How my mind and body have learned to cope with trauma

When you think about it, the human mind and the human body are amazing things. I’ve been thinking about this more lately, as the topic of connecting (and disconnecting) from my body have come up in therapy quite a bit lately.

I think of all the ways that my body has dealt with trauma. In response to damage in my foot, my body built bone on top of bone to strengthen what was already so weakened and damaged. When I had surgery two years ago to remove some of the excess bone, the doctors discovered a mass hidden underneath. The bones had literally formed a protective cocoon around it in a way that my doctor had never seen before.

I also have extra bone in other parts of my body, in response to fractures that were never properly treated. When they get really noticeable, I would give them names. Before it was surgically removed, I lovingly called the cluster of bone spurs on my foot “Humphrey”. As the same thing began to grow on my opposite foot, I called it “Humphrey II”. I have a palpable spur on my hip that I call Hipsley. It seems rather silly, and probably not quite normal, but it helps me not think about the damage that led to these growths in the first place.

To tackle the physical, sexual, and emotional trauma I endured as a child, my mind fractured to help me cope, leading to the development of DID. Many people don’t really understand DID, but it is truly one of the mind’s greatest coping mechanisms. It helped me get through childhood and the early part of my adulthood. It kept me alive and able to function without coming completely undone. If I never dissociated, I don’t think I would have been able to handle the trauma that had been occurring every day of my life.

Some of my mind’s and body’s coping skills are not so safe in the long run. My therapist and I have talked quite a bit over the last couple of months about my disconnection to feelings and sensations in my body. Sometimes, I can feel. Other times, I am completely numb and oblivious to any sensation.

There are times when I don’t feel hunger even when I haven’t eaten for days. There are days when I don’t feel any pain, even though I know that I have problems that should be causing me to feel pain. I also have periods when I cannot feel the temperature. It’s something that has been occurring for awhile now. It actually served me well when I was working in a warehouse in somewhat extreme weather conditions (100+ degree weather, below zero temperatures). I was able to work in the loft, where temperatures reached well over 100 degrees Fahrenheit, and not feel the heat at all. My coworkers used to joke that I didn’t even break a sweat – they were right. I wouldn’t have been able to tell the difference if it was 110 degrees or 50 degrees.

I had (and still have) the same issue with the cold. There were days where I’d go to work in a tee shirt in the middle of winter in freezing temperatures. I didn’t feel cold at all. Other people were concerned, however, because I would turn blue and red from the cold. I couldn’t feel a thing – cold or hot. I just didn’t feel. I still have this problem. Last week, I was waiting outside of my work for the manager to come. A coworker said I could wait in his car to stay out of the cold. I told him it wasn’t cold and that I was okay. Except that the temperature actually was cold. It was 12 degrees outside, and I was wearing a hoodie. But I felt fine, because I couldn’t feel anything.

I had an incident several years ago while cooking. I leaned over the front burner, forgetting that it was on (I was reaching for something in the cabinet above). As I was fiddling about in the cabinet, I heard someone shout, “move, you’re burning!” I didn’t really understand what was going on because I hadn’t put anything in the pot yet. Then I looked down and realized my shirt was burning. I quickly patted out the fire. My shirt was completely ruined, half of it had disintegrated from the burning. I had a coil-shaped burn across my abdomen. And I didn’t even know it was happening. I was so disconnected, I didn’t even realize I was burning.

It may seem like not being able to feel is a great thing. I assure you, in the long run, it’s not good at all. I try to make an effort and check the weather and dress appropriately, even though I may not feel the temperature at all. I’m always afraid of overheating in the summer, because I’m not connected with my body enough to know when it’s reaching a danger point. When I broke my foot a few months back, my mind blocked out the pain and I was able to walk on it, even though I shouldn’t have been. I ended up causing even more damage. I’d rather not accidentally set myself on fire again.

For the last six months, I have been experiencing pain off and on in my tailbone. I appreciated the days that I was able to block out the pain completely and move around like nothing was wrong. Some days, I can’t block the pain and I feel it intensely. I use those days when I can’t feel pain to rationalize that nothing is wrong with me on the days when all I feel is pain. I feel like if I were to go a doctor and tell them that I feel great some days, and horrible other days, that they would minimize the pain just as I do. Doctors won’t understand that cutting myself off from feeling is how I have learned to cope with trauma.

