Why the Focus on Gratitude? (Part 3)

Thanks for the love and support on my previous post! It’s meaningful to hear (or read) your messages and comments. I share because I know I’m not alone on this journey; but at one point, I thought I was and that felt awful.

If my sharing helps even one person to know that they’re not alone, or if it helps explain what it’s like to live with this aspect of mental illness to someone who doesn’t understand, or if it raises awareness or even opens conversation, then it’s worth it.

I previously mentioned all the things I use to help me cope. Things like therapy, medications, exercise, diet, journaling, sleep, nature, being present and gratitude all contribute to a healthier, happier me.

I could spend a long time talking about the journey from where I was to where I am now, and how I got here. Maybe I will add to this series but the point was…

Why do I Focus on Gratitude?

Why? Because I believe that practising gratitude has made a HUGE difference in my life.

I have had my share of struggles and challenges. In Jan 2005, our 4th child, Nathaniel, was stillborn. That rocked my world. We never got a clear reason why. It was “just one of those things that happened” according to the drs. It was devastating. After that, we tried to have another baby. I got pregnant 4 more times over the next 2 years and lost them all. Again, Drs had no answers. The 5th time was the charm and Josiah was born in 2007.

To say that my mental health was challenged during this time was an understatement. I was sad and grieving but also, anxiety was at an all time high. It was not a great time for me. I spent the 9 months of Josiah’s pregnancy terrified that he was going to die. I had brutal rumination every waking moment of the day. Combine that with 9 months of “all day” sickness and you have yourself a serious party. I was desperately wishing for a dr. to admit me to the hospital because I felt insane, all of the time.

I was so thankful that Siah was born healthy and was finally earth side but the years of intense anxiety had done a number on my brain. I was terrified that something might happen to him; and that we might lose him too. I was severely anxious all the time and basically white knuckling it to make it through each day. At this point, I didn’t have an anxiety diagnosis. I wasn’t on meds. This was part of my, “it’s normal to feel anxious after you’ve lost a baby and I should be able to handle this better than I am.” period of life. I just had no clue what “better” could look like.

In June 2010, our eldest was diagnosed with Leukemia, one week before Judah (our 5th child) was born. Talk about holding space for conflicting emotions, we had the immeasurable joy of one child being born combined with the heart wrenching pain of seeing another fighting for their life.

The birth wasn’t what I had planned. Going home alone after the birth wasn’t what I had planned. Parenting 4 kids alone wasn’t what I had planned. Nothing was going according to my plans.

I’m a hard core planner. Well, I was. Now I’m more of a loose planner who hopes for the best but is willing to flow with whatever because I’m aware that I have absolutely no control in this life.

One afternoon, a couple of months into the cancer journey, I felt like I was approaching rock bottom. I was exhausted, depressed, hopeless, devastated, I felt alone and unsure as to how I was possibly going to do “this”. It was too much. Way too much. I couldn’t fathom carrying on but I didn’t have any other choice.

I have no idea why, but I picked up my camera. I determined in myself, to capture 10 photos of things around my home that brought me joy.

A Rainbow of Cloth Diapers

I purposed to take pictures of the beautiful things in my life, no matter how mundane or ordinary. In fact, I was looking for the things that most people would gloss over.

A sleeping baby

My life felt like it was a run away train barrelling towards a cliff and there was nothing I could do to change where I was at.

Perfectly clean floors

I had no control over anything. I was helpless and hopeless; or was I? I couldn’t change my circumstances but I could change what I was focused on. Even if it was for just brief moments of time, I could focus on the beauty around me.

Perfectly moist Banana Muffin

I could shift my focus from the chaos, devastation and difficulties surrounding me and seek out the good, the beauty, the light. I could choose to be thankful for any little thing that I could find.

It took a bit for me to get started because I was so used to seeing all the bad things that were happening; but once I got started it got easier.

My gorgeous backyard

I honestly believe that practicing gratitude saved me. It didn’t change my circumstances. Things were still SO tough. I was still overwhelmed. I was still exhausted and had no idea how I was going to carry on but purposely shifting my focus from negative to positive, even for a moment, gave me a brief moment of respite.

My Sweet Jeremy – age 10

That brief moment of gratitude filled my heart and soul with happiness. Even though nothing had changed externally; internally, there was a shift. A minute and fleeting shift but a shift none-the-less.

I’d love to say that from that moment on everything was sunshine and roses. Um…but it wasn’t. And honestly, that was just the beginning of my gratitude journey. It was a brief foray into the world of living with gratitude.

The “cancer years” were a pretty dark time. And although I did practise gratitude sporadically, and mostly when things got really dire; it wasn’t until a couple of years later that I attempted my first 30 days of Gratitude.

That’s when I really started to realize how powerful and life changing it could be.

46

Dear 16 year old me,

You’re gonna be okay. These overwhelming feeling of insecurity and intrusive thoughts are part of a life long anxiety disorder, probably a chemical imbalance and you will eventually figure that out. You’re not broken or awful.

It’s okay that you’ve not had a boyfriend, yet. You’re going to find an incredible boy who will grow up to be an even more incredible man. You are gorgeous, smart and powerful. It’s okay to be a strong woman. Your strength will serve you well in the future. You don’t have to pretend to be something you’re not and who you are, is incredible. You’ve got this!

