Chronic Pain is No Joke

Chronic pain is no joke

It has been a while since my left foot has been acting up. The last two days have been really bad. I think it is because of the weather changes, temps going from 30 to 60 always wreck havoc on me.

Though I have had a rough day, my thoughts right now are focused on my foot and its throbbing. I seriously want it to stop but there is nothing I can take to calm it down. I already took my pain meds two hours ago and can’t take another dose for another two to four hours. I am in such agony that I want to cut my foot off. I don’t have any power tools in my room so that is a good thing. And I can’t bear weight on my foot so I can’t get to the basement where there are the tools that I need. I hate being in so much pain.

I didn’t do much today, in the way of walking or standing. I did stand a lot yesterday, which is probably why my foot is killing me. There were a bunch of kids at the bus stop yesterday and I couldn’t sit down like I normally could. And it wasn’t like the kids were going to let me sit down. They were running and jumping all over the place. One little kid was actually looking at me like I had ten heads when I decided to move to another spot while waiting for the bus. It was like I wasn’t supposed to move. Now I am paying the price in increased nerve pain and physical pain. Plus my foot is swollen so that is NOT helping my case at all.

I am so tired but I can’t sleep because of the pain. My foot needs to settle down to at least a 5 on a scale of 1-10. Right now it’s a 9. I am glad I already took my night time meds because to get up again will be torture. I just hope I don’t have to go to the bathroom any time soon. Going down the stairs will kill me.

Why does my foot hurt? Because it is an asshole. But seriously, no one knows why. I have nerve damage in my foot and a little of what is known as Complex Regional Pain Syndrome (CRPS). I got the nerve damage from a ruptured disc thirteen years ago. Then I got another ruptured disc five years later but at a different level. I have had many problems with my left leg, mostly stemming from my back. I have herniated discs throughout my lumbar spine. I just hope that me lifting and carrying three cases of sprite didn’t hurt me in anyway. I will find out tomorrow. I know my arms are going to be sore.

THROB THROB THROB. That is all my foot does to aggravate me and put me in a bad mood. And there is nothing I can take for the throbbing. I just have to wait for it to settle on its own. Sometimes, if I feel like it, an NSAID gel will calm it down. But right now, I can’t touch my foot. Just the sheets on my bed are bothering it. It is that sensitive. I also love how all the veins in my foot are popping out like no tomorrow. Another sign that it is CRPS. And my foot is so hot, like it is on fire. I wish I had a fire extinguisher for it but none exists. That is what kills me all the time, the burning sensation in my foot. So I have the throbbing, burning, stabbing, bone-crushing pain going on. I really want to lob off my foot. I could cry but I am not a crying guy.

day gone wrong

I had a long day. I thought I had an appointment with my neuro but apparently due to major miscommunications, it was yesterday, not today. I went there for nothing. No matter because I am cancelling the appointment on Monday. I am not going to miss an appointment with my therapist because of an incompetent office staff. I even called to confirm that I had an appointment today was told I did. I am beyond pissed and this isn’t the first time this has happened.

I started writing about the darkness and then got so aggravated I couldn’t think of what I wanted to write other than what an asshole staff my neurologist has. I will work on it this weekend. I am still in a bleak mood and as long as that doesn’t change, I think I will be fine for writing more on it.

In my frustration, I emailed my editor and blasted her with an ultimatum, either work on my stuff or I want a refund. She said that she will be working on my stuff this weekend. I hope so. I had to wait so damn long and she better be pristine. Or I am going to be more pissed than what I am right now. If we work this weekend, I can still get this hopefully printed by the second week in April. I won’t be able to have copies of it for the AAS conference but that is ok. I didn’t think production would happen anyways for that. Looks like I can’t back out of it now.

Last night I had some hallucinations that were not fun. Ever since my cousin told me about pink slime, I have been having paranoia about eating hamburger meat. Last night I was hungry as I skipped lunch and I bought hamburger patties. The voices got so insistent that I was going to die from eating this burger it took the enjoyment of eating a burger away. I still am having the same voice telling me there is pink slime everywhere. I am trying to ignore it but this voice is one of the annoying kind. I have to take some trilafon to make it go away. Or I am not going to be able to eat anything, even if I make it. Even as I was eating my burrito today, the voices were calling the guacamole pink slime. I was getting disgusted so only hate half of the burrito. Now I don’t know why these voices have crept up. I know I am a little stressed with my book and all. And today was a real annoying day. My cousin kept on calling me three fucking times just to bust my balls. I kept telling him I was annoyed and didn’t feel like talking but he kept on calling. And no use trying to just have him talk to voicemail because he will start calling my mother’s phone and bother her. I kid you not. He is the literal meaning of pain in the ass.

