Confiscated

My doctor took ALL the pills I had stockpiled and didn’t use during my suicide attempt.

All of them.

And then he destroyed him.

I hate my whole team right now. 

I don’t want to recover I want my damn pills back so that I have an out in case I need it. I had hundreds of pills saved up sinc I was in late high school and college. From every surgery and injury bc, well, my pain threshold is high and I didn’t need them for that purpose. 

And now they’re gone. 

And I can’t have them back.

And I’m so pissed. 

I have no clue how I am going to go to work tomorrow. I feel like I need to go to therapy. Ironic since instead of going inside at this very moment I’m in my car typing this. 

But I can’t go in. I DONT WANT TO HEAR ABOUT EVERYONE ELSES ISSUES. I have enough on my mind without all their Bologna. I don’t need to hear about their problem with their job or their family or their day. I want to not hear about how awful everyone’s lives are because right now ALL I WANT IS TO END MINE. And that will NOT be helpful. 

I texted my IOP therapist (one of them) that is running group and said I’m not coming. She promptly replied with “yes u r” to which I have yet to respond and clearly, yet to abide by. 

Part of me is wondering if they’ll even care if I don’t show up. I’m a lost cause. I’m a burden and a mess. I’m complicated and hard to handle with therapy because I don’t trust anyone fully with my feelings including my conscious self. 

Anyway. I’m tired. I hate me. I WANT MY PILLS BACK. On a scale of hate my doctor is on the top. He’s a nice guy and easy to talk to but he is evil and awful for taking them before I was ready. My whole team is actually bc I wasn’t ready and they still forced me to do it. Well now I am just BEYOND depressed again and not going to treatment and I really don’t see how that’s at ALL useful. 

I hate them all. I hate them, I hate them I HATE THEM. 

All I want is to punch something right now or scream or nth or to run and exercise but noooooo I can’t exercise because that would be breaking the rules and even though I am overweight- despite what they say- I am not allowed to do it. Well eff this I am so done listening to people who lie about my weight and won’t really tell me if I have gained. I’m tired of people not letting me choose anything for myself. I hate this whole stupid process and I hate my life. Why did I even go to treatment in the first place??? If God really had a plan he’d have stopped all this madness a long time ago. 

I’m done trustin people. I’m done trying. I am just relying on myself from now on. The end no one else but me. 

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Facing My Fear of the Scale

Got my weekend homework for IOP: Bring my scale to IOP on Monday.

Anyone with an ED can probably figure out why: we are getting rid of it.

Thing is this isn’t hard for me because I am getting rid of it, it’s hard because, well, I haven’t touched it in over 2 years. I haven’t weighed myself on it. Haven’t turned it on, haven’t anything.

Why?

(Trigger Warning Begin: Suicide, Depression, Self-Harm, Eating Disorder)

Because the last time I touched that scale I almost attempted suicide.

The number had gone up. I was a failure. I hated myself. My life. My body. Everything. I couldn’t live with myself anymore. I had to die. I wanted to die. I had failed and I deserved to die.

I prepped everything. I was in the bathroom, I figured it would be easier for them that way, easier to clean. Plus, there were no pictures, no reminders of what there was left of my life. I got the pills, I got the razors. I was done.

I didn’t go through with it. As I laid out the pills and brought the razor closer to my flesh I thought about them- my 4 year old niece and nephew. What would my family tell them? Would they remember me? Would they be at the funeral? Would they forget me eventually? Would they hate me for what I had done?

Touching the razor to my wrist and seeing the faces of those two little “babies” was all it took. I looked down at the razor, looked at myself, at that scale 2 feet away, at the pills in my palm and then fear surged through me, my thoughts racing through my mind so fast. It was like my mind was trying to get out everything that was rational before the depression, before Ed took back over.

(Trigger Warning End)

What are you doing? This is not okay? You need help. Don’t do this. They need you.