Dear 26 year old me,

3 kids, eh? You’re a rockstar!

That littlest one you’re holding?!? He is going to teach you more than you ever imagined was possible. You are going to learn patience and compassion, communication, persistence, gentleness, love, and so much more.

You’ve got a lot of life ahead of you and lots that I wish I could protect you from. You’re in for a world of heartbreak, trauma and devastation; but the flip side of all of that hurt is the most glorious awareness of grace and mercy. You are going to learn to love, have compassion and care for others in a way that will rock your world, in the best way possible.

That strength I mentioned earlier, it will do you well as we navigate these dark days ahead. You will survive. I promise. Even though it may feel like you could die from the pain and heartbreak, I can promise you that you won’t. You’ve got this!

Dear 36 year old me,

Can you believe that we have 5 incredible kids? Those 2 miracle boys born after all those losses…..AMAZING, eh? It’s a lot of work, but this second round of parenting is so much easier than the first round, isn’t it?

You thought the losses were tough but you’ve got another decade of unfathomable heart break. Between 3 years of Pediatric Cancer treatment, the physical, mental and emotional fallout from the treatment, mental health issues, trauma, school issues, and so much more – this is the decade that is going to really test you. Even though you will feel that you are walking a fine line between surviving and breaking, you will survive.

This is the decade that you learn just exactly how strong you are. Even if you wish you weren’t as strong because you’re exhausted and sometimes you wish it would all just go away or stop – you’ve got this. One day, one hour, one moment, one breath at a time. Breathe girl, breathe! This season won’t last forever.

Dear 46 year old me,

I truly wonder what this next decade will bring. I’d like to believe that the pain of the previous 2 decades will lighten up some. It’s been intense enough to last a lifetime. But the gifts that have come along side the pain have been glorious. In spite of all that we’ve been through, we’ve had the most incredible life and it’s not over yet!

You are wise! You are strong! You are brave! You are beautiful! Trust yourself! Trust your instincts! Believe in yourself! Believe that you have a voice! Believe that your dreams are valid and important! Believe that you can affect positive change in the world! Believe that you are a strong and powerful women. Know that your strength is one of your super-powers. Keep going to counselling! Keep reaching for inner healing! Have patience with yourself! You are a work in progress. You’ve got this!

Why I Choose Joy

This is not my first rodeo with social distancing. In June 2010, our daughter was diagnosed with Cancer and just like that, isolation became our new normal.

On Chemo, her immune system was compromised. We had 4 younger children and we all know how kids are incredible carriers and conductors of germs and viruses and basic filth. It’s like their super power. Anyhoo…..we basically holed up and all social life halted for the 2.5 years that she was in treatment.

There are differences between then and now. One, we’re all in this together. That’s HUGE. Do not underestimate how incredible it is to have others know what you’re going through. Two, back then we were fighting only for our daughter. Today we are fighting for our world. Again, knowing that you’re not the only one going through this situation is incredible for the mind, body and spirit.

2.5 years of isolation is a long time. It’s long enough for friends to move on. It’s long enough for you to lose so much of yourself in the monotony and loneliness that you’re unsure you if you will ever find yourself again.

I’m not some naive “Pollyanna” and my life is not in any way, all rainbows and roses. Social distancing and isolation can either destroy you or make you; and I fully believe that you have a say in how you respond and move forward.

I remember the feelings of helplessness and hopelessness that I felt back then. I remember standing in my living room, trapped in my home, with no end insight. I remember feeling so incredibly powerless and out of control. my only option was to hold on tight and ride this journey, until it was finished. I felt like I had no control and no power. I felt like a victim of the whole situation. I was miserable, scared and lonely.

I remember the day that I decided that I would reclaim every bit of power that I could. The sun was shining. The warm air floated in through the window. Geli and the baby were both sleeping and the other kids were occupied. I pulled out my camera to find something good, something beautiful, something that was full of life. The situation had taken so much from me, from our family. We were surrounded by the hardship and struggles ; but I was determined to balance the scales and shift my focus.

I couldn’t change the immediate situation but I could choose to look for and see the good things that were happening in spite of, or even as a result of the hardship. That was the day that I was reborn. I didn’t realize it at the time, but now I see it so clearly. It wasn’t an immediate change. It was a slow, gradual process but looking for the good. Searching for the light. Finding the joy even in the middle of the darkest times, was life changing for me.

There are studies about the practice of gratitude rewiring the brain. I didn’t know this at the time, I just knew that practicing gratitude was like air to my drowning soul.

It is a practice. It requires effort, at first; and then it becomes a part of you; a glorious, life giving, transformative part of your very being.

I’m not encouraging that you lie to yourself, or that you pretend that everything is perfect. BECAUSE IT’S NOT! These are tough times that we are living in. Acknowledging the difficulties and finding the joy are compatible.

What I am encouraging is a shift of mindset.

My kids and I are trapped in this house and fighting like idiots because they are anxious and uncertain; but I am so thankful that we have this time together and that we are healthy.

I didn’t get my complete order of food because of panic and hoarding and now I don’t have any orange juice or Mr. Noodles; but I am so thankful that we do have food to eat and that I have time to bake and make meals for my family.

I can’t go out and be with my friends right now; but I’m so thankful that we have technology that enables us to connect through the internet so I can still see and chat with them.