I cried today because I was so upset with my neurologist’s office staff. I know I am going to get charged for missing the appointment but I am NOT going to pay it as they gave me the wrong information. Plus no one called to confirm the appointment and they usually do, 48 hours before the appointment. So they can just stuff the payment up their *****.

I am relieved the editor got back to me and will start working on my book tomorrow. I was really starting to think she took off with my money. Now I can relax a little bit, least until the edits come in, LOL

Pink Rectangular Pill

It begins with the shakes. The creepy crawly feeling that you hate. You are not shaking but it feels like you are. All the side effects of the one pill that keeps you sane. Small price to pay for if I miss a dose or don’t take it, I end up in the hospital because the psychosis strikes with a vengeance. The voices have gotten worse as I get older. Luckily, there is something I can take to stop the quivering and restlessness that I feel. But I have to wait till it takes effect thirty or so minutes after I take it. Thirty minutes is a long time when you are feeling like you are crawling in your skin. It drives you crazy. Sad part is that I am not even tired despite today being a long day for me. I watched a movie for the first time in months and actually had the attention span to watch it beginning to end.

The small pink rectangular pill. That is all that makes me sane and crazy at the same time. And it sucks being like this, this crawling in your skin type of feeling. I rather deal with the elastic ball type of feeling where I am being stretched out. That is more tolerable. But I can’t pick which side effect I want. I rather have none but, like I said, it’s a small price to pay. And as long as this isn’t permanent, I am good. I think tonight it started when I noticed the increased in saliva production. I have been drooling a little bit for a while but it stopped too, for a bit. This is the stuff I go through that no one really knows about except for my therapist and psychiatrist. No one else really understands when I say I feel like a rubber ball being stretched out. That I feel like I can’t stand being in my own skin. I have not felt this way in sometime. But then I also have been lax in taking my other white pill to counter act these side effects. I only take them when I need them so if I am not having side effects or feeling symptoms of PTSD, I don’t take it. My doctor trusts me with this judgment. She is not a pill pusher like some docs are. We have a good relationship.

When I feel this way, I can’t help but think bad thoughts. Thoughts that are self destructive. Thoughts of how I wish to be dead. Thoughts that if I only had killed myself before now I wouldn’t be going through this. I still don’t know what my purpose is in my life. It’s not like I am an aspiring country singer. I just am struggling with mental illness. And that is a battle I don’t wish upon no one. It is difficult dealing with these thoughts and feelings when you feel so crummy. It makes the world seem dark and gray. But then my world is dark and gray even on a bright sunny day. It’s hard to see anything else when you have a black cloud trailing you all the time. But that is what depression is. Only dark gray skies can be seen. And within this darkness there is no hope. That is the toughest part of this illness is feeling hopeless all the time. You try not to let it get to you but it sinks into your veins and you have no choice but to accept that things are never going to change. Sure you might be happy that one day but it never lasts. Too bad that pink pill can’t help with that.

write the pain

Write the pain.

For those that are frequent blog readers, you know I write about my pain, physical and emotional, most, if not all, the time. It has been the cornerstone of my blog. I can articulate what few can and my readers like what I write because they can relate.

Writing about pain has been a staple of my blog. It seems I cannot write without some measure of pain. It can be the pain associated with depression. It can be the pain associated with the chronic pain condition that I have. It can be a pain that keeps me awake at night. The pain that tears at you and is unrelenting. Whatever type of pain that I have been feeling, it has caused frustration, anguish, despair, suicidal thoughts, and agony. It makes you dread waking up in the morning. It makes you want to sleep forever, to have this escape of no consciousness. It wears you out. And exhausts you. It causes you to be unmotivated. To want to stay in bed and not face the day. But for me, it also has been the stimulus behind so many writings. I write about my darkness that is a short story. I write about the chronic pain and suicide ideation that happens frequently.

Pain has been sadly, the inspiration to write this blog because it causes such dark thoughts, and by dark thoughts I don’t mean just depressive thoughts. I’m talking about suicide ideation. Thoughts that make you think you would be better off dead than to continue living. Dark thoughts of suicide, the ones where you cannot express in normal conversation. Most of my dark thoughts are expressed in this blog because the therapist hours do not occur between 11 PM and 3 AM. It’s hard to find any here to listen between those hours. So I read about the pain. I write and I write till I am succumbed by pain meds or psych meds or exhaustion. I write the pain. Because if I did not have this outlet, the dark thoughts would take over. And I would cease to exist.

Pain is exhausting, be it physical or emotional. And to have both occur at the same time is just torture. When the meds don’t work, when the pain is overwhelming, when all you feel is anguish and misery, that is what causes you to feel like life is not worth living. Writing helps to express what I cannot it sort of makes life more bearable as the father of suicidology has said many times, decreased the psychache (pain), decreased the suicide. I have found writing the pain decreases in my dark thoughts. This doesn’t mean I have found a life worth living. It just means life is more bearable for me.