In true form, it has been a while since my last post as an inconsistent-mom-blogger, but I have suddenly found myself with more time to write as I am off on a bit of a leave from work and school. The good news is, I am not bored because I have a lot to reflect on, especially as a parent left trying to make sure their kid has what they need to be safe for next school year.
I usually try to err on the side of support vs. advice giving, but I’ve had so much floating around my head these days that I have 10 considerations that due to my current circumstances, I have come to recognize as worthy personal considerations worth sharing with other parents of kids with disabilities:
1. If you feel like giving up, surround yourself with a tribe of people who ‘get it’ and that you can vent to.
2. It is more work to raise a child with a disability because of how the world does not understand or plan for disability, this is not your child’s fault.
3. Take on the ‘big system fight’ when you can but don’t feel guilt if all you can do is fight for your own child.
4. You do have allies within these systems, but sometimes you have to look really hard to find them. They could be a lunch program supervisor, an educational assistant, a School Trustee, teacher, superintendent, etc…
5. Remember that your child is a precious human being, just like those without disabilities, don’t let all that talk about what your child can’t do or does inappropriately keep you from seeing them as precious.
6. People will always have advice for your, if you feel it’s unwelcome, judge people more by their intentions and less by the quality of their advice. It might be good to keep your distance from those with ill intentions. You don’t have to make everyone happy, but those with ill intentions can cause undue suffering if you give them too much room in your life.
7. Take care of yourself. Burn out is a real thing. Your health is important. If you are not around to love your child and help the world understand your child has a place in it, that would be a huge loss for everyone.
8. Celebrate what your child with a disability brings to your life, and let others hear about it. So often when working with professionals involved in our children’s lives, we forget they are not a problem to be dealt with. Their value is not based on report cards or how many IEP goals they attain in a year, don’t let anyone forget it ❤️.
9. You will fail at being everything your child needs. This includes what educators, child care providers, health care practitioners, mental health providers and other practitioners might request of you. You are not super human and at the end of the day, you may not be able to do it all. It is better to change one’s expectations than to die trying to meet the unrealistic gold standard.
10. Cry when you need to. Life can be hard enough without kids! Take a moment and let out what is causing you suffering somehow (maybe not crying if you are not a cryer) find someone to talk to if you need to. There is no shame in getting external help. Just make sure it’s the right kind of help for you.
That’s all I have for today folks. Much love to y’all.
#parenting #parenthood #motherhood #disability #childhood #autism #adhd #asthma #anaphylaxis #coldinducedurticaria #mentalhealth #burnout #advocate #advocacy #safety #socialmodel
This time around I will also give my children names to make writing about our family easier; we will call my oldest son Napoleon and my youngest son Coyote. Napoleon is now in 5th Grade and loves to build complex structures, swimming and collects all things unusual, Coyote has entered Kindergarten and loves Taekwondo, skateboarding and cracking the most hilarious jokes.
Since I last wrote, so much has happened…far too much to contain in the words of a single blog post. Life has ranged from absolutely amazing to incredibly dark and uncomfortable. The Coles Notes version sounds like this though: I finished my social work degree and started working for an awesome non-profit organization. I survived something very wicked that caused me PTSD and left me damaged but stable. I lost one of my best friends to a difficult parting of ways. My husband and I celebrated 10 years of enjoying the calms and surviving the storms of life and marriage together. I have gotten to know some of the most amazing moms that I am happy to count as friends. I celebrated 18 years of friendship with two women I call sisters. I have embraced the chaos our family brings to the world and celebrate our differences. I have had to suck up my desire to avoid conflict and fight for my children to have their educational needs met. We officially went from poor to not poor. You can trust me when I say I have spared you many details, but you get the gist of what you missed.
I am so glad to be back writing here. Our life is not perfect but it is never really dull and I enjoy sharing stories and thoughts about what goes on in our family. I will not sell you lollipops and rainbows here. I won’t pretend that we have our lives all sorted out or that we are the best example of how things are done. Our life is chaotic, fantastic and still less than perfect but I look forward to sharing it with you.