My therapist suggested that my disconnection from feeling is related to my history of trauma. I am so used to it, that I never really thought about the reasons why I am that way. It makes sense. I just wish there was an easy fix. As much as I’d like to not feel anything, I also need to eat like a normal person, to fully experience my environment, and to feel when something is wrong with my body. Right now, I can’t do that fully. It is something I need to work on, along with the 8 million other issues I have thanks to life.

The ongoing battle: Why I deny my DID and why I know that I have it

I’d like to think that, as I am now six months into my official dissociative identity disorder diagnosis, I wouldn’t still be struggling with accepting that I have DID. But the truth is that I still have doubts. Some mornings I wake up in complete denial. I try to rationalize my denial my pointing out the differences between myself and others with DID I’ve come across, even though I know full well that the dissociative spectrum is so diverse that no one’s DID is the same as another person’s. Yet I still try to convince myself that this all just a misunderstanding.

Reasons I use to tell myself I don’t have DID (note that I am not saying any of this is true for all people with DID – these are my irrational rationalizations):

Medication: I am not taking any psychotropic medications, and I haven’t since September. Every person I’ve ever come across with DID (and mental illness in general) takes at LEAST one psychotropic medication. I tell myself that since I am functioning without medication, I must not be ill at all.

Functioning: I function decently well. I’ve held jobs (and excelled at them), I’ve always been one of the highest achievers in my class (from elementary school through college), and I am able to live independently without assistance from anyone. I know many others with DID are not that fortunate. They are unable to hold jobs, unable to focus or stay present long enough to manage an education, and many are in supportive living.

No inner world: In my reading and through my participation in DID support groups, I’ve come across so many people speak of an inner world that they can actually picture inside of their minds – filled with different rooms and places for alters to go. I don’t have that. I find it difficult to imagine having that.

Trauma: This is difficult for to me admit, as I would tell a client to never compare his or her pain to another person’s. Yet I find myself regularly comparing my trauma to other people’s traumas, insisting that my experiences are minor in comparison to what other people have gone through. I tell myself I don’t have DID because what I went through just wasn’t that bad.

Lack of alter involvement: I realize in typing this out that it is one big oxymoron, because admitting that my alters exist actually supports my DID diagnosis. Many of my DID friends have actively participating alters: alters that use the computer and social media as themselves, alters that perform certain life tasks, etc. None of my alters use the computer (that I know of). None of them have their own accounts. As far as I’ve realized, I’m the one putting the work into daily tasks, not any of my alters.

Memory: Although I don’t remember everything, I do have memories of quite a few traumatic experiences I have endured. I tell myself that if I really had DID, I would have dissociated during these events and blocked them out from my memory. Why didn’t I dissociate all of the time?

Reasons I use to counteract my denial:

Medication: Funny how I use this both as a tool for denial and a tool for acceptance. The fact that psychotropic medications don’t affect me actually supports a dissociative diagnosis. DID cannot be treated with medication. The symptoms that may coincide, such as depression and anxiety, can be treated with medication, but DID itself must be treated through therapy. It explains why anti-depressants never helped me, and why even the strongest anti-psychotics never stopped the voices in my head.

Outsiders have met my insiders: When I told a good friend about my DID, there was no sense of shock or surprise. In fact, my friend had suspected something long before I even realized it. When I asked why he never said anything to me, he said it didn’t matter to him – it was just who I was. I even found out he had met one of my younger parts. My therapist has also met several of my parts, even before they were comfortable enough to come out to me.

Recognizing differences: Two weeks ago, I had a disagreement with a coworker. We were discussing an issue with boxes that needed to be shipped out, and I insisted that I didn’t pack and label the boxes. I couldn’t recognize my own handwriting. As I stood there vehemently denying that these boxes were mine, my coworker reminded me that I was the only one who knew how to do it, and no one else would have written those labels out. He was right. It could have only been me. But that was not my handwriting. Someone else had taken over for me, and it wasn’t the first time. Over the years, I have come across many notes that were not in my usual handwriting, but I knew that they must have been written by me. These differences are never subtle, either.

Ending up with things I don’t remember buying (or liking): I’ve been known to carry around a pink and white polka dot bookbag. My therapist commented on it once, and I mentioned how I hated the color pink. And then she asked me why I had a pink bag. Truthfully, I don’t even remember buying it. I don’t remember buying a lot of things I end up with.

The voices in my head: I can’t ignore it. Hearing voices is not normal. Yet I’ve heard them for years. Sometimes I can understand what they are saying, and sometimes I can’t. Medication doesn’t make them go away because they are parts of me. They are not auditory hallucinations. They are my alters.

