Writing difficulties and dealing with shit
***warning long read***
I have been having trouble writing my blogs. I have been going through some turmoil about my psych leaving. I have been in contact her with email but it isn’t the same. I feel like I lost a parent. Because of this, I have lost my words. Past few days, I have not been able to write because even though there is stuff to write about, I just can’t get it. It is really difficult. Before I left seeing my psych we talked about my writing and writing in general. I half want to send her a message telling her I have been having difficulty writing since she left but not sure that is appropriate as I don’t want to make it seem like her leaving is the reason I cannot write. I am so mad at the place she and I worked at because they forced out for obviously different reasons. I think this anger is what is getting in the way of my writing. She wants me to continue my care there. And frankly, I really don’t want to leave as I finally found a doctor that can work with me and has a good team that cares. That is rare to find these days.
Day before yesterday (the 2nd), I had my appointment with my TG doc (transgender). We discussed how things were going and I am pleased with the results. I sort of have a hair explosion which I knew was going to happen but damn, my legs are really hairy now. She told me that T can cause increase in sweating and OMG that hit me like a ton of bricks. I sweat really bad anyway because of my nerve injury and now it is worse. The weather has been really muggy and hot and because of the sweating, I had to go through like 3 shirts in one day over a couple of days. I couldn’t understand why I was so damn hot and now I realize it is because of hormones adding to my already messed up temperature settings. I asked her if she was going to increase the T dose and she said no because my testosterone blood level is in the “male” range. I had my blood drawn yesterday and I guess I made the cut off for running hormones as my T result came back. It was nearly double what it was in Jan. Holy crap. I looked up the normal range for males and I am close to being in the middle of it. So I will stay on the dose. My hematocrit has increased though my energy levels haven’t. Hematocrit levels shows if you are anemic or not. I was always in the 30s range. Now I am in the 40s. Thing is my numbers have steadily increased and she told me that she doesn’t want my blood to become viscous due to increase in blood production in the bone marrow. I am fine with the dose as it is. She also said that it is a time process so the longer I am taking the T, the more it will build up in my system. I felt good about that but also am a little impatient!
Before I started my blog, I had a chat with my nephew. I am so glad I can talk to him about men stuff. I had asked him about the facial hair and he said that shaving it will make it grow faster. I had wanted to hold off shaving the rest of the month to see what will grow as the fuzz around my face is becoming more noticeable but is not really dark enough yet. It is there but kind of faded. So when I take a shower today, I will shave. I might trim my sideburns a little bit. They are now past my earlobes so it will be only a matter of time before the rest fills in. One day I really want to go downstairs with facial hair just to freak my mother out. She has not been accepting of transgendered people. My brother in law’s nephew is trans and there was a period of time where we didn’t see him. When we did, he had almost a full beard and my mother exclaimed, “what the hell is on your face?!” I nearly died from embarrassment and also felt the sting of it because I knew then she would not accept me when I did grow a beard or when I came out to her. I was right about it and it still hurts. I have tried talking to her about it but she is adamant that she is “accepting.” When I was in the hospital, I had asked her during my last weekend there when is she going to accept me. Her response was in a strained voice as she said “she has accepted since I was born.” The other stuff we talked about I knew was making it uncomfortable for her. I can pick up things, I always have as I have been empathic and sensitive. We haven’t talked about it since, though she is trying to use my pronouns and name more, unlike my sister that moved in. She has yet to call me a him/he and will call me my birthname. I am glad my youngest sister is more accepting but if she messes up, she will correct herself. I am not sure if my brother in law knows I am or not. I haven’t told him and I am not sure my sister (youngest) has either. The kids (nieces and nephew) have been more accepting and I think knew before I came out to them. It has been a process for everyone. My online friends have been the most accepting and supportive. They really like the transition photos as they can see the changes. I had recently done a ten week transition post and even then you can see a change. I really don’t like my day 1 pic anymore. But I think that has more to do with me hating myself and being uncomfortable with myself for basically two reasons: I am not congruent to what I am and that my father called me ugly and fat my whole life. I do think I am ugly and obviously I am fat. The TG had the “weight talk” with me. Even though I had lost 12 pounds since I last saw her and I told her it was because of me not eating, she still wants me to lose more. I have no idea why doctors feel they have to say the obvious. I cannot stand it because it makes me feel more ashamed of myself.
