Four Skills I’m Pretty Good At #Write31Days

Welcome to day 15 in my #Write31Days challenge on personal growth. Today, I have another list post for you. One of Lisa Shea’s journaling prompts on self-esteem has us write about our skills. What things are you pretty good at? Here goes.

1. Writing. I’m by no means a bestselling author – I have only had one piece of writing published in a book so far. I also make a lot of typeos in my writing. Overall though I consider my writing to be pretty good.

I started writing at about eight-years-old, wanting to become a children’s fiction author once I’d grow up. Now my husband is one of my worst critics when it comes to my children’s fiction, saying my stories aren’t very imaginative to say the least. Then again, when he compliments me on my blog posts, I take it all the more to heart.

2. Calendar calculation. You didn’t know that’s a skill? It is! My husband can’t tell whether October has 30 or 31 day without looking at the calendar, so I’ve got to believe that calendar calculation is a skill. It refers to being able to tell what day a given date in the past or future falls on. I’m not nearly as good at it as I used to be some twenty years ago, but am still pretty good.

3. Researching topics of interest. When a topic captures my interest, I can research it for days on end and will quickly get to know a lot about it. As such, I know a lot about psychiatry – more than some so-called professionals would like me to know. The flip side si that I cannot convert all my knowledge into practice. For example, I know a lot about soap making, but after those first few attempts, I haven’t tried making soap on my own again.

4. Relating to other people in a unique way. Particularly to people with cognitive, intellectual or developmental disabilities. I consider myself pretty good at relating to my fellow clients at day activities. As such, I have been known to come up with some ideas for sensory activities.

What skills are you pretty good at?

Book Review: Where Has Mummy Gone? by Cathy Glass

I bought Where Has Mummy Gone? by Cathy Glass on Kindle right when it came out early last month, but didn’t finish it till yesterday. Not because it wasn’t a good book, but because I struggled to make time for reading. Today, I’m reviewing this foster care memoir.

Synopsis

The true story of Melody, aged 8, the last of five siblings to be taken from her drug dependent single mother and brought into care.

When Cathy is told about Melody’s terrible childhood, she is sure she’s heard it all before. But it isn’t long before she feels there is more going on than she or the social services are aware of. Although Melody is angry at having to leave her mother, as many children coming into care are, she also worries about her obsessively – far more than is usual. Amanda, Melody’s mother, is also angry and takes it out on Cathy at contact, which again is something Cathy has experienced before. Yet there is a lost and vulnerable look about Amanda, and Cathy starts to see why Melody worries about her and feels she needs looking after.

When Amanda misses contact, it is assumed she has forgotten, but nothing could have been further from the truth…

My Review

The subtitle listed on Amazon for this book is “A Young Girl and a Mother Who No Longer Knows Her”. From this subtitle, I already guessed that Amanda, Melody’s mother, might’ve suffered some form of brain damage. Perhaps she was in an accident and had gone into a persistent vegetative state? The thought of dementia also crossed my mind, but I dismissed this when I found out early in the book that Amanda was only 42.

Despite the fact that I had some inkling of where this book might be headed, the twists and turns did surprise me. It was heartbreaking to read about Amanda’s decline. The book ended on a really bittersweet note.

I loved Cathy Glass’ narrative style. I developed a liking for each of the characters. Amanda, of course, elicited pity with her illness, but I also got to appreciate the attempts she’d made at caring for Melody before she was taken into foster care. Cathy maintains a mostly unbiased yet positive attitude throughout the book. I thoroughly enjoyed the book, despite its emotive subject matter.

Book Details

Title: Where Has Mummy Gone?: A Young Girl and a Mother Who No Longer Knows Her
Author: Cathy Glass
Publisher: Harper Element
Publication Date: September 6, 2018

Ways to Take Better Care of My Body #Write31Days

Welcome to day 14 in #Write31Days. Last week, I wrote a post on the topic of what my body is telling me. Today, I’m writing on a similar theme. The prompt from The Self Exploration Journal I’m using today supposes that your body is a temple. How could you better take care of it?

There are many ways in which I could take better care of my body. I’m already doing a lot better though than I used to. Like, until I was eighteen, I wouldn’t touch toothpaste and would brush my teeth with just water. Then, I went to the dentist to find out I had seven cavities. Filling them (without anesthetic) was horrible. From that point on, I started using toothpaste, buut I still had trouble sticking to a regular teeth-brushing routine. I struggled with this for many years to come and have only recently been able to consistently brush my teeth twice a day. I’m still not doing it very well, but I’m getting better.