As our family life changes and becomes more challenging, I am finding it more and more difficult to write about life. Yet, I’m sure the things we have encountered as a family are not unique. So I am going to push myself to write about them, knowing that as ‘different’ as our family is; we are not alone.
As parents we often start with these expectations of how things are going to be, how our children are going to be and how we are going to be with our children. We enter into parenthood with ideals, pictures and examples of what we want our lives to look like. We buy or do things because they are supposed to help, we avoid things because they may harm, and most of all we stack ourselves up against how other families are doing. Unfortunately, it’s these ideals and expectations that can cause rude awakenings for families who are less-than-perfect.
I’m not exactly sure when my rude awakening to our not-so-perfect family occurred, but I do know it was followed by depression. I never wanted the same struggles for my children as I had, and I certainly didn’t want more challenging ones! When you first discover that the mental pictures you have painted of your family are not quite accurate- disillusionment can ensue. Rude awakenings can occur, crushing parental expectations for many reasons: whether your child has to wear glasses, has anaphylaxis, asthma, juvenile diabetes, acid reflux, still wets the bed, has wicked temper tantrums, a learning disability, adhd, autism and any other type of disability, or even something that makes them just a little more ‘challenging.’
Upon realizing that one’s family is less-than-perfect you begin the process of becoming comfortably uncomfortable. For me, this process started off slowly, beginning with acknowledging that my first born did not like to sleep and that I, in turn, was not rested and losing my footing. Eventually we added more less-than-perfect’s to our lives some of them drastically impacting the way we socialized with others. When you’re forced to ask people who are around your son to not bring snacks or serve food that might have peanuts in it, or asking people to wash their hands before they play with your son’s toys, it often becomes easier to withdrawal than risk being treated as an inconvenience. For me, this fear was further magnified with the emergence of behaviour that didn’t always fit the mould or environment our son was in. We became that family that others stared at in the grocery store because their child was having a meltdown.
The second part of my journey to becoming ‘comfortably uncomfortable’; was accepting that it’s okay to be different. I was a quirky child, my husband was quirky child, we are quirky adults and our children are…that’s right; quirky. It’s not that everything about being quirky is difficult, but the difficult things need to be acknowledged and honoured. For myself, being able to acknowledge the things that were not going well, was made easier by looking at the difficult and amazing parts to being ‘different’ at the same time. For instance, I would say: It is painful when my son has melt downs over pocket lint, but it’s hilarious that he loves to dress as the Undercover Boss. Framing struggles with a bit more context often helps to make things a little less depressing. I love both my sons, and they do not have to be perfect or like everyone else for me to accept and love them.
The third part of this process that I really needed to go through, was to accept help when things were beyond me. It does not make you a bad parent to admit you don’t know how to deal with something. Once you are able to acknowledge the ‘differences’ in your family; it becomes easier to embrace support when the difficult parts of these differences interfere with your family functioning. Whether the help comes through family, friends, counselling, occupational therapy, specialists, medication, etc., there is no shame in admitting the challenges may be a bit bigger than you thought. It’s scary to get help, because sometimes getting help means being judged or giving a label to a struggle; As much as this potentially opens the door to a lifetime of preconceived notions and criticism from others, it is important to push through until you have the support needed to improve things. One of the things I want for my children as they grow up, is to become the most well-adjusted adults they can be, but to do this we may need help along the way.
The part of the journey to becoming a comfortably uncomfortable parent that I am currently at is where I am learning to embrace people who cherish my children for who they are. We are so lucky to have people in our lives that understand what being different is like and get a kick out of it. Usually these people can take the difficult parts to being different in stride. They don’t talk about how awful your child(ren) are behind your back, or about how you as a parent have failed or are doing things wrong. These people are the ones who find joy in playing a role in your child’s life, and who don’t treat your child as a half human due to their differences. I feel so fortunate to have these people in our lives; they make it easier for us to embrace both the good and bad parts to being different.
