TG short post

Hi all my lovely readers,

I am really sore and in a middleweight now so today’s day 1 post will be tomorrow.

Injection went well. I am just mentally and physically drained.

Thanks for reading

Anxiety and not knowing it (my list of worries)

Anxiety and not knowing it (my list of worries)

Last night I was up due to a flare. I had done way too much and was hurting. I couldn’t sleep so I was thinking a lot of things. I pondered about stuff that happened during yesterday’s PT session. I realized then that I have a shit ton of anxiety that I am not even aware of most of the time. I think about things and think often of the worse. Like my PT was telling me, I didn’t re-injure myself, that it was just the muscle being overworked because I did too many reps of the strengthening exercises she was giving me. It took her most of the time to reassure me that I was okay. I didn’t resprain my ankle. What I was feeling was the muscle hurt because of overuse. She also reassured me that I was NOT getting CRPS in that foot because I injured it.

I never knew how much anxiety I was feeling. I never do. It’s always a million thoughts and worries and last night I started writing about them in my journal and there was a lot in those three pages I wrote. I am sure if exhaustion didn’t kick in, I could have probably finished the journal off. There are only about 10 pages left and then I will start another one. I really need to write more about this because I don’t think it is going to get better otherwise. I was reading an article about anxiety and ways to reduce it. One of the things mentioned was writing in a journal. I have noticed that when I can’t sleep and write down my thoughts, whatever they are, either in my blog or journal, but mostly journal as it is pen to paper, I feel more relaxed and can often go to sleep afterwards. I had been in the habit of writing in my journal since being disabled. Sometimes I would write three times a day, between my day and night journals. I have one I take with me and write in when I am at Starbucks or have some down time between appointments. Then I have one on my bed so I will write when I get home if I am frustrated and before I want to sleep. I kind of got away from it and it was only during times I couldn’t sleep that I would write.

Thing is, I am not really aware how my thoughts are affecting my emotions and causing me to be tense. I really have a disconnect between my emotions and feeling them. Most of the time, I don’t feel anxious. I feel calm but just worried about things. Like my mother and her rehab, my upcoming pain doc appointment, being in pain, wondering what my PCP is going to do/say when I see him next, etc. I also worry about my sisters and what is going on in their lives. I have a lot of these thoughts and then dealing with my cousin last night that pissed me off because he was flipping out over the weather. Not kidding, he was cursing because it was going to rain today. I have never seen him flip out before over something so stupid. He just made me so annoyed. I knew I shouldn’t have picked up the phone.

Then I worry about my country and the assholes that are ruining it. Also because of the Supreme Court nominee, my sexual abuse stuff has been stirred up big time. I can’t seem to stop the memories and the feelings attached to them. I haven’t told my therapist this. I want to get through this pain doc appointment first. And then you have the worry thoughts of going on hormones next week. While I am thrilled about it, I am thinking of every little detail of how this shot is going to be played out. I have a few hours before I see my therapist after the nurse shows me how to do it. I kind of want to give it before the appointment but worry I won’t do it right. My biggest concern is how to extract the contents of the vial without bending the needle and not breaking the vial because the damn needle is bigger than it. I am not supposed to bring the med with me but I am so the nurse can advise me on how to do this. I will feel better if she sees how small this vial is and how big the needle is. I might be worrying for nothing (anxiety talking) but I think it is a legit concern. I have spoken to a few of my friends who were nurses before they were disabled. They say it will be fine. I would kind of feel better if I had a smaller needle so I can extract the stuff, especially the last bits to make sure I get the correct dose when the vial is almost gone. The syringe I have is okay. I can figure out how the markings and stuff. I used to be a medical assistant so know how to draw but fuck. This is not for a patient. This is for me. And I will be injecting into my muscle!! I am kind of worried about that, too. I know it is better than gels or creams but fuck. I never gave myself an IM injection before. Subcutaneous, yes. We did that in school. It was nothing. I am not afraid of needles but this one is directed toward me. UGH. Sorry, I just realized I am going on and on about this. I must be more nervous about this than anything. But hell, it is got to happen if I am want to be more masculine. I am in the wrong body. I haven’t told my mother. I am not going to because I don’t want to hear what she has to say on the matter, which I know won’t be positive. I can’t deal with her about it.

I have been listening to Mary Chapin Carpenter because she can calm me down. She has such a soothing voice. I haven’t done a thing all day. My mother made pancakes so I will have that in the morning. Maybe I will make some bacon to go with it. I haven’t had her pancakes in quite some time. Only three games left in the regular season. We play the Snakes (NY Yanks). I am hoping for at least one win in the series. Post season starts next week. It will either be Oakland or Snakes. Hoping for Oakland, sort of only because I don’t want to play the snakes!!

Feeling tired after a long day

Feeling tired after a long day

I woke up early, a few hours before my alarm because I had to move but it was not easy. I was in pain from the position I was in. I turned over carefully and slightly went to sleep, only to wake up because that position caused my elbow to hurt. I moved it to stop the hurt then my med alarm scared the shit out of me when it went off. I was not expecting it at that moment. I got up to take my meds and use the bathroom. I have no idea if I brushed my teeth or not. I was so groggy and just wanted to sleep but I had stuff to do.

