ADDventures

mommy noodles

this is why i love my kid.

they can drive me nuts through the day fighting and whining, and making  ABSOLUTE mess of the house, having temper tantrums over sensory issues, being cranky from lack of sleep etc.

But today, she had a fairly decent day, though she was whiney and cranky from the heat….then after a lovelery swim in the pond we come home hungry and the girl makes her own supper wth some help… a can of alphabet noodles.

In the middle if eating she asks “can I borrow your DSi for a minute?” I say ya, but give it right back. She did, and I never looked until just a few minutes go to what she wanted to take a picture of… and this is what she borrowed it for!

Planning lessens my anxiety

So planning things is helping me not have so much anxiety.

becoming more aware of my high anxiety times is helping me avoid total add/aspie meltdowns.

all my life I’ve been a sort of “fly by the seat of my pants and see where I land and deal” kind of person.I think one of the reasons I avoided it like the plague is because I fear needing to be very rigid and have strict planning to function. it’s almost like dealing with the chaos feeds my ADHD need for stimulation, and my aspie side of me is cringing, and having anxiety the whole time.

So planning things, and using a day planner/to do list has not been natural to me, nor has it it been easy to start as a habit.

I’ve finally come to some habits that are making things easier for me, though if I get interrupted/sidetracked in my routines, I forget things lose things etc.

Slowly I’m trying to fix the mess I’ve made of this place since our move and my mental burnout. Your looking at someone who has taken 11 years to remember hubby needs his bread toasted to be able to eat it ( oral sensory issues)

So, I have a day planner I write a week out in, in an overall plan, and then each day of the week after the general plan I write out info that is important as those days come, like who I called, recipes, my master to do list for the week, and next steps in those projects .. really it’s just a composition book, with blank pages, so I have no worries of needing to remain neat, or confined to a certain amount of space.  it IS my brain it holds everything.

and I have a calendar I write out meals on for a week or more to have a plan.

On Sundays I plan the weeks meals ( generally, sometimes they change)

This week, my menu plans are

Chicken taco crockpot w/home made Naan bread

Salmon Croquettes w/dill sauce

beef crock pot & gravy w/mashed potato

Veggie Lasagna

Pizza

Crock Pot Pork with orange and Videlia onions & rosemary rice.

This Collage makes me Cry

This collage makes me cry.

These are pics of my kiddos. This makes me cry, not because they are some of the cutest frackin’ kids you’ve ever seen, but because this collage even exists.

I didn’t make it, and it is not on my wall.

My friend SJSH made this collage of my kids for her wall…from my facebook pics. she had asked me for the better pics of originals to get it done, and waited a long time… and I never got around to it.

She reminded me over and over, but she knows me.

And I know her.. we just connected and have known each other now for 7 years. she was my neighbor when we moved into our building when the girl cub was 2. I baked homemade bread and brought it over, and from there, a friendship budded. establishing and maintaining a friendship has never been so “right”…like puzzle peices, we just fit.

no matter how long we go without talking since I’ve moved an hour and a half away, we fall right back into as if we were right next door. when we lived next door to each other, we’d talk in the phones across the hall. while doing housework, I could hear her defrost her freezer through the door, while we gabbed on the phone.

So…. she got her son to get the pics she wanted and help her put this collage together for her wall.

I LOVE that and it makes me cry, because she loves my kids, and thinks they are so smart and beautiful and she has the biggest heart! The Cubs love her, and not a day goes by that they don’t talk about her :)

I’ve said it here before, she was at the boy cubs birth for the three whole days, she helped us move ( move from hell) and she is always a phone call away for a laugh or a .cry, or gossip.. we never fall short of things to talk about.

In short…I love this woman, and her family. they are awesome people, and I’m glad they are our friends. Family is not the people you are born to, or give birth to, or are stuck with at easter dinner out of obligation… family is there through thick and thin, and laugh and cry with you, share your joys and your sorrows with you.

I’m glad I have SJSH as part of my family… she’s the best kind :)

Cherries!

"I'm the bestest cherry picker in the whole world mommy!!!?"

Time doesn’t heal

they say time heals….i say bullshit.

Time doesn’t make the death of someone you love hurt less. You don’t heal. you just learn to live with a gaping hole in your heart, and learn to live with the pain.

It’s like acquiring a disability from a sudden car accident that will change you forever.

the initial grieving is like rehab, a period of time that teaches you how to go on through the day to day for the rest of your life differently.

sure you get so used to the gaping hole in your heart you kind of have a new normal, and go on about your life. But it’s always there, you never really forget, even if you can go a day or a week forgetting your disabled now, you will see something, hear something, and be smacked in the face by how much it still hurts.

Today is the anniversary of the day my brother died 13 years ago.

It is hard to believe it has been 13 years! some days it feels like yesterday. live in his basement that I rented from him. I came home from work at 3 in the morning to be greeted by the blunt news on the driveway… “Paul’s dead” with a somber, no emotional expression on my then husband’s face.
i fell to the ground, I screamed, i refused to believe it, i demanded they take me to the hospital to see my sister in law, and  see this apparent reality for myself. I’ll never forget. I wish someone had warned me what I’d see. they still had all the tubes and wires attached to him from trying to revive him ( which was futile, he was dead before he fell to the floor at a resturant.) i keep this picture out and framed where I can see it, because if that memory pops in my head, I NEED to look at this picture to get that image out of my head. I used to be angry at my first husband for how he told me, but I realize now that he was just as shocked, and that he is a “fixer” kind of person so he was trying to be strong for me, and my brother’s children, and my sister in law, and my parents.

