Writing to Discipline My Thoughts

Disciplining My Thoughts By Writing

This morning I attended an OC Writers’ write-in. I haven’t attended a writers’ group in a long time. Been isolating myself and focusing on my son rather than my writing, rather than myself. Today, I left him home in bed, then left the meeting early to get him to class on time. When I got back home, he was dry-heaving in bed. Crap.

Hate spending my mornings trying to wake him up to do his homework and go to school. He will be seventeen next month. Time to wake up and do homework on his own. Unfortunately, his private school is not within walking distance, nor would it be a safe bike ride, and my kid has no interest in getting his drivers’ license yet. So, I’m still driving him to and from school.

The first week of June, during my son’s summer break when I didn’t have to act as alarm clock and chauffeur, I started cleaning my house with help of my next-door neighbor. She did most of the cleaning and organizing. I chatted and did a wee bit of organizing. We tackled the kitchen, spending two hours on Monday and two hours on Friday.

The second week of June was my son’s first week of summer school, so I took the week off cleaning and organizing. He has a full schedule this summer. He attended most of his classes last week, perhaps because I offered him $10/class/day. He’s motivated by money. It costs more to reschedule his classes than it does to pay him to attend.

Hypomania Raises Its Head (Again)

Last Tuesday in therapy, I said I no longer felt hypomanic. At the time, I seemed relaxed, at ease. By Wednesday my mind was racing. At night, when it was time to fall asleep, to slow down my mind – instead of thinking in my usual monologue, as an orator narrating my life – I heard a cacophony of voices.

I wondered if, when those voices crowded my mind, I should have written them down to see if I was thinking in dialogue. Were the voices characters wanting to be heard, auditory hallucinations, or thoughts racing so fast, I could not make heads or tails of them? Most likely speeding thoughts.

When I couldn’t fall asleep, instead of writing, I medicated myself to sleep. I force sleep when it won’t come on its own.

As I wrote last week during the day, while my son attended school, I could not hear the noise. Instead, I focused on my voice and that’s what I thought. Writing disciplined my thoughts.

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Silent Lately

Silence - background of clouds over Saddleback mountain range formation and trees in foreground

I haven’t written in a while, nor have I read or commented on others’ posts. I used to write brief reviews after reading a book. Recently, I’ve simply left stars on Amazon and Good Reads.

Why? Because I simply needed to recover. Recovering not from an episode of bipolar disorder – though I do live with that illness and must take care of myself – but from exhaustion, physical illness, and the demands of life.

Sometimes I need silence. Sometimes I must do less. I must NOT do.

Since my mother had her stroke November 2015, I’ve had added responsibilities overseeing my parents’ finances and care. My sister helps me make decisions and offers emotional support, but she lives in another state and has her own life to live.

I parent a high-needs adolescent who gets sick A LOT and has struggled throughout his life with migraines, ADHD, depression, and anxiety.

My husband, son, and I have all been sick.

All this weighs on me.

So, I’ve pulled back.

I’ve been silent.

I’ve binge-watched TV.

I’ve done lots of jigsaw puzzles on my iPad.

Hope - yellow hibiscus background

Starting Monday, I’m hiring my neighbor, who has been a caregiver to seniors, to help me with my chaotic physical environment. Together, we will organize and clean my house. It’s cluttered and dusty. The floors and refrigerator need cleaning. Hopefully, that will improve both our physical and emotional health.

Spring Brings Hypomania

SpringBringsHypomania

This year, as winter has ended and spring has begun, I’ve taken it slowly and protected myself from overstimulation. You have not heard from me as much, as I’ve not been as active writing here or on social media.

You see, springtime triggers hypomania in me. Now I’m experiencing mild hypomania, irritability, and some mixed features. I feel myself internally crying, and on the verge of tears. I have good reason to cry, but my feeling of emotional vulnerability and instability goes beyond my current life circumstances. Perhaps, for I’ve never experienced losing my parents to dementia while raising a chronically ill teenager and living with bipolar disorder type II. Sounds pretty stressful.

My response is to cocoon, to reduce stimulation, to take sleep meds if I must, to reduce stress. When I haven’t been busy caring for my son or visiting my parents, I’ve relaxed and let my husband spoil me.

Hopefully I’ll feel much better once tax season is over. Exhausting and stressful.

