Tuesday, June 9, 2009

The "Wash Out" period

Well, we are in the midst of letting the drug "wash out" of Sara's system. While the rash is better each day, we can tell she is coming off the drug. Last night she wouldn't eat dinner and dinner ended when a bowl of applesauce went flying off the table and dumping onto my carpet (yet another reason we will be getting hardwoods installed before the end of the year). Bedtime was fine, except that she didn't fall right to sleep when she went to bed and called for daddy once (something that hasn't happened in the two weeks on the drug). Last night she woke up in the middle of the night for the first time in two weeks. She came to bed with us, but was awake for about two hours (or so it seemed in my half awake brain) and was very emotional and defiant. She slept "late" this morning and seemed to be in a good mood, but we will see how today goes at daycare.

I spoke to the nurse that oversees our case at the phsycartrists office yesterday. They can't get me in until the 18th to discuss a new drug therapy, so we are just going to have to wing it until then. I think daddy and I are going to have earlier bed times so we don't get behind on sleep again. She did give me a list of drugs that could be possibilities for our next try. I researched all of them, and while each carry their own risks and side effects, none of them have the sun sensitivity like this last one. That is good news for a family that will be spending a lot of time at the beach this summer!

Tonight Nigel has a work thing, so sissy and I are on our own. I need to grocery shop, so we may do that. The other part of me wants to blow off the grocery shopping and snuggle on the couch with my sissy... we will see what wins out!

Sunday, June 7, 2009

Starting over

UGH.... everything was going so well and yesterday we spent the day at the beach. Yesterday morning, we noticed that Sara was starting to get a rash. She has such sensitive skin, we chalked it up to the sunscreen I put on her as it started shortly after that. We gave her some Benadryl, bought different sunscreen and laid around on the beach.

Last night she came home with a good bit of sunburn, even after gooping her up with sunscreen over and over again yesterday. This morning, the rash was now covering her from head to to and I was started to get concerned. We went and had bagels and while sitting there, we realized that it was time for her to get looked at.

After waiting forever in the ER... Ok, it was less then two hours... but it felt like forever, a dr took one look at her and said she definitely has a drug rash and we were to stop her medication immediately. BUMMER.

After getting out of the ER, I called the psychiatrist and the on-call dr told me to stop immediately, give her a dose of Benadryl and call the office in the morning to get something else. Total bummer, because I think we liked this medication.

It will be interesting to see if she sleeps tonight or not when she doesn't receive her regular dose tonight. In the meantime, we are all going to lay done and take a nap. This sucks.

Friday, June 5, 2009

Such a good girl!

Today my Sara had to have a blood draw to test her medication levels. While that seems so routine to most, having a child with several issues... we were prepared for a fight. Early this week, I went back and forth on if I should tell her before hand or not. I decided to tell her.... and then doubted my choice. Tons of screaming and tears about getting shots. For the last several days she has been telling everyone she is getting a shot. Lots of tears and whining (and a little screaming on top of that) every time the subject came up.

We recently found out that Sara will eat refried beans from a little Mexican place on the way home from school. This is actually a good thing because with her sensory issues and the texture of refried beans, we are surprised she would eat them. Additionally, they are pretty fattening and Lord knows my little stick of a child could use the fat. So, we told her that if she was good (meaning no screaming... we are ok with tears, but not screaming) we would take her to get refried beans on the way home from school today.

This morning was a struggle. She knew it was the big day, but did not like that she couldn't have her beloved juice cup this morning (it was a fasting blood test, so no food or drink). So, lots of tears and screaming this morning. I let her choose a snack to eat once we were done and she got in the car finally and sucked her thumb and didn't make a peep all the way to the lab.

When we got there, she was glued to me. We had a bit of a wait, so she climbed up in my lap with bunny, blankie and her thumb and was very quiet, but asked several times to make sure she could have juice and a snack when we left.

When we were called back, the staff was SUPER!!! They did their job quick so she didn't have time to throw a fit. She sat in my lap, they put the rubber band around her arm and found a vein. Another tech came in, held her arm (which is when the tears started... she hates to be held down) and POKE! BIG tears, and then they were gone. They took four vials of blood and the tears were gone before those vials were filled. She watched intently at her blood filling them up. A neon green band-aid and she was done.

Then we got another surprise... time to pee in a cup. Anyone ever tried to get a kid to pee in a cup on command?!?!? In the past, this has been a HUGE struggle for us. It usually requires me to get pretty inventive with putting a bowl in the potty to catch the urine and then pouring it in the cup. But, of course, my little girl shocked me. I got her giggling about not peeing on my hand and she filled that cup up! YAHOO!!! Success!