Memories: There are entire chunks of my life missing from my memory. Sometimes I can’t remember what I did last week or what happened in therapy. These are clear indications of dissociation. When I am present, my memory is exceptional. There is no other reason for my memory to be that shitty, even with the drugs and alcohol I’ve taken in the past.

Trauma: This is another dual-purpose tool for both denial and acceptance. I know through my research and involvement with other survivors of mother-daughter sexual abuse that the incidence of DID seems to be much higher with survivors of this type of abuse, so inevitably my risk is higher. I also endured physical, sexual, emotional, and psychological abuse by both of my parents, increasing my risk factor for developing DID even more. As much as I don’t want to admit it, I had a traumatic childhood and early adulthood. Saying that my life was fine won’t change the fact that it really wasn’t.

As I sat in therapy last week and insisted that I never went through any trauma, my therapist reminded me that that just wasn’t the truth. She told me that if I continued to deny my experiences, I was also denying everything that my parts went through, all of the trauma they endured. It’s not just about me; it’s about them, too. I realized that I was doing the same thing to my parts that other people had done to me: denying the reality of my/our experiences.

Sure, I wish I didn’t have DID. No one wants DID and all of the shit it comes with. But for every reason I come up with to support my denial, there are even more reasons that support my diagnosis. I can try to maintain my dissonance, but that will never work in the long run. Maybe one day I won’t have to fight myself anymore on this issue. We’ve done enough fighting already.

Silenced in shame

I tend to be a very open person. I tell my therapist nearly everything on my mind and in my heart, good and bad, happy and sad. I’ve shared my thoughts and experiences with others by writing this blog.

But something came about last week that I could not talk or write about. The memories left me confused, angry, and ashamed. I hated myself. I hated the world. And I couldn’t tell anyone about it because I feared that would only make it worse.

When I went to my therapy session on Thursday, I tried to deflect talking about everything I was feeling by denying everything. And by everything, I mean everything. I told my therapist I had a good life, no trauma, and no problems. I didn’t want to deal with any of this shit anymore. But denying it doesn’t make it go away. I could’ve said I had a good life until I was blue in the face, but it wouldn’t have changed the fact that I was seething on the inside.

I finally admitted to my therapist that I was full of anger, but I could not tell her why. It’s not that I didn’t know; it’s that I didn’t want to talk about it. She traced back the last few days trying to pinpoint when and where my feelings originated. I went over each minor detail of my life starting with Thursday morning and working backwards. Eventually I muttered “I checked Facebook.” That was when it all began.

I didn’t expect to feel anything when I checked Facebook that time. Then, I read a status that came up in my Facebook memories from six years ago about being admitted to the hospital. I instantly realized what happened in the days after I wrote that status. I felt as if I were right back in 2010, going through it all again.

My therapist asked me what happened and I burst into tears. All of emotions came pouring out and I couldn’t stop crying. I couldn’t even tell her all that happened. I told her that I cried for help and no one helped me. No one knew what had just gone on just minutes before the nurse came in my room. No one could translate my cries of desperation. No one could feel the pain I was in, the disgust and shame I was filled with. No one. I was completely helpless. I was entirely ashamed.

I remember laying in my hospital bed day after day just wanting to go. I couldn’t even eat. The numerous visits from nutritionists could not take away the sickness that was eating away at me from the inside. I was so disgusted with myself. I felt so unclean. I couldn’t shower for weeks, which only magnified how gross I felt. I wanted to scrub away the dirty. But no shower would have been enough. Nothing would have been enough.

It was at that point, after that incident, that I realized that nothing would ever stop my mother. She was sick; sicker than I had ever imagined. In my most helpless state, she took complete advantage of me, all the while putting on an Academy award-worthy performance of a concerned mother. No one knew how badly I needed to be protected from her. Instead, they inadvertently helped her terrorize me. I was completely alone. Despite the numerous flowers and gifts, and visits from coworkers and friends, I felt isolated and alone. Physically, my heart was trying to give out on me. Emotionally, my heart was already dead.

Despite my realization that my mother was (and still is) sick, I blame myself for what happened. I could have told her to stop. I could have gotten away. I could have told the nurses. But I didn’t do any of that. I let it happen. That’s all I could tell my therapist. I let it happen. As if I could have done anything to stop her. I had an oxygen mask, a heart monitor, and numerous IVs, but yet I expected myself to, in some way, fight back or resist; something I had never done before when I was in much better physical condition.

