weeks from the first vet visit for a cough to the day we took her in for her last visit. In between was medication, tests, an emergency drive two hours away to an ER vet for a transfusion (where she had to stay locked in a cage overnight without us) during a bad hurricane, there was a bad reaction to the infusion, more tests…and pain. My sweet, loving, gentle girl snapped at a vet tech who barely touched her, snapped at our vet when he tried to help her, and cried. She’d never done any of those things in the nine years we’d known and loved her. She’d never snapped at anyone, ever, over anything. Man or beast. And then there were the eyes. She watched us every day, with these big, sad eyes. Pain seemed to radiate from her gaze. We hesitated to touch her because we thought it caused her pain. I laid on the floor with her in our dining room…the softest carpet in the house, and I stroke her paw. I stroked the spot from between her eyes down to her nose, so lightly I barely felt her fur. I wanted to hold her and hug her close, but I couldn’t. I wanted her to make the decision for us, but she refused. She refused to stop caring for us. She refused to let go, because she knew it was her job to see to us first. We had no choice. We had no fucking choice.

We took her in to the vet. I talked to her from the moment they put her on the table until long after she was gone. I told her that we were letting her go, and that her job was over. That it was our turn to take care of her the way she had taken care of us for the last 9 years. I told her it was all right, that she could go, she could be free of her body that was betraying her. And I cried like I’d never cried before. I told her how much we loved her. I told her how thankful we were to have her in our lives. I told her how much we would miss her. I sobbed and I petted her and I held on to her. I smelled her fur and her feet and touched her ears. And I cried. And inside, a part of me curled up and died with her.

We took her to our property and laid her to rest in a pretty spot near my parents’ dog, who had died one year prior. It was incredibly hot and humid, but my family–my brothers and my parents and Hub–dug a hole. Deep and wide, so there would be no concerns about the animals in the area. And it was so hot out, but they did it. And they put her in the grave, wrapped in her two favorite bed covers, with a couple of her favorite toys and an unwashed shirt of mine that smelled like me.

I can’t tell you the tears I’ve cried for my girl. I can’t tell you the hole in my heart from the loss of her. I can’t tell you how much I’ve changed because of her. I can’t explain how much I’ve changed with the loss of her.

I’ve written about her a lot. A lot in the first year she was gone. Not as much during the second year, though I’ve talked about her often in a professional and personal setting. I think about her every day. I’ve gone back and read the things I’ve written about her…and cried like it was the day that we let her go. I did it today in preparation for this post. It was incredibly painful. It IS incredibly painful.

I posted this on her six month anniversary, elsewhere. I re-read it earlier and every word is still the truth for me today.

I woke this morning early, looking directly at the clock by my bedside. The clock shows not only the time, but the date…and I almost felt my heart stop. I had been crying most of the night after I turned off all the lights. Images of the day we let SP go were running through my head, making me sob like it was the day it happened. I am crying now as I type. So when I woke this morning, I was fuzzy-headed, and I could swear the clock was telling me today’s date was 3-3-12. How could that be? I knew today was the six month anniversary, and that SP had left us on 9-2-11. I couldn’t believe I had missed the day, although I have been feeling the pain of this date for weeks.

I stayed in bed for hours, long past my husband let Le Moo out and went on his way to work. I stared at the clock, tears clogging my throat as I berated myself for missing the 2nd. It wasn’t until I was standing outside with Le Moo, staring at the trees in our back yard, when I realized that my clock must not have allowed for leap year. I KNEW today was the 2nd…I knew today was the day. I had spent hours thinking about it, not knowing how I could have been mistaken.

I feel whipped and beaten. I spent most of the hours crying last night and early this morning thinking that I desperately wanted to go to the basement and bury myself in the dog bed SP slept on in our old house in our bedroom. It’s an atrocious 70s orange color, something I found at overstock and bought merely because at the time it was the only memory-foam dog bed I could find big enough for her that we could afford. She loved the bed and we put up with it because of that. I mean that color would burn your retinas and I have no idea why it was ever made, but she loved laying on that thing. I suspect before the afternoon is over, I will be sitting with that bed, trying to find her smell and looking at the dog hair I hope it still clinging to it.