Another way to take better care of my body is by getting off my behind. As a child, I was fairly active, but my activity level declined sharply in my teens. I got a computer, which meant hours upon hours of screen time. At this point, I’m still pretty sedentary, although I love walking. Since I cannot leave the house on my own, I need to think of ideas to fit in more activity at home. I already go on the elliptical regularly, but I’m thinking I could be dancing too.

Sleep is another aspect of body care that I’ve improved in. As a child and teen, I’d get no more than five to six hours of sleep a night. Now, I make sure that on week days, I get eight to nine hours of sleep. On week-ends, I get much more. That probably means that I’m still not fully rested from those eight to nine hours on week days, but I do’t know how to fit in even more sleep.

An aspect of body care in which I really need to pick up the pieces again, is food. I am doing better than I was when in the institution, when I’d binge on candy twice to three times a week. However, I’m still snacking a lot more than I should.

In what ways could you take better care of your body?

The Most Important People in My Life #Write31Days

Welcome to day 13 in #Write31Days. It’s getting harder and harder to keep up with the challenge, but I was reminded by my husband not to give up now that I have nearly two weeks’ worth of effort put into it.

Today, I’m making a list of the most important people in my life. I’ll also explain why these people are so important to me. I tend not to come across very appreciative of wht people mean to me. I mean, the people in my life right now are mostly very supportive, and yet I don’t tell them so that often.

1. My husband. Do I really need to explain? I first met him in 2007, when I was struggling to hold on living independently. He supported me throughout my 9 1/2 years in the mental hospital and through the nearly eighteen months we’ve been living together now. He also fully supports my choice of trying to get into supported housing, even if it means we can only see each other on week-ends. He’s also just the most loving person around. Hubby, I love you!

2. My in-laws. As regular readers know, I am in low contact with my own parents. For this reason, I’m all the more thankful to have my in-laws. My mother-in-law particularly helps me with important meetings and with other decisions I need to make.

3. My home support staff. I first met my support coordinator in August of last year, when I finally got approved for home support. At first, she mostly just monitored my care with my old support worker, but eventually, she had to step up more. She now sees me usually once a week. My new support worker – the old one was moved to a team in another area – sees me twice a week. They’re both very supportive and skilled and especially my support coordinator goes out of her way to help me.

4. My day activities staff. My assigned support worker is one of the nicest staff working at that group. Not that the other staff aren’t nice, but she is the one who most truly gets me. The other staff truly try too. I am so glad to be here. Now I must say my old day activities staff were nice too, but they weren’t equipped with the information to properly support me. Besides, the manager was probably more stacked against my “psychiatric” needs.

Who are the most important people in your life?

20 Things I’m Grateful For in Life #Write31Days

Welcome to day twelve in #Write31Days. Man, I’m late writing my post today. I really planned on writing two posts today, one for #Write31Days and the other for Ten Things of Thankful. I may write a #TToT post for this week tomorrow anyway, but I also found a great topic that fits both #Write31Days and #TToT. It is to list twenty things (or people, I assume) you’re grateful for in your life. Here goes.

  1. My husband.
  2. My family. Even though my family of origin isn’t very supportive, they are still there. My in-laws are especially importantt to me.
  3. My great team of home support and day activities staff.
  4. My online friends. I don’t have any real-life friends other than my husband, but I appreciate the network of supportive people online.
  5. Our cat, Barry.
  6. My relatively good physical health.
  7. The fact that I’m mentally stable.
  8. More than enough food in the pantry.
  9. A roof over my head.
  10. My computer and iPhone.
  11. Social security.
  12. Never having had to worry about money.
  13. A relatively good health care system. It could be better, but it could also be a lot worse.
  14. Psychiatric medication.
  15. The sensory room at day activities and sensory supplies at home.
  16. Sleep.
  17. Being a lot fitter than I used to be.
  18. The readers of my blog. I can’t seem to stick to just one blog project forever, so I’m glad some people keep following me.
  19. The weather. It’s really good for October right now, but generally speaking it’s never all that bad.
  20. Being alive!

I must admit that in writing this post, I did cheat a little by checking back at a similar post I’d written several years ago. I could probably think of enough things without cheaitng, but that would take me longer, and it’s now time for bed.

The Greatest Life Lesson #Write31Days

Welcome to day eleven in #Write31Days. Today, I picked a prompt from 100 Self-Help Journal Prompts by Francie Brunswick. It asks us about the greatest lesson we’ve learned in life and what makes this lesson so important.

