I Found Some Hope!

Have I mentioned that I’ve been struggling with depression for the past month or so? I’m trying to avoid going to the hospital and it has been tough, but today I discovered a potentially helpful community resource.

My day started with 3 fillings at my dentist. With 2/3 of my mouth numb, plus my right eye, ear, and my nose, I sat in my car after my appointment and tried to figure out what to do for the rest of the day before dance practice. I had 7 hours to blow. I sat in my car for a good 45 minutes, basking in the sunlight on Michigan’s first warm spring day of the year and farting off my unfortunate breakfast choice, as I tried to decide whether I should drive home (a 30-minute commute) and sleep off the anesthesia or parade my crooked smile around Salvation Army, looking for deals on stuff that I didn’t need. I finally left with no plan, but then remembered that I had seen a mental health office on my drive in. I would pop in and see what they offered!

With a VERY wonky face, dental chair hair, and (probably) a faint eau de fart aroma about me, I walked into Pine Rest Christian Mental Health Services. No, I’m not Christian. But I am desperate and I would hope that my treatment wouldn’t be heavily peppered with religion. Anyway, the receptionist kindly informed me that their office only offers therapy, med management, and a substance abuse group. I’m looking for bipolar and/or depression groups and possibly partial (day) hospitalization. She made it sound as if the other local branch offered day hospitalization, so I drove there. I could have just called, but I have a stupid aversion to talking on the phone.

The next place was the same story, but they were kind enough to suggest the Elizabeth Upjohn Community Healing Center. So I drove there. This place was the same deal as the first, but with more substance abuse options, plus child therapy. Have I mentioned that every time I open my mouth to speak, the right side of my mouth and face doesn’t move? The reaction from the various people that I interacted with was pretty comical. Usually a look of slight confusion and then terror. Anyway, this time I was referred to the local DBSA  (Depression and Bipolar Support Alliance) chapter. I had to call :(. Nobody answered, but there was a message stating when their group meets (Mondays from 7-9 pm). I was really hoping to find something during the day, when my husbeast is not home with me. He works a lot of hours and I usually only get to spend 3 hours per night with him + Sunday and sometimes I see him on his day off, depending on which day that falls on.

So, feeling like I was at a road block, I got on my phone and tried to see if there was a DBSA chapter in the neighboring county. I’m not clear on the answer to that, but I stumbled across the local NAMI (National Alliance on Mental Illness) chapter, which listed several support groups in my area for family members of individuals living with mental illness (a good find, although not sure the husbeast will ever be able to do it due to his work schedule) AND I read about the Recovery Institute of Southwest Michigan, Inc.

Sorry that this story has gotten so long! Here’s the point: this sounds like exactly what I need right now. The Recovery Institute of Southwest Michigan, Inc. is a peer-run non-profit organization for individuals that are embracing recovery. There are weekly peer support groups for substance abuse, addictive behaviors, mental illness, for veterans, and for members of the LGBTQ community. There are ongoing wellness classes such as “whole health action management,” tobacco reduction, writing about recovery, meditation, yoga, and even an “open studio” time, when people can play games, play music, and share skills with each other. There is individual peer support and recovery coaching available, as well as special events and activities like computer lab, reading and writing tutoring, access to the local YMCA gym and pool, movie screenings, workshops, luncheons, and field trips. All of these resources are available to me for FREE, thanks to individuals like myself who volunteer to make the Recovery Institute work.

I picked up the March and April schedules, and I have so many good options! And all of them are during the day. I look forward to embarking on this new leg of my recovery. I’m sure that I will meet some great people and learn a lot about myself and others.

Do you participate in any groups to help you manage your mental illness? What are you doing on your own to manage your symptoms?

Advertisements

Dr. Copeland’s Concepts Essential to Self-Help

Concepts that are essential to self-help, according to Dr. Mary Ellen Copeland:

  1. There is hope. It is only when you feel and believe that you are fragile and out of control that you find it hard to move forward.
  2. It’s up to you to take responsibility for your own wellness.
  3. Education is a process that must accompany you on this journey.
  4. You must advocate for yourself to get what it is you want, need, and deserve.
  5. Support is essential.

Source: Copeland, M.E. (2002). The Depression Workbook: A Guide for Living with Depression and Manic Depression (2nd Ed.). Oakland: New Harbinger Publications, Inc.

I wish that someone had told me these five things the very first time that I experienced symptoms of bipolar disorder. I kind of want to have them printed on a card that will fit in my wallet so that I can remind myself of these concepts when needed and even share this knowledge with others that may benefit from it. I was going to talk about which aspects I think are the most important, but they are equally crucial. What do you think? Is there anything that you would add to the list?

Holding My Breath

Picture a person in a scary movie who is hiding from a bad person. What do they do when that bad person is within very close range? They hold perfectly still, doing their best not to make a sound. They hold their breath. No movement.