I cannot tell you how often I ache over the fact that I do not have a pawprint from her. I know there is one embedded in my heart, but I wish I had one to look at and touch. I have finally put one picture of her on my wall in addition to the polaroid picture I keep next to my bed. I want to put up so many that I fear it would cover the entire wall…but then I think it would kill me to see them.

I feel like I cannot get past this loss. I feel like I will never get past it. I still think of her every day. I still wish that she was here with us. I still look to step over her next to the bed. I cannot believe I have woken up without her every day for the last 180 days…how is it possible? How have I made it?

SP, I carry this pain of your loss every day. It is a part of me and will always be. I miss you so much that sometimes it hurts to breathe. And he misses you, too. I see it in his eyes and I feel it in his heart, even though he doesn’t show it the same way I do. You know how much he adored you, how he lived for those early morning and late night conversations with you. How he looked forward to coming home from work every day to see you waiting for him at the window, or at the top of the stairs, wagging that gorgeous tail of yours. How we both loved your big brown eyes and the “eyeliner” that Mom swore you woke up early every morning to put on. I miss touching your soft fur, feeling you snuffle my face and my eyes and my hair. I miss hugging you and calling you Sweet Pea. I miss singing to you when we went downstairs every day for lunch. I miss you, dammit. There isn’t a thing about you I don’t miss. The way you would eat your food, then come find one of us and burp right in our face like it was a “thank you”. The way it felt when you leaned against us, sharing your love with us. The way you used to run out into the yard to see neighbors walking by the fence…the way you used to run back to the house looking happy and “lighter” after you poo’d.

And as I sit here, I remember your last days, and I sob for the pain. I remember sitting on the floor in the dining room, on that atrocious pink carpet you loved to use as a scratching post for your toenails…I was already in pain as I considered what lay ahead of us. That we would have no other option but to let you go, to take away the pain of your disease. I remember posting here, asking for guidance and support, knowing that we had to do the right thing. I remember laying there with the laptop nearby, wishing I could hold you close and never let you go, but knowing even the smallest of caresses could cause you physical pain. I remember touching your paws, hoping it would not be too much for you. I remember using one finger to stroke the spot between your eyes and down your snout, praying it would not bring you pain but give you comfort and show you my love for you. I remember sitting in the family room, begging him to take a picture of the two of us because we had NONE….but only hovering over you because I was afraid to touch you. I hate those pictures. I remember taking you to the vet hospital, and sitting in the car with him, both of us dreading the moments because they were our last with you. Your beautiful gorgeous face, watching us, looking so tired and old and sad…the pain from the meds and the disease having beaten the life from you. And when we arrived, how you tried so hard to get out of the car on your own, but we wouldn’t let you. We were so afraid you would hurt more. The moments when we stood with you in the exam room, as the vet gave you treats to say his goodbye to you. The way you laid there on the table, so trusting and loving, but so tired. I hated every second of it. I hated that we had to do it. I hated that it had to happen. I hated that we had to let you go. It was so bittersweet to see the pain lift from your body as your life ended.

I am literally doubled over in pain, sobbing with the pain of this all. Of the memories. Of the loss. Of the regrets.

I love you, Sweet Pea. I love you, Sweet Pea. I love you my precious beautiful Sweet Pea.

It’s been so many years without my Sweet Pea. 2,190 days…the Polaroid picture of her is still in the exact same place next to my bed, on the corner of my dresser. Every now and then I go look at pictures (other than the one that is the background on my laptop) and a few videos we have of her. On the landing going upstairs, there’s a picture of her front and center on a console table…I never want to forget her smile, or what she brought to my life.