Here I’m going to be a bit repetitive, as I covered this topic already in my letter to my younger self. The greatest lesson I’ve learnd in life is that you need to stay true to yourself.

I have some codependent tendencies. In other words, I tend to be a people-pleaser. For years, I thought that to make up for the burden that I was due to my blindness and other disabilities, I’d need to let other people make everyday decisions for me. In that sense, at age seventeen or eighteen, I definitely would’ve met the criteria for dependent personality disorder. Not because I wanted others to do stuff for me or because I claimed support I didn’t really need, but rather because I allowed others to take responsibility for my life. Conversely though, practically, I thought I had to be extremely independent, never asking for help, for fear of losing other people’s approval.

Until my mental crisis of 2007, I let my parents rule my life. That may be normal’ish for someone at that age, but it wasn’t healthy. Then when I went into the mental hospital, I let my social worker make decisions for me. She was a very authoritarian person, threatening me with forced discharge from the hospital or guardianship if I didn’t do as she wanted.

Then, of course, I let my psychologist on the long-term care unit make decisions for me. Ironically, when she diagnosed me with dependent personality disorder in 2016, she used as one of the reasons the fact that I wouldn’t openly disagree with her. I told her half-jokingly that I assumed she’d remove my diagnosis again if I fought her hard enough on it. She wouldn’t. Her diagnosing me as dependent was based on her screwed beliefs about disability and mental health.

I am now 32. I have the most supportive care team I could wish for. However, if I ever get to deal with less supportive staff in my life again, I know I can and must stick up for myself. I cherish Leonie, my fights-like-a-lioness insider, who emerged when I most needed her, when fighting my psychologist on the DPD diagnosis. I have a right to be myself. I am not dependent on anyone for making my decisions.

How My Friends and Family Would Describe Me #Write31Days

Welcome to day ten in #Write31Days. Today, I’m writing on how others see me. The prompt from The Self-Exploration Journal I’m basing this post on asks how my family and friends would describe me. They probably assume that my family are mostly supportive. My parents are not. But it still helps to look at how tey’d describe me to get to know myself. I am going to list a few qualities I’m told I possess.

1. Strong-willedness. Most of my family and friends agree that I’m pretty strong-willed. This can be a positive thing or a negative thing. I tend to fight fiercely for what I think is right. On the other hand, what I think is right is not always what others want.

2. Intelligence. My father pretty much reduces me to the three digits of my measured verbal IQ at age twelve. It’s 154, if anyone’s interested. My IQ was measured again last year and was down to 119, but my parents feel I wasn’t trying my best then.

3. Determination. Some of my friends view me as quite a go-getter. Other people tend to think I’m quite the opposite. It tends to depend more on their view on my disabilities than on me.

4. Humor. Way back in like 2005, my psychologist asked for my parents and sister to each come up with three qualities of me. My sister came up with my sense of humor. It tends to be pretty dark and cynical. I remember, when I had just been hospitalized on the psych unit, already cracking jokes about the differences between the patients and the staff.

5. Manipulativeness. I just had to list this one. Particularly my parents describe me as manipulative. In a sense they’re right. Then again, what strong-willed, determined person isn’t manipulative in the face of authority figures telling them what is best for them? I think that being manipulative isn’t necessarily a negative thing. All communication is in some ways manipulative, as its aim is to influence others. So can I just say I possess a bit of healthy manipulativeness?

What qualities would your friends and family say you possess?

A Letter to My Younger Self #Write31Days

Welcome to day nine in my #Write31Days series on personal growth. Today, I chose yet another prompt from The Self-Exploration Journal. It asks what one piece of advice you would give your younger self if you could go back in time. Ths question couldn’t be more timely, as I’m facing a lot of regrets from the past right now as I face the decision to apply for long-term care. I am spinnning this questioon around a little and going to write a letter to my younger self. I don’t have an idea for the age of this younger self, but the piece of advice should be the same anyway.

Dear Younger Self,

This is your 32-year-old self writing. I want to reassure you that I see you. I see your struggles for autonomy, for self-determination. And yet, I see your struggles with your limitations. You have yet to come to terms with the fact that you’re multiply-disabled.

I see that peope try to control you. Your parents consider you worth parenting only so long as you prove that you’re going to give back by contributing to society. Your support staff try to please your parents, sending you out to live on your own despite knowing this isn’t in your best interest. Your psychologist in Nijmegen, no matter how helpful she is in some respects, still doesn’t provide you with the opportunity to go into the right type of care. She, like eveyrone before her, values your intelligence over your need for support. Your psychologist in Wolfheze blames you. She robs you off your last bit of self-determination by kicking you out of the institution without proper after care.