In this journey, my children have been my main teachers as I learn to be comfortably uncomfortable. They have shown me that life doesn’t have to be perfect to be good. Sometimes all it takes is the simple pleasures and small victories to bring us joy. I accept and expect that there will be many bad days to come, which I suppose makes it easier to be grateful for the good ones. I embrace that our family and my children are not what I imagined them to be- and I am okay with that. I acknowledge that for me, parenthood will be an ongoing challenge, but for now I will remain a comfortably uncomfortable parent in my less-than-perfect family.
P.S. If you feel alone because of what makes you different, remember; different is the new normal.
We have lived without peanut butter in our home for the last three years. If you had known my partner and me three years and two months ago, you would have seen peanuts and peanut butter as a daily part of our lives. Peanut butter and butter sandwiches , peanut butter and jam sandwiches, peanut butter and bananas sandwiches, peanut butter and crackers or apples, peanut butter squares (or as my partner would argue, butterscotch squares), peanut M&M’s, Reese’s peanut butter cups, peanut butter and chocolate ice cream, thai food with, you guessed it- peanuts! Just writing about them makes me hungry.
Shortly after having my first, I remember being with some fellow moms/friends and they were talking about the idea of introducing peanuts to your toddler in a vehicle just outside the hospital; I thought this was the most paranoid idea and giggled to myself a little at the image of feeding my son a peanut butter sandwich in the emergency parking lot. I thought to myself, why bother being paranoid there is such a slight chance of a child being allergic.
A year or so later over Christmas holidays we flew out to see my brother in California. On our way there we had a lay-over, and since most air lines were no longer serving meals we picked up a meal to tie us over on the next flight. I went to a really cool Thai restaurant and got myself a delicious peanut-y stir fry. I had barely eaten all day and I was starving! After getting our family seated but before they safety exit spiel, I took out my delicious peanut-y stir fry and dug in. Now I know what you’re thinking, my son ended up having a reaction and we were forced to get off the plane and go to the hospital and I can assure you this is definitely NOT what happened. But the flight attendant got on the loud speaker and asked all passengers to please refrain from eating peanuts for the flight as there was a “little guy” with a severe peanut allergy on board. I finished chewing my mouthful and lidded my delicious peanut-y stir fry. I was a little disappointed and starving, if I had only known earlier I would have got something else to eat!
A month later I tried feeding my son a peanut butter cookie for the first time and he was not interested, a few days later I was able to get him to eat a pint size amount of peanut butter and no reaction! Hooray for us! Oh wait, reactions usually happen on the second exposure!?! The next day I slathered apple slices in peanut butter but he would only eat a miniscule bite! That’s when I realized the joke was on me. I spent the next few months in denial, saying “It could have been the apple… right???” Once diagnosed we began a purge of our home, threw out jam, ice cream, a food processer that I used to make our own peanut butter in, all things that could have been cross contaminated and anything that said “may contain traces of…” or “contains traces of…” or “contains…”
Which now brings me back to the three years later, or as I like to call it; now. One of our other peanut free families in our son’s class gave us a sample of this soy butter to try saying it was just like peanut butter. Now, we have tried almost every kind of soy nut, sunflower, blah blah blah butter you could think of and nothing has even come close to passing the test. I opened up one of the samples and dipped my pinky in it, “WOW, you need to try this!” He did the same and gave the same response. It smelled, tasted and even looked like peanut butter.
You could hear our youngest in the background parroting one of his first words, “Wow, Wow, WoW, WwwwooooowwwW” I grabbed the bread and jam and made my son’s sandwiches for lunch. We held our breath as our oldest, Mr. Anaphylaxis to one bite after another, hoping this wasn’t some cruel joke and his face would start swelling up because we had actually just given him peanut butter. But the only thing that happened was that he finished his whole sandwich and asked for a drink. WOW.
