I’ve done my errands for the day. Now I can take my pain meds for my ankle. I don’t have to drive anymore. Today is National Burger Day so I am thinking of ordering my favorite burger from my pizza place. It has avocados in it and I love it. But the rest of the Chinese food that I had for lunch really filled me up and the heat is making me sick. I don’t know if I could eat anything right now. Maybe later. It’s close to 90 degrees in my room. I have to bring that temp down if I am going to be comfortable. I feel like I am burning up.
I was talking with a fellow blogger today. We get a long really well. I hope the situation she is in gets better. She suffers from depression, like I do and it’s interfering with her getting well, or at least doing stuff around the house. I just want to tell her to leave it, so it doesn’t stress her out but I understand how things can pile up and then become unmanageable. I did some cleaning around my room today, which made me feel good. If the recycle bin wasn’t already overflowing, I would throw out what I have collected. It’s just old water and powerade bottles that have missed the basket. I didn’t realize I was such a bad shot until I moved stuff around so my brother in law can install the AC. Good thing I don’t play professional basketball! I’d stink like yesterday’s garbage.
Meeting with my father was interesting. He was in an aggravating mood. Damn guy just wouldn’t keep his hands to himself. Kept fake punching me or moving his papers so I couldn’t see my phone. God, he is so fucking annoying. But he needed to have his blood drawn today. I probably will get results hopefully tomorrow. I hope they are normal. Last time they were high. Before that, it was low. I give up. I just do what they tell me and then relay it in child speak to my father. 83 going on 5. Bastard is probably going to live to be 100. And why not, he has me doing all his medical stuff for him to keep him alive. I bring him to the best doctors (aside from his PCP, who is a jerk). But to him, I am just his secretary. Next week starts his other stuff that I won’t be too happy about. Every Thursday in June there is a medical appointment for him. God help me.
I really am feeling low and sick. Heat is not my friend. Since my nerve injury, I have grown intolerant to high temperatures. I hope this doesn’t mean I am stuck in my house until the heat wave is over, once the AC is in. I will venture out for my mocha. I think it’s going to be cooler next week. I hope so anyways. It’s not even June yet and it’s humid and yucky out. So shoot me if I am the first person to complain about the heat. Least there is a cool breeze now and then. I have my window open to try and air out my room and get the air circulating. I am really miserable.
I called my therapist today and asked her to answer my text about the abuse and whether I should write about it to her. She still hasn’t answered me. I hope she got the text. Both our phones have been acting up lately. My phone is having trouble answering phone calls. I ordered a new phone today. I will get my glasses next month. I need a lifeline and it is my phone. If I can’t get phone calls, what the hell is the purpose of the device? Today I was trying to call my father and the damn launcher crashed. I couldn’t do anything until it went through it’s shut down phase. Then things were alright again. It just kills me that this is happening just three years after my last upgrade. I guess the phone is only as good as the OS (operating system). I know they came out with a newer Android OS. It is on the newer phones. My cousin has the S5, which is what I will be getting. I can’t wait to use it. But it won’t come until possibly sometime over the weekend of next week. I had to order it because they didn’t have the phone in stock. It was kind of a hassle because they wanted me to “lease” the phone and I didn’t want that option. I wanted a 2yr agreement. Turns out I saved a dollar by ordering it in the store rather than online. Too funny. I complained about the customer service being not too friendly with my request. I hope that I have everything the same as I do. I know that I will be paying a little more each month with the new upgrade, but to me it’s worth it. It’s my phone and I can do what I want with it. I just hope I can do what I want with it, like putting music on it and such. The phone is going to have a 64GB external SD card so I can load my pics and music. I should probably do that tonight so I don’t have to do anything when the phone comes in. Just plug in and hope it all works!
Therapist just got back to me. I have some writing to do that is not going to pleasant. Writing about past abuse rarely is pleasant. I won’t go into graphic details because that could be triggering. And I am already a little post, PTSD with my foot. Because I couldn’t move my toes the other day, it set me off big time. My anxiety was through the roof. I just am now back to my “normal” level of heightened awareness. Plus, bruising my last toe pretty good really got me freaked out. I think I will wait a few days. I don’t have to have this done till at least Tuesday. That should give me time to think about what I want to write and stuff. I just hope it is helpful to me. I also know that I don’t have to do this. My Ativan supply is limited until I get a refill next week so I really have to think about what I want to write. Ativan is the only med that helps with my PTSD symptoms, which is mostly anxiety and overthinking. I used to really be on guard every time my foot swelled up and I couldn’t move my toes. I would think that I was getting CES again but I would have no other symptoms such as numbness, pain in the legs/back, loss of bowel/bladder, etc. But I would just go nuts and flip out. The Ativan has helped me so much that I don’t flip out as often anymore. I don’t take it all the time, just when I need it. The funny thing is, it really is just my brain on fire when the symptoms of PTSD occur. I really have to ground myself with distraction, or talking with the voices (mostly because my agitation level is up) or I have to take pain meds to quiet the pain flare. It doesn’t happen as often anymore, but when it does, I am a wreck. I have to continually tell myself it isn’t going to happen. It’s hard because the brain wants you to go crazy and you are fighting yourself with not going crazy. I hope this makes sense.
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