I went back to my room and laid down for a bit. Then I remembered I had to do an errand for my mother and I cringed. I had to get up now if I wanted to shave my head and get ready to go out. I did and left the house around 11. I didn’t get home till around 1730, a good 6 hours or so later. I swear my ankle had gone out on me at least two times. When I got to my psych appointment, I had to take off my aircast.

The orthotist fixed my brace a little bit. He gave me some moleskins and some sticker things for the grummets so they wouldn’t cause me sores. He encouraged me to find a taller sock but I think I have a few old socks that I can just cut the foot off and use the tube part so the AFO rubs against that rather than my leg. It will add some worth in the winter months. Not so great in the heat though, should we have another heat wave burst. I had woken up with my back aching because the temp dropped like 20 points. My spine didn’t like that one bit. It is supposed to be in the 70’s the rest of the weekend and I hope I can bake.

After I saw the brace clinic, I went to get Thai food for lunch. I almost ate the whole thing. What I have left is just a snack. I thought I would eat it after my psych appointment but I was still full. My psych appointment went well, though our next appointment won’t be in a month. I am shocked. I said I can still contact you, right? She said yes. She refilled my scripts. She was worried about my weight as it was up a few pounds since last year. I am not worried because it goes up and down. I have been gaining and losing the same five pounds for years. Since the Invega I did gain a little but I seemed to have leveled off. I just haven’t been successful in losing weight, which is hard to do when you can’t walk. We talked about weight and she wanted me to get weighed the next time I see my PCP. I told her I would. I hate getting weighed. It always leads to uncomfortable conversations. I have no idea how to diet or “eat right”. A friend of mine said that I should cut carbs. I have no idea how as I eat a lot of bread. She said that instead of having two slices of toast, eat one. Being Italian, bread is like part of the 4 food groups. We have bread with almost every meal. I have been trying but it’s hard to break out of the habit, especially when my mother or sister buys bread that is fresh from the bakery. Last night I had crackers with cheese. Crackers are carbs. So see, I got a carb problem, but the human body needs carbs so…I am stuck with weight.

I asked my psych if I could go ahead with the transition now that my pain is somewhat controlled. It might not be what I want it to be but it is better. I just wish the flares and ankle give outs would stop. So Monday I will be calling the LGBT clinic and making an appointment with the doc I was seeing there. I just hope they have an appointment that isn’t in Nov. I don’t think I can wait that long, again.

transition appt and other things

Transition appt and other things

I’ve had an early day as I woke up around 5. I decided to stay up as I needed to get up at 7 to shower and get ready to leave the house the latest at 815. I played with my phone, talking to a fellow tweety buddy about stuff. I had woken up with spaghetti arms and she never heard of the term. I explained that it was a side effect of my antipsychotic medication. It doesn’t happen often but it does happen now and then. Around 6 I decided to heat up a burrito and then shower. For some reason, my heating method didn’t work as well as before as parts of the burrito were cold. I might have to use the second side at 40 seconds rather than 30. I had a glass of juice and then hit the shower.

By the time I was done, I was wiped out. I had about 45 minutes before I had to get dressed so I decided to risk laying down. I set my alarm and when it went off, I didn’t want to get up. I laid in bed for another ten minutes before getting dressed and leaving the house. It was sunny out and a little chilly but it would warm up a little by the time I got home. I just caught the bus to the station. While I was on my way, my friend texted me saying that she couldn’t meet me because something came up. She felt bad as she was looking forward to seeing me. I told her not to worry. I will be having frequent trips to the health center so there will be other opportunities.

The appt went well. I asked him what to do with the one female hormone I am taking to stop my periods. He said once I start testosterone, I can switch to a progesterone only pill until the T builds up in my system to adequately stop my menses. I might have a period or two while adjusting. He needs to talk to my psychiatrist and therapist and then I think by next appt, I could be ready to go for T shots. It will be weekly and could take as long as 6 months to show changes because of my age. I asked about top surgery and he said that can be discussed once I have begun changing. He asked if I wanted bottom surgery and I said no due to my nerve injury. I still don’t know how T is going to affect my sex drive or how it is going to be. I am kind of worried because when I was sexually active (some 15+ yrs ago), after my nerve injury it was very painful and I hated it. Since I have been out of that crummy relationship, I have not been with anyone. It’s so damn hard because even my urine is fucked up some days. Like the other day it was like all I did was pee. Then the next day, I hardly peed at all, no matter how much I drank. It’s so frustrating.

With the length of this transition, I am kind of thinking of how my plan is going to be and what to do about it. I haven’t put anything in motion, mostly because I haven’t been up during business hours to place phone calls. I emailed my psychiatrist in a kind of panic email about all of this as I was in a pain flare and basically going nuts like I do. I just get so overwhelmed with anxiety during a flare, like the world is ending kind of feeling. I also become more suicidal as I want to escape the pain. I don’t want to live anymore if I am supposed to spend the rest of my life in horrific pain every single day. I don’t know if it will be worthwhile going through the transition or to start it. I don’t know what to do. I keep thinking it will pass and I can manage the pain again, but then there are days where I am set in my ways and I want to go through with it. I still have time as it will take some time to organize things. I have no deep rush. I do know it will be sometime this year. I just don’t know when, specifically.