Behind starburst eyes

Corona’s Effect on Mental Health

It’s been months since Covid-19 became a worldwide epidemic, and while I am truly, deeply thankful that my family has not experienced this virus directly, sadly it still has had an impact on my children through their mental health.

He used to be gregarious, he used to be fearless, he used to be happy and confident…Used to be…

It makes my heart ache to see the changes in him, to see how scared he is to even leave the house because as he puts it “It’s invisible, I can’t see it, I can’t fight it” He used to be thrilled to pop over to the store for me, and he’d always ask if he could pick up something for dessert for everyone in addition to the bread or milk I was usually asking for. Now, his first response is “Or I could not go” with a pleading face as he says it. He used to love going for runs, now he says “there’s too many people”. He would rather forgo takeout or new toys if he has to go outside for them.

So instead I don’t ask him to go for me, but I do ask him to go with me. I’m willing to walk with him, because I’m determined to make him go out (while of course allowing precautions such as a mask and hand sanitizer) because he can’t stay locked inside for the next however long. It’s not healthy for him.

I know this might be a long road for him, but I remember when he was 2 and would have uncontrollable meltdowns when we’d walk different routes home from Airzone, he’d cry that it “wasn’t the right way home”. Back then I knew he had to learn there were many ways to get to somewhere, physically and metaphorically. I would hold him and tell him over and over he was loved and safe and I understood and he was my wonderful brave boy as he cried for hours even after we got home.

This is no different, I’ll be there each step of the way offering him love and support as I help him walk this hard path. I love him enough to do the hard things because he always has been and always will be worth the effort to help him thrive.

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Coronavirus Pandemic and Our Emotional Health

We live in Ontario, Canada and our premier has officially declared a state of emergency this morning. This means in addition to primary, secondary and post-secondary schools being shut down for the next 3 weeks, now our daycare centers, restaurants (dine in portion), bars, cinemas, libraries, museums, major venues such as the science centre, and recreation centers are all shut down until at least April.

We homeschool our 3, but my two stepdaughters attend public school at their mother’s insistence. So this changes some things for us, but not all things. Obviously daycare facilities being closed doesn’t effect us. However, everything else being closed does.

One of the ways all of these closures effect us is through fear and anxiety. My youngest son has asthma and has had to be on oxygen and nebulizers in the past, so I am in a heightened state of anxiety. But I’m not the only one, my children feel it too. Not just through me, but also because news of the virus is everywhere and both kiddos understand the potential implications for their brother, and he understands the implications for himself. To that end we have been working a great deal with the concepts of fear, anxiety and powerlessness.

Acknowledgement of Emotions:

We’ve spoken about how scary it can be to feel like you’re powerless in a situation, and how to work with that feeling to acknowledge it but not let it overwhelm us (a thing I am struggling with myself as well).

Then, I attempt to teach them how to work through their scary thoughts. We talk about their feelings, how their real and valid first. But also that even though their valid, we don’t have to be ruled by them. We can focus on the things we HAVE done, the things we ARE doing, and the things we CAN do during this time.

Breathing Techniques:

Once I’ve validated their emotions we do breathing exercises. Five deep breathes in through the nose and out through the mouth. This helps to calm the nervous system down and allow the pre-frontal cortex to come back online (center of logic and reasoning).

Mindfulness Exercises:

Mindfulness exercises such as finding 5 things they can see, touch, and hear can also help to refocus on calming the mind enough to work through any scary thoughts.

Positive Actions:

Finally, we focus on something positive, such as on gratitude, love, giving to others, or constructive actions. We do this because in allot of ways our thoughts are like roads, the more frequently their used, the more deeply they become entrenched and at times like this we NEED the positive perhaps more than ever.

For one child, focusing then on how grateful they are for the healthcare professionals or our ability to have things delivered to lessen our chances of exposure is helpful.

For another it’s expressing love through acts of kindness such as offering to play another siblings favorite board game or reading a book to a younger sibling.

For another it’s writing a card to send to someone they can’t see in person right now, or walks in the conservation area to be in nature.

For me, it’s constructive physical acts that help, for example organizing cupboards and labelling jars with our supplies or sorting the kids clothes for donations (I’ll wait to donate, but I’m happy to pop bags of donations in a closet ready to go once this is all over). Each person is unique, so choosing the positive actions that work best for them should be specific to them.

