April 4, 2017

Update

So things have been quiet around here lately but it’s not what you probably think. I have been doing great – I am feeling much better. I think being on insulin has helped immensely. I am not feeling so tired and foggy all the time. I am actually getting some housework done and making meals at night doesn’t feel like I am barely able to make my way around the kitchen. I’m still working on eating better and getting more exercise. I went and got my hair done and I love the style. I bought contacts and new makeup. Today I got my eyebrows waxed for the first time since my wedding 22 years ago. lol. In a few weeks we are […]
March 22, 2017

My Husband – I See You

A new article over at Her View From Home
March 14, 2017

Post-Adoption Depression is a Very Real Thing

I have a post over at Her View From Home, check it out http://herviewfromhome.com/post-adoption-depression-is-a-very-real-thing/
March 3, 2017

Remembering Stuart McLean

On February 15, 2017 writer and radio personality Stuart McLean died from cancer.I was saddened by the news of his death, deeply saddened.For him and his family and friends. But also in a selfish way I felt sad there would be no new volumes of work. No more new books and CD’s for Christmas. I wanted to do this post right away but honestly it was hard for me to admit he had died, kind of like when Robin Williams died. Grief and pure disbelief. I first heard of Stuart probably around the year 2001. Adam and I had been trying to have a baby with no luck. I was heartbroken and trying to see the good in things but […]
January 31, 2017

Respite

There are 3 things that I feel helped Corbin and our family the most when he was in early years of elementary school. One was Camp Winston ; then there was Occupational Therapy and then respite. According to the Family Respite Services website We are a Windsor-Essex community organization that works with families caring for children under the age of eighteen who have intellectual, physical and mental health disabilities. We facilitate the provision of respite services that contribute to: The sustaining and enriching of a family’s quality of life. Seek the fullest participation of the child in the community. We have always felt it important that respite be viewed more as a way of connecting   Corbin to his community than a break for […]
January 26, 2017

The Words That Almost Take My Life

  Thanks for the concern – the following is an example of how I feel when depression overwhelms me – I am NOT feeling this way now. *** Failure Loser Incapable Unwanted Unworthy Words my mental illness plants in my brain. They sneak in under the cover of dark, rearing their ugly heads when I least expect it. Defences down, I am bowled over by the intensity and severity of the words. I do my best to fight. I do positive self talk and affirmations. I stay away from sad movies and TV. I seek out my husband who counteracts the force of the words. But sometimes, sometimes I can’t fight. They overwhelm me, those words. They tell me I […]
January 24, 2017

The Silent Killer

Diabetes is kicking my ass Really I know I have type 2 so the onus is on me to eat healthier and exercise more. I also have central sleep apnea which doesn’t always respond to my CPAP machine and often leaves me exhausted all day. Who feels like exercising when you have had no sleep? I also have Polycystic Ovaries which wreaks havoc on my hormones and leads to weight gain.  Which then makes the Diabetes worse. I also have depression – at times crippling depression and anxiety that make it hard for me to get out of bed in the morning let alone exercise on purpose. I use food as my emotional crutch.  Feel sad. Eat. Feel scared. Eat. […]
January 21, 2017

A Journey Through Family Centred Care

A few months ago I mentioned that I gave a 1.5 hour talk at a conference. It was at the Ontario Association for Infant and Child Development (OAICD) and the topic was Our Journey: Finding Hope and Courage within Family-Centred Care. The audience was small but perfect for my first solo presentation at a conference. I received the feedback from the conference in late November but was swamped with work and home stuff and didn’t get a chance to post.   Here is what people had to say: Fantastic! Definitely valuable insight that is needed to hear Best presentation in the whole conference! I’ll definitely be checking out her blog. Moving! Absolutely fantastic that Tina would or could share her family’s […]
January 14, 2017

A New Place to Write

I stumbled across a new site – Her View From Home – and if you click on the link it will take you to an article I wrote for the site. Please comment and share – the more unique pageviews for the next 30 days the more I get paid. Thanks in advance ?
December 14, 2016

Advocacy is not a 4-letter word

There are times where, as the parent of a child with a disability, you will be told to fight for what your child needs. Us “special needs moms” – we tell each other “fight for him, you know him best” and “the squeaky wheel gets the grease”. People get worked up hearing other parent’s stories. At times I too have believed this way of thinking and engaged in my fair share of fights.  Last week I read a piece that spoke of being a Mama Warrior for your child with special needs and it just seared my heart.  I genuinely felt very saddened by the notion that as a whole, it is thought that parents of kids with a disability […]