Tag: transgender

Daylight saving time sucks!

by Midnight Demon, posted in Bipolar Disorder, blogging, Chronic pain, chronic physical pain, CRPS, depression, mood disorders

Daylight saving time sucks!

Last night I was just reading. I finished Langford’s Leap by Ted Boone. It was such a good female hero book. I cannot wait for the second book to come out. After I finished that, I read this memoir that I started in December. I might have mentioned it before as a “sugar-coated” book. It is terribly written and I just couldn’t finish it. It was getting me so damn frustrated because of the drops and not explaining then going on to something else. It also used mental health and mental illness like it was interchangeable (sorry, it most definitely is not). The author never went into her symptoms so I find it hard to relate to something when this was similar to what I have been writing for a while now. It was like she was putting it out there and then just left it there. Like she would say she was suicidal or had a suicide attempt where she didn’t care if she did or didn’t die but no background to what lead up to that point, no talk of depression or despair or frustration, nothing. I especially didn’t like where she was talking about mass shootings and there was a KEY word missing in the sentence. I had read it three times and it was just bad. Terrible editing on whoever did it. I just decided to write a review and called it a day.

I then went to Harry Potter and got sucked into the wizard world. Around 0030, I finally put the book down and tried to sleep. It took a few tries to get comfortable and then out of nowhere, my damn right instep was killing me. I took some ibuprofen and Tylenol. I couldn’t figure out why it was hurting so bad. I had only got up once to stretch the whole time I read, and there were at least 3 or 4 hours where I was just on my bed. I finally decided to put some diclofenac gel on and then I realized why I was hurting. The golf ball size swelling had moved up my foot and was very inflamed. I don’t know if while lying down the weight of my other foot set it off or what. I had got up around 0130 and realized that in a half hour, it was going to be 3 am instead of 2 due to the time change. I wasn’t looking forward to that because it was going to throw me off. Next thing I know it is 4 am because I decided to read Harry again to wait for the meds to work their magic. I fell asleep somewhere around 0430.

I woke up a few hours later because my mother got up. She is not quiet and her breathing is very labored. As much as I hate the woman, I care for her wellbeing, though I try not to as she doesn’t listen to me anyway. Her breathing is like she is puffing the air out of her lungs. Her COPD is worse (though she will say her knees are causing it). She doesn’t use her inhalers at all. She had paid for a nebulizer and used it maybe a week or two. Now not using it all. Her breathing was slightly better than it was but now without the medication, she is back to her huffing and puffing. I have to listen to her as she climbs the stairs every night just to make sure she doesn’t collapse. I am hoping that when my sister lives with us, I don’t have to worry so much. I wish she would just move her bedroom into the dining room but nope, she doesn’t want to give it up despite her not using it for anything other than her gatsies (little trinkets and things just used for display). I understand her mother gave her those things, or rather were my grandmother’s things before she died but all it is doing is collecting dust. Today she refused to yield me any fucking space to put my mugs yet wanted them in my room. Fuck, seriously? Seriously. She wouldn’t allow me to keep things even though I would like space to. She is just so fucking selfish when it comes to the house, this is mine and that is mine so you can’t use it. Meanwhile she nearly burnt the crap out of my new kettle because she didn’t put enough water in it for making her coffee. She leaves water in it so the bottom of the thing is starting to rust. That is okay though…because she didn’t buy it. I am ready to buy an electric water kettle just so she doesn’t use mine and can do what ever she wants, which she does anyway. I just get so fucking frustrated because she tells me how to live my life, doesn’t use my changed name, doesn’t respect me in any way, shape, or form. Today she had the gall to say G or my birthname or what ever you are. I got mad and said what am I to you, two different people? Then she spewed that she has been calling me my birthname for 40 years so isn’t going to change. Fuck you too. I don’t know why the fuck I bother. I get so hurt and she doesn’t care. She is so transphobic.

I wanted to change my sheets today but my CRPS foot is giving me grief. It has been snowing and raining most of the day so that is probably why. I ordered take out for the first time in a few months. I wanted a burrito but the place didn’t have drivers so canceled my order. I was disappointed. I ordered a burger from another place. Now both feet are killing me just from going up and downstairs. I fucking hate being in pain all the fucking time. It is the biggest trigger of my suicidal thoughts. I am still thinking of my plan. I don’t know if I will go through with it but it is on the backburner. Tomorrow I am seeing my PCP’s social worker to work on some financial planning and things. I hope that she can maybe speed up the process for therapy as I am really needing to talk to someone about things. I know I have this blog but sometimes actually talking to someone helps unload things. I don’t want to call my friends because I don’t want them to worry or be mad at me. Just sucks that even though the majority of my friends accepts that I have depression, some are not so accepting that I have suicidal thoughts and plans, even if it is just to hear me out. I no longer bring it up with them. I guess it is a “don’t ask, don’t tell” situation, which really bugs me. As many times as I have had trouble with therapists, it is the same. No one wants to truly hear how dark my thoughts are. Makes me feel more alone with each passing day. I know there are people out there that say “you aren’t alone” but when you are chronically suicidal, you really are. I just wish I would go through with it so it will end.