Even finding the beauty in little things, helps to shift your focus from what you don’t have to what you do have.

That tiny bud on the tree that’s just emerging shows us that everything moves according to seasons and where there is a winter time, that a spring will follow with new growth. That the desolation of winter is always followed by the glory of spring.

Food spilled on the floor by your children is so annoying but it also means that you have food for them to eat.

My windows might be dirty but the sunlight shining in, is glorious.

There is good. There is always good. Sometimes the good things are easy to find and sometimes you have search harder. What I know is that searching “the good” is life changing. I do find that if you can acknowledge what you see in a tangible way, it seems to imprint on your soul. Whether that’s making a list on a piece of paper or in a journal; taking a picture to save on your phone, sharing your photos or thoughts with a friend or posting on social media…..there is power in acknowledging the good. It encourages you and it encourages others.

This is why I choose Joy and why I encourage you to choose Joy, as well. There is so much benefit from a shift of focus and a bit of perspective, right now. We are all in this together.

My Autistic Daughter

Today is my Darling Girl’s 22nd Birthday. I had BIG PLANS to post this earlier today but true to our chaotic lifestyle, today was chaotic.

Jude decided that he wasn’t going to school, so I attended Grade 3…..it was about as awesome as it sounds. We came home after recess and then I had to leave for an appointment with our psychiatrist regarding Jeremy moving towards adult supports. It was epic. As soon as we got home from that, I threw dinner in the oven for Gelica‘s Birthday’s Dinner and then ran out for a chiropractor appointment. We’ve finished dinner, sang happy birthday and now I’m banging this post out.

I asked Geli to share a bit about living as a autistic women. She self-identifies as autistic and I guarantee that if we knew more about how Autism presents in girls that we would have had her tested, when she was younger. In hindsight, there are SO MANY indicators but we just didn’t know. It explains SO much and would have been incredibly helpful information as we parented her.

Without further ado, to continue on with Autism Awareness Month….here is Gelica sharing about what it means to her, to be Autistic. It’s not a bad thing, or something to hide or be ashamed of. She’s incredible just as she is. She just happens to have a brain that processes things differently than a typical person’s brain…..and that’s okay! In fact, it’s fantastic!

I am Autistic.

It’s not something I usually lead with.

If I do, people are generally confused. There’s the whole “you don’t look/act autistic”, “don’t worry, I don’t think you are”, “are you sure…?” statements. I’ve gotten quite a few of these, and I only started self-diagnosing, like, 2 years ago.

But I am. It was a puzzle piece I didn’t know I was missing. But once I got that piece, so many things started making sense.

I look back at my childhood, and I just remember being a confidently quirky kid. I knew I was different and weird, but it’s who I was. So I ran with it.

But knowing that I’m autistic has just shifted a few things into clearer focus.

Horse Obsession

Like how I could wear the exact same outfit, every day, for almost 2 years of school.

Or how I was reading grade 11/12 books in grades 2 and 3. Which is frustrating when you go to a traditional school that filters what it puts in their library and you end up with 5 books in your reading level; or you can take three Geronimo Stilton books home and finish them all in one day and have to go back the very next day, because you can’t take out more than 3 books at a time

Or how I was obsessed with horses. (Mentally.) They used to actually frighten me a bit in person as a child

If you ask my mom, she has a whole list of things that actually make a lot of sense when you look at them through Aspie glasses.

I think being autistic played a huge part in me being able to stay caught up in school while going through cancer treatment

I can remember in elementary school, asking the teacher for more homework. I believe my mom even has video proof. But I can remember the homework I was getting wasn’t ever really a challenge. I had heard the information when it was first taught to us, so I didn’t understand why I needed to regurgitate the information onto worksheets. And so, I didn’t put any effort into making sure the worksheets were correct, so the teacher had no proof that I deserved more challenging homework. I was told to put the effort into the work I was being given, to aim for 100% if I was so smart. But I figured that was wasted effort, and so I just continued on with the boring homework.

But, because I wasn’t challenged or moved up a grade or anything, I was in a decent spot to teach myself grade 8 while going through chemo. In fact, I taught my tutor math, so she could teach her other stuck-at-home students

Granted, the school only gave me the bare minimum of all my coursework, and I don’t know how much of any of it actually counted towards the school barely passing me through grade 8. But I had done enough work that when I returned to school, it didn’t take too much extra effort to catch back up and raise my grades back up to almost A’s.

Currently, I think the biggest thing that discovering I’m autistic has given me, is the information.

I have an explanation.

For my introversion;
for my small-talk aversion;
for the way I think; the way I communicate;
the way I process;
the way I experience emotions and empathy.
It explains why I can not be a receptionist, but why I am amazing at my current job.

I don’t mind coming to this conclusion in young-adulthood. I think if I had been diagnosed as a kid, I would have been challenged more in school, and maybe moved up a grade. I would not have been able to keep up with my class through chemo, then.

But the one thing I think I did miss out on, was a more serious effort to teach me social skills. I seemed to always have at least one friend. But as a kid, I put no effort into making new friends. People came up to me, and made me their friend (and then they were stuck with me). So I pretty much always had someone to play with, but it was never intentional on my part; I would have been fine to sit and read by myself, honestly.