My therapist reassured me that there was no way I could have stopped her. I did what I could in that moment. It wasn’t my fault. But part of me was still angry. Part of me was still disgusted and ashamed. I left session that day wanting to destroy the world. All of that anger I was holding on to for so long was trying to get out.

But I couldn’t direct it at my mother. So I directed it at the branches I passed by on my walk home; the branches I ripped out from the bushes and broke into pieces, much in the same way I felt my heart had been ripped out and broken into pieces. I smoked, but not even 100 cigarettes wouldn’t calm me down. I drank, but no amount of alcohol would wash away my disgust.

It was only in today’s session, nearly a week after my memories and feelings resurfaced, that I was able to tell my therapist a piece of what happened to me that day. I still find myself overwhelmed with shame. I still fear that other people would not understand. I still fear that other people would think it was my fault. My therapist asked if there was anything she could do to lessen the shame. But I don’t know. As much as I know I need to talk about it, I can’t. Not even to the person I trust the most. I remained silenced in shame.

PAFPAC Support Forum

The PAFPAC support forum for survivors of female-perpetrated abuses is up and running. There are a few members, but no one is really comfortable with posting yet. If you are a survivor of any type of female-perpetrated abuse, please consider joining the PAFPAC Support Forum.

It is a private forum, so you will need to ‘apply’ – I receive a notification and can approve you the same day. This is so members feel more comfortable sharing and it helps weed out people who may be there for the wrong reasons. The forum is really for anything, not just talk about abuse, but also healing and everyday struggles.

If you or anyone you know can benefit, please pass on the information.

Thank you.

 

23 weeks

How did I end up here? What forces have driven me to be the person I am today?

I’ve been thinking about this a lot in the past week. Like nature versus nurture, I wonder how much of an impact my experiences have had in shaping the person I am today.

If I was never told I wouldn’t amount to anything, would I still have striven for academic excellence, or would I have been complacent with being average?

If I never had to endure physical or emotional pain, would I still be working to alleviate this pain in others, or would I just be focused on my own needs?

If I never had to muddle through 14 years of therapy and a failing mental health system, would I still find it my purpose in life to become a therapist, or would I have ended up being a (much more financially stable) businesswoman?

If I never grew up being hurt by the very woman that gave me life, would I still be fighting for the countless others that have been abused by women, the countless others that have been ignored and disbelieved because our society doesn’t want to believe that women have the capacity to be abusive?

In many ways, I’ve beaten the odds. Despite being raised by a psychopath, I’ve developed a strong capacity for empathy. Despite experiencing abuse and violence, I’ve chosen to stop the cycle. Despite being programmed not to talk, I’ve become a voice not only for myself, but for others.

Perhaps innateness and experience aren’t that separate. I truly believe there had to have been something in me at birth that allowed me to survive. I know my DID helped me survive, but it had to be something else.

How did I learn what goodness was when my own parents were the complete opposite of goodness? How did I develop morals? How did I know that violence and abuse were not acceptable behavior?

During our last therapy session, my therapist and I talked about the role of my father in the family dynamic. I have realized in the last few months that, as a child, I idealized my father because he was the least horrible of my parents. I modeled some of my behaviors after him, especially the aggression and the physical violence. That probably explains why I never got along well with girls as a child. My rough nature fit in so much better with the boys. Then I guess there came a point when I realized that being like that wasn’t socially acceptable, so I changed.

My therapist asked what role models I had growing up. There had to have been someone positive in my life, someone that I modeled myself after. She asked if I remembered any television shows or movies that had an impact on me. I couldn’t think of anything. Truthfully, I can’t really remember a lot of my childhood. I wish I did.

Then my therapist told me “women who have experienced what you have end up in places like Chowchilla, but you haven’t.” (For background, Chowchilla is a women’s prison in California. The organization has worked with many of the inmates who were victims of mother-daughter sexual abuse as well as non-maternal female-perpetrated abuse). “I could have,” I responded as I thought about the countless times I imagined killing my mother and father, the countless times I researched how to kill a person without leaving evidence behind. I’m probably not that different from those women. The only difference lies in that I never carried out the action. My tendency to over-analyze and my anxiety saved me from ending up in a prison cell. Nothing more, nothing less.

This next week will surely be difficult for me. Holidays were a rough time for me before. I imagine they will still be difficult for me now, even though I’m no longer a prisoner of my own family. I’ve been trying to keep busy and not think about it, but that’s hard to do. I will get through it, though.

 

 

It wasn’t their fault

I used to hold a lot of anger against the people in my life that did not help me. Then I realized that was a lot of anger to hold onto, and a lot of people to be angry at.