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Dear Mental Health Professionals:

dsvm cover

I am aware that the DSVM (all editions since the 3rd) include Autism as a mental illness/disorder. However, just because they are included does not make the mental health field correct in their assessment of Autism as a disorder. It is included because Western society has a serious lack of acceptance of anything different. All things different should be treated and minimized to the greatest degree possible, is often the misguided thinking with Autism and many other neurodiversities.

The Ontario government has released a statement that they are pledging $333 million dollars towards treatment, but that the maximum age for treatments of IBI will decrease to 5 years old. This is said to be because the greatest chance for changing these children is until they are 5 years old. After that, it becomes harder to help change their behaviors to mirror neurotypical behaviors.

Autism is looked upon as something to correct, or at least to help intervene as much as possible and push towards encouraging the person to act as neurotypical as possible. I’d like to ask you why this is? I’d like to ask you why someone has to behave the way you do for you to see value within them? I’d like to ask you why biodiversity in the world is a plus, but neurodiveristy within humankind is not? I’d like to ask you why someone has to live in a predetermined manner for it to be the right way to live? I’d like to ask  you what is so bad about allowing someone else to live their version of a happy life, even, especially if it’s not the same definition of happy as yours? I’d like to ask you what will it take for you to see that my sons do not have a disorder, they have a different neurological structure. What are the words you need to hear to understand that their value is not to be based upon how well they can become chameleons in society, but that their value is based upon the person they truly are when they stop trying to fit into your rigid, substandard predetermined cookie cutter shape of humanity…The Autistic Person they always have been and always will be does not need to be fixed, they just need to be loved, respected and appreciated for who they are, just like every other living creature on this biologically diverse planet.

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Depression, Suicide, and Pills

I had what I’ve read is one of the “hard” talks with Mr. C tonight. We talked about bullying, depression and suicide. We talked about how sometimes some people that are being bullied feel like they have no other option to escape their situation than to take their own life. I promised him that there is always a solution. That if we had to I would pack everything and everyone up and move 500 km away to get him out of that kind of situation. (I also explained there are other less drastic solutions we’d try first) But to never ever think he was trapped in that scenario, because if all else failed I’d hire a moving truck. I meant it. I wouldn’t want to move because of something like bullying, but I’d sure as shit do it if I knew it would make the difference between having Mr. C with me and not. See there are lots of studies that show a correlation between Autism and depression. But more importantly I know his family history, including his maternal medical history.

We then talked about depression. We talked about how sometimes for many different reasons (including but not only because of bullying) some people end up feeling like they’ve “lost their happy.No matter what they try to do, including activities they used to love, their happy seems just out of their reach. I explained that it could be because the brain isn’t making the right amount of certain chemicals. It could be because of a really hard time in a person’s life. I also explained it could happen with no obvious cause in sight. I told him it was important to talk to me or another grown-up he trusted if he felt like his happy was gone. We talked about the difference between being sad, having the blues, having the blahs, being upset and being depressed. I told him it didn’t matter which one he was feeling it was okay to talk about it and that his feelings would be respected. I promised him I would never slough off his emotions when they weren’t “happy/shiny”

I’ve read that these were hard conversations to have with your child, but for me personally that wasn’t the case. Instead I was grateful to have them with him. I was glad to hear him say that he knew suicide was never the answer. I was thrilled to hear him say he trusted me to help him find a solution should he be bullied or feel like he’d lost his happy. I’m glad because I’ve struggled for 11 months to find my happy. It’s been since we lost Joy that I can’t seem to find it. I try, and I have brief moments where it seems almost within reach, but then it slips through my fingers again. I end up staring off in the distance trying to remember how to smile like the woman I was in the hopes that if I go through the motions long enough I’ll finally BE her again. Only it hasn’t worked. I see her staring back at me through the mirror, so clear I could almost touch her, but really she’s like a faded photograph, because she’s just a reflection of who I used to be. So I went to my doctor finally and I am now taking something to help. Because I tried everything I knew, but I still couldn’t find the happy woman I used to be. Which is part of the maternal medical history I know of for my children. The part that makes me aware of how needed conversations like tonight’s was to ensure should he ever be facing a rough part on his path he’ll ask for help in walking it. Because that’s what I’m here for, to help each of them in whatever way they need. I acknowledge a part of that is also taking care of myself. In part so that I CAN be there for them, and also to show them it’s OK to ask for help when you truly need it.