When I finished with cancer treatment, and re-entered society, it was a bit of a culture shock. I had been diagnosed as a pre-teen, when I was most upset about not being able to join a baseball team, because games were on Sundays and my parents were assistant pastors. So when I got back to school, and all that the girls were interested in were boys, make-up and grad dresses; I could not have cared less. But there was suddenly this huge, noticeable divide between myself and all the other students my age. And I suddenly actually felt like I was different.

I spent the rest of high school trying to figure out exactly how and why I was different. And nothing seemed to click just right. And forcing me to go to the church youth group was not going to suddenly fix the problem.
What I’ve come to realize, is that I was never taught social skills. I was never taught how to make friends. So now, as an adult, the one thing I wish I could go back and change, the one thing that might have made an earlier diagnosis more worth it, would be the ability to make friends. Because learning these skills as an adult, is really really hard.

I don’t know if I’ll go through with getting an official diagnosis. I’m still contemplating that. But I definitely am Autistic. And I am so thankful that I now know.

Pain, Coping and Recovery

Today is a special day. Five years ago today, my sweet Xandra decided to make a change in her life.

She told us that she wanted to talk to us. We knew she’d been struggling for years with depression and anxiety.

It’s hard not to when your sister was diagnosed with cancer, your baby brother was born, your brothers have autism and you’re unsure how to deal with it all. You don’t know if you should bear the weight of everything because your mom and dad are overwhelmed. You don’t want to burden them any more, but you still have needs.

Xani told us that she’d been cutting for a year. That she’d been using this self-harm as a way to cope and alleviate the emotional/mental stress that she had been feeling. She showed us her arms and her legs. She wanted help to stop cutting and knew she couldn’t do it alone.

I was in shock.

She was so badly wounded. Her physical body was a outward representation of how wounded and how much pain she felt internally.

As a mom, it’s a horrible place to be in. To try to hold it together and be loving and compassionate and understanding.

To offer unconditional love and acceptance to the hurting person in front of you, while at the same time feeling absolute helplessness to know how to move forward.

Wondering how to get your child help, to give your child help.

Feeling terrifying rage at the person who mutilated and hurt your child, all the while knowing that it was YOUR child who did this to themselves. Knowing that they must have felt unimaginable emotional and mental pain to have even considered this as an option.

The dichotomy of emotions was huge.

I’d love to say that we had a well thought out game plan. That we rocked her recovery. But the the truth is……this was Xani’s journey.

She determined that she didn’t like where she at and that something needed to change. She reached out for help. She was open about the pain she had been and was currently experiencing. She recognized and identified the harmful things she was doing to cope with and escape her pain. She chose to walk away from those harmful coping mechanisms. Did she struggle on her road to recovery. Absolutely! But she reached out for relationship and community when she felt tempted to cut. When she felt the pain and stress rising up internally – instead of hiding and coping on her own, she reached out. She brought her feelings out into the open and allowed us to walk with her.

We……..we were there. We were available….to love, to accept, to champion, to talk, to just BE there.

Today, I’m SO VERY thankful.

I’m thankful for so many things. I’m thankful for this incredible woman that I have the honour to call my daughter. I’m thankful for courage and her strength and her vulnerability. I’m thankful to be on this side of this journey. I’m thankful for the perspective that this journey gave me. I’m thankful for the opportunity to love and accept. I’m thankful for the knowledge that we as people experience pain and look for ways to treat the pain and cope; often how we “cope” is in unhealthy ways….but that doesn’t make us bad or unloveable or unworthy; it just makes us human.

We are all worthy of love and acceptance; not in spite of who we are, but because of who we are.

ps. I have Xani’s permission to share about her journey. But I’ve also shared my perspective of it because this is my life, my journey and my perspective.

Perspective

Challenges are what make life interesting. Overcoming them is what makes life meaningful. Joshua J. Marine

We’ve had a fair number of challenges in our lives. Enough that, I had to make a choice. I could allow the sorrow and despair to crush me. I could surrender to the devastation and lose myself…….or I could choose to live and see the light regardless of what was happening around me.

I think this is one of the reasons that I resonate so strongly with Leonid Afremov’s paintings. There is such depth and even darkness within the paintings but there is light everywhere; and it’s glorious. It glows from within the scenes.

That’s what I want my life to be. Regardless of how dark a time is, I want the light to shine. I want to glow brightly whatever the scene around me is. I want to see the light shining and reflecting in the darkness. I want to BE a light shining and reflecting in the darkness.

It’s easy to see the light when it’s bright, but I choose to look for the light when it’s darkest out.

I refuse to allow hard times to define me. I don’t like to ask “Why me?” More often, you’ll hear me ask, “Why Not Me?” There are no guarantees in this world in regards to hardship and trouble. Life is not fair.

One benefit of looking for the light is that you find the good that comes from every situation.

Cancer is not good! My 13 year old daughter being diagnosed with Leukemia is not good. The 2.5 years of treatment is not good. The side effects of the chemo are not good. The long term physical, and emotional effects are not good.

But there is good! Having community surround you and carry you, is good. Realizing that you are stronger than you ever thought possible, mentally and emotionally, is good. Learning a deeper level of compassion and understanding for the suffering of others, is good.

I wish we never had cancer touch our family, but I WILL find the good things that came from that experience. I will hold onto those things, tightly. I will learn and grow from that experience.

I will stare at cancer, defiantly, and proclaim that it didn’t win. It didn’t destroy me. It didn’t crush me and if anything, I grew stronger.