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I miss her so much.

 
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Posted by on September 2, 2017 in anxiety, crying, death, dogs, grief, loss, love, Sweet Pea

 

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Shock and OW!

I know that I said previously that I wouldn’t be seeing the neurologist for my EMG until September, but that changed.

I had such a terrible weekend. Saturday I basically did nothing because I felt so weak and tired. We went to bed at our regular time that evening, but at 12:30am Sunday morning, Hub and I were awakened by SCREAMING smoke alarms. In our house, all our smoke alarms are interconnected, so if one of them detects something every single alarm goes off. Not only does it make that horrendous alarm noise, but it also yells “FIRE! FIRE! FIRE!” I literally sat straight up in bed and hit Hub in the chest to wake him, then I turned the overhead light on. The dogs were freaking out, I was trying to get dressed, and Hub was trying to unhook himself from his CPAP machine, all while the alarms are screaming and yelling, and the dogs are running around the bedroom (we keep them closed in with us at night). We finally are semi-dressed and have shoes on and we open the door to the hallway and the screaming gets louder because there are more alarms in the hallway and in each of the bedrooms. I tried to get the dogs downstairs to give them treats (they always get treats when there are loud noises) while Hub tried to silence the smoke alarms (the dogs are still freaking out and Butthead races into her crate and won’t come out even though there’s an alarm nearly over her head still screaming). We don’t see or smell fire anyway, but Hub goes to investigate the whole house while I retrieve Butthead and rush the dogs outside and away from the noise. When Hub comes outside he tells me he has ripped down several of the detectors and the noise has stopped. I’m not happy, I’m afraid that there’s a fire in the attic or in the walls or there’s CO2 somewhere and that’s why the alarms went off. So at about 12:45, I find and call the non-emergency number for the fire department, and I explain what is going on. They take my address and say they’ll be out to the house shortly…and while we’re waiting the alarms go off again, so Hub rips MORE detectors off the ceiling and when the silence reigns again he takes the dogs into the basement so they can’t get out of the house and I go outside to wait for the fire department. To try to shorten this story–which really has nothing to do with this post–the firefighters come out to the house in the middle of the night, and after inspecting the entire house, they figure out that ONE of the smoke detectors has malfunctioned. And because it was wired into the “system”, it sets off all the other detectors in the house. Bless them, the firefighters were pretty awesome, and by 1:30am, they were walking back down our driveway in the darkness to load back up onto the firetruck they had left in the street. We were awake, trying to re-settle the dogs and ourselves, until about 2am.

Okay, so Sunday night I pretty much had a bad breakdown. I was just sobbing over how bad I was feeling and how tired I was and how afraid I was. I felt like I was getting worse, that my weakness was worse, my fatigue was worse, my imbalance was worse, and that now I was having trouble with my hands/arms and not just my legs.

For only the second time in the four and a half years I’ve been seeing T, I actually contacted her to seek guidance and help after-hours (or out of a normal session). The only other time I’ve done that is when my mother died. I am so grateful and so lucky that she took the time to talk to me in email (which is how I contacted her). I can’t say anything got resolved or that I even felt “better” in that moment, but knowing someone was out there to reach for–and who would reach back–was enormously helpful. Yes, Hub was here and he was being supportive, but this time it took a more confident and experienced communication.

When I finally caught my breath, I was so exhausted from struggling during the day and crying for hours that I went to sleep at 9pm. When I woke up the next morning, I called to see if my primary doc could see me, even though I didn’t think it would be helpful. They were able to fit me in just before lunchtime, and Hub took time off of work to go with me. After that phone call, I called the neuro’s office to see if he had any cancellations where he could fit me in for my test. The receptionist said no right away, because she had just gotten off the phone with someone else asking the same thing. So I asked to leave a message for my doctor, and I told him I was feeling worse and that I was having trouble with my hand/arm. He called within thirty minutes and fit me in for the EMG for two days later (that’d be today).