My sister in law ( ex husband’s sister) had taken me to the hospital, then she took me home and I never slept,I changed clothes and she drove me from Toronto to Hamilton so I could tell my sister. I didn’t want her to find out over the phone. That was the hardest thing I have ever had to do in my life.

Paul was 32, and had a heart condition that runs in the males of our family. Until his death, they didn’t consider it a pattern. officially dxed cause of death was Arrythmia.

I could tell you so many things about him. but I’d be here all day.

as a young girl, he was my hero.

as an adult he was my friend.

he was un dxed ADHD,( looking back it is obvious) and he was awesome.

he was a motorcycle racer and a greatly sought after motorcycle mechanic and go cart builder in Toronto in the racing circuit

He was a great dad, a great brother and had a great sense of humour. I wish my kids could know him.

he had his flaws. I have not put him on a pedestal because he’s dead. But we all have our flaws. The thing about him was, you could never hold his flaws against him for too long, because everything else about him was so great.

I’m wishing I had more pictures of him. whenever I look at this one i can just hear him laughing so hard. It was taken at the reception of my wedding to my first husband. He had danced and danced and partied all night. that’s why he is glowing. it was August, and it was a muggy day, so he was sweating from dancing, and they hauled him off the dance floor for candid family pictures. it was 2 am.

He had such a deep chortle. My son chortles, but it is high pitched since he is 6.  Sometimes the things my son does, remind me so much of him it makes my heart ache.

There has been a hole in my heart for 13 years…today it is more noticeable. today it aches, and makes me cry.

Poke the Chicken

lol..I just realized that “poke the chicken” might sound like I’m saying to poke the chicken, but really the chicken’s name is Poke.

ADDventures of Parenthood

a short, but much needed break at the beach

We live on lake Ontario. We have always enjoyed going to the quite beaches during off peak days/times, and taking walks.  we are in a very touristy area, so some times it can be jam packed. We love it on quiet days after a hard rain when no one is around. We have not done it in quite some time…I hope we can do it more often.

TMO’s guest post of the week…Chickens!

Peck & Poke

It was too rainy today to do much of anything outside with tools, but we had a break for long enough to take a few pics.

The first is our two girls standing on their roost watching me. These chickens are called Red Shavers, and they are a Canadian breed developed somewhere near Cambridge. Their colour is sex-linked – the pullets/hens are red and the cockerels/roosters are white – so sorting chicks is really easy. At least we know we’ll be getting all hens when the chicks arrive next month! Poke is on the left, and Peck is on the right. It isn’t the sharpest picture, but I was hurrying since it was sprinkling.

Next shot is of the back of the coop. Poke is still looking out the window being curious. I always heard that chickens were a bit thick-headed, but these are very bright and curious. They aren’t budgies by any means, but they’re definitely friendly and interested in us, and not the stupid birds my great uncle had in his coop. Maybe it’s because he had 30 or more and didn’t see people as part of their flock, while we have only 2 who think we’re just funny-looking chickens.

The last 2 shots are the front corners of the coop. We’ve got a padlock on it because we’re a little concerned about a couple of neighbouring kids – one in particular who comes across the back field and climbs the fence. After all the work, we don’t want the chickens getting out and lost. The other shot shows the nest-box side. Our two girls are using an old kitty litter pan for laying eggs at the moment, but when we have more pullets we’ll need more space so I’m making a box which can be attached to the side for them to share. I haven’t made the pegs for securing the door/holding the box yet, so the blocks of wood will keep it tight.

The roof isn’t weather-proof yet, and couldn’t be done in the weather we had today, so the tarp is keeping the rain out a bit. Tomorrow, we’ll get the roof done properly and put the whole thing up on stilts (it’s currently resting on the base without the legs attached to the bottom.

Anyone wanna chicken-sit tomorrow while we finish?

SIT. I said SIT.

-The Mundane One

Garden and Chickens and MS

so in all this chaos the last week or so with a garden to put in, and now a chicken coop to build, and gathering needed materials to build the garden fence in the coming weeks, I’ve not talked to my mom much.

I spoke to her on my dad’s birthday for a few minutes.

So, i didn’t know she had gone to see a neurologist for more tests with the arm tremors, and full back numbness etc.

I’ve been worried about her because she has fallen down 3 times in the last 6 months in a significant fall, seemingly for not much reason , other than walking on a “uneven surface” from one block on a sidewalk to the next for example.

she found out yesterday that she has MS. I’m the first child she has told of the family. only my father and her parents  know. she’s pretty upset, though we’ve talked about it before, and have suspected it. they don’t know which kind yet, and she has to go for more tests, which scares her a lot.

I felt so helpless on the phone with her trying to be positive and supportive. I wish I could have just been there in person to give her a hug.

So, I’m pretty bummed right now, worried about my mother, and how much she has deteriorated over the last few years. 4 years ago she had symptoms, but no lesions. now she has “several” high up on the base of her skull/spinal cord.

Funny tho, she was more worried about me, and my similar symptoms i’ve had over the last 2 years, and is urging me to go demand I get checked closer for MS right away.

I admit I’ve had my thoughts and concerns with the twitches and numbness on my back, and my seemingly clumsiness sometimes when walking and misjudging my steps etc… but, I think we have our fair share of disabilities in this family, so it’s probably fine. Given that when i exercise regularly he twitchs slow down, I’m pretty sure it is a disk degeneration pushing on nerves in my spine.

sigh….

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