The fear coursed through my entire body so strongly that I threw up out of fear. I flushed the pills, I flushed the razor and then I turned and looked at that scale. I was hysterically crying at this point. Terrified to look at it, to touch it. Half of me was scared I couldn’t withstand the screaming voice in my head to stand on it, the other half was terrified that I would see the number again and not be able to stop myself against the suicidal thoughts.

I flipped the scale over with my foot, fumbled with the battery component because I was shaking so hard that I couldn’t steady my hands enough. I tore the battery out violently and flushed that too. And then I put the scale away, in the back of the closet. The “junk” closet. The one with the stuff we never use. And I NEVER touched it again.

Now, one of my IOP therapists wants me to bring it on Monday. Wants me to touch it during treatment and then get rid of it for good. I’m not even sure I can touch it to put it in the car so she said to have someone else do it for me and she’ll come get it out of the car.

That’s how bad my fear is.

Even getting weighed at the doctor’s office, daily in treatment and weekly now during IOP causes such anxiety that I have to take my anxiety medicine beforehand. And if it’s a scale that makes noise (like ones that aren’t digital) it’s almost too traumatizing to handle. (Case and point: Tuesday when I had to be weighed at IOP because my therapist wasn’t here to weigh me and it took my dietitian 15 minutes, music, stepping on the scale to hold it steady and a double dose of anxiety medicine to get me to even comply.

So that’s my homework. Bring my scale. Touch it on Monday. Getting it into my car will even be a challenge so I have to ask someone to do it for me- which is also hard because I feel like that’s embarrassing to admit and I hate asking for help but at least I have a few days to figure it out.

But oh gosh, I have to touch it. I don’t want to do it, I really don’t want to do it.

The REAL feelings I hide

My therapist is back in town (thank goodness) and I saw her today for the first time in 3 weeks which was a longgggg time considering I see her at least once a week typically.

I have a hard time with feelings. Like a really  hard time, in fact it is nothing short of hate toward feelings. Today, Dr. B asked me what feelings I am trying to avoid so much. After attempting to get around that conversation I reluctantly answered with two (of the many) feelings I try and avoid sadness and anger.

The truth is, those are only two of the feelings I am trying to avoid. And not even the top 2. The real emotions I hate, the ones that I am so embarrassed to really say out loud, I have yet to tell her, to tell anyone. Why? I don’t know. I guess it’s because I am so incredibly ashamed of the feelings and thoughts I have that I have a hard time bearing the idea of actually saying them out loud. I mean they are bad, really bad. Like think of the worst thing you’ve ever thought about yourself and then repeat that in your head 24/7 for dozens of years in a row.

The truth is, I have hated myself since I was 9.

The truth is, the feelings I harbor for myself are horrendous. I am self-loathing, hateful, spiteful, ashamed, embarrassed, appalled, disgusted, angry, sad, depressed, uncomfortable and anxious about my body.

When I was 9 I began picking on myself, self-bullying I guess it can be called, the first thing was about my epilepsy. I hated myself for it. I felt defective, like a freak and convinced that people would make fun of me at school if they ever found out. I wanted to keep it a secret, I was so ashamed of it I didn’t even want my teachers to know, couldn’t look them in the eye because they knew and refused to go to meetings with them and my mom where it was discussed.

Things only got worse when the medication I was on caused weight gain, a lot of it. Couple that with the changes of puberty and it was a firestorm for a disaster. I was shy, uncomfortable, insecure, self-hating and refused to acknowledge my true feelings about myself.

Time continued. The hate grew. Even after I was taken off the epilepsy medication and told my seizures and resolved and medication was no longer needed I still was highly insecure and mortified, disgusted and appalled at what I looked like, weighed, my personality, style, everything. Nothing escaped my self-hate. College brought tremendous growth in my personality. I became extremely outgoing, friends with everyone, involved in everything, willing to try new things and put myself out there. But the hate I harbored for my body and my intense shame about my past, my weight and my entire self was still there.