Hypomanic Episode Symptoms

By Steve Bressert, Ph.D. for PsychCentral

  • Inflated self-esteem or grandiosity
  • Decreased need for sleep (e.g., feels rested after only 3 hours of sleep)
  • More talkative than usual or pressure to keep talking
  • Flight of ideas or subjective experience that thoughts are racing
  • Distractibility (e.g., attention too easily drawn to unimportant or irrelevant external stimuli)
  • Increase in goal-directed activity (either socially, at work or school, or sexually) or psychomotor agitation
  • Excessive involvement in pleasurable activities that have a high potential for painful consequences (e.g., the person engages in unrestrained buying sprees, sexual indiscretions, or foolish business investments)

Source: psychcentral.com/disorders/hypomanic-episode-symptoms/

Who Do I Care For, Really?

Definition of caregiver: a person who provides direct care (as for children, elderly people, or the chronically ill) https://www.merriam-webster.com/dictionary/caregiver

I spend way too much emotional and physical energy toward the care of others, aside from myself. Why do I care so much, too much? No doubt due to my upbringing, to my relationship to my parents – trying to please, to earn their love and approval. Why, after decades of therapy, do I still feel and act as an enmeshed parentified daughter? I’ll just leave that question hanging there for now. Not up for explaining alcoholic family dynamics. Too tired. Adult Children of Alcoholics has a good concise description.

Who do I really care for? Good question. My husband and my son are the most important people in my life. I have devoted a great deal of time and energy trying to help my son. Too much, perhaps. No, not perhaps, without doubt. Now, I need to step back, to neglect a bit, to allow for more independence. Time to do just enough. To be just good enough. Just enough. Enough.

My sister, trying to help me set boundaries and stop taking on too much emotional responsibility, reminded me that I am not our parents’ caregiver. They are in memory care. The memory care facility provides their daily care. That’s what we pay them for.

I am not my parents’ caregiver. I am my son’s caregiver, and even he could use less of my care.

Now that my parents both have dementia and live in a memory care community, aside from being their daughter, my role is to be their power of attorney. With my sister, I make decisions on their behalf. I pay their bills. I coordinate their care, which is not the same as giving them direct care.

Before my mother’s stroke, I did not visit my parents regularly. I did, though, talk and play Words with Friends with my mom daily. I miss communicating with her. I miss my parents as they were before dementia. I’m grieving.

Living with bipolar disorder, I must take care of myself. This season, springtime, is a time when I often start mood cycling. I’ve feel particularly vulnerable and fatigued. The longer sunny days trigger hypomania and irritability.

On a more positive note, in January and February and again next week, I’ve been a NAMI Provider Educator for the staff at the hospital where I received both inpatient and partial day treatment twelve years ago. I enjoy educating their staff on what it is like to live with mental illness and to be in mental health recovery. Wish me well next week. We’re increasing the time that we devote to our personal trauma stories, so I must rewrite mine. I may edit my In Our Own Voice presentation for content, or I could take a look at what I have shared here.

Reunited and Learning ASL

My mother has moved back in with my father, back into the same Silverado memory care community (which is lovely), again sharing a room. I hope and pray it goes better this time round than last when they isolated and refused medication and care. They love one another very much, so it is wonderful to see them together.

Missing his old home, my father asked about his old beach house which we sold last year to pay for their care. The staff has told my dad “therapeutic white lies” about the house, such as saying that the plumbing is being repaired.

Instead of using a “therapeutic white lie,” I skirted the issue, telling my dad that since my mom had her stroke, she needs care and that the house was too much work. He asked her if she wanted to live in the memory care community, she nodded her head yes (since the stroke, she hasn’t been able to speak).

I told him that it was no longer her job to cook, clean, or take care of him. Up until the stroke, she was his caregiver, as he’s had progressive memory loss for years. I told them that their individual needs differ now. Mom cannot use language, but dad can and should take part in community activities designed to exercise the brain and fight memory loss.

The community’s social worker has started working with my mom to help her communicate her feelings. My mom didn’t like using communication boards. I knew from previous attempts at using them that my mom doesn’t seem to understand what the drawings on the boards represent. She didn’t want to try writing either, as she knows that she simply cannot.

BUT… the social worker discovered that my mom responds to ASL (American Sign Language). So now my mom, dad, and I are using simple ASL signs to communicate. Not sure how much my father will remember due to his dementia, nor how much my mother really understands due to her stroke and vascular dementia. At least, my parents seem to enjoy learning it.