I’ll be honest, it almost did destroy me. BUT…….it didn’t!

I choose to live a life filled with gratitude regardless of the circumstances that come along.

One thing that I am SO grateful for is life. Life is a gift. Knowing firsthand, the fragility of life and the reality of death puts perspective on EVERYTHING. My daughter could be dead, but she’s alive. That’s incredible. So what, that my car broke down or I’m having a bad hair day, or I’m late for an appointment or I’m 10 pounds heavier than I’d like to be……compared to life and death….it’s all frivolous. The reality of that perspective is a HUGE gift. Something I will forever be grateful for.

I’d love to hear what your grateful for.

ps. it doesn’t have to be as heavy as this post is. Gratitude is gratitude!

What if……

But what if I can’t do it everyday…….

So?

What does it matter? There is no right or wrong with gratitude. There is no failure. Imagine that, being a part of something where there is only success……

If you are thankful or grateful for one thing, you are winning!

If you are in a tough situation and you look for the light, you are winning!

If, even only once, you find the good within the bad, you are winning!

You can’t lose. I guarantee it

When you start to become aware that you are looking for the light, you can’t miss it. Picture a pitch black room, with no light. Now if someone, turns on a spotlight, will you see it. Yes! How about a flashlight? Yes! How about a match? Yes! If you are looking, you will see the light no matter how small!

Once you start to look, once you are aware that there is light, always…..you will find it and it transform your outlook on life. It’s crazy and awesome and mind blowing.

Imagine trudging through your day, at a job that’s difficult and thankless and just overall hard. If you focus on that, it all sucks. If you start to look for the light, it all changes. It’s not that it magically becomes easier but it changes. Your perspective changes. You see things that you may have missed or just might not have noticed and all of the sudden, it’s a little less horrid. The situation didn’t actually change. It’s still full of challenges, But your perspective changed and its amazing how much of a difference that makes.

June 27 2010

This is day that I left Jon and Geli at BC Children’s Hospital, and drove myself and my newborn home. I could not see any light, in this day. The next day I wrote this post, and while I was miserable and struggling, I was also so aware and thankful of the love and support we were receiving. Knowing that I had support of a community, helped to keep me going.

It wasn’t some “joy filled” thankfulness but it helped me to shift my focus from the immediacy and intensity of the moment and widen my gaze to include those who loved us. This brought an awareness of the love and kindness and encouragement that was available to us. That awareness helped to bolster my strength so I could keep putting one foot in front of the other. It helped our family to get through a very long 2.5 years of cancer treatment.

I’m excited to start this Gratitude Challenge on March 1st and just be more intentionally aware of the things that I have to be grateful for. Obviously, I’ve started already but I do hope you will join me in looking for the light and share how it impacts you.

My Journey with Food Addiction (part 1)

It’s said that knowledge is power and when it comes to food addiction and me, that saying is so true.

Here is a decent explanation of Food Addiction and how it relates to me…….(just click on the underlined words)

I’ve struggled with my weight for a really long time…..I’ve had issue with food for even longer. I remember sitting down as a child/preteen/teenager and pounding back cookies or chocolate bars or candy or to a lesser degree chips…..any kind of junk food specifically those with sugar and/or flour.

I’ve never really understood people who could take “just one”. As far back as I can remember, it was kind of an all or nothing deal. If I had a bag of M&M’s….I’d eat until they were gone…..and it was never the small bag – always the BIG ONES. I’d never just buy 1 chocolate bar…it was 3 or 4. I’d grab a handful of cookies and most likely head back for a second or third handful.

While I was a teenager, it never seemed that big of a deal because I was a tall, big framed person and weight wasn’t ever an issue for me.

I was 170lbs when I got married and definitely was not overweight by visual standards.

I still struggle because according to different standards like the BMI or other weight calculators, I was overweight based on my height vs weight ratio….but in no way was I overweight back then……I was thin, I modeled. I firmly believe those standards are flawed…

As far as my weight goes, I did ok until after I had my second child and then things started changing……I didn’t lose the weight as fast as I did after having Angelica. Literally, 10 days after having Geli, I was back in my pre-pregancy clothes and I could see my hip bones and everything. It was not the same after having Alexandra and from then on I began to actually “struggle” with my weight.

But this whole issue is about SO MUCH MORE than weight……and that’s where the “knowledge is power” aspect really comes into play for me.

I remember my sister telling me about a friend of hers who was eating a certain way and she briefly mentioned “food addiction” when she was telling me about this “way of eating”. I briefly looked into it but mostly because I was desperate to lose weight. I didn’t particularly “like” the food eating plan and so I dismissed it…..after all, I wasn’t an addict and I most certainly wasn’t addicted to food…I only had 10 pounds to lose and then I’d be happy……

I’ve spent a huge portion of the last 20 years dieting or eating according to a “food program”. I’ve eaten low carb, sugar free, fast metabolism, 3 day diet, and so many more gimmicky eating plans to try and lose weight. And while some of them worked for a bit, in the end……I’ve gained the weight back and felt more miserable and like a HUGE failure on top of it all.

I think that there have been 2 periods of time over the last almost 20 years where I’ve been close to a healthy weight. Neither lasted very long and between the different traumas and stresses in our lives, its been a brutal battle.

