That’s not even a question, it should be are they ready for him?
The visit with the preschool went well. We visited a 4/5 year old class just to walk around the room to see what will work and what won’t. It was determined a lot of the interactive things like the easel and sensory [...]
| Things have been relatively quiet around here (outside of the bank auctioning off my home and bombarding me with daily phone calls…)
The kid’s are doing well and I think they have reached a new level of appreciation for having a little brother. Hannah, in particular is spending more time playing “mommy” with Knoah and he [...]
| My posting on POLP and here have given me so much relief and comfort!
I worried about sharing it because no one wants to be considered weak or “can’t handle” life. It’s not that I can’t handle life, life just has a way of sneaking up on you and makes you deal with it at [...]
Things around here are chugging along as normal.
Knoah is suppose to have a sleep study the 19th, but I am debating if I am going to take him. I want to take him because I want to know how he;s really doing at night, but Dr. Pauli thinks it’s not really necessary. So, I [...]
We have a few new blogs to add to Knoah’s ARC!!
We start with Stacey and Grant! Grant was born November 5, 2008 and was diagnosed with Diastrophic Dysplasia. He is little brother to Emmalyn and they live in Utah. Please go over and welcome them!!
Then we have Kasia and Amelia. Amelia, affectionately called Mimi, was [...]
Look what he did yesterday….
Knoah falls. He falls a lot. He seems to ALWAYS gravity toward corners, which ALWAYS makes me panic. The swelling went down quickly, but still. Hannah said to me today…
“Mom, instead of getting Knoah a new brace for his back, we need to get him on for his head. He hurts [...]
Recently, I did a post about Little People, Just Married. The Oprah Winfrey show was looking for LP parents and kid’s who had seen the show and was willing to share their story with them.
Samantha, the little girl featured on the show with Bill and Jen did a wonderful job! She was excited to meet [...]
There comes a point during blogging or sharing information that one must ask themselves “how much do I want to share”?
The answer is not always an easy one to come up with, especially when we’re talking about a child with dwarfism. With the hit show like Little People, Big World, people are naturally curious as [...]
| Well, the excitement from the last week’s appointment’s have calmed down. We did receive information regarding our ENT appointment from Dr. Pauli and…
1. Knoah need’s PE Tubes. No question. He doesn’t want us to wait six months to see how many ear infections he has, he wants us to find another ENT who will preform [...]
Make sure you watch Little People, Big World come Monday!!
Me and Amy Roloff, one of the stars of LPBW!
This episode is suppose to feature scenes from the National Convention held in Detroit!!
Let’s see how many of our little one’s we spot!!
The families that I know were there from our blogging community were:
Knoah, Kaela, Owen, [...]
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