I want to reassure you. I see your needs. I’m fighting for them to be met. I don’t have enough support yet, but I have people around me who are fighting for it with me. I can’t promise you that you will ultimately get into long-term care, as that’s up to the funding agency to decide. I can however assure you that I’m fighting for you.

If there’s one piece of advice I could give you, it’s to fight for yourself. No-one can live your life but you. You don’t owe your parents anything. You’re past that point. Care staff do only their job. This isn’t to discount the good work my current care staff do, but it’s just that, work. They will eventually fade out of our life. Even your husband, the only person who will most likely stick by you for a long time to come, doesn’t have the right to control you. I know you want to please him, because you love him, but that is different. Pleasing your husband is founded on love, not authority, and it is mutual. Even so, your husband does not live your life. Ultimately, the only person who will live the entirety of your life with you, is you.

I don’t mean this to criticize you at all. I see how hard it is for you to stand up to controling people. But you’ll learn to do so in time.

With love,

Astrid

What one piece of advice would you give your younger self?

What Emotions Drive Me to Bad Habits? #Write31Days

Welcome to day eight in #Write31Days. Today’s post, like last week Monday’s, is yet again focused on emotions. I took another prompt from The Self-Exploration Journal. It asks what emotions drive me to bad habits.

I have a few self-destructive habits, some of which I engage more regularly in than others. For example, I overeat on average at least once a week, but only self-injure by cutting occasionally. Then there are these little habits that I engage in so often that I barely even notice them anymore, such as nail-biting or most recently teeth-grinding. Just a few minutes ago, my husband asked me to stop grinding my teeth.

Basically, I can be pretty sure that the type of emotional state that drives me to engage in all of these bad habits is stress. Stress is usually thought of as a type of anxiety, but it is not necessarily fear that drives it.

I tend mostly to engage in the little bad habits, like nail-biting or teeth-grinding, when not feeling much of a clear emotion at all. Rather, I tend to be in a state of worry, thinking in circles.

When emotions do reach the point where I notice them, they are pretty close to boiling point already. When this happens I may engage in self-harm behaviors or overeat.

When I look closely at what emotion causes me to engage in these self-destructive behaviors, I see that it is usually a sense of loneliness. Loneliness is not an emotion or so I’m told. At least it isn’t a primary emotion. Sadness is and that’s often what’s underneath this sense of loneliness.

Anger can also drive me to engage in self-destructive habits. Usually though, I am angry at something too minor to matter. The emotion underlying this anger is once again sadness.

What emotions drive you to bad habits?

What Is My Body Telling Me? #Write31Days

Welcome to day seven in #Write31Days. Man, I’m getting tired of this challenge, as it doesn’t look like any of my readers care for it. However, I try to remember what the challenge organizer said, that this isn’t about gaining followers. It is instead a writing challenge to get you writing every single day.

Today I picked yet another prompt from The Self-Exploration Journal. It is: “What is your body telling you?”

I find this a really hard question to answer. I don’t focus on my bodily sensations much, yet when I do, they tend to overwhelm me. I regularly have a meltdown because I simply need to use the toilet. Usually this happens when I am not in a position to find the bathroom independently and the need-to-use-the-toilet sensation has robbed me of my speech. I also commonly have meltdowns because of hunger, pain or being cold.

As I focus on my body, I notice how my mouth hurts from having burned it on a hot snack I just ate. I notice my nose is a little runny.

I have distressing pain in my neck and shoulder muscles. It’s not as bad as it was yesterday, but still bad enough to distract me as I type this post. Good thing that this post is focused on my body.

If I have to guess what my body is telling me with these sensations, it’s probably to take a step back. I was impatient with my snack, thinking I’d need time to write this blog post too so I’d better eat my snack fast.

I’m not sure what the neck and shoulder pain are from. My husband says it’s most likely stress, but is that from doing too much or giving in too easily?

I know about the spoon theory, which describes the limited energy levels of people with chronic conditions. My support worker, who works mostly with people with acquired brain injury, reminded me of it on Monday. This morning, I was quite tired from the mere acts of showering and getting dressed. Yet I still can’t shake that little voice that says that, before I had support, I did these things too and never complained.

So my body tells me to take a break. Now I need to decide whether to listen or overpower its noise with my own and go on.