There have been a lot of people throughout my childhood that failed to act when they should have, or they acted in a way that just made my situation worse.

My elementary school teacher severely underreacted concerning my sexual inappropriateness. I don’t have to tell you how that went over. Knowing what I know now, I don’t think my teacher’s response was appropriate.

Perhaps if someone had intervened, I could have been rescued. Then again, who would believe that a child was being sexually abused by her own mother? In the 90s, mother-daughter sexual abuse was just beginning to be studied. I was so programmed, I doubt I would have had the courage to tell the truth.

Then there were all of the teachers and guidance counselors who I begged not to talk to my parents, the ones I expressed fears of going home to, the ones who didn’t really know how to respond. No one ever got involved. No one questioned why I regularly peed my pants throughout elementary, middle, and high school.

The doctors and nurses never picked up on my panic whenever my mother was in the same room. They saw my unwillingness to be examined as just being shy rather than my feelings of fear and disgust. They never questioned why I seemed to have a UTI at every physical.

Family members either never realized what was going on, or chose to remain ignorant. My parents were very skilled at appearing somewhat normal, so I don’t blame people for not noticing, or not being 100% sure what was going on.

Was I that good at hiding the signs? I doubt it. Looking back on the times I remember, I think there were multiple instances in which something should have been reported. But nothing ever was. I continued to endure the pain and people continued to turn away. Maybe they were confused. Maybe they didn’t know it could happen. I don’t know.

But none of this matters now. I can’t change what happened to me. I can’t continue to hold on to the anger I have felt towards these people for so long. I hope they never feel like they were at fault; I hope they never feel guilty. It wasn’t their fault. It wasn’t my fault. It was my mother’s fault, and it was my father’s fault.

I can only use my experiences to initiate change. No child should have to endure abuse. The signs should not be ignored as they were in my case. People should not be afraid to report their suspicions. Ignoring it does not make it go away.

21 weeks

I’ve spent much of the last few days crying.

Not because I’m sad, but because I recognize where I’m at right now and where I’m going.

I received an e-mail late Wednesday that said that after reviewing my application, I had been invited for a final interview with the Psychological Counseling department on Saturday. I just assumed that everyone got a final interview, but when I told my therapist about it the following day, she said they only interview you if they are interested in you. Both therapists seemed more excited about it than I was. My therapist asked me in session if I wanted to go over some preparation for the interview, but I told her I would be okay. I wasn’t going to prepare. I was going to just wing it.

My anxiety started to kick in shortly after my therapy session was over. I was sitting in the lobby waiting for the next bus to come when the other therapist saw me and stopped to sit next to me. We talked for a little about my pink bag (because I mentioned that I hate the color pink) and laughed, and then we started talking about the interview. She told me what to expect, what questions they might ask, what questions I should ask, etc. She even shared some hilarious answers that she had people come up with during interviews. We ended up talking for almost half an hour, and she gave me a hug and reassured me I would do great.

I felt a little better knowing what to expect, but now I was anxious about needing to prepare. I had no nice clothes, no dress shoes, and no makeup. I had to make myself look presentable. I bought the cheapest drug store makeup I could find, bought dress pants, a shirt, sweater, and dress shoes (which I was sure I would never find in size 12). I definitely looked the part. Now I just needed to act the part.

I stayed up late looking up information about the program, how it ranked nationally, and how it was rated by other students. I made sure I got more than 8 hours of sleep, which never happens for me. I woke up early to make sure I’d be ready in time. I made it there a half hour early, which is always better than being late.

The interview was not nearly as bad as I expected. There were 10 people including me, with two professors leading. We introduced ourselves, learned about the program, and asked questions. Then we were split into two groups and had to discuss how we would respond to certain ethical dilemmas. I think I did pretty well. We then had a discussion about informed consent and confidentiality and I was the only person that mentioned mandated reporting when child/elder abuse is involved. I’m surprised that more people did not know that, as I thought it was common knowledge.

At the end, everyone had to write a short essay on a hypothetical situation while utilizing the ACA Code of Ethics. Once that was written, we were allowed to leave. There were no one-on-one interviews. I was nervous for no reason. I shook the professor’s hand and told him I hoped I would see him again soon. I will hear back within the next week if I have been accepted or not.