Canada:

If you are contemplating suicide, please contact your doctor, or go to your local emergency room, or dial 911 from any telephone.

If you are being bullied, depressed or just need someone to listen and you are under 20 you can call Kids Help Phone 24/7 for free: 1-800-668-6868.

If you are an adult and find yourself in a mental health crisis: Canadian Crisis Centres is a list of crisis centres across Canada, with local free phone numbers.

You can also dial 211 from any phone and ask to be connected with your local crisis service.

In the USA:

Crisis Service: 24/7 for free help 1-800-273-8255

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Teenage Mutant Ninja Turtles

tmnt

I have agreed to speak at a local event called “The Heart of Ajax” this coming Wednesday. The really cool part is I’ll be speaking with a bunch of youths from all over the town of Ajax who will then devise a plan to take back to their school that will do one of the following: Raise awareness, Teach other kids how to be an Ally, Raise funds for an organization or in some form bring about positive change and positive impact in the lives of others. I was asked to speak about mental health, the stigma surrounding mental health and how to be an ally to those not classified as neurotypical.

I have thought extensively on what I wanted to say. I have started a dozen speeches, and threw each one away. Then tonight as I watched my son gently lean in to kiss his sleeping cousin’s forehead I saw her wall decals. She adores Teenage Mutant Ninja Turtles (TMNT) and I knew right then what I was going to talk about.

I hate TMNT. I hate what they remind me of. When I was in Grade 5 there was a boy in my grade who loved TMNT. we’ll call him “Shawn”. He would talk about them every single recess, and lunch hour. It didn’t matter if other kids really paid attention our not, this boy would still talk about them. See he didn’t really catch social cues all that well. He wore clothes a bit different from the rest of the boys my age, instead of jeans he only wore sweat pants, and his shoes had Velcro instead of laces. He would go into a special room with a special teacher than none of us had seen before for allot of his day. He didn’t always brush his teeth, enough so that the other kids really noticed the build up on his teeth at times. He was never mean to anyone. He would smile and say hi to everyone every day. For quite awhile, the first few months at least he tried to play with the other kids at our school. Every recess, and every lunch hour he’d try to insinuate himself into our games and our conversations. Most often his addition our conversations was to change the subject to TMNT. There was a girl in my class who was not very nice to allot of kids. She was especially mean with this boy. She would laugh at him and make fun of him and purposely exclude him from games and interactions on the school playground.

I never said anything mean to him. I never really said anything at all to him. I never stood up for this boy. I never tried to be a friend to him. I stayed silent when he was being slighted or shunned or made fun of. 22 years later I still have a lump in my chest when I think of him. I still feel bad that I wasn’t strong enough to stand up for him. I didn’t know why he was different. I didn’t understand it. I didn’t understand him. Do I know what his official diagnosis was, no I don’t. In part because we didn’t talk about that stuff back then. We didn’t get presentations or custom made books in our classroom to explain why someone was a bit different, and that we should accept them as they are. We didn’t have Autism Awareness Day or many of the other Awareness Days we now have for mental health/neurological diagnosis’s. But those are just excuses I tell myself when I look at my two sons. Pat answers for why I wasn’t the type of person I now want other children to be towards my own Autistic boys. The truth is, acceptance is taught. Acceptance is learnt, through being open, through conversations and presentations and through real life moments with someone who only wants to talk about TMNT.

My goal is to help these kids see how to be better than I was at their age. My goal is to help them develop their own school’s plan for increasing awareness of, and acceptance of persons with, various diagnosis’s. I want for the “Shawn’s” of the world to be invited to a birthday party when the entire class is given invites. I want their additions to conversations to be valued, even if they’re not agreed with I want them to feel like their peers are listening when they speak. I want for these kids I’ll speak with tomorrow to learn and in turn to teach others how to be an ally to those different from themselves. And maybe even to be open to the possibility of friendship with people with all different neural structures.

That is why I hate TMNT, because they remind me of when I failed at being an Ally. I failed at being open to someone different than myself. That is why I also love TMNT, because they remind me to be better, to be the type of person I would want in my own child’s life.

P.S “Shawn” I doubt you’ll ever read this, but if you do: I really am sorry.