I went to my primary, who said she didn’t know what else to do for me except to send me to see a sleep doctor to see if I was having some kind of sleep disorder, and also to an infectious disease doctor to talk about Chronic Fatigue Syndrome. We were sitting in her office and I was so damn tired and frustrated that I literally put my head down on the edge of her desk and tried not to cry. She asked me what was going on and I told her, I was exhausted, frustrated, and scared. She immediately asked me if I was depressed. I was both annoyed and frustrated with this, because ANYONE in my shoes, with this length of exhaustion and weakness, and not knowing what was wrong, would be afraid and sad and upset. I thanked her for the offer but said I wasn’t ready to do that right now. She told me to try to stop focusing on my symptoms because I would surely make them worse by doing so, and to continue with my neuro appointment.

After that, we ran off to get my blood work done for the neuro and then we went home. Fast forward (cuz this is soooooo long), I spent most of today trying not to think about the test and/or what it might or might not say. I semi-obsessively check my laptop to see if my blood work has come in while trying not to spend time searching Dr. Google. We finally head off to the neuro office and within about ten minutes we are back in the testing room. I had read a little about the test(s) and heard both that it was no big deal and that it hurt like a mo’fo. I think I ended up somewhere in the middle.

The neuro doctor is very quiet in general, so there was almost no talking. The room had to be like 85 degrees, which I assume was on purpose because some of the testing is on muscles and maybe the heat keeps them relaxed? The first part of the test was where they put some thingys on you and then send an electric shock through certain nerves. The second part they use needles, stuck into your muscle, to record some kind of feedback. I asked what the needles were like and was told they are thinner and shorter than acupuncture needles. When he started zapping me with electricity, I asked if the needles hurt more or less, and he said “there’s no electricity with the needles” and went back to his zapping. So after another few minutes of silence and him randomly saying “zap here”, I ask him if his patients say the electricity is worse or the needles, and he says “it goes both ways.” *sigh*

The zaps range from a slight sting to a full-on-stick-your-fingers-in-an-outlet zap to OH SHIT THAT HURT LIKE A MO’FO. Fortunately, they are pretty quick zaps–up and down both legs in multiple places and along one arm and hand–and within about forty minutes we are moving on to the needle part of the test. He actually started with my arm and it really wasn’t all that bad, as long as I didn’t look at what he was doing. When he moved to my first leg, it was fine until he went into the inside of my calf and then it HURT. Especially he had trouble finding the right spot to be in and he had to sort of shift it around and push harder and that was pretty bad. The same issue happened with the other leg, but then we were pretty much done. After I got dressed, I asked him if he saw anything and he only said, “nothing jumped out at me” and said he’d have to go through all the data that had been collected during the test in the computer. I asked if there was anything I should or shouldn’t be doing, and he only said to stay hydrated and to rest. He scheduled us to come back for a follow-up for next Wednesday, so I have a week to sit and wait…

Tomorrow morning I go in for my CT Scan for my cancer follow-up. My father is driving me because Hub has to be in the office and I feel so weak and off-balance that I am afraid to drive myself. Friday I have a massage therapy appointment, which I hope I can get to, and I might have to have my father drive me again. I had cancelled my PT appointment for this past Monday because I didn’t think I’d be able to do it. I hope I can return to it this coming Monday, because I need to continue to try to make progress on my shoulder.

For now, I have a headache and I think I need to go to sleep. I have to get up early to start drinking the crap for my CT Scan, so off I go.

 

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I need a minute

I had my hair colored yesterday (more in another blog), which took about two hours. This morning I had to get up early to go to PT (her first appointment of the day) so that I could get to my neurology appointment on time.