I e-mailed the therapist that helped me as I was waiting for the next bus. I told her everything that happened and thanked her for her support and encouragement. She e-mailed me back and mentioned that she was proud of me, and how she was really rooting for me, not only for this grad school stuff but in every area of my life. I started to cry again because I know her feelings and care are genuine. It’s difficult at times because I don’t have very many people on my side that I can count on (excluding online support). But she has been there, my therapist has been there, and my support group has been there for me through all of this.

I’ve accomplished so much in these 21 weeks. I have a job that I really excel at. I started this blog and have continued to write. I write professionally. I’m (hopefully) going to start graduate school next month. I’m getting more involved in advocating for mental health and other issues. I was recently invited by NAASCA to be a guest on their program and share my experiences recovering and healing from the abuse I endured as a child. I’ve also been approached about my thesis on mother-daughter sexual abuse, which I am currently re-editing for a more general audience.

I have so much going on, but it’s all good. I’m in such a better place right now. I could never be where I am today if I was still with my family. I made the right decision. For the most part, I am happy. So many people tell me how much better I’ve been looking, and how much happier I look. I’m starting to realize that they are right. When I take a picture, I no longer have to fake a smile. I’m struggling, but I’m no longer living in fear. I’m no longer waiting for the pain to come. I’m finally able to live. I am worth living.

18 weeks

I can’t believe I’ve made it 18 weeks.

This journey has been anything but easy. But I’m still moving through and moving on. Not everyone would be able to do that. I never thought that I would be able to do that.

My coworker has told me numerous times that I have “found a home here.” I know that he is referring to our workplace as home, and I agree. I fit in so well at work, even being the only female among so many men and boys. I can be myself…my sarcastic, funny, cursing-like-a-sailor self. I’ve also learned that I don’t have to put up a wall there. It’s okay not to be happy all of the time, and they accept that and embrace it. As much as my workplace is a home for me, I feel like I’ve also found a home here, in the city where I now reside. I’ve met so many people and done so many things here that I would have never done in my old home. Being free feels so different, so scary and yet so rewarding.

A friend of mine reached out to me yesterday. It was strange because I had just been thinking about her, realizing that her birthday was coming up and wondering what I could mail to her just to let her know I still care. My best friend showed her some recent pictures of me and she noticed how much better I looked. She said I looked good and relaxed. I thanked her and told her it’s still a struggle, but I manage. Then she told me she was proud of me. I put my phone down and tried to hold back the tears, but they came through anyway. Someone was proud of me. I know it’s such a simple statement, but it’s something I wanted and tried for so long to get my parents to feel towards me; of course, that never happened. I’ve recently heard it from other people in my life and rejected it, as I tend to do with positive compliments given to me. Hearing those words from her just…I don’t know how to describe it. It meant so much to me.

I’ve been working on acknowledging my denial of my DID diagnosis and trying to get past it. I think I am in a better place now – not all the way there, but close enough – to accept everything. I’m not going to lie, I’m still scared of what will happen in the future. As I get closer to my parts, I know that I will have to deal with new memories, and those memories will not always be good ones. I think I have a good support system in place to help me through it, though. I’m not alone. We’re not alone. We don’t have to feel like we’re all alone anymore. I don’t want my parts to feel like they have to hide anymore. They’ve been through enough.

There is a DID conference coming up in February through An Infinite Mind. I’ve thought about going to a conference for the last two months. There was a conference given by another organization just a few weeks ago, but it was on the other side of the country and just not feasible. This conference is probably the closest and most accessible to me, as it’s taking place in Orlando, FL. On a whim, I asked my best friend if he would go with me (the conference is for people with DID, their supporters, and therapists). He said he would. I feel so much better about going there with someone I know and trust. I think it will be a good experience for me. I still have to figure out exactly how I am going to manage it financially, but I’ll do what I have to do. I’ve already gathered some things to sell online to earn some extra money that I can put towards the trip. I think I deserve it. I know I deserve it. It will work out somehow.

I have a little more than two weeks left to get my graduate school application completed. I’ve ordered the transcripts, mailed out recommendation forms to be filled out by my professor, and filled out the FAFSA. All I have left to do is the essay. It’s funny how writing comes so easily for me until there is something that I need to write. Then I put it off for as long as I can because I feel that my writing will be inadequate, or that I won’t have anything substantial to write. I’ll get it done. I need to get it done before life gets so crazy that I just won’t have the time.

I felt a little guilty today because I had off from work and didn’t really do anything except wash my laundry. I haven’t really had a day off to myself in a while. I probably needed to sit at home and do nothing. I’m tired, physically and mentally. I’ve had a headache for four days. I need a break. But there’s really no time for breaks. I just hope I don’t burn out.