Not the funny thing in all this (and I’m not really one to promote brands of anything via blog) is the name of this stuff, Wow Butter. That’s right! So the aftertaste gives off a very slight hint of soy, but we had never tasted something so close! We got online as fast as we could and looked it up to see where we could find more. It took a half day to track it down, and when I finally found it, I bought 4 jars.
Now for the scary part: As much as we were in awe of this stuff, a knot formed in our stomachs… how are our teachers supposed to know the difference between a peanut butter and Wow butter sandwich. Obviously a teacher wouldn’t question the sandwiches we have labelled and sent with our son, but what about non-allergic children? We thought they should maybe make it green or blue, but then you look right on the jar’s lid and it says to label all sandwiches made with wow butter and the website encourages parents to send information from their website to their school. The other scary part: is our son supposed to know the difference? If it smells, looks and taste like peanut butter, is there a risk that he will get confused? It’s amazing how something that has been created to help us also forces us to adjust our family rules for the sake of risk reduction.
We have decided that this fear of potential mix-ups will not keep us from recommending Wow Butter to others, but we will ask kindly that if you do find a use for Wow Butter; please oh please label your children’s sandwiches every time. If someone has to ask please don’t take it personally because it’s really that amazing.
Check it out: http://www.soybutter.com/
P.S. Did you know that hand sanitizer does not get rid of peanut residue?
Like many bloggers before me, I have been on a bit of a hiatus. I hate to do this “since the last time I wrote…” business, but seriously since the last time I wrote…
About a month after the passing of our beloved GG, my husband was in an accident at work. Without getting into too many details he had a serious fall that could have left him paralyzed or worse, but instead he amazingly landed on his feet and left hand after falling from over 17 feet. While the last three months have consisted of Physio Therapy and Doctor Appointments, I am very aware that things could have looked much differently and not a day goes by that I don’t know it. While having my partner home has been difficult at times, it has indeed made us stronger. He has healed up quite nicely and has recently returned to work. He would credit his cat like reflexes or skateboarding skills for landing on his feet, but we both know that things could have turned out much worse!
As the famous Dr. Seuss has written, “that is not all. Oh, no. That is not all…”
We took advantage of my husband’s time off over Christmas and drove out to visit my dad’s side of the family. It was great to see my grandmother, my aunt, uncles, many cousins, and cousin’s children! While out there, the kids caught some crazy super cold that was filled with puking and coughing. Since our youngest son’s bout with Pertussis (whooping cough) he has become a germ magnet and gets sick very easily. So while on our 14 hour journey home, his crazy super cold got much worse. By the time we got home, he had a really bad fever and was coughing up junk. We took him to the hospital and chest x-rays confirmed that he had developed pneumonia. Now the kicker in all this was that it was right over our oldest son’s 5th birthday. Thankfully he didn’t notice this fact until only a couple weeks ago, after he went to another child’s birthday party. Our youngest has since recovered (though he has another cold and an ear infection right now) and our oldest has been spoiled enough to make up for the lack of presents or party on his birthday.
Two weeks following our oldest son’s birthday, our youngest son turned 1! Lately we have kept all birthday’s low key and I have been able to let go of my guilt and replace it with appreciation for my family’s existence! Looking back at our youngest son’s life I amazed that while being sick with all the many illnesses he’s experienced, he has been able to hit all his milestones! He was walking (and I mean WALKING!) shortly prior to 8 months, he was climbing weeks later and has been a happy little boy that doesn’t let much interfere with his play time. I have been inspired by his resiliency and tried embracing it in my own life. This is the boy that I would wake with many, many times a night pounding on his back as he stopped breathing due to pertussis, this is the boy that would cough and choke on his own phlegm several times a night because of pneumonia; I remember holding my breath in until I would hear him take his first breath in. It is amazing that such a little person can have so much strength; his illnesses have made teething seem like a mosquito bite.
