Monday, December 28, 2009
Talking & Shopping with Olivia
Olivia: (pointing to boxes) Tigger!
Me: No, that's not Tigger. Its a Tiger. Someone the Tiger.
Olivia: Its Tigger.
Me: No, he's Tony the Tiger.
Olivia: No, its Tigger.
Me: Well, of course
Olivia: Mom, he's not a horse, its Tigger.
Me: Okay!
End of Discussion.
I am easily persuaded. Or poorly persuading.
More Skating Today!
When not riding around in her parent powered stroller, Olivia was prancing around.
We got to watch the Junior National short track speed skating team (I think?) practicing.And topped it off with frosty's on the way home. Lovely afternoon.
Sunday, December 27, 2009
Ice Skating

Austin and Nyah had a blast!
Kurt and I took turns going around with them . . .
. . . and sitting with the little two. Olivia was mesmerized by the zamboni clearing the ice for a hockey game. Jolie just like hanging and pulling at the gate. Saturday, December 26, 2009
Hurray Keshia!!
So I've been doing a little research:
LDS Country Profiles: Slovenia & Croatia
Location: Maps of the Balkans - Slovenia & Croatia are across the Adriatic Sea from Italy
Interesting Facts about Croatia
Intersting Facts about Slovenia
She reports to the Missionary Training Center in Provo, Utah mid-February.
Christmas Day
Friday, December 25, 2009
Merry Christmas!

Jolie, 19 months, is growing up faster than a speeding bullet! She is in a hurry to catch up with all her siblings, and can’t stand to be left behind. Some of her favorite things are dogs, babies, shoes, and her Dad. We love how helpful she is- from switching laundry to unloading the dishwasher, she always wants to be a part of what we are doing.
Olivia, almost 3 years, is excellent! About a month ago she fell from a shopping cart and ended up with a fractured skull and small bleed in her brain. Within an hour she was on a life flight to a children’s hospital, stayed a couple days, and caused lots of worry and stress for everyone. Thank you for all your help, kind thoughts, and prayers for our sweet girl. She is back to her happy, joking self, running and playing, laughing and screaming, and squabbling with her siblings. All efforts to keep her on ground level and doing walking-paced activities are failing miserably—we wouldn’t want it any other way.
Nyah, 7 years, is still the firecracker in our family. She is part rebellious teenager and part helpful sweetheart, and loves tricking us with her different personas. She speeds through her daily work and assignments so she can go outside and play with her friends. She enjoys her home school club and being in Girl Scouts. And despite the many complaints about little sisters, I know she secretly loves being the ringleader.
Austin, 8 years, is our ever dependable and laid-back boy. He is a great big brother and always looks out for his sisters, though he also likes being the one to tease and torment them. He can spend hours playing with his legos and action figures, but he also likes playing video games and hanging out with his friends. He likes his home school club and is thrilled with all the exciting things he gets to do in Boy Scouts.
Kelsey—I am busy with all the usual details of being a mom, homemaker, homeschooler, and scout leader (boys & girls). When I have free time I am learning to play the piano, reading books, blogging, or trying to squeeze in a nap. We are expecting a new baby—my due date is July 5, 2010.
Kurt—has been working as the VP of Corporate Development at ASEA for a little over a year. He is busy and gone a lot, so we love it when we get to spend time with him. When he has free time he enjoys being with his family, practicing guitar, playing video games, or shoveling snow! HA, just kidding.
Merry Christmas and Best Wishes for the New Year!!
Lots of Love from the Richards’ Family
Thursday, December 24, 2009
Sledding
Graham Cracker Houses
Tuesday, December 22, 2009
Its Almost Christmas!!
Because it takes forever to get all the kids ready, find everyone's boots, gloves, & hats (putting things in the same place so you can find them later being a totally alien concept to kids), I don't take Olivia and Jolie out very much. But we made the effort today.
Building a snow fort
Sunday, December 20, 2009
Saturday Highlights
Austin & Nyah singing at the ward Christmas party. Kids ended the day sliding in the living room while we watchedA Muppets Christmas Carol (my favorite Christmas movie!!!)

Friday, December 18, 2009
Christmas Trees
I admit to chickening out when it came to decorating this year. We put up the tree and trimmed it, and I have spent everyday since picking up ornaments and putting them back on the tree, only higher, which is why the bottom part is empty.

