All packed. 

Taking a huge leap of faith tomorrow. I’m getting on a flight, heading to Illinois and well, going to residential treatment Monday.

I’m a bit stressed over the situation but it’ll be okay. I think. 

I’m going for the right reasons, my behavioral specialists at my current center trained with those ill be working with up north; I’ve got the inside scoop on the treatment center, I’ve been through some treatment so I kinda know what to expect and yet, I have no clue what it is really like. That scares me.

On top of that I went to the doctor on Friday, asked the treatment center if he needed to run tests and was told no, last night they called and said yes. Ugh. So now I have to go to the local ER by the center and get those done on Monday before I admit to the actual center. It’s really not a big deal just I would rather be at my doctors office when they do it. Oh well, I’m considering it an introduction into my new life in an ED residential facility 😏.

Anyway, after Monday I’ll be MIA for who knows how long. I’ll be finding myself, unplugging and getting better. So hopefully soon I’ll be back. I’ll try and post tomorrow and Monday before check in but I guess it depends on how overwhelmed I feel. 

Until then, my bags are packed, I’m all checked in to my flight (with an upgraded seat because, well, something should be extra comfy), I said goodbye to my niece and nephew who think I am on “vacation”, and to a few others who know about my ED and tomorrow my sister and mom will take me to the airport and drop me off. 

I’m not thinking about that part. 

Yesterday I had to say goodbye to my current treatment center. The hardest was to the 3 teens who are like little sisters to me. One was being discharged for good-for which I was psyched- the other 2 will go back on Monday except we won’t get to catch up and bond we will instead be separated by half the country. It sucks. They cried, I held it together until I left and cried the whole way home. They are so sweet, they don’t deserve this disease, they are fighters though and they will conquer this, they inspire me. So T, S and B if you ever read this I hope you are well, that you stayed on recovery’s sometimes bumpy path and I hope you know I cannot thank you enough for being the brightest part of my day in treatment. 

And J, my friend in the adult program, got moved to IOP but she was really my guardian angel in PHP. I have no clue how I would’ve survived without her or have been strong enough to accept my fate and come to terms with going to residential. J I can’t wait to get back bc we are so going to catch up at the cafe our EDs have kept us from ☺️☺️

But to do all that I have to go, my behavioral specialists say the center is stellar and like a family,so while B, S, T and J and our behavioral specialists S and M and dietitian C are all back here, I’ll be thinking of them and working hard to get home to them. I am going to make the most of it though, I actually do like unplugging for a while and I have wanted to live up north for a while so this is sorta like a trial run, sorta. 

Until then, I am excited to see my aunt and uncle tomorrow and have a mini sleepover with my mom and sister tonight before they take me to the  airport 

Going to Residential…

I am officially too sick.

That’s a thought I never once had before seeking help for my eating disorder.

It only became a faint thought when I talked to the admissions officer at PHP and then once I got in, I figured I was good. But starting with my tears over a pineapple cup and the realization that I wasn’t lying about my food intake they instantly began to raise concerns while simultaneously raising my calorie count as rapidly, safely and efficiently as possible.

To get me to the minimum 1000 calorie amount per day I am on 2 Ensure Plus’ a day and they let me bring my own safe food for lunch and dinner (which is the same 1 thing) and they work with me to get my snacks and other intake up higher. I purge too. Which has caused an abnormality on my EKG that is consistent and is requiring me to get EKGs every single week along with getting my blood drawn. The purging is scaring them, in addition to everything else, because they fear it will cause me to have a heart attack. I am scared but I can’t stop, I’ve lost control of everything. I can’t see what I look like, comprehend what I am supposed to eat or how much, know what’s normal and not about feelings toward food, know how to stop the instinctive purging and restricting. I just don’t know how.

So with that, they have officially recommended residential treatment.

I am too sick for PHP, I need more advanced care at a place with a doctor 24/7 and a full time staff to keep me from purging and restricting while I am not at the clinic like I am now. I have to uproot my life, go to Wisconsin (probably) and give up the “freedoms” I have (really they are my ED’s freedoms) and give them to someone else to try and save my life. It’s odd. I am technically not getting rid of my freedom since I guess I don’t really have any while living under this ED but still, it feels like I am giving up everything whereas right now I at least have the pseudo feeling of control and freedom.

My medical director at PHP has called the medical director at their residential facility in Wisconsin to see about getting me in ASAP. They will have a timeframe on Monday so I’ll know when I’ll be flying up. This will be an interesting flight. Instead of going on vacation to Chicago and DC in 3 and 5 weeks like I was supposed to, I am going to be in Wisconsin and not exactly on vacation. I guess that’s life.

Until then, I am on watch. My little sister is staying at my apartment. My therapist and dietitian and psychiatrist have all talked to her and my mom about how much I eat and how I am not allowed to use the bathroom for 30 minutes after meals and for the 30 minutes after that if I do, I have to talk to her the whole time (so she knows I am not purging). I have to eat multiple times a day (I eat small meals due to my GI conditions and because I have less urges to purge when I never feel full) and drink 2 Ensure Plus’. We try to keep me on the same time schedule as at PHP because they are trying to make this easy on me transitioning between weekend and weekday.

I feel like a newborn that they are trying to get on a schedule.

On top of that I went shopping today with my sister after lunch to distract me from food thoughts. I tried on a sweater that is long like a dress and would look good with leggings and I was showing my sister in the dressing room and she looked taken aback. I asked her if it looked okay and she said that you could see how skinny I was in it. She said to get the larger size, much to my EDs hate and the negative self talk went wild, but I did because she said the other one was scary how thin I was. The saddest fact is that I don’t see it. And she knows I don’t so she didn’t fight it but just said that they are supposed to be looser and it’ll be more comfy in residential and in winter so I did.

I wish I could see what she sees though.

So that’s how it is right now. Residential is my fate. I have both come to terms with this and not.  I waver back and forth but feel a lot better than I did Thursday when I deduced that the psychiatrist was recommending residential  after they asked if my mom could come to a session. That, I didn’t handle well because there were still so many questions. But I talked to a friend, we will call her M who has been to residential before we met and J, who is currently in PHP with me and who I’ve become friends with quickly, and she has also been to residential in the past and they both really made me feel better about it. So for now, this second, I am okay with the prospect of residential. Maybe it’s a chance for me to reassess my life and live somewhere new for a bit. I’ve been wanting to move up north for a long time now anyway.

But honestly, I never thought I would ever be too sick for treatment, I always thought I wasn’t sick enough to even complain about my situation but I guess, that’s all part of the illness.