While we have had some of the less then helpful opinions on the causes of our challenges, we have also been very fortunate to have such awesome people in our lives that have helped make our year a good one. I believe that when you live in a supportive community, it becomes easier to be resilient; and our family has had to be resilient. I will abstain from listing all of our struggles of the year, because I’m set on moving forward. I love our family’s capacity to deal with challenges and our resiliency when it comes to struggles. We have not always been able to hold it all together, but we have definitely managed to stay and grow together; which is the best possible outcome in the face of adversity.
So, I will end with this,
To my family: I love you to the moon and back and I am proud of you and proud to be a mom, wife and daughter!
To my friends and community: I have so much appreciation for the way you have supported us in both simple and large ways.
P.S. It’s hard to make supper in the dark; So to make it easier, if you are able, turn on the lights.
We recently said goodbye to Great Grandma (GG) as she left us very suddenly a couple weeks ago. Our oldest son (almost 5 years old) had the opportunity to visit GG in the hospital before she passed away, and her illness gave us opportunity to prepare him for the inevitable loss of our beloved. He had many questions and thoughts on the idea of GG dying. Upon her passing, everyone had their own input to offer him about where GG went and what happens next. At one point my son and I had a long lasting disagreement in the grocery store about whether or not GG was a zombie.
My husband and I struggled with whether or not to include him in the funeral, at one point we were going to bring him until my mom made a really good point. Her thoughts were that instead of trying to fit Ajax into an adult way of saying goodbye at a funeral, we create our own way of helping him say goodbye. What a brilliant idea. So over the next few days we encouraged him to draw some pictures and write some notes of what he would like to say to GG on our Goodbye GG Day. We answered his questions about what will happen to GG’s body now that she was dead and allowed him to express his sadness.
On the day of the Funeral, my parents watched both the boys, so that we could be there for my husband’s family. The funeral was a traditional French Catholic ceremony, at the end I didn’t feel I had the closure I needed in saying goodbye to GG, so I’m not sure why I thought our oldest son would.
The next day we proceeded with plan Goodbye GG Day. Our oldest son asked if he could bring his camera and we agreed. We gathered the pictures that our son had drawn and the messages he had written and loaded the four of us into the van. The destination was the graveyard where GG’s ashes were buried. We made two stops on our way; one to purchase some flowers and another to pick up some balloons in GG’s favorite colour.
At the graveyard we walked around talking about the headstones and why you shouldn’t step or climb on them. He played in the leaves and took some pictures; finally we walked over to where GG was buried. At GG’s headstone we pointed out that Great Grandpa was buried there a long time ago and now GG was too. We talked about how GG’s body turned into dust and would eventually become part of the earth and help plants to grow. We laid the flowers we brought and our oldest left his pictures and “GoodBi GG” note in a plastic bag with some rocks in it. We walked around some more, and visited with a lady and her Theo Dog (daschund) whose property bordered the graveyard; while our oldest played in the thousands of leaves that had collected at the edge of the fence.
Just before it was time to go we took the balloons we had gotten and attached one of our son’s notes that read, “Sorry GG that you died.” Our son let them go and we said good bye as the balloons floated away. On our way home we had some hot chocolate to warm our insides, as it was a chilly day. On the drive home I asked our son if it was good to say goodbye to GG, “Yes Mom,” he said in his sad voice, and then he proceeded to ask if he could watch a movie when we got home.
Everyone grieves differently and children are no different. Early lessons in death are sometimes the hardest ones for children to grasp, but I feel we did right by GG and our family. When it comes to death, it is easy to take ourselves very seriously, but I am grateful for children who have a wonderful way of lightening even the darkest moments with laughter. Whether it’s questions of zombies, why robots are helping Grandma breath, or them wondering why you can’t see someone at their grave site; their innocence can keep us from getting to caught up in the traditions of saying goodbye while forgetting to actually say goodbye.
So with that I say goodbye and au revoir GG, we love you and are missing you!
I understand this post is going to be somewhat controversial.