Have you ever tried holding your breath when you are scared? That’s essentially what I do every time that I am afraid to make a move because of my mental illness. I’m doing it right now.

It is painful! But not in the same way as when you are actually scared for your life and forced to hold your breath for as long as possible and then slowly let it out because you can’t hold it anymore without passing out and now, instead of holding your breath in, you have to breathe as slowly, evenly, and shallowly as you can so that it is QUIET. It is the slow, even, shallow breathing that hurts. It hurts because your heart is pumping a million miles an hour, ready to fight or fly, but you are forcing your lungs to pretend like nothing is wrong. They want to suck in as much air as possible and propel you into victory, but you’ve chosen to make them do something that doesn’t feel natural to them.

For me, normal life is halted when I am severely depressed. If I make a decision, it is usually a bad one, so this is my coping mechanism. I become lethargic, with almost no interest in food or the activities that I usually enjoy. I cancel plans, push people away, skip showering, and more. I don’t like doing this to myself. It hurts me to see myself falling into these patterns. But I don’t know what to do differently. I am the scared victim in the movie, hiding from myself. Putting life on hold so that I can survive the next 30 seconds.

I’ve spent countless hours learning coping skills from therapists and self-help books. Some really helpful stuff, but my memory is awful and when things start to go sour, I can’t remember what to do to help myself. I’m 34. Maybe my memory sucks just because? Maybe it’s because of years of different psychiatric drugs? Maybe it’s due to past trauma? I don’t know why, but my memory sucks, which sucks.

Because I’m terrible at helping myself in these times of severe depression, I rely heavily on my husbeast and my mother for support. I become so tired that I fall asleep in the middle of the day and sleep for up to 6 hours. I wake up dazed, hungry, and thirsty, but can’t muster enough energy/willpower to walk myself to the kitchen to get food and drink, so I lay on the couch until my husbeast comes home. He finds me cold (I usually don’t have the foresight to grab a blanket) and starving. But food doesn’t sound good. We both know that I need to eat, but it’s difficult to do so when nothing sounds good.

I don’t like putting that burden on my support group. I see the toll that it takes. I fucking hate that sometimes I need to be rescued. Sometimes = multiple times per year, often for weeks at a time. I have always been the empath/caregiver, and don’t like being on the other side. I want to be able to take care of myself! I’m screwed if there’s ever a zombie apocalypse, WWIII, etc.

My condition affects other things like my part-time job, my small business, and my friendships too but I’ll write about that later. Not really sure where I am going with this, I guess this is a status update. I’m holding still. Doing my best to survive another hour. It hurts, but I’m doing okay. Today’s accomplishments:

  • eat (orange for breakfast, ramen for lunch)
  • drink water (only did 1 bottle, but better than none)
  • put on more than just a bathrobe (I did undies, sweats, and a t-shirt)
  • take care of something other than myself (baby chicks)
  • channeled bipolar energy to create art
  • nap
  • blog about feelings/progress/whatever this is about
  • avoided going to the hospital (keep telling myself one day at a time)

I hope that your day is going well.

Annoying Sound Frequencies

I don’t know why, but certain sounds irritate me and this seems to be amplified when I am “off-balance.” My husbeast likes to watch YouTube videos on our tv about guns, military history, etc. and it seems like 95% of the narrators (not sure if this has anything to do with it, but they are all men) have a voice that gives me brain trouble. My mom’s voice does it sometimes too. She has a deep voice for a woman. The people on YouTube don’t have particularly deep voices. On the contrary, I would say that they are not deep. I call it a headache, but my head doesn’t hurt per se. It feels like I have slightly increased intracranial pressure and all other sounds become annoyances too. Certain vocalists and musical keys do the same thing, as does the sound of the water spilling from the filter in my aquarium.

I call it a headache, but my head doesn’t hurt per se. It feels like I have slightly increased intracranial pressure. When this happens, my ears feel sensitive and other sounds become annoyances too, such as certain musical and vocal keys (although I couldn’t tell you which ones) and the sound of the water cascading out of the filter in our aquarium.

I don’t know how to make it stop other than to remove myself from the situation. I feel bad asking my husbeast to choose a different thing to watch and it sucks when I’m at my mom’s house and I have to leave.

Does anyone else experience something like this? How do you handle it?

 

Back at it

I don’t have a stellar track record of keeping blogs that aren’t related to belly dance going, but I’m going to do my best to not delete this one. Stick around if you want to read about my life with bipolar disorder. I’m just bouncing back from a breakdown, so I’m going to start right where I’m at: working my way through The Depression Workbook: A Guide to Living With Depression and Manic Depression by Dr. Mary Ellen Copeland, which I snagged from Barnes and Noble two weeks ago.