I had appointments all week. Today and the rest of the week I am not doing anything. My legs are so sore from everything. Monday when I went to PT things looked good. I have two sessions left and then I will “graduate.” I have been going for nearly six months trying to get my right (good) ankle/foot stronger. I don’t think I can get the calf to loosen. It has been the most aggravating part over the course of treatment. Every time I try to stretch, I hurt the next day in a big way. I pretty much have given up on it. I have also given up on trying to get my balance better only because I need to be standing and my CRPS foot/ankle doesn’t like it. It can trigger a flare. Tues after I saw my TG doc, I had a flare and for the first time, a few hours later, I dissociated. I felt like I didn’t have a foot/ankle anymore and the pain was not there. It was very fucking weird. This lasted until this morning when I woke up at 2 am because of back and hip pain. I have gotten into this habit while sleeping to twist my upper body is one way and my pelvis/hip is the opposite. I had some pain that was about an 8 so I took my breakthrough meds and some Neurontin. When I was having difficulty going back to sleep, I took some melatonin. I now have a hangover from it but that is what coffee is for. I still don’t have mega pain and this worries me. I had emailed my psych about this but never got a response about it.
Yesterday I saw my eye doctor, which I am not going back to again. She didn’t really help me and I feel like she didn’t get what I was telling her as I really couldn’t see the letters out of my right eye clearly. No matter how I told her that, she just kept adjusting the lenses on the thing and nothing worked. Then she went to the other eye. After that she just said my prescription changed a little. I was like WTF. How the hell could it have changed a little when I cannot see out of my right eye from far away??? I had gone to see her not only for a regular eye exam but also due to my having double vision. I had told my psych as I thought it might be the Lamictal and she said it is. I needed to be under supervision to taper down the dose so she is trying to speed up seeing another psychiatrist. But after the exam, it turns out that my right eye is “lazy” meaning the muscles are weak and get worse when I am tired, hence the double vision. The problem is not problematic enough for me to have a prism in my eyeglasses, but if it gets worse, I will need it. I feel like I might need it now as I could not see just one frame the whole time she was trying to get me to see one. I kept on seeing two or the corner or half of the other frame. Again, she did not listen to me and just went on with her business. I will be seeing my mother’s eye doctor. He is an ophthalmologist which is what I sort of need. My mother confused me because she said a “nurse” did the eye exam and then he went over what they did to okay it. I tried to get more information out of her but she doesn’t know who the person is that is testing her vision. She never asks the questions just goes along with it. I am sure if the doctor said that if she jumped off a bridge would help her, she would. So now I got to get another eye exam, which needs to be on Medicare, not my eye insurance. I am not sure Medicare covers eye exams. I know the insurance that I have does but they will not cover it because I have Medicare. I am so annoyed at this. I won’t be getting new glasses until I get another eye exam. I want to make sure the prescription is right and won’t cause my eyes to strain or get tired while reading on my phone or while I am on the computer or even looking at something far away like a street sign or something. I have always known my right eye has been weak but hell, least listen to me when I say I cannot see the letters!
After the appointment, I sent an email to my psych telling her the double vision was likely not due to the Lamictal but having the lazy eye problem. I never got a response back. I then emailed her about still being in a dissociated state. I wish she would have responded but she didn’t. I miss her and it has only been a week since I last saw her.
I guess that is all. I might do a weekly blog if I don’t write every day or every other day, like I am doing now. I know it is long and I apologize. I just wanted to write how things are going for me. It has been a real struggle and my pain has not helped my suicidality. I still have my plan and I know one day I will go through with it. Just not now.