doctors | Lessons from my daughter

I know, that’s not my typical blog title

But recently, I saw 2 blogs who made me laugh and think about poop in bathtubs.

Just When Things Are Looking Up, Someone Always Shits In The Tub. This girl is awesome, go read her posts… unless you are easily offended, she’s not shy with words. I love her!

And here the second post: It’s all fun and games until someone poops in the bathtub

It’s poop week!

From day 1, Emily had serious tummy issues.

I have heard many parents over the years state that they would take a constipated baby over the poop machines they had.

Only a parent who has never seen their baby, the love of their life, suffers through constipation would say that. The cramps, the discomfort, the squirming, the cries, the screams…

A constipated baby is no jokes.

We gave our tiny baby many baths hoping that she would relax enough to make things move.

A poop in the bathtub was reason to celebrate!

Yes, you read that right.

We would be really quiet, let it happened, take Emily out of the tub, drain the tub, dispose of the poop, clean the tub and fill it again.

If we got a second poop, awesome. If not, at least we had a clean baby.

Yes, we washed the bathtub a lot but for us, a poop in the bathtub was awesome because it meant our baby felt a little bit better!

Perspective!

Is there anything in your world that makes you appreciate what others take for granted?

💜💜💜💜💜💜💜💜💜💜

NEW!!! We have a facebook page: 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.

You can also find me on Twitter at @plebrass

And on Pinterest too: Lessons from my Daughter

I just discovered StumbleUpon but I have no clue what to do there: I believe you can find me under plebrass but I need to spend quality time there.

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

February 29th is Rare Disease Day

In my own way, through writing about our experiences raising Emily, I continue to spread the word about Cri du Chat Syndrome (CdCs)

I do my best to share experiences that are positive, fun and inspiring. I don’t shy away from writing about struggles but I will always respect Emily’s need for privacy on some more personal topics.

Did you know…

Only 1 in approximately 50,000 born will miss that tiny part of their 5th chromosome…. chances of knowing or meeting another child with CdCs are really small.

Emily was diagnosed before facebook, the information available was outdated and scary. It took us 15 years before we met others with Cri du Chat Syndrome.

Now with facebook, association and blogs, our reach is far greater and parents find up-to-date information much faster.

That being said, it is essential to increase awareness to promote acceptance for any child with special needs.

I would love for Emily’s blog “Lessons from my Daughter” to reach as many people as possible…

Would you help me by sharing this post? Please help Emily and I raise awereness for Cri du Chat Syndrome!

Thank you for being part of our journey!

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 too… one day I will figure out what to do there other than finding cool recipes but meanwhile, you can find me here: Lessons from my Daughter