Dream house – long term plan

I’m not sure how far away it has to be to count as long term…

All I know is that 3 years from now, we are planning to be ready to move into our dream house.

Our dream house will be the place where all 3 of us will have private / hobby space as well as enough common room to be able to live comfortably.

I read this recently:

This has reinforced my belief that not only we need to plan for all of this but we need to live comfortably and continue to grow as a family and has individuals.

So here I am, reworking our family budget to pay off debts and save some money while at the same time listing all the little things we can fix around the house to slowly make it ready to sell in 3 years.

So, we now have a board with pictures of things we want in our new home to keep us motivated.

Gourmet kitchen, central vacuum, hot tub, a bath big enough for an adult…

Tonight, Emily started to add to it.

When she was little, we moved quite a bit.

Now, we’ve been here 12 years and Emily never wanted to move to another house but now she’s getting into it.

Look at what she added:

She’s dreaming with us!

And look at her printing! 🀩

Afternoon tea in Bermudas

When I was pregnant, I was hoping for a healthy little baby girl!

I had those images in my head and in my heart.  My daughter and I walking, chatting, going to the book store and sitting around a coffee shop with our books and magazines.  My baby would turn into a beautiful young lady, polite and respectful, she would love me the way I love my mom.  We would go shopping and we would travel the world together….  She would probably dance, be really good at school and grow-up to be an amazing woman…

After Emily was diagnosed, I had to fill some paperwork detailing her handicap / her disability.  I looked at the form, all she could do was see and hear…  She was severely affected physically, mentally and her gross & fine motor skills were non-existent…  I knew I had to sign the form and send it to the government but I sat there and looked at it for days…. I didn’t want to admit it to myself.

Emily didn’t die when she was diagnosed but my dreams did!  All of them were shattered!

Regularly I had to go back to those calls that changed my life and remind myself that I could do this, that all I had to do was look at my daughter for who she was not for who she could have been.  I had to adjust my dreams.

November 2012, my husband, daughter and I traveled to Bermudas!  While at the Fairmont Hamilton, I noticed they were offering afternoon tea… Emily likes tea, her Nana introduced her to tea.

I asked Emily if she wanted to come to afternoon tea with me.  Explained that it would be like pretend tea but for real….. we would pick our tea and tiny sandwiches, we would wear our pretty dresses and try to drink tea with our pinky up…  She agreed to try.

I reserved a table, we got all dolled up, said goodbye to daddy and we went for tea!

Most people looking at us saw a mother-daughter (and a doll) having tea.  I saw a dream, a dream I wasn’t even allowing myself to have anymore.  Emily picked a jasmine butterfly tea and I can’t remember what I picked.  We took both trays of sandwiches and every other little finger food they would bring us.

We tried everything, some things she liked while others she didn’t.  She had an opinion, on the tea and the food.  She had an opinion on the live music.  We had small chit-chat and she tried drinking with her pinky up…  We laughed!

I discretely wiped tears from my eyes….. I didn’t want Emily to see how happy I was, I didn’t want to confuse her.

Sometimes, our dreams are so big, so far away that we can’t imagine getting there….  I had given up on this dream of enjoying a beverage with Emily while talking…… When it happened, I was speechless.  I wanted to hug her and tell everybody around us how special this moment was but I didn’t.  It was our moment.

I do have that daughter from my earlier dreams, she is polite, she adores me, she is beautiful inside and out.  She is determine to learn and work hard on learning to read and understand math.

But the most important thing is that she is herself and has opinions…..

Do you allow your kids to be themselves and build their own opinions?  Do you allow them to be kids and to dream?



Find more about about Cri du Chat syndrome at 5p- Society

Emily has a her own page in the family stories , you can find it here: Emily

If you want short updates and timely pictures of the little things that are happening in our life, please like and follow Lessons from my daughter‘s page on Facebook.

You can also find me on Twitter at @plebrass

I am on Pinterest… one day I will figure out what to do there other than finding cool recipes