Last night we all went out to dinner to celebrate the end of a long project for me. She did great and ate like a horse (still not gaining any weight according to her weight last night, but at least she is eating). She has been sleeping well, actually she has been sleeping AWESOME! While we notice an increase in a lot of good behaviors, we also notice that the tears and whining haven't really stopped either. Not sure what that means exactly, but I meet with the doctor again on the 18th, so we will see what they have to say then. She is just VERY emotional, although the outbursts usually don't last very long.

As a another note, she had a GREAT day at therapy yesterday. She actually squished Jello between her fingers and toes. This is a HUGE, HUGE thing as she is usually very reluctant to have anything weird go on with her feet. Very awesome. Since starting therapy several months ago, we have seen an increase in the amount of times she is willing to "try" something. More often then not, she will try new foods now instead of simply turning up her nose. She has zero fear of water (a good and bad thing), and has even started going under water. She still has a lot of issues with going in circles on a swing, but is at least willing to try it each week in therapy, which is progress.

It has been a long week for this family. A work project has kept me at a high anxiety level and cranky and tied to my desk for long hours. Nigel has had work issues of his own and is not his usually joking self. And Sara has had her own worries this week with this blood draw. On top of that the painter was here earlier this week, so our house has been in shambles. Very soon the older kids will be here and there is a lot to get done. BUT, tomorrow, we are taking a break from it all and heading to the beach again. The three of us had such a great time last weekend, that we are going to do it again. It was super relaxing and so nice to soak up some sun. This time I will slather on the sunscreen so I don't get as much sun myself, but all of us need some time where the phone isn't ringing we are only focused on being a family.

Much Love to all who read this.

Tuesday, June 2, 2009

Emotions... or going thru the motions

It's a busy week in our house. I was hoping to be able to blog every day at least until we were sure this was the right medication therapy for Sara, but I am already falling behind.

Work is kicking my ass this week with a super, huge project that will be over soon, but in the meantime, late hours and load o' headaches. On top of that we are having the upstairs painted, while it's WONDERFUL to have some color in this house finally, not sure why I picked this week to do it! It is beautiful though. Walking upstairs feels like you are slipping into a warm cup of hot chocolate. Super nice.

As for my Sara... we heard that she had a great day at school yesterday, but she told Nigel that she got sent to timeout for calling someone an alien?!?!? Not sure that was a true story or not. :) We did spend a few minutes in the pool last night and she slept great again. The sleep seems to be doing wonders for all of us right now.

Sara is VERY, VERY sensitive to change, so when she came home last night to the upstairs being painted and the house in disarray, I was hoping that it wouldn't spark some sort of a meltdown. She was totally fine and was happy 'cause Mr. Paul (the painter) was here to "play." WHEW!

Now my only worry for this week is a blood draw. I have made an appointment and made sure they knew it was for a toddler.... one that has an issue with shots and needles. Do I tell her before hand, wait until we get there, wait until that morning? SIGH.... I just don't know. What I do know for a fact is that this is not going to happen with out a struggle, so that should be just dandy. Oh, and it's a fasting blood draw, so that just makes things that much more fun to look forward too.

I have a nasty sunburn that has blistered in a couple of spots... but come hell or high water, my arse is going to be on the beach again this weekend!!! Time for relaxation and fun times with my little one (and Nigel too! LOL!)

Sunday, May 31, 2009

Today was a good Day

Today was a good day. Ms. Sara woke up at about 6:15 (again, the ass crack of dawn) and ten promptly took a small tumble down the stairs. Most of the time, she sits at the top of the stairs and yells for DADDY until he goes and gets her and brings her to our bed. Yesterday morning, she yelled a couple of times and then we heard her say over the monitor, "NEVER MIND!" and the next thing we know she climbs into our bed and tells us to "WAKE UP!" (Yes, every thing is at the top of her lungs, or so it seems when you are still trying to pry open your eyes and figure out what day it is). :)- Well, I have a feeling her new found Independence was short lived after taking the last two steps of the stairs in one fell swoop! Oh Well.

So, of course, this got her started off in a foul mood. But, we went off to experience a Kolache (for those non-Houston folks, that dough with eggs and sausage or a variety of other things stuffed inside) and then made our weekly trip to Wally World. Walmart at 8:30 on a Sunday morning is a fab time to shop. In fact, we can even let Sara out of the cart, and she held the list and "helped" with the shopping.