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Nation Swell

My Facebook feed often has different videos in it, and this was one that I felt compelled to share. It’s about a doctor that treats homeless people, not in a shelter, but out on the streets. For the last 22 years he has been going out 5 nights a week and offering health care to homeless individuals including providing antibiotics, inhalers, cold medicine, splints, bandages and more should he feel the patient needs them.

At one point in the video he says that he can see himself in them, that they are just people and that he too could have been homeless if for different circumstances. He then says at the end “Everybody matters, we need to look out for the people that are the most ostracized” Here’s the thing, according to Canadian Alliance on Mental Health and Mental Illness 66% of homeless persons in Toronto, Ontario have a diagnosis of a mental illness. Furthermore, according to them 1/3 of homeless persons are without a home directly due to their mental or physical illness preventing them from obtaining and or keeping housing for themselves. This makes me angry, why because he’s right, and most of society isn’t paying enough attention to the simple fact that we as a society should be helping one another in constructive ways. It also points to me at least to the disparities in what is needed for those with various mental illness diagnosis’s to thrive compared to what resources are actually readily available and easily accessible. It points to me to at least to the fact that mental illnesses or disorders or whatever word you want to use are still stigmatized and this makes me want to talk more about things like Autism, it makes me want to be louder about my real life with my kids, to be so loud for as long as it takes to stop the stigma, to push for better services (not just for Autism, but all persons not classified as “neuro-typical”)
Be loud with me, and together we can change the stigmas attached to not being neuro-typical, we can change our society one step at a time, because we ARE our society. Just as Dr. Withers has been changing it with his nightly walks.

 

Dr. Wither’s video can be found here: http://www.nationswell.com/making-house-calls-people-without-homes/

The Canadian Alliance on Mental Illness and Mental Health page that I mentioned can be found here: http://camimh.ca/mental-illness-awareness-week-english/about-mental-illness/what-is-mental-illness/homelessness-and-mental-illness/

 

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Summer Solstice Strawberries & Our Virtues

Every year we pick strawberries on the first day of summer. We make various jams from them, and put some in bags in the freezer for delicious smoothies. We also talk while we’re on our way there, and during it about a few things. We talk about how it’s the first day of summer, which means it’s the longest day of the year. We talk about all that Mother Earth has grown since the first day of Spring. As well as all that we have grown in our lives. We discuss that which is ready for harvesting in our own lives as well as what we need to further nurture and grow more before it’s “ripened” in our lives. We talk about the unintentional “plants” we’ve sowed (such as being argumentative, or jumping to assumptions, or whatever it is that each of us has been “growing” in our lives.) The good and the not so positive all get reflected upon. Then we decide what we shall continue to nurture and what we shall “pull” or “weed out” of our lives and ourselves. I started doing this with the kids as well as myself when C was very young, because I feel that regular introspection and honest reflection about ourselves is one of the ways we can help ensure we are growing in the ways we want to be. Conversely, it means that the things we don’t want to be “growing” within ourselves can be “pulled out” faster, when it’s had less chance to grow unchecked. It’s easy to say we’re going to do _____ and ____. It’s a bit more challenging to really look at oneself and see where we’ve perhaps gone off the path we’d prefer to be on and admit ownership of our “flaws” or less than virtuous aspects. But with regular honest, open reflection on who we truly are at that point in time and how it fits with who we aim to be we can foster the traits we most admire like honesty, patience, selflessness, honor, etc with better results than if we leave ourselves “unchecked”.

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Pick me up

When I’m in a bad mood I’ve long been of the practice to do something for someone else to help lift my own spirits. Years ago before they had to start refusing such offers I’d bake for homeless shelters and soup kitchens as a way of creating beauty or good energy when I was upset about things I could not control. (They now have to refuse them due to health code regulations, unless you are an actual business that has been okayed by the health department)

Tonight I was not in a great mood. Nothing really wrong per say, just feeling blah and a bit down, a touch of restlessness had settled in and I felt a bit constrained. SO I thought I’d take the boys for a walk, and on our walk we brought sidewalk chalk. We had an amazing time! C and I wrote inspiring messages at random spots, things like “You are special”, “Life can be GREAT” “You are loved exactly as you are” and so on. N “helped” us to write the messages and was fully loving being completely included, so a few of the messages may not be super clear lol but it was a lovely experience for them and for me.