We put a few things on the mantle, but not our stockings yet. We use some cute Santa statue hook things for our stockings that we didn't want our little girls pulling over on top of their heads-- no more head injuries!!! We'll hang them Christmas Eve.

I also bought a poinsettia this year, but I don't know why I torture myself with potted plants-- they start to wilt and loose their leaves because I forget to water them, so I water them and they perk back up only to be neglected again. Sigh.

P.S. to Karla- I changed the settings so you should be able to leave comments now.
UPDATE:
My mom has posted about her Christmas trees (yes, there has always been more than one!) and beautiful decorations. Check 'em out!
Thursday, December 17, 2009
Doctor Blather
I saw Olivia Richards today who as you know was diagnosed with a left optic nerve glioma on recent scans that were done incidentally because of an injury that she got from falling out of a shopping cart in November. (A little fancy doctor talk but so far I'm with him)
On Olivia's exam today, she has very slightly reduced vision in the left eye compared to the right but no clear-cut afferent pupillary defect and no optic nerve atrophy or edema on the left. (I'm lost, are you?) She has no strabismus. Her ocular rotations were full. Her cycloplegic refraction did show hyperopic anisometropia with more hyperopia on the left, compared to the right. I think Olivia is not having any impact on her vision thus far because of the optic glioma (That sentence I understood). I think she does have hyperopic anisometropia and mild amblyopia in the left eye secondary to it, but I recommended glasses wear and I will see her again in two months to check her vision. (Glasses and go back- check!)
We certainly could do a visually evoked potential in the future if we suspect that the glioma is a problem with her vision but I am not sure that we would do any treatment anyway. I hope this letter is of help to you and I will keep you updated.
Warmest regards,
blah, blah, blah.
Obviously there was a lack of communication/understanding on both sides for him to think this would clear things up for me.
I have been looking up all these terms on MedicineNet, if you want to try it I suggest using full terms such as "afferent pupillary defect" instead of single words. Or you can go to this Eye Glossary. Or you can wait until I have it explained to me by someone else and I'll try to explain it again here.
Wednesday, December 16, 2009
Monday, December 14, 2009
Announcing . . .