Once home, she played by herself while I read for a bit and daddy passed out for a nap. She then took a 2 1/2 hour nap and then spent the remainder of the afternoon playing with me in her blow up pool. Nigel just put her to bed and we will see if the streak of good bedtimes continues tonight.

Another thing I am starting to notice.... she has eaten me out of house and home today. Usually getting my tiny little bird to eat is a challenge (along with most other things). Today is actually asked for lunch and dinner and even once helped herself to a snack from the ice chest.

There was a small fit when it was time to get out of the pool for bed, but much better then it could have been, so I will call today a success.

As for me, this week is going to be a work challenge. I have a MAJOR project that will be completed on Friday, but between now and then.... it's going to be ugly. I am doing what I can to keep my stress from rubbing off on her and even promised a short swim in the pool after dinner tomorrow night if she has a good day at school (precious time I do not have), but it will be worth it to see her smile.

Still many miles to go, but the increased number of hours we have been able to sleep has helped keep things in perspective. This weekend is just what this family needed. We have one last weekend before the older kids begin to arrive for their summer stay. Two weeks to see how this medication works before we introduce the 8 weeks of controlled chaos of summer. :)

Saturday, May 30, 2009

Before I get to far behind...

I want to keep up with Sara's medication therapy and use my blog to document. She started her new meds on Wednesday night. She has been sleeping thru the night since then (which is super HUGE good news for Nigel and I). While she still wakes up at the ass crack of dawn, bedtime is MUCH easier as she falls right to sleep instead of an hour of doing whatever she can to avoid going to sleep. However, I have noticed that she is EXTREMELY emotional in the mornings. Even after sleeping 10-11 hours, she is very quick to whine and cry in the morning when things don't go her way.

This morning, we almost didn't go to the beach for fear of a day of meltdowns in public. BUT, after getting her something to eat and popping a DVD in, she was pretty quiet all the way to the beach. Even without a nap, she did well. A couple of times she crawled up in Nigel's lap in the shade and just about nodded off, but then would pop back up and be ready for more sand, sun and waves.

The girl has NO fear of water, and we had to keep a close eye on her several times. The other thing that struck both Nigel and I was that she played by herself for quite some time. Usually she wants one of use to entertain her, but today she sat at our feet and played in the sand for at least 30 minutes all by herself. That ended when she realized she was hot and was ready to head back to the water.

Tong ht when we got home she was EXHAUSTED. Bath time, at best, is usually filled with a lot of whining. Tonight, she let me take out her pony tails without a fight (usually a HUGE issue) and only cried when washing her hair. Bedtime was shortly thereafter, and Nigel and I haven't heard a peep out of her.

So, after a morning that was not looking good, the day turned out well. In fact it was so fun, we are hoping for good weather next weekend so that we can do it again. This time, mom and dad will be more frivolous with the sunscreen! :) We were so worried about Sara and the sun, we didn't take care of ourselves. Her new medication makes her sun sensitive, so we were SUPER, SUPER careful with her. She only got burned on one hand and one little butt cheek near the bathing suit line.

It was a good day. I think we all needed some sun, waves and sand.

Thursday, May 28, 2009

My husband, my rock

Nigel is a dream come true. This July we will celebrate three years of marriage. What a freaking CRAZY three years. We were living and married in New Jersey. Moved to the Portland area after Sara was born and then moved to Texas.

Thru it all, Nigel has always made me laugh, kept me on track, and has always made me feel like I was his one and only! If I had to describe him in three words they would be: funny, compassionate, dedicated. Nigel was also married before we met. He has two fabulous kids from his first marriage.

Working in IT, he is a computer geek by day, but his passion is music. He is a talented DJ, and has open my eyes to the world of music and the joy it brings to people. While there are times it drives me nuts (we have a laptop on our coffee table at all times so that he can be downloading music and working on CDs while he is watching TV.... that laptop on the coffee table drives me bananas), I LOVE, LOVE, LOVE being able to sit in my office on Friday afternoons (his office closes early on Fridays) and listen to him in his music room playing on the turntables.

Getting pregnant with Sara was a total surprise to the both of us, but he is a super dad. Without Nigel holding down the home front I would never be successful doing what I do for work. I can walk away from this house for weeks at a time and know that when I come home, my littlest sweetheart will be well loved and well taken care of.

Nigel is the biggest blessing in my life and I would never trade him for anything!