Festering. Growing. Being buried by myself. Forcing itself into every crevice of my soul.

And then came life, my eating disorder and everything finally had an outlet. But even in treatment, those 3+ months I spent with 24/7 care I couldn’t bring myself to really truly, honestly express how absolutely deep and bad my self-hate is.

Treatment now, at IOP, has touched on it recently. Forced it out of me. It makes me want to quit. It makes me feel SO awfully insecure and embarrassed. But maybe they are right. Maybe it’s time to deal with it. It is after all, as I identified it, the one thing that I know will 100% cause me to relapse.

The thing is, sometimes I am not sure I want to recover.

Still, after months and months of treatment. I am still ambivalent. And that, that just makes this self-hate infinitely worse.

So when my therapist asked me what feelings I want to hide from I said saddness and anger. I have other reasons why I don’t like those but I don’t know how to say it out loud. How to tell her how BAD it really is, what I am REALLY afraid of. I feel like a failure, an idiot, someone who is weak, can’t handle emotions, is overly conceited and like a loser. A loser. Something I have always considered myself to be. How do I admit that? How do I tell someone that out loud and not expect them to judge me. Or for me to judge myself so bad that it becomes unbearable. The truth is I can’t, which I guess is why I haven’t.

Just add that to the reasons why I hate myself.

MEDICALLY CLEARED for Treatment!!!

This GIF pretty much sums up my feelings: a touch of relief/excitement mixed with sheer horror. One hurdle down and closer to getting into a program. My doctor (or rather, Nurse Practitioner since that is who I see) is the bomb dot com and called me back and said although my labs are consistent with being malnourished and she is concerned that they are still stable and she can clear me! I am both terrified and relieved.

I am going in tomorrow afternoon for another set of follow-up labs to check my potassium and other levels (because they are pretty out of whack) and I can get the letter and paperwork I need too. It’s all getting so real again whereas the last 10 days have had me living in a neutral state where I have been allowed to exist with my ED. Not that I mean anyone supports the ED, but where they are just trying to be supportive toward me while I get everything sorted out and they’ve been trying to encourage me to eat more but haven’t given much push back when I struggle or give into my ED brain. But now, now that I can get medically cleared it’s one step further. Now, I am going to have to talk to the treatment center again, have the case re-reviewed by the medical board, hopefully get this cleared by insurance (that’s my next major hurdle that I am freaking over) and then beginning treatment. But tomorrow, tomorrow is the next step and it feels horrifying, scary and slightly relieving at the same time.

Could “Not Sick Enough” be “Too Sick”??

“I’m not sick enough,” that’s frequently what I have told myself leading up to where I am right now but never ever did I think I might be too sick for recovery. That’s right, too sick.

That’s what happened today on the phone with the PHP/IOP program I called. The guy I spoke to was so incredibly nice and really was very understanding and patient when I wouldn’t know the answer or rambled or whatever. I felt, oddly comfortable talking to him which is rare for me because I am not an outwardly emotional person about my deep dark secrets (I am not a stone cold person either I just prefer to not talk about my personal issues with others). We talked about a lot of the same things I discussed with the doctor on Thursday and about my eating habits, what I am scared of, how it is affecting my life, what types of programs they have, do I have symptoms of a plethora of other mental illnesses or issues. It lasted just over 1 hour. One of the questions was about my side effects,

(trigger warning)

I decided to be honest, totally honest and told him that I have passed out 6 times in the last 2 1/2- 3 weeks and collapsed about 5 more times. I told him about the chest pain, about the night blindness, numbness in my limbs, crying in the grocery store, everything i could think of.

(end trigger warning)

Then came the Concerned Voice. The “you may need a higher level of care” conversation.