Feeling ill with no sleep and little appetite

by Midnight Demon, posted in Bipolar Disorder, blogging, Chronic pain, chronic physical pain, CRPS, depression, mood disorders

Feeling ill with no sleep and little appetite

I realized when I got on my laptop today that it has been almost three days since my last post. It has been difficult to write because I haven’t been sleeping well and pain has been a bitch. Also been feeling under the weather the past few days and not sure if I am getting a cold or what. My voice has been all over the fricken map. I think I am going to email my doc and be like when is this going to stabilize because I can’t stand one minute I have vocals and the next I don’t or sound like a frog! I know this is a process but I thought it would be gradual progression not a constant up and down thing. I did a pic on IG. You can definitely see a change and my chin is being more defined. Just wish I could lose a little weight to get rid of the fat under it.

I have been trying to eat but lately I just don’t feel like it. Not sure if this is mood related or because I am just not feeling well. One minute I feel fine and the next dizzy and weak. I’ve been at least trying to increase my fluids but even that is difficult. I was supposed to see my psych today but I didn’t fall asleep till almost 7 am this morning. My sleep has been so fucking awful. I am not sure if my last post said that a social worker called for a phone eval for a therapist. I thought the social worker that works with my PCP was just going to outright refer me to someone and then they would call me. Now I got to wait six weeks to find out if they will take me on. Fuck. It doesn’t really matter any as right now I am having so much trouble walking and going out it isn’t funny anymore. Since my double appointment last week, I have been recovering. I thought I was okay but Tuesday I had gone out after putting my groceries away and I guess that was too much. My right calf is just horrible and the more I try and stretch it or walk, it just kills. I also had cramps in my foot the other day which freaked me out. I have been sleeping with a pillow between my legs since because I think my left foot has been pressing on the golf ball, causing it to cramp because I have overused the muscles so much. I really don’t like this going to one appointment or go out for something, like getting my haircut, and then being immobile the next few days. I really can’t limp on either leg for support because that just makes it worse. When I am downstairs I use the walker to get around so I am not putting so much weight on my legs. I still sort of limp unconsciously. Then the heel pain jacks up and I really am done. For two days, my CRPS pain was down the lowest it had ever been. I think it was because the heel pain was so high it couldn’t process the other pain. Well, last night while moving the pillow under the sheets, I “hit” my big toe on the CRPS foot and set it off. Then I moved my ankle two hours after taking the breakthrough med and I was up all night. I was so fricken tired I couldn’t get comfortable. I was playing with the pillows, turning it this way and that, then switching to the body pillow but couldn’t get that right either. I was so fucking annoyed.

I was supposed to go do an errand for my mother today but because I haven’t been feeling well, my mother did it. I forgot to renew my T-pass for the month so will have to pay when I go out again. I am hoping I can go to the Square tomorrow to get the ground beef I need for my barber’s dish I been promising him. Then I have been waiting for two bills to clear my checking account only to find out I never paid them. I think I paid the majority of my bills in the early morning on Wed when I got paid, went back to sleep with the thoughts of doing it when I got up, and forgot. Oh well. I am glad I paid today because one of them was due tomorrow. Oops!

Because I am not seeing my psych, I have been emailing her to try and get the Lamictal called in. I’ve sent her two emails because Sunday is my last dose and I don’t have anymore. I hated cancelling but I really didn’t feel well and will being up all night, I didn’t think it was a good idea. If I have to, I will try and Uber to my PT appointment Tuesday. I hope that this PT regimen will pay off because I didn’t have as much calf pain as I do now since the whole stretching bullshit. I have had to modify how long I hold the stretch to just ten seconds and rest a bit before doing another. Last night I got so annoyed, I just did two stretches and think I positioned the belt wrong because my ankle flared up. Like WTF. Seems like every time I do something I have one step forward and ten back! I just decided I am just going to do what I can to try and get my ankle and foot functioning but it is so damn hard when pain stops you. The heel pain is so fucking intense it literally consumes the whole of you. I’ve never had pain that bad before, aside from the CRPS pain, but this is probably worse! Least the pain meds are controlling the CRPS pain. I have been taking ibuprofen and Tylenol for the heel pain. Nothing else seems to work. There was a study on using these two together to reduce pain after hip replacement surgery. Pain relief was only for three days but I will take it if it calms it down enough for me to do the exercises and not flare it back up. Standing after I have been reclining in bed for a while is the worse because my CRPS ankle bones feel like they are being crushed and that pain takes a while to subside before I can put my right foot down, while then my heel starts hurting. How I have been walking is beyond me. Maybe I should consider a cortisone shot though it goes against my beliefs. I had one cortisone injection in my wrist many years ago and it helped the tendonitis pain I was having. Maybe one shot will do the trick and then I won’t hurt so much. I got the new ankle brace (the 4th one I am trying). I didn’t realize it had straps to go underneath. That might aggravate the golf ball and heel. I will have to try it out. Just getting up the nerve to use it. LOL