2014 has been an extremely difficult year for me and yet……..it’s been an amazing year.

We are exhausted.

And that’s putting it mildly.

Over the past 10 years, we’ve had numerous job changes and losses, a stillbirth, 2 second trimester losses, an early miscarriage, the long desired arrival of Josiah, a crazy long, difficult and exhausting journey to an Autism Diagnosis, children with special needs, cancer and the birth of our sweet Judah in the middle of it, serious Mental Health Issues, and 2 BIG house moves…..there is more that I’ve not accounted for, but that’s enough….it’s just too much. We are tapped out.

I feel like I’ve been fighting a battle for a long time. I have been…….. but what’s worse is that I really didn’t understand what or who I was fighting.

Earlier this year, I committed to 100 days of investing in myself. When I look back, I see that I was searching for answers and that I was close to finding them but just not quite there….

See, in the past, my focus has been for the quick fix….

– If I lose 10 pounds, I’ll be happier and then I can go back to doing whatever I want.

– Ok, realistically, I should lose 20 pounds, but that’s a lot and so difficult so if I eat no/low carb for a few weeks, I should loose a ton of weight, and then I’ll be happy and be able to do whatever I want.

– OK!!!! So I should probably be REALLY SERIOUS and just go for an entire month and hopefully lose more than 20 lbs and then I’ll be happy and can do whatever I want……….

It was all about losing the weight as fast as possible – which for me typically meant no sugar, no fruit, no carbs……just veggies and protein….and then something would happen and I’d “cheat”………. cause everyone deserves a cheat now and then, especially when you’re being SO GOOD. That cheat would typically turn into more than just a little treat and BAM…….soon I’d be stuffing my face with whatever I could find.

The “100 Days” challenge was difficult for me and yet amazing, when I look back on it. I’d decided that it needed to be more than a quick fix. I needed something longer term, because the quick fixes were not working. I needed a shift from “short term/quick fix” thinking to something that was more a “lifestyle/long term” plan.

So I started back in February….on Valentines Day to be exact…. my plan was no sugar, no gluten, low carb, only natural foods that I could eat in whole form or combine to make something. I’d started running in 2013 and planned on combining that exercise with my food eating plan to be able to lose weight and really get control of my life which felt so chaotic and out of control.

It started out pretty good. I started 2014 at 230 lbs…..

Towards the end of March, I was doing pretty good. I was down to 208 lbs. I’d run over 100 km in the month of March….and then I stalled.

March-April-May…nothing shifted and I was getting frustrated. I started eating things that were outside of my chosen allowable foods and my running slowed down and by the start of summer….I crashed. it probably didn’t help that I was anemic over the summer.

Summer of 2014 was an absolute out-of-control, gong show. I ate whatever I wanted, whenever I wanted. I didn’t exercise. I felt lousy. I was trying to just survive. It was so bad, that even walking upstairs to my bedroom was a colossal effort and so once I came down stairs, I avoided going back up until I had too. Lotta couch time over the summer and anything I did do, came at a huge price as I’d crash the next day.

Every time I walk upstairs now, I flash back to how bad it was over the summer and I’m amazed at the difference from then till now. It’s pretty drastic. I went up on my anxiety meds and even added another one into the mix. There were days that I contemplated hospitalizing myself because I could not get the anxious thought under control and I’d spend the entire day fighting thoughts….crying…..it was pretty bad.

September’s are always like a new year for me….a new start……so I kept looking forward to September and the kids going back to school and routine and…….when it came…..everything was still brutally difficult and nothing changed except that I didn’t have the kids home all day…..I didn’t do anything. I couldn’t. I was so exhausted. Just existing was difficult….it was bad!

I went to give blood in September. I’ve been donating blood since I was 18 and while it’s not been as regular as I’d like and been broken up by pregnancy, breastfeeding, and different meds that I’ve been on….I could finally give and so I did….only to be denied because my hemoglobin was too low. While at the time I felt pretty embarrassed to be denied, that was the start of something amazing…….like the catalyst that kick started this next phase in my life.

I went to my dr and asked for some blood work. I started taking iron…..went and saw my naturopath, got a few supplements…… Finally towards the end of October, I started to feel a bit better.

I honestly cant remember why or how the whole concept of food addiction came to me but right at that same time, I started doing some serious research and reading about food addiction.

It was like my whole world exploded into tiny shards of hope and shame, exhilaration and denial…….

What does THAT even mean?

I mentioned that I felt depressed about my life yesterday.

I thought I might take a moment to clarify what exactly that looks like, feels like and means to me.

I ran into someone yesterday who had read yesterday’s post and gently asked me how I was doing. I threw something back at them saying that I was ok and that I was just keeping on, keeping on.

Anxiety speaking here: I’m not sure if they were expecting me to be a huge mess of tears, or if they were thinking that I’d be fragile, or really off, or shaken, or…..maybe they were thinking none of the above and that’s just the anxiety saying that they were “thinking” or “expecting” something.

Regardless, it got me thinking….because I’ve written posts before and had people very cautiously approach me wanting to cancel a get-together that was planned because it might be too much for me, or talking to me as if I couldn’t handle things and they were not wanting to upset my delicate balance.

I’m not saying that I don’t appreciate people’s care and concern……NO! Actually, it’s exactly the opposite. I feel so cared for and supported and loved, when people care enough to step outside of the emotional distance that we, as humans, like to hold ourselves to and try to bridge over into my problems and stresses. It’s HUGE and I’m so grateful.