By the time we came home I was in much better spirits, and both boys were in lovely moods. It’s funny the messages were supposed to be for other people, random strangers to see, to take in and to perhaps offer them a spark of positivity. While they just still might, those messages definitely gave the 3 of us writing them a whole slew of positivity too. 😀 

I’d like to think that they did, and that the ones C and I wrote together will do the same for someone seeing them come morning. 😀 Have any of you dear readers seen sidewalk affirmations at one time or another? If so, did they indeed offer you a spark of positivity that day?

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Autism is NOT a death sentence

Just over a month ago C and I made cookies for his home school group at the YMCA to help promote Autism Acceptance. With how positive of a reaction we received from them I asked one of the people who helps to coordinate the Orientation for Parents of Children Recently Diagnosed with Autism at Grandview Children’s Center if they would be interested in having some at their next orientation. She spoke with the her colleagues and they said yes. So today I went and got more business cards for the packages I’ll be dropping off Saturday morning. I’m happy that they said yes to them as I feel they do have a positive message to them. So often I hear of parents being absolutely desolate about their child’s diagnosis, and I think our perception as a society needs to change about that.

Last year on C’s 8th birthday his father and I were not with him. The night before, I called everyone that was supposed to come and told them that we had to post-pone his birthday party. Why? He’d done NOTHING wrong. We had to cancel his party and leave him with his Nana because we had a funeral to attend. A close friend’s 23 month old daughter had passed away. Now that was something to be absolutely desolate about. Her’s is a place that will forever be empty at their table, the memories of that beautiful precious little girl are what her parents get to hold instead of her. That is a truly devastating loss. One that those two parents must bear.

But to perceive a diagnosis of Autism as the same level of tragedy as the loss those parents deal with every single day is in my mind an insult to both the little girl who will never have a second birthday, as well as to the child diagnosed! It is NOT a tragedy that one’s child has been diagnosed with Autism, it is not something they will die from. Will there be some areas of their lives that are more challenging because of how their neuro-pathways work? Yes. But that’s what parents are for, to help their children to thrive to the best of the child’s abilities. Now I understand that some people would argue that a child classified as “Classic Autism” or as “Low-Functioning” does not have the same level of abilities to function as a child that is classified as “High-Functioning” I’m not arguing levels of abilities, but I am arguing that Autism is not a death sentence and should not be approached as one.  Yes there will be times that are hard for both parent and child. There will be times when as a parent you might not be sure how best to help your child. There will be times when they are judged negatively by others, when your parenting choices will be called into question by others, but all of those statements are true for parenting of any child!!!

To mourn the loss of the child you thought you had, the one that won’t _______ because they have Autism is unfair to your child. They are still the same child as they were prior to a diagnosis. They still have feelings, thoughts, dreams, wishes, fears, hopes just like any other child. Will they need different kinds of help or parenting than you originally thought you’d have to provide when you learnt you were going to become a parent, perhaps yes. But our job as parents is NOT to dictate what they need, but to observe them and their ways of communication to understand what each unique child needs us to provide them with and help them with.

These children can and do go on to lead lives that are happy and fulfilling for them, perhaps it’s not your definition of happiness and that’s okay because it’s not your life, it’s theirs. As long as your child is alive, and happy what on earth do you have to mourn???

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To My Children

From the moment I knew each of you was on your way I have spent every moment of my days and nights devoted to you.

I anxiously awaited your arrivals,

I have pondered for countless hours a million different aspects of your upbringing, from the largest facet of child rearing to the most minute of choices,

I have made countless phone calls for counsel on the best way to handle various situations I found myself immersed in due to being your mom, searching for the best solutions for each of you,

and I promise you that I shall continue each and every day to be the best mother I can to each of you…

I’ll go hungry so that you may eat,

I’ll go cold so that you can be warm,

I’ll go without sleep so that you have time to dream,

I will fight for you so that you are safe,

I will stand in the shadows so you learn how to shine,

I will find time when none exists to do whatever needs to be done to see your faces light up with joy,

I’ll endure whatever hardships are necessary so that you always have what you need no matter the cost to me,

At the end of it all, I will let you go with a smile upon my face when it’s your turn to fly; Knowing I did every single thing that I could to help each of you reach your fullest potential as the amazing individuals that you are…

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