tg issues, weekend, and sleep

by Midnight Demon, posted in Bipolar Disorder, blogging, Chronic pain, chronic physical pain, CRPS, depression, mood disorders, transgender

TG issues, weekend, and sleep

To my regular readers, I apologize for not writing as often I should. I am in the throws of another depression brought about by who knows what but I am pretty sure it has to do with my mobility issues and not being able to go to Starbucks as much as I would like. To further complicate matters, there will soon be a bridge on the main road taken out to accommodate the new public transportation line that the scum bag mayor wants. It will be a longer route to the Square (I am told by a friend). This will be the middle of March and will supposedly last for a year. I have never seen bridges taken down and rebuilt in a year’s time so we’ll see.

I also have sort of lost interest in blogging. I knew if I stopped blogging every day this would happen. And it happened. I think there were three days where I didn’t blog or just posted a pic. But it is hard to continue to write when there is little to no feedback. For a while I was writing just for the sake of writing. I kept track of my stats and there were few people who read the blog for that day or the day after. But no likes or comments. I thought I was okay with it and part of me is, but there are some days where I feel like no one will care if I just stopped writing. Hence my little hiatus every now and then. Some days I just write to give an update on what is going on. I hardly every write a blog about the chronic pain and how awful it is. I might but not in the moment because I can get suicidal very quickly, if I am not already suicidal. So if you don’t see me post, this is why. I am either in a rut of depression or I just am not up to blogging.

I’ve been thinking more about top surgery. I asked my sisters what did they think and my youngest was like if you have it done, I need to know so I can take off work. She didn’t care, I guess. Then she asked me if I wanted to be in more pain than I am in. This further made me realize she has no clue about CRPS and how it is. I most likely will be in pain post op from my surgery. But it won’t last forever and I will eventually heal, maybe have to go to PT for a bit, and then be who I am meant to be, provided everything goes according to plan. So, in reality, the decision is mine and only mine to make. Still would like to have some support on the issue, which is what I was looking for. I don’t think “hurry up and give me a date so I can take off work” was what I was looking for.

My middle sister will soon be living here with one or two of her kids. I am not sure. But this is going to be stressful because my sister yells at her kids all the fucking time and has no respect for others but herself. I am hoping she will be living with us just long enough for her to save up the money she needs to get an apartment for herself. I also hope they don’t think they can turn my office into a bedroom because that isn’t going to happen! I am not looking forward to this. The only benefit will be that she will help my mother more than I could, in regards to doing the laundry and dishes and maybe dusting. With these changes, I am not sure I will go ahead and have surgery as it will be quite crowded in the house.

Since Thursday, I have been recovering. Yesterday I went out to get a few things at the grocery store. Last week my sister bought me 5 powerades and they were bad. They were supposed to be lemon-lime but tasted like orange. One I had to throw out because I felt like it was burning my tongue. Another one or two, I diluted with water and that was okay. So yesterday while I was at the store, I bought a few more and looked at the lot number to make sure it wasn’t the same. It wasn’t so I bought three. I also bought my coffee that I was out of.

I pretty much had a resting weekend. Yesterday when I was doing my PT exercises, I still couldn’t move my foot outward without pain. I haven’t tried to do my exercises today yet. I still need to fill my meds boxes for the week. I am officially off the Trileptal. I am kind of sad about this because I have been on it for so long and now I am no longer on it. I hope I won’t have withdrawal symptoms from it. My psychiatrist and I went very slow with it, like we are doing with the Lamictal. I started with 100 mg last week. I think it is adding to my constipation as it has been really hard to go since I have started it. Usually fiber pills save me but even then it takes a few days to work and then I feel awful. I still haven’t found the right combo. I had take two senna today and still nothing! Hope I go later tonight or tomorrow. I hate being backed up.