On one hand, I don’t like to appear weak, on the other hand, I don’t like to be needy, but so often I am both weak and needy……..and I’m recognizing that having a “community” or a “family” that can help to lift you up and carry you when you feel exhausted or worn down, is an incredible, INCREDIBLE thing.

When I share about feeling depressed about my life…….I think what I’m trying to say is that I’m in a tough place and I don’t have a clear vision as to how to move from this difficult place into a better place. I don’t like NOT KNOWING……..I like to have a plan, to be in control, to be working towards a goal, to be able to make things better……

There are somethings in my life that I cannot change. I cannot remove the emotional or physical marks that cancer has left on every person in my family. I cannot remove the anxiety that all 5 of my children seem to deal with in varying degrees, from severe and debilitating to mild. I cannot change the fact that autism is a very real, exhausting and difficult neurological disorder that we deal with, as an entire family, EVERY. SINGLE. DAY. I cannot change the fact that ADHD has impacted 4 of my family members intimately and the trickle down effect of that disorder effects the rest of us.

I can’t “just fix” those things. They are here. They are real. They require HUGE amounts of effort mentally, emotionally, physically, and spiritually. They affect each interpersonal relationship within my immediate family and many outside of my family.

There are moments when “the reality” of my life seems WAY. TOO. REAL…….and my options are to keep on keeping on….or give up.

I cannot give up.

I mean, I could. That was something that my counselor said to me at one point. I could give up. I could check out. I could run away or end up in a hospital somewhere…..unable to “handle” things and that it was my choice to carry on.

I think she was trying to tell me that I “held power” in my situation and that many people did/do check out and that I was doing well, in the fact that I still had the ability to CHOOSE to carry on.

I think I get what she was saying and yet……oh there is always a yet or a but, isn’t there……..I don’t feel that giving up is an option. Yes, somedays, it’s all I can do to just get up and get dressed and put my make up on……

That’s my thing…..my gimmick…..the one thing that signals to me that the show must go on….if I get up and get dressed in real clothes (not pyjama wanna-be’s) and do my hair and make up……..then I accomplish so much more. Very rarely, do I ever, stay in pyjamas and not do my hair and make up. I get “ZILCH” done on those days and I simply cannot afford to not accomplish things……

The 2.5 years of cancer treatment was brutal. It taxed me to my extreme limits as a person, and definitely as a parent. I am still not recovered from the toll that it took on me.

I find that I feel a bit like I am a hollow egg (Humpty Dumpty, if you will). I have a very thin and fragile shell and as long as things don’t shake me or bump me, I exert every bit of energy that I have to hold my broken and cracked self together. One little bump and the precariously balanced pieces start to fall. I fall apart……

Jeremy has a bad Autistic day……….BUMP!
Geli has an emotional day relating back to cancer crap………BUMP!
Josiah has an ADHD frustration flip out…….BUMP!
Judah is 3 (enough said)………BUMP!
Xani experiences extreme anxiety for unexplained reasons…….BUMP!

So many bumps……so much energy expended trying to keep all the pieces in place…..so many pieces falling…..so little left at the end of the day.

I can’t make these things go away, and so I must learn how to live and carry on and continue with pieces of myself broken and fallen apart.

Some of it will get better….or at the very least different, with time. Some of it will never go away, but the kids will grow up and learn coping skills. And my hope, my prayer, is that I do a good enough job of training these amazing blessings of mine how to deal with life’s challenges with grace and dignity; and how to keep on keeping on even when you are unsure of how to proceed and what the best course of action is…..

But………

………sometimes, the enormity of my job weighs heavy on me. Sometimes, I’m unsure how to best help these ones I love so dearly. Sometimes, I feel like I don’t have the emotional or physical strength to deal with “even one more issue”(…and there is always “one more issue”). And then I feel discouraged…….

We have had a few BIG BUMPS recently. Ones that I’d love to share, but it’s just not the right time…….and the added pressure and stress weighs very heavy and makes “coping” that much more difficult. And so here is where I am at today……..

I’m dressed. I have my make-up on and my hair done(sorts of, if a messy pony tail counts…). The kids are off to school, except for Geli – who is still feeling sick (Thanks to Xani for bringing home a stinking bug from New York) and Judah. I’m needing to make a list and see what I can actually get done today. I know I have a mountain (probably 8 large loads) of laundry to fold, sort and put away. I know the main floor is a disaster and the kitchen needs to get put right. If I can accomplish any (not all, but ANY……) of that before the kids come home; as well as planning dinner for Angelica’s 17th Birthday (which is today) I will consider today a success. I have LOW standards…..

So, my “feelings of depression” are an exhaustion, a feeling of uncertainty and brief moments of hopelessness, a sense of constant pressure and chaos, an insecurity of my abilities to adequately parent these amazing children who have been presented with striking challenges to overcome……it’s a little bit of acknowledging a desire for some easy days, yet not wanting to stay in a place of discontent with my life, because that helps no one. It’s a tough place. At times it’s a wonderful place…..but right now, it’s mostly a tough place.

It won’t stay that way forever. I know that I’ll feel stronger and stronger again….I always do, but it is tough.