This was my second PT appointment, the first with full treatment since initial appointments include lots of time for evaluation and pre-treatment measurements. I’d been doing the stretching exercises she assigned me since Friday, so I have been doing some work. Today, though, she did some more stretching…and it hurt. The physical therapist is a very nice, very low-key woman, who spends most of the appointments so far reassuring me that I will make progress and I will feel better. I’ve told her that I am VERY familiar with PT, as I’ve been multiple times over the years. Even so, she seems intent on keeping up with the reassurances…I guess she thinks she is being encouraging, I’m not sure. Anyway, the appointment was painful and I left feeling sore and tired.

When I got home, Hub told me he couldn’t go with me to the neurologist because he had a big meeting come up at work. My father offered to go, but I really didn’t want to have to deal with my dad’s pushiness, especially with a new-to-me doctor. So I said I’d be okay, and when the time came I headed off to the doctor’s office.

The doctor was on time, which was shocking to me, and his space in the suite was a combo office and exam room. It was a little odd, I’ve never seen anything like that. Normally you are in an exam room or you meet with the doctor in a separate office space. We sat down and he asked me what was happening. I gave him my history as best I could–including the recent bloodwork done that had all come back normal–and told him the issues I was having recently. He asked me a ton of questions, most of which I gave negatory answers to…it almost looked like he was reading from a list on his laptop! He then went through the litany of physical neuro tests–most of which I’ve been through before. When that was done, we sat back down at his desk and he stared at his laptop for a minute. Then he started saying that I didn’t fit in this category (ALS) or that category (Myasthenia gravis) or even that category (Guillain-Barré)…and each time he described WHY I didn’t fit. Having been alone, I tried to remember every reason why I didn’t match those categories, but I was busy thinking “oh, but I do have trouble swallowing!” (but I don’t REALLY) and “oh, my upper body IS weak” (but not REALLY) and “oh, I do have tingling!” (but probably that’s when I overdo or my limb falls asleep). It’s like he was giving symptoms (more than I just described) and I was latching onto them, worrying that maybe I really did have those symptoms and they were just on the mild side and what if I had missed the symptoms??

It was hard. I don’t remember which disease was ruled out by which missing symptom(s). I know he didn’t specifically rule out MS (multiple sclerosis) and I don’t know why.  I was afraid to ask. The final result was the he wanted to start with bloodwork for some muscle thing, and that he wanted to do an EMG (electromyogram). He said he had time to do it later that afternoon or tomorrow because of cancellations, but I didn’t want to do something unknown when I had the wedding this weekend. I said I wasn’t available and at that point the best they could do was schedule for the end of August. So I put it on my calendar and left the office.

I drove home, feeling weak and tired…and so disappointed, even though I really had no hopes for the appointment. I guess some part of me thought something would come of it, but it had to be pretty far buried in my subconscious. When I got home, Hub was still on the phone for his meeting, so he slipped over to greet me briefly. I said I was going upstairs to change my clothes, then decided I wanted to lie down for a while. I called my father to update him, had to listen to him talk about the time HE had some sort of muscle electricity test thingy twenty-plus years ago for a possible pinched nerve, then I stripped and got into bed. I barely settled in when Hub came in to check on me…he wanted to know if something happened that I hadn’t told him.

I cried. I don’t want to be sick again…or more than I already am. I’m tired of being sick. I’m tired of being tired. I’m tired of not knowing. I’m tired of having to change my life because I’m sick again, or more. I’m tired of having to grieve for the life I had, or the one I’ll never have, because I’m sick again, or more.

Hub hugged me, and even though I knew he wanted to hover and smother because that’s his M.O., he left me to rest. I just wanted a minute to mourn, you know? I needed a minute to come to terms with the disappointment, with the fatigue of it all. No one ever knows what is wrong with me. I’m always a syndrome…a catch-all that I’m dumped in because I don’t match any known disease or medical terminology.  I’m tired. So fucking tired.

I laid in bed for several hours–though I got up briefly to eat some soup because I hadn’t eaten or drunk anything prior to that–and just did nothing. I just couldn’t get up the energy to participate in life. My body and my soul didn’t want to body or soul.