When we had our first child, we struggled with whether or no to get him vaccinated. It wasn’t that we believed that vaccinations caused autism or other learning or behavior problems, but rather that we were not satisfied with the amount of research that had gone into vaccinations. We struggled with the idea of adding something into our son’s system that could potentially mess with his tiny little body. We struggled with the idea of giving our son something that may change him before we even got to know him. We never judged other parents for deciding to vaccinate their children, however we always encouraged parents to do their research and know about what they were getting their child vaccinated for.
One of our beliefs was that with better access to clean water, health care, and careful hygiene practices we could take on many of these diseases if our children were ever so unlucky.
As our first son got older it became apparent that he faced some serious illnesses that directly impacted his immune system; Anaphylaxis, Asthma and the much less serious eczema became constants in our lives. Not to mention the occurrence of a seizure, and the chronic diarrhea our son had dealt with from day one. With his emerging hyperactive immune system we believed it better to wait until we had figured out and dealt with some of his health concerns before adding something new and foreign into his body. With our doctor, we decided that we would put him on a delayed schedule for some of the highly encouraged vaccinations, but there were a few we were definitely still uncomfortable with. A few months after his fourth birthday, he received his first set of vaccinations.
When our second son was born, we had the same dialogue, but determined we would not wait as long to get him vaccinated. We could tell right from the beginning that his little body was the different from his brother’s. We still had our major reservations about vaccinations but, we knew that we would be getting his much earlier than we did for his brother.
Now one thing to keep in mind is that children under one, whether vaccinated or not, are at risk of contracting the diseases that vaccinations cover. A child following a regular schedule for vaccinations is not considered fully immune before the age of one and there is still at risk of contracting certain illnesses. For children not vaccinated the risk increases.
If you regularly read my blog you would have noticed that there are no entries for the month of September, this is because of one awful word: PERTUSSIS. Last month our seven months old son contracted Pertussis. Pertussis, also known as whooping cough, is highly contagious before being treated with a full course of antibiotics. Most of the time infants who contract the disease get it from an adult. Most adults who have received the DTaP vaccinations in childhood are no longer immune to Pertussis as it requires a booster shot in adulthood. As a child, I was vaccinated for Pertussis, but in spite of this I contracted the illness. Pertussis was our first run in with a disease covered by vaccinations.
It took one visit to our family doctor and two visits to children’s emergency before we received a confirmed diagnosis and by then the illness had progressed so far that the only thing antibiotics did was make the Pertussis not contagious. Infants under one year old are most at risk of complications leading to serious implications. If you ever have an infant that contracts Pertussis you will learn the words “spontaneous recovery,” in reference to your baby continually stopping and starting breathing. The fact is that it’s been over 5 weeks and he still has many fits of coughing a day followed by short periods of time when he cannot breath. I wish I could say that things have gotten better, but the fact remains that our son is still quite sick, though his disposition has improved greatly.
With the Pertussis everyone in our family and our neighbors’ family was treated for it with antibiotics, but the complications have been Mike getting Bronchitis, myself getting pneumonia and our entire family getting a virus. It has been a long, expensive and exhausting journey. The reality is that we now have both boys on a schedule for the full course of vaccinations. Our youngest will have to wait until his health has improved, but I am less comfortable with our son stopping breathing than I am the unknowns of vaccinations.
We have received a lot of criticism around not vaccinating our children, I understand the concerns but as a parent you need to be comfortable with what goes into your child and if you’re not you need to understand why. It is not good enough to simply trust your Doctor or the advice of other people. Our first visit to children’s emergency I asked the Doctor if it could be Pertussis, the Doctor told us it was definitely NOT Pertussis. Doctors are well educated, but they are humans just like you and I and it pays to do extra research. However, be aware that in doing this research you may move from being indifferent to becoming more or less comfortable with what you are researching.
With this I will sign off and hope that my time this month is filled with less illness and more writing.
P.S. I wonder what would happen if all people regularly washed their hands, coughed into their elbows and didn’t go out when they were sick.
