Posts filed under 'Parenting'
Dear Mama,
I love you so much!
Thank you for your smile and for all the hugs and especially the snuggles. Thank you for reading me books and playing games, for taking me on adventures, and even for the tickles. Thank you for letting me eat yogurt and cookies and beets and green beans. Thank you for helping me wake up when I’ve had a bad dream, and for coming and sleeping in my room when I’m not feeling well.
Thank you for spending so much time with me. I love being around you so much! Thank you for teaching me to do things with my left — I know that’s important even if it makes me frustrated sometimes. Thank you for your confidence in me, and for teaching me how to be big and good.
I hope someday I can be as big and good as you.
I love you Mama.
Anna Rose
May 11th, 2008
Not us! Last night was a very long night for Anna and me. Anna seems to have picked up some bug (or already had a bug) that took advantage of the fact that she had no sleep yesterday. She had a fever last night of 102 degrees. That, coupled with the fact that she’s in strange place in a pack-n-play, didn’t make for a particularly good night last night. I ended up sleeping with her in her room. There’s a queen-sized bed in her room, but I certainly wouldn’t know, as I was clinging to the very edge while Anna took the rest. She just wanted to be close, and kept insisting on sleeping on me. I generally like to sleep in a cool room, with a cool pillow, etc. The heat generated from Anna’s hot little body was not really conducive to good sleep for Tara.
So far today, Anna’s been a bit of a mess. She’s obviously exhausted, but not really wanting to take a nap. We finally insisted on the nap, and she’s going on 3 hours! She even managed to sleep through a pretty loud thunderstorm (I felt like I was in Kansas again! You just don’t get storms like that in Colorado.). Hopefully she can sleep off the worst of this bug. If not, we’ve been googling the nearest urgent care.
When she finally wakes up, we’re off to Target to spend some big bucks. You really take for granted the fact that you have condiments, spices, and what-not in your pantry. We don’t even have any dishwashing detergent to wash up the pots we’ve used.
February 17th, 2008
I posted some pictures we had taken recently of Anna and Henry in their Halloween costumes. I’ve got some other photos to post, but I have to get them off of the camera first. Too few hours in the day.
We had Anna’s neurology appointment on Monday, as well as her preliminary evaluation for this second round of constraint therapy. The neurologist thought Anna looked great, and commented on the fact that if you didn’t know Anna had hemiparesis, you couldn’t really tell. Whereas this is GREAT news, it is going to turn into the bane of our existence vis a vis receiving medical services. Anna still has quite a ways to go in terms of her therapy, but we are reaching a point where the medical community says “oh, she’s functional, so we aren’t going to treat her anymore.” It hasn’t happened yet, but I’m seeing that as an issue coming up.
The OT at Children’s who will be working with us during this next round of constraint therapy believes the botox injections could really help Anna gain more functioning in her left arm/hand, so we will be proceeding with the treatment. This is not really a cut-and-dry decision for us. Because Anna’s tightness is more in the deep tissue of her shoulder and smaller muscles in her forearm, the botox injections will be a bit tricky. There is no way that the doctor is able to help the tightness in the deep muscle tissue, but she can do an injection in her forearm. These smaller muscles are harder to isolate and if she is not precise in her injection, she could end up causing decreased functioning in her fingers (for grasping). Of course, if this happens the constraint therapy is really going to be difficult to continue. I’m of the opinion that if her fingers are affected by the botox, we will call off this round of constraint therapy completely. The OT believes there are still gains that can be made, even if her grasping is affected…but at what cost!? A completely frustrated little girl? I don’t think so.
Neal is rightfully concerned that if the botox does affect her grasp that we may lose ground during the time that the medicine is blocking the signals to the brain (botox’s effects usually lasts about 3-4 months). She is beginning to use her left so much in her daily life (unprompted, no less), it would be a shame to see her disregard it once again. Needless to say, we are quite nervous about the procedure. Not only are we injecting a dangerous neurotoxin into our baby-girl’s arm, we are also exposing her to the risk of decreased functioning of her left hand. To minimize the risk of an unintended muscle being injected, the doctor will use an electronic stimulator on her needle, which will show her which muscle she is in contact with. I’m not sure how this will work, but I’m sure we will learn soon enough. Anyway, it is not an easy decision. These are the times you can’t help but think about how unfair life can be.
October 30th, 2007
Since my last entry I’ve posted at least a couple batches of photos. Make sure you check them out! They extend far beyond those found on the front page of this site.