I got up and had dinner later, and I talked with Hub like I was “normal”, but inside I’m hurting and I’m disappointed and I’m lost. Again. And writing these things has me crying again…

 

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One year.

I love you, Mom.

Every moment, even the difficult ones, were a blessing for me because they were spent with you.

I mark this day in honor of a woman whose life mattered.

I mark this day in honor of a woman who loved her family beyond what words can express. It was immeasurable.

I mark this day in honor of a woman who is loved beyond her time on this earth.

I mark this day in honor of a woman who was generous, intelligent, compassionate, and downright amazing.

I mark this day in my heart and soul, like a tattoo that can never be removed.

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March not better

I thought February was bad. March has been worse.

I’m feeling so shitty, I can’t even. Period. I spend much of my days fighting the nausea and the fatigue…I’m exhausted before I get going. And now…and now, my imbalance is back in a big way. I’m struggling to walk without falling over, and I’m back to touching walls and handrails and tables and whatever in order to keep myself stable. This is a huge slide backward for me, as I haven’t had this kind of imbalance in quite some time.

I went back to the doctor AGAIN because I’m still exhausted and I’m still nauseated. She told me I was acting better this time versus the last visit, but she’s still thinking I have a virus that I need to just “wait out”. She sent me for more blood work (ANA, rheumatoid arthritis, lyme, iron, b12), but everything came back normal. My b12 is a tad on the low side for my history but still in the normal range. I’ve ordered my b12 sublingual pills and will start them ASAP. Maybe it’s that, maybe it’s stress and grief, maybe it’s something else. I have no idea and apparently neither does my doctor. She said to drink more water and walk outside for 20-30 minutes a day. She says dehydration can cause nausea–and maybe it can–but my drinking habits haven’t altered much. Except now I feel like shit and so I don’t want to do anything, including drink. If I go walk outside my allergies will get worse and I’ll have more breathing trouble and more snot and more post-nasal drip and more nausea. The doctor didn’t care for that and told me to do it anyway, that being outside and walking will make me feel better and get rid of my fatigue. I’m not eating much because I’m so nauseated all the time. I rush through eating what I can before I feel like I can’t put anything else in my mouth at both lunch and dinner, then I leave my dishes in the sink and go back to the couch.

I spend most of my days on the couch, barely even bothering to look at my computer. I try to stay upright, but I’m so exhausted all the time that I end up stretched out and wishing that the day was just over. I don’t know why I wish for that because at this point tomorrow will be much of the same. I feel like I’m sliding into this despair of thinking that I’ll never feel better. That it will always be like this. I am trying to push past the exhaustion and do stuff–I did three loads of laundry on Sunday–in the hopes that if I ignore what’s going on it will go away. But by the time I do anything, I feel this crushing fatigue again and I end up on the couch. Or in bed.

Sleeping is a negatory. I try to sleep but it doesn’t work, and when I wake up in the morning I can hardly haul myself out of bed. I don’t feel rested or refreshed or like I even closed my eyes. I want to cry but I’m too fucking tired to cry.

I was supposed to go see my massage therapist on the 14th but our local snow canceled that appointment. I was also scheduled to go tomorrow morning, but I literally got an email at 9:30pm saying she’s sick and has to cancel. And for sure I’m grateful because I do NOT want to get sick and it sounds like she has the flu, but I’m so disappointed. For one thing, I was hoping some trigger point release would help with my imbalance and nausea (hoping, though not confident)…for another thing, getting onto her schedule is a bitch and even though I rushed I struggled to get back onto her calendar. It’ll be two weeks before I can get back in to see her, which might not be horrible because if she DOES have the flu I wouldn’t want to be back in her “hands” too soon. But it’s hard to miss appointment after appointment when I’m feeling so poorly. Hub tried to send me a link to a list of massage therapists in the area, but none of them do trigger point AND it’s hard to just find a new massage therapist. It’s like a mental therapist…you have a relationship built up. It’s not so easy to walk into someone’s space and get naked and let them rub you for an hour.