Me??? Need higher level care than partial hospitalization or intensive outpatient?!?! I never thought I was even bad enough for IOP!! How could I be worse than PHP!!? These thoughts raced through my mind, overwhelming my emotions. Then came the next thought: They aren’t going to help you. My biggest fear. I mean granted, I always thought they wouldn’t help me because I wasn’t sick enough but now, now I am facing possibly being too sick. My biggest fear is not being helped because, quite frankly, when the doctors couldn’t figure out my GI issues they said “use trial and error.” No joke, those were the words. That’s how I ended up here because I was so scared of the error that I eliminated any chance of error (and every single food except 1 between that and the ED taking over).

The guy I was speaking to could tell I was taken aback. At the end of the conversation he said he would bring it to the doctors and treatment team to see if they would consider the case given that information or what they would recommend. My head was going nuts, I was almost completely in tears. They aren’t going to help was blaring in my mind, racing a million miles an hour. He asked me, “Do you have any questions?” I couldn’t think straight with my head yelling at me, my ED brain screaming at me that of course telling was the wrong decision and this is what I knew would happen and all I could muster was “if you can’t help me then what do I do?” And tears. He assured me that if they couldn’t help me in my current state that he would come back with some kind of referral to another treatment center to another doctor or someone who would be able to provide the level care they thought I needed. I confirmed I understood but I didn’t. I didn’t understand anything.

How could I possibly be too sick?!?!? I’m not sick. I’m not that bad at all, that’s all I have thought for so long that maybe I was wrong. Maybe I really am too sick to even see it.

After I hung up, I just laid down in bed (I was already in bed) and cried. I felt, defeated, lost and hopeless. I felt the exact same way I had after I realized no one could help with my stomach. I felt dead. I had no idea what to do but I had promised my mom to call her. I called her. I cried that no one was going to help that I was all alone, that I might not be “medically stable” and that I didn’t want to do this anymore (both have the ED and seek help).

To be honest, I think part of how upset I was had a lot to do with the fact that it kind of all hit me hard. Here I was facing something much more serious than I thought I originally was. It’s scary to admit you have a problem, it’s even scarier when they tell you that you are much more critically sick than you can see, feel or realize on your own. PHP/IOP are terrifying, the thought of inpatient or residential is downright horrifying. I don’t feel skinny enough or sick enough still and I am still coming to terms with the words ‘eating disorder’ coinciding with my name and coming out of my mouth. It’s a LOT to take in, to come to terms with, to get straight in your mind when you are already aware that your mind is lying to you. So I think my crying, frustration, loss for words, patience and exhibition of sheer terror was just me trying to finally deal with everything and sort it out, something I normally do in the gym or on a run- which I currently can’t function long enough for.

I miss running.

The good news, however, is the guy called me back within a half hour because he was able to get with one of the docs immediately. The doctor recommended going to the ER. I couldn’t fathom that, after all it’s been a few days since I passed out last and honestly, I can’t handle the stress of explaining the situation to MORE strangers. Telling my doctor, my best friend and him all in 6 days is much more than I can handle right now. It’s all moving too fast. They said if I downright refused the ER I could have my doctor do it. Yes. Manageable. Much more manageable. After all she ran blood tests and an EKG while I was there on Thursday. I can handle calling her.

In the end, that’s all I have to do. Provide them with proof I am medically stable (still can’t believe I might not be, so scared) and they will look at the case to see about PHP/IOP. I am still so terrified they will say I am not medically stable but I am trying to stay calm. I called my doctor and left her a message and my mom was really concerned after talking to me and emailed her and she also sent more resources for possible therapy because when my mom emailed her the guy from the center hadn’t called me back about getting medically cleared by the doc so she sent the information just in case but did say we might want to consider inpatient depending on the complications and if they continue. But, I called her office and left a message (it was late in the day about 4:00ish) so I expect a call back tomorrow and hopefully she’ll be able to calm me down or rationalize the situation for me.

I’m just so anxious and realizing how deep into this I am and I both angry and scared with what I have done to myself. Although, thinking about it for a while has helped calm me down I just still feel so confused and scared with where my life is at and what it all has come to.

I’ll keep y’all updated!