I hesitate to write about politics, as I like to remain somewhat impartial to those readers who don’t know me personally. However, our family was recently impacted by a politician this week in a way I never thought possible. Jack Layton was the leader of the opposition in Canada, and no matter what your party preference, most Canadians can agree that he was a genuine and sharp politician. Jack was the leader of the New Democratic Party of Canada and while he was not our Prime Minister he helped keep our Prime Minister accountable. It is easy to view politics as exhausting, futile, crooked, and pointless- but for us, Jack Layton made politics personal and refreshing while challenging Canadians to work towards a better country and world. Jack Layton was the only politician that kept our family going back to the polls when election after election was called, exhausting many Canadians by leaving them questioning the value of their vote.
Jack was 61 when he passed away on Monday from an ongoing battle with cancer and we will feel his loss for the months to come. Thank you Jack for renewing our faith in politics and men with moustaches. Thank you for showing us that good can come out of the government and that there are people that genuinely want to see a holistically healthy Country and are willing to work for it. As my husband says, “You were the best Prime Minister we never had,” and I wholeheartedly agree.
I’ll leave you with quote from Jack Layton in his last letter to Canadians and a moustache tribute from our family,
“My friends, love is better than anger.
Hope is better than fear.
Optimism is better than despair.
So let us be loving, hopeful and optimistic.
And we’ll change the world.”
In a small capacity, I have recently been humbled by experiencing life as a single parent. Minus the extra income and having to worry about daycare, I have seen what our life without a father and partner would look like. The number one word I would use to sum up this experience is EXHAUSTING. I love my children, but simplest things become a challenge, especially with a newborn; Grocery shopping, mowing the lawn, making supper, bedtime routines, socializing, taking time for oneself, finding constructive ways of dealing with anger all become more complicated and emotionally taxing.
I have so much respect for parents whom are raising their children on their own, for whatever reason. Taking the time to listen to your children is hard when all you feel like doing is locking yourself in the bathroom and crying. I’m sure it gets easier but in cases where parents have limited outside support, the wear and tear to the soul must be immense at times. I love being able to share my parenting joys and frustrations with my partner, and I love hearing his thoughts and feelings on what is happening in our family. In my partners absence, friends and family helped by filling in the gaps in order for me to stay a sane parent.
In my experience, one of the only things that got easier in being a pseudo single parent was the cleaning. It’s no secret that my partner is a clutter bug and in his time away I have found that my housework load decreased substantially. With that said, I would still much rather have his involvement in our family in exchange for a few more messes to clean (I do have my limits though).
To those who are parenting on their own, I pay homage to you! May you find the support you need to breath, the patience you need to listen, the money you need to eat and the time you need to sleep.
P.S. You can wear your baby doing many chores, but draw the line at mowing the lawn.
I have two sons. One I have known for over four years and the other I have only known for six months minus a week. My oldest son was a highly active baby that made himself known all hours of the day and night. He would not fall asleep unless my husband or I rocked him for a good half an hour before bed, and even then he’d wake up ever hour or two. I suffered from intense postpartum, which looking back, was made worse by the overwhelming lack of sleep. Though I wanted more children, we put off having a second for fear of a repeat performance of that first year.
Finally, a month after my thirtieth birthday and over three years after having my first child we went for it; nine months later my youngest son was born. It may sound far fetched, but from in the womb I could tell he was an easy going baby. Unfortunately for him, “easy” has sometimes meant getting lost behind his brother’s larger than life personality. Through no fault of my oldest son, we have sometimes neglected to spend the same “getting to know you time” with our youngest as we did with our first. It’s not that we are ignoring our youngest, I am just aware of the struggle over ensuring that his growing personality does not get overshadowed by his older brother.
Finding the balance in love, time and energy spent is a tough job for most parents, especially when children compete for your time. A good teacher tries to find ways to engage not just the eager to participate but the children who are acutely quiet. As a parent, I want to see both my boys have a platform to express themselves while feeling heard and valued. While my youngest isn’t even talking yet, I am excited to get to know his personality. For now I take comfort in that I am committed to finding a balance for my children as I want them both to have voices in our family.
P.S. If you sit in silence long enough even whisper sounds like yelling.