I see T on Friday, which is the day after the one year anniversary of my mother’s passing. Just happens to be how it worked out. Considering how things are going at the moment, it’s going to be a long, sobby appointment.

I can’t stand this constant nausea. Every time I swallow I feel sick. Every time I move I’m wobbly and off balance and that makes the nausea worse. If I didn’t have the dogs, I’d be in bed all day. I gave thought to going back to bed after lunch today because Butthead had peed and pooped after HER lunch so I knew she’d be okay for a while, but I didn’t want to give in. I’ve been in that place where I didn’t get out of bed for weeks (with my prilosec fever) and that’s a bad road to head down. It only makes me weaker and makes me feel worse.

Hub’s birthday dinner with his family is this coming weekend. I don’t know how I’m going to go…by 3pm, I’m so exhausted I can barely sit at our kitchen table for dinner, how am I going to get out and go to a restaurant and be “on” for his family? For hours… We didn’t go out on his birthday because I couldn’t get up the energy. We didn’t go donate the dolls and bears I crocheted to the police station because I didn’t have the energy to leave the house.

I don’t know what to do now. I don’t know what path to take. I don’t know how to do anything right now.

 

 

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Sleep? Why bother…

Apparently this is what my body and brain has decided. Sleep unnecessary.

I know that for real it has to do with my mental, emotional, and physical pain. All of those wrapped into one, split into pieces, kneaded into each other, and then rolled into a throbbing ball of oneness. I’m so on edge that one small scrape and I’m raw and bleeding profusely, figuratively.

I cried on the way to the grocery store this morning. Not because I had to go to the grocery store, not because I was worried about being able to afford the trip to the grocery store, not because I was afraid I was going to have an anxiety attack in the grocery store… I cried because I couldn’t not cry. I’m tired, I’m not sleeping, I’m worried about Hub and I’m worried about Butthead. I’m worried about myself, too. My grief is overwhelming every part of my life and I can’t seem to dig my way out of it.

Hub is agonizing over a job offer–in part because it might mean less flexibility and he worries that he won’t be able to come home if I need him–that he received on Friday. I’m worried for him because I don’t feel that the company was being up front with him…they kind of bait and switched the job position (which they apparently did to the guy before him, someone Hub knows). I am concerned he won’t have any backup on his work, and I’m worried because if this is how they treat potential employees, how do they treat current employees. But Hub is unhappy in his current job and looking for a way out. Our health insurance changed due to the buy-out, so he’s both unhappy with the new corporate owners and unhappy with their shitty health insurance. Unfortunately, the potentially new company has equally shitty health insurance…so that kind of cancels out the pro/con in that category. Now they’re not budging on a concession he asked about (a minor concession on their part!), so that might be the end of that. I only hope that his current corporate overlords don’t decide that he’s no longer needed before he finds something else.

Butthead is randomly puking again. I mean, it’s good news that she’s not persistently puking like the last episode where we ended up rushing her to the vet hospital and coming home with anti-vomit pills… But this randomly throwing up (twice in the last four days…one of which was this morning which was another reason why I was so upset) is so frustrating. We don’t know if she’s sneaking and eating bad things outside or has gastritis and so her stomach hurts her or what… We’re at the point where we’re acclimating her to a basket muzzle that she’ll have to wear anytime she’s outside so she doesn’t eat crap off the ground and make herself sick. It’s hard and sad to make her wear a muzzle because she’s a good dog, not aggressive, shouldn’t have to wear it. I know it’s uncomfortable and bulky and just plain weird for her, but we don’t know what else to do with her. We can’t figure out what is wrong with her. And if it’s that she’s eating stuff outside that’s making her sick, there’s nothing else we can do other than the muzzle. For the past month or so we’ve been out there with her every minute, following her and standing over her and making sure she’s not eating things. But with the snow and ice, and my physical capabilities being limited at this point…I couldn’t keep up with her and I think she might have eaten something that made her vomit last Thursday when I wasn’t standing over her. We just don’t know what to do with her… So I’m worried that she’s going to vomit again like the last episode. Ugh. So far it’s been these two random episodes and today I spent time on and off modifying the basket muzzle to try to use a quick-snap collar to hold it on her head versus the old-fashioned buckle which is a pain in the ass to get on and off of her, especially with her floppy ears and long hair.

