By Ox Drover
Yet Being Someone Other is the title of one of my favorite books and sometimes I think that title applies to me as well, at least since I recognized the post traumatic stress disorder (PTSD) that has become such a part of my life these last six years. Now I’m “someone other” than who I used to be. I’m not the same person at all. I no longer think like that other person did, that FIRST ME as it were. The NOW ME is different.
This was a very disturbing thing for quite some time as I had to get used to things being gone that I had depended on previously. I had to make adjustments to the changes in myself, sort of like a teenager has to make adjustments to larger feet and longer legs, and for a while becomes quite clumsy as they learn to use these appendages which have suddenly changed in dimensions. I felt very clumsy for a while, and still do to some extent. In other ways, I feel like an amputee that is having to relearn to walk with only one leg, or to use a prosthetic leg. To me, this is quite unsatisfactory. I want the old me back, the familiar me.
Worst of all I think, is that my mind doesn’t work the way it did, and it keeps on changing. At first I couldn’t read at all, not even one sentence, as I was in shock and couldn’t retain the words from the first of the sentence long enough to add them to the last words of the sentence in order to make sense of it all. That was frustrating and scary. I’d watch a movie and enjoy it, and then put the same DVD in the next night and not realize I had seen it the night before until maybe near the end when some specific line would make me realize I had seen it. Then I would feel so stupid that I had watched it again, not remembering.
I talked to my psychiatrist about this and she reassured me, “It will get better, it will come back,” but I didn’t believe her, and even after six years, she is only partly right. It has gotten better, but I realize and finally accept that it will never be the same. I am Someone Other than who I was before. I still have word finding problems like a stroke patient, seeing the image of a tree in my mind, yet not being able to find the word “tree.” It is as if my brain is now made of Swiss cheese, with large empty holes at random within it. I stutter when I talk, trying to find the words I want to express myself, and sound to others as if I have the early onset of dementia. I apologize to them for not being able to find the word I am seeking, and explain why, or try to, but not really knowing if they believe me or not, or if they are simply humoring me to be polite. I don’t talk as much to strangers now, the New Me doesn’t want to have to explain. The Old Me never met a stranger, or was reluctant to exchange conversation with someone they just met.
I have found that for some strange reason the muscle memory of typing which the Old Me always did well, though not quite intact, is actually better for producing words and thoughts than verbally doing so. Though I now have problems spelling, and will use the word “here” instead of “hear” and not realize it until I read back through the typescript. Sometimes my spelling is so bad on more complex words that even spell check doesn’t know what I am trying to say to fix it, so I have to go back and find a simpler word that I can still spell, so my vocabulary has decreased by a large percentage.
Reading, which has always been one of my passions, is still a passion for me, but now instead of reading at breakneck speed, reading by phrases at twice or three times the rate most people read, I am again reading word by word at about 200-250 words per minute which is about average speed. I also know that my memory of a series of numbers, which was once quite extraordinary, can’t even extend to the seven digits of a phone number long enough to dial it.
Through the last six years the Now Me has gone through many changes, some quite painful, and has had to navigate through the rapids of multiple episodes of grief, make decisions while not fully functional as far as logic is concerned, and reinvestigate what my core beliefs are, and which direction my moral compass should point.
The feelings have been sometimes like that feeling of unreality you have inside a house of mirrors at the county fair! You end up holding out your hands in front of you to touch the things you think you see in order to navigate because you learn you cannot trust your eyes to navigate your way out. The Now Me must learn to use other senses besides sight to move by. Sometimes I’ve had to close my eyes and grope in the dark to find the path out of the maze because if the Old Me tried to find her way out by sight, she would confuse the Now Me.
Time has helped to calm the fears of things being different, of be being Someone Other than the Old Me. I’m learning to adjust, and to accept the Now Me and not grieve the way the Old Me was. There is really nothing in this life that is constant except change, and though the PTSD does seem to cause this change to accelerate at what seems like a breakneck speed, in many ways the Now Me has adapted well to these changes and is learning to care for herself in ways that the Old Me never was able to.
I saw a video a while back of a two-legged Border Collie working sheep at a dead run. One of the things I’ve learned in my years of having and raising collies is that they are a “can do” breed and ”working,” which to them is play, is very important to them, and if there is any way they can succeed in doing that, they will find it. I didn’t see that two legged dog sitting down whining on the side lines, but running as hard as she could go, doing what she loved. It was only when she sat down that she fell over, so I intend to keep on running and being and appreciating that the Now Me, while not identical to the Old Me, is still able to do what I really want to do.
Oxy, This sentence from your above post struck a chord with me:
OxDrover: “After my husband was killed and I was still very actively in the PTSD I couldn’t answer the voice mail or answering machine and listen to the messages”.just couldn’t make myself do it.”