New PCP and of course, pain

by Midnight Demon, posted in Bipolar Disorder, blogging, Chronic pain, chronic physical pain, CRPS, depression, mood disorders, transgender, writing

New PCP and of course, pain

I had two appointments today, one for PT and then another with a new PCP. PT went okay. By the time I reached the train station after, I had to take off the support for my ankle I was wearing. It was causing too much heel pain. When I got to the hospital for the pcp (primary care provider) appointment, I took some pain meds and ibuprofen. My heel felt like it was being split in half. I have no idea how I endured this much pain without passing out. I used the walker as I navigated the hospital. I only went in the hospital rather than the streets because it snowed last night and I wasn’t sure how the sidewalks would be. I also didn’t want the wheels to get salt on them.

I was seen rather quickly. I was met with a social worker and the doctor. They introduced themselves and told me more about the transgender program as well as the services they provided. They offered counseling and I asked if I could meet with someone as I was having difficulty with my current one. I did mention that I was having mobility issues so it was okay if I didn’t see them right away. I also asked her if there was a way to deal with financial issues as I really would like to start saving some money a month but currently I can’t because I am an impulsive spender due to my mental illness. She said we could meet to work it out. She said she would set up the time and then send me a message when she did as she didn’t have her calendar in front of her.

She left and then the doctor examined me while talking some more about things. He agreed to take over my pain management. I was so happy. He asked about top surgery and we talked about it for a bit. He said I would need a note from my psychiatrist before I could have it. Then it would be some working with my insurance to pay for it. I am excited about this but as I was emailing my psych to tell her about him, I kind of realized I don’t know if I am as ready as I think I am. I mean, things have been moving so fast since Oct. I am not sure I want to have surgery after being on testosterone for only four months! I haven’t really thought what it will be like after my chest is gone. Don’t get me wrong, I want these guys gone, but I am sort of attached to them! It is weird. I have to think about it some more. I do kind of wish I had my therapist to talk to just to bounce ideas off him. But I don’t right now. I don’t have anyone to really talk to about it that isn’t coercive about it. The social work did mention a group that is at the hospital that is just transmen to talk and support one another. I am going to look into it. It would be nice to meet others going through this that are around my age. We joked about it as I often get the younger look and I am not that young! She said she was a few months older than I was. I found that funny because she didn’t look her age either!

I haven’t heard back from my psychiatrist but I see her next week. I feel like she is my only support right now as I am not seeing my therapist due to mobility issues. This is the first time I have been without a therapist because I couldn’t walk to their office. Makes me miss my former therapist all the more because we had phone sessions. I have no idea what kind of therapist the social worker has in mind that I see or where. The hospital is a huge place with office space all over the area. I can talk to my psychiatrist, she is easy going about it. I just don’t know if I am ready for the conversation with her. We have never discussed this subject before though when I asked her to change my sex on my license, she was more than willing to do so. She is okay with me being a different sex for than when she first met me 26 years ago. I really wonder if they ask kids how they feel about themselves if they have problems. I know that if I was asked when I was 19 or so if I felt comfortable being a female or not, I know I would have answered yes. I remember having to go through a pap smear even though I wasn’t sexually active and then being placed on birth control pills because I have polycystic ovary syndrome (PCOS). I asked my psychiatrist treating me in the hospital if it would change me into a woman, basically, but I couldn’t bring myself to say that because I didn’t want to sound crazy. When she read my memoir a couple years ago, she said it made sense now rather than then and I saw her for three years. I don’t know if I would gone through transition then as my mother was not cool with my sexuality. But she isn’t happy now with me being me either. I just don’t know about what will happen when my boobs are gone. I have thought about it in passing but now that the surgery is like yeah when do you want to talk to the surgeon, I am taken aback. I guess part of me is still waiting for someone to say to me you are a female not a male get with the program or something. But I can’t help but feel masculine. I don’t like being female. I am not female. I am a male. I just don’t know about things right now. I think I want to wait till I feel comfortable talking to my psych before I talk to a surgeon.

I have my friend’s husband reading my Darkness Always Wins book. He is giving me some insights into it. He is honest about it but I can tell it is hard. I just bluntly write shit. I guess that is why my story hasn’t been written. It also doesn’t help that the T is redoing the bridge on the main street that takes me to the Square. I am so upset that I won’t be going to Starbucks as frequently as I was. Since my therapist and I have halted sessions, I haven’t been to the square as much. I am so depressed about this. I don’t know what I am going to do about it. I might have to seriously have money put aside for Uber (and stick with it!) just to go to another Starbucks that is hard to get to due to a long walk. On days I am okay, it might be okay to walk that far but on a regular basis, no way. And I would seriously have to commit to writing on my story and not play on my phone while there. I want my brain emptied! So to speak…