Even though I’ve been feeling ultra shitty and exhausted, we had to do a bunch of things this weekend. Most of which we accomplished. Unfortunately, one of the things was cleaning up the caulk in our master shower which seemed to be growing mold behind the caulk at the joints of the floor and wall. Hub is not flexible, so he had trouble sitting on the floor and scraping at the caulk, so I did 90% of it. Which, of course, hurt my arms, shoulders, and hands more than they were already hurting. The end result, though, is that we need to call in a professional to look at our shower because this is the second time in a year that we’ve ended up with this problem. Last time my brother helped me strip and re-caulk the shower, but now we’re in the same place again… There’s something wrong if there’s mold and mildew growing behind the caulk, especially since we bought mold-resistant caulk. This all means that we don’t have a shower in our bathroom and we have to haul ass to the shower on the opposite end of the house…past all the windows in the front of the house and over the foyer area of the house. It also means we have to haul all our paraphernalia into the other shower, which is smaller than our master shower. It’s not a huge deal, it’s just more stress. And more stress in having to find someone who knows what they are doing to come into the house to fix whatever is happening. The stupid sub-contractor that our builder hired to do our bathrooms did not know what they were doing. They screwed several things up in our master bathroom and ruined a lot of our shower floor tiles by having to go back and chip out all the wrong grout they put in. So we were left with grout over top of grout, and chipped tiles. And the slope of the floor is really bad, which causes water to pool in different spots in the shower and leaves our grout with water stains where the water sits. It’s shitty and depressing and frustrating. That’s all in addition to whatever this caulk situation is.

I have my mammogram on Wednesday. We finally got our health insurance cards from Hub’s new corporate overlords. I opened the mail, found the card, and called for my appointment all within about ten minutes. The first they had was a week away (now this Wednesday) and I took the appointment. I am pretty paranoid about keeping up with my mammos, so I’m glad that it’s only about ten days overdue from the day I had it last year.

I was supposed to have a relaxing massage last week. I had it scheduled in between two trigger point appointments…I normally go to TP massage therapy once a month (ish). So I scheduled the relaxing massage exactly two weeks after one TP appointment and two weeks before the next TP appoint. And then it snowed, and my relaxing massage appointment got canceled. And I really really wanted it. I mean, not enough to endanger my therapist or myself, but I’m so disappointed. I knew this was going to be a difficult month (technically, it’s been a difficult year so far), so I had planned for the relaxing massage–which I never get–and then plans went pfffft. Since my massage therapist only works two days a week, there were no openings for me to do a make-up massage. I don’t know when I’ll be able to fit it in again.

I told T on Friday that I want this grief to have some kind of end date. But with every day, every month, it stays. It’s a solid burden that I carry with me every. This month is especially difficult as it’s the (one year) anniversary of Mom’s death. And with every calendar day I think of what I was doing on “this” day last year. How we had no idea what was coming. How we took her to an arboretum in the city trying to perk up her spirits…not knowing how soon it would get so bad. How it happened so fast. How I was late to Hub’s birthday dinner last year because I was with Mom and Dad helping them with something. How it was only days after his birthday that she was in the hospital and then hours later that she was gone. Grief has no end date. It plays by no rules. It doesn’t give a shit who you are or what you want. It lives and breathes and grows and growls and harps and hammers and changes and does whatever the hell it wants. And it sucks.

 

 

 

 

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