I hate waking up alone in the morning. It’s almost a panicky feeling. When the S/P first devalued & discarded me in May, I was actually fairly good. I found a wonderful Christian radio station to use for an alarm, with first a sermon, and then people talking. It was so much easier than having music haunt me…
After listening to that to wake me, I would read the Bible or one of the other spiritual books from the library. Another thing I do is listen to my iPod while I work around the house or in my studio. It makes me sing, dance, feel good, and induces some really positive things in me.
For about the past 3 weeks, I have not been able to do either. The thought of music makes me cry. The thought of the Bible makes me nervous and apprehensive. Those are things that got me through the last 2 times he D&D’d me.
It’s just strange that I am just paralyzed now… But I am forcing myself to get with things and follow through….. Starting tomorrow. After I run him over with a shopping cart. Then I’ll feel SOOOO much better!!!
Dear sageegirl,
Yes, it is “odd” isn’t it the things that somehow don’t seem connected to the trauma we have endured, but all of a sudden you realize that you can’t stand something that never gave you a bit of problem before….I still don’t see the connection of my traumas with the answering machine, but for some reason that phobia is there, the anxiety that goes with it. I make myself do it, but don’t WANT to. LOL
Your idea about a station like that is a good idea, better than music. I too don’t like waking up alone, or sleeping alone either. I have quite a large bed, so I put things on the top of the other side from where I sleep…so the bed doesn’t feel so “big” I guess.
Each step we take in identifying things that are different about the NEW ME and find a way to adjust for that is a step in the right direction. Just keep on walking toward the light and keep one foot in front of the other and you will continue to make progress. (((Hugs)))) and my prayers!
I went to the neurologist this afternoon and I STILL don’t get to go back to work yet. I thought I would go in and get cleared and be on my way. This doctor claims that I have pathological reflexes in my ankles and I had to get an MRI and check back with him on Thursday. I told him that I don’t have the sick time to sit around home doing NOTHING when I am totally fine. My strength is strong and equal in all four extremities. I want a second opinion. I had to get an MRI of the brain and cervical spine. I am terribly claustrophobic and made it through the test without sedation. The Tulane neuro department has a history of being dumb as a box of hair. I’ve worked with them when I worked trauma. This is total BS! I have to stay home AGAIN tomorrow!
Oxy, yes the talking is such a nice way to wake up. It’s as if someone is there with you. You need to get a BIG dog. I have a Golden, and she is wonderful. Not the same as a man, but at least she’s always here for me. Maybe she knows that if she D&D’s me, she’ll never find anyone to give her Goldfish and sing “Who stole the cookies from the cookie jar” to her in the mornings when I get the coffee! Thank you for the hugs and prayers. I give you hugs and prayers back!
Erin72, Oh no! I thought you were ready to head out there and knock their socks off! OK, well maybe you have to wait till Thursday. But at least you FEEL better- and that’s half the battle. Good luck!
erin72 – are these folks incompetent or are you just frustrated (or both?)
it won’t last forever. breathe.
associations with the ppath – i have been thinking about this lots. i have lots of triggers. especially tied to seasons.
this time last year we were just working up to the big D+D+D (an extra ‘D’ for me…for the fake death. grrrrr)
it’s the cell phone. i have changed the number and i rarely use it, but it still reminds me of the fake boy. it’s an old phone, the n dad bought for me at xmas a few years ago. never used it until last summer…so i look at the damn thing and i think of them both. the battery kept falling out of the back so i taped the back on. i usually take good care of things. this thing i could care less about.
fake boy used to text me. all his messages are off the phone. all my sent messages are off the phone, every time i look at it i am weirded out. so, this week, i have started to say – she will never call this phone. she doesn’t have the number…a little litany to break the fucking spell.
ouu, just remeered the incomprehensible text message she sent me when the fake boy was supposed to be dead. at work. thanks very much. really appreciated that.
found out about another heinous con she pulled. caused someone to have a break down and almost kill themselves – convinced them they were the child of rape – and that she was the mother…and she also pretended to be the father….i am sorry, i cannot, i who live to, even swear…there is no word strong enough, vile enough, damaging enough to levy against this woman. makes my head hurt just to think of it.
truly, if anyone ever needed killing.
.
hens – it was 2 seconds in the micro wasn’t it? 🙂
i was hoping you would show up tonight. she’s so sick hens. one of those things was new, the one i mentioned above. was a sack of shit she is.
i have never paid to watch horror shows. never liked them. those icky ones you are talking about.
my phone does have a sim card – any reason i can’t take it out and put it in a new phone? i did change all the tones on the phone…still want to smash it though.
i will send a note to donna – thansk hens. it would be releif to let this go…well, smash it actually. 🙂
she really hurt me. deeply deeply.
how is boo doing?
sim cards can be switched easily, alot of new cell phones dont have sim cards….the Saw movies are not really horror movies but somebody playing with peoples minds..anyway Boo called and left a message thanking me for a lovely day and for lisrening to her etc..she sounded better too me…goodnite