Baby Richards due July 7, 2010
Ultrasound pictures at this stage always remind me of those orange, candy, circus peanuts. Baby's head is the circle-y blob inside black oval on the right and baby's toosh is the other end. Baby was kicking legs and waving arms during the ultrasound- so adorable. Totally made the 2 hour wait worth it (my doctor had to go deliver a couple babies- some excuse).
Sunday, December 13, 2009
Christmas Concert
It was magical!!!Saturday, December 12, 2009
Penny MIA
Thursday, December 10, 2009
Wednesday, December 9, 2009
Olivia NF1 Update ~ Dec 09
So, November 30th Olivia had an MRI to check on her head injury, but primarily to get a clearer picture of the optic glioma. We've suspected she's had NF1 from when she was 3 months old and she was officially diagnosed around 9 months old. Because she doesn't have any major outward signs and she has been developing normally, its the type of thing that just doesn't come up in conversation, so I know it has been a surprise for some of you to find out about it.
In March 09 I did a post about Olivia's yearly check up. Basically there are 7 major signs for NF1--A listing of these can be found here.
Olivia has:
(1) cafe au lait spots- basically birthmarks. She has several that are bigger than two quarters placed together and lots of smaller ones of different sizes. These started appearing when she was 1 month old and will likely continue to appear. I asked her pediatrician about the first of these when she was 2 months old and he recommended we see a genetics specialist.
(2) surface neurofibromas- if you look at pictures of these online they are freaking scary and Olivia's don't even remotely look like them. The doctor pointed out 2 possible ones, they are small, slightly raised bumps, maybe about the size of a grain of rice. I'm never sure I'm even looking in the right place. These were found at her March '09 visit.
(3) freckling- in her armpits and groin, pretty much where the sun doesn't shine. Also started appearing from a very young age. This was the 2nd sign that confirmed the diagnoses when she was about 9 months old.
(4) Optic glioma- this is what was found in the CT scans we did for her head injury, on the optic nerve of her left eye, Nov 09. This picture is similar looking to Olivia's.
(5) Lisch nodules- small, raised bumps on the iris of the eye which don't interfere with sight or cause problems. Picture here - These were also found at the March '09 visit, and aren't visible to the naked eye.
There were also a few other things that the doctor talked about in March '09 that he attributed to NF1, such as low muscle tone. The doctor felt her belly was sticking out more than a toddler's would naturally, a result of the muscles not being as strong. I will also say that she isn't as physically coordinated as my other kids. She's a really awkward runner. But I've never felt that this is completely due to the NF1, because not every kid is going to be an athletic super star. There can also be learning disabilities, but she has been meeting milestones for her age so we aren't worried about this.
Soooo, the MRI results- we did the MRI on Monday, I talked with Olivia's neurologist on Tuesday, and we saw her pediatric opthamologist on Thursday.
The neurologist said her optic nerve looked slightly enlarged or thickened, and as long as its not affecting her sight or pushing her eyeball out she wouldn't need any form of treatment (treatment options would be surgery, radiation, or chemotherapy- but these would only be necessary if its affecting her in an extreme way). Also, because we know she has NF1 she wouldn't need a biopsy.
The opthamologist. Hmmm, I will start by saying that by the end of this doctor's visit I was thoroughly tired of doctor-talk. He was so technical that all his explanations just didn't stick in my brain. So, I still can't remember all he was trying to tell me, and I plan on requesting a review of this appointmet, and I think he usually sends out follow-up letters for each visit anyways.
Here are some of the main points I do remember:
(1) The optic glioma is not affecting her vision or pushing her eye out. He said we would just continue to monitor it, see how fast it grows, if it begins to affect her vision, etc. So we will go back to see him in 2 months. He made it seem like it is really small, and it even could have been there on her previous MRI (at 9 months old), but just undetected. I really wanted to see the MRI for myself, and the other doctors involved had given me the impression that this doctor would show it to me, so I was really disappointed that he wouldn't let me look at it, and this seemed to be more of a "not enough time" issue for him more than anything else. I was shown CT scans while Olivia was in the hospital and the optic glioma looked HUGE to me, and I was able to see left eye vs. right eye, so I really wanted to look at the MRI with someone who could say "this part is the glioma, this is the nerve, this is how it might affect her vision, etc." Very disappointing, but I'm thinking when we go see her genetics specialist we'll be able to do this.
(2) Treatments (surgery, radiation, chemo) are avoided, unless the risks of the treatment would outweigh leaving the optic glioma alone. He was really the first doctor to make this clear. Everyone else (neurologist, oncologist, and all the others we saw when she was in the hospital for the skull fracture) acted like this was something that needed to be treated ASAP!!
(3) Her left eye isn't focusing correctly so he gave us a perscription for glasses. He said this is unrelated to the optic glioma/NF1, but I don't think that makes sense. ???
Anywho, that's the gist of it all for now. I'll post more when I get more info.
Thank you everyone for your thoughts and prayers for our sweet girl.
Sunday, November 29, 2009
Decorating for Christmas
Jolie, of course, immediately starting un-decorating the tree. Now she has figured out how to put the ornaments back on and she does her "I did it" dance when she is successful. Kids are sooo entertaining!!!
Friday, November 27, 2009
Thanksgiving Week
Austin reading
Nyah and Olivia painting- I leave the room for one minute right?
Nyah was actually mad at Jolie for stealing ponies, even though she's smiling in this picture.
Jolie and her favorite person in the whole world.
Video of Olivia getting back to normal-- playing "cooking show" with Nyah. One of those rare moments this week when they were playing nicely together. All three girls are driving each other nuts-- wanting whatever some else is playing with, taking it away, hitting each other, yelling and fake crying-- I'm going crazy too.Olivia is much better. She is up and playing most of the time. She gets tired quicker and is hit with headaches throughout the day, but that is to be expected and overall she is doing good. As long as her mom isn't trying to cram her head into a bike helmet-- in my defense she asked me to help her put it on so she could ride her bike around the house, but I really did fail to think about possible consequences before popping it on. Total mental lapse.
Monday, November 23, 2009
Olivia Update
Hiding under her blanket when she saw the camera out -- She also does this when she is tired of being asked if she wants something to eat (she's living off green beans and apples) or if she's okay or when people stop by to visit her.
After breakfast she sat up and colored for a while.






