I would encourage you to look around you and encourage each other…..it doesn’t matter whether you are a single parent by choice or by circumstance, or whether you have special needs children or a child with a long term or chronic illness, whether you have a difficult or challenging child(ren) or need to work multiple jobs to make ends meet, whether you or your loved ones struggle with any kind of mental illness or disability, or whether you seem to have a fairly smooth go of things at the moment……

Be Kind.
Be Compassionate.
Be Loving.
Be Encouraging.
Be Understanding.
Be Gracious.
Be Merciful.
Be Caring.

Understand that everyone is doing their best, and while “our bests” may differ depending on our circumstances and experiences and abilities……..be gentle with each other. Your care and support may make the difference in someones life today.

Moving Forward The Morning After

So I posted last night…..

I was tired and emotional and probably if those two factors had not ganged up on me….I may have filtered myself a bit more or even just made less typos…..maybe….maybe not?!?

I don’t know that this morning brought any new clarity with it.

I woke up with a killer headache……….at 5:30am.

Yah, it’s been a long day already and it’s only noon-ish. Did not get back to sleep after that. BLERGH!!!!

On a side note….It’s gorgeous outside.

That is the view to my right….

and this is my view straight ahead…..

She’s not supposed to be on the couch….but I haven’t exactly kicked her off.

It’s the last day of school before the Christmas Break….and probably my last quiet (ish) day for the next two weeks.

So, I’m taking advantage of it. I’m sitting. The house is a mess, and I made Judah pancakes for lunch. He is currently trolling Netflix….I believe Ninjago is the show of choice at this exact moment.

I’m currently staring at my Christmas Tree trying to figure out what I’m thinking, but again with the 50 million thoughts going in 50 million directions.

I had a few people send me private messages of encouragement and those were so nice to hear.

I wonder if it’s about perspective.

I’m in the middle of it all. From my position, I look around me and I see children who are unique and amazing and challenging in their own fantastic ways. I see the screaming and the bickering and the squabbling and the challenges to get them to do their chores and take care of their responsibilities. I see their shortcomings and I want to work with them to strengthen those areas while at the same time encouraging them in their strengths. I see these amazing individuals with really great hearts even in spite of all the challenges that we’ve faced individually and as a family……. But it’s a constant effort to keep these 5 bodies moving in a forward direction.

We were so isolated over the “cancer years” and before then….doing almost anything with Jeremy required HERCULEAN effort and sometimes it was easier to just not do anything. Again…..very isolating.

It is hard when you’ve had it said to your face that people can’t be friends with you because your child is too difficult. Or to hear from others that you shouldn’t subject your children to people because they are too much effort to have around and be around.

Just typing both of those down….I realize how brutal those two comments are. I mean, I know how brutal they are….I’ve lived though both of those said directly to my face and more. But I can’t imagine saying those things to someone…..EVER!!! I love children. I especially love the challenging kids. The ones that make you think and keep you on your toes. The extremely smart kids that say the most incredible things but require a little more attention and focus……I love the regular kind of kids too, but somehow, the ones that people seem annoyed with or bothered by….the ones that talk and talk and talk and talk and never shut up……I LOVE those kids. I want to go out of my way to make sure that they feel special and included and NEVER EVER a bother or an inconvenience….

I get it. I know how much effort it is. I live it…..EVERY. SINGLE. DAY! Jeremy has not been the easiest child. He requires some effort. Well, he requires a lot amount of effort. So does Josiah in a different way and Judah….well, he’s a 3 year old. What 3 year old doesn’t require some attention and effort. My boys require effort……I know this. I guess, it would just feel really good to feel like others “want” to be with my kids. Do you know what I mean? I think that in spite of their particular challenges or maybe even as a result of them….that my kids……all 5 of them are pretty amazing. I’d love to feel like others felt that too and wanted to spend time with them….not cause they HAD to, but because they WANTED to.

So, to those who have said something…..THANK YOU. Really! I appreciate it more than you may ever know.

I’m not sharing this in the hopes that people will “do” something. I am just trying to unravel some of this mess inside myself. Part of that is dealing with the hurts and wounds that I have or have gotten.

I realize that I’ve been hurt and I definitely have some sore, open wounds when it comes to my kids and how they are perceived and received.

And this OBVIOUSLY colors how I hear people comment on my kids.

So the school wanting to help Siah….turns into….HE’S A PROBLEM…..which I can’t even fathom….cause he’s freaking sweet kid who can read and write and wants to please…….and then I go…WHAT….WHAT do I even do with that….

How could be he a problem…..which, when it comes down to it….that is not even the issue at all.

He is a great kid….who has some quirks and may require “some individualized strategies” to help him succeed and how do we (parents & school) as a collective team help him to achieve success?

So we met, and talked through some things and I think I have a better perspective. I think we are more on the same page than I “felt”.

Which is great.

Not that the whole things doesn’t still stress me out….but the Principal….she’s an amazing lady, encouraged me to trust them and to just “plug my nose and JUMP!”

I believe this school and these people are amazing people…..I believe they truly care about Josiah. I really do believe that they want the best for him. That they want him to succeed. And so…..I jump.

I’m scared.
I’m nervous.
I’m sure I’ll need reassurance again.

But…..

I want to trust.
I want to believe.
I want to be in “community.”

and so….

I carry on…

one step after the other…..hopefully in a forward direction. 🙂