Just a quick update…yes, we are all still alive and kicking! I know it has been a long time since I updated the blog; I guess we’ve been a little busy. Here’s a brief list of what’s been going on: Anna’s been walking around a lot lately - it’s become her primary mode of locomotion at this point; she’s had another ear infection; she’s been fitted for a new Dynamic Ankle Foot Orthotic (DAFO) for her left foot, so that she will hopefully walk correctly (heel-toe, not toe-heel); I was sick for a couple of weeks; Neal was sick for a couple of weeks; Granny and Papa came to visit; Anna played a lot with Henry; she’s been increasing her vocabulary substantially; Neal received a promotion; and we recently purchased a new car. Doesn’t sound like a lot when you write it down, but it seems like we’ve been very busy lately.
September, October and November are gearing up to be extremely hectic months. If she isn’t already, Anna will be fed up with doctors and clinics (I’m sure I will be too, and I’m not the one being poked, pulled and stretched). We have Anna’s 18 month check-up coming soon (she’ll be 18 months in a little more than a week!). And then we have all of her specialist appointments - neurologist, opthamalogist, neuropsychologist, and physiatrist (rehab doctor). We’re coming up on the one-year anniversary of Anna’s diagnosis. It’s hard to believe that it has been only a year. Sometime in October we’ll also be having Anna’s 6-month reevaluation for her IFSP (Individualized Family Service Plan). This is basically a powwow among Anna’s therapists, our early intervention service coordinator, and us where we discuss Anna’s progress and our goals for the next 6-month period.
In late October Anna will be receiving her Botox treatment. No, she doesn’t have wrinkles. Doctors often use Botox in children with cerebral palsy to relieve/reduce spasticity (high muscle tone) in select muscle groups. The physiatrist will be injecting Botox into several of Anna’s arm muscles. This will hopefully allow her to strengthen the opposing muscles that aren’t able to do much because of those muscles with high tone. Of course, this makes Neal and me more than a little nervous. I mean, the stuff is poison. And she’s still so little. They say that the injections are painful, which makes me feel terrible for putting her through this. I guess the one saving grace is that she probably won’t remember this (?). I certainly hope she doesn’t.
After the Botox treatment, Anna will begin her second round of constraint therapy at Children’s in Denver. As a reminder, this is a 3-week intensive therapy program where Anna’s good arm is casted in an attempt to make her use her affected arm. We see an occupational therapist down at Children’s 3 times per week, and we do a lot of work at home. She wears the cast from the moment she wakes up until she goes to sleep. Fun!
Anna has made a lot of progress since her last round of constraint therapy in March/April. Since we finished up the first round in April, we’ve continued to wear the cast all-day for 2 days per week and during each and every evening meal. It will be interesting to see what goals we establish for this phase. The treatment period will last right up to the Wednesday before Thanksgiving. I’ve been joking about the fact that this year we will have something for which to be truly thankful: a few cast-free days!
September 7th, 2007
Busy busy busy. That describes these last couple of weeks since our mid-April post. Both Neal and I have been crazy-busy at work lately; simply not enough hours in the day. I have to wonder where the last 2 weeks have gone, though.
Update on Anna…shortly after Neal’s last post on the 16th of April, Anna either developed another ear infection or had a flare-up of the same one she’s had since…oh, I don’t know, the first part of March! She had an ear infection when she went in for her 12-month check-up. She was given a 10-day course of antibiotics, which didn’t clear it up. We went back to the doctor and were given a different family of antibiotics - 6-day course. And we most recently went in and received yet another family of antibiotics - 10-day course. We’ve been off the antibiotics for 4 days now…so far, so good. We have an appointment next Friday to see if this round of antibiotics actually killed it. I hope so. If not, there is talk of ear tubes. Let’s hope that we do not have to go that route.
Otherwise, Anna is doing well! She is gaining weight and growing tall. At one of her last doctor’s appointments she weighed in at 21 lbs 7 oz. She gained 1 lb 4 oz in about 2 1/2 weeks. We’re less concerned with her weight these days. We’ve discovered that the things on the edges of table tops are now fair-game. Anna can now peek over the edge of a table and check out what’s on top. Yikes.
We’re still actively cutting teeth. I know I’m tired of all the drool and fussiness - I can only imagine how tired Anna is of the entire business. We’ve pretty much got all the first year molars now and the 4th front tooth on top is pretty much in. I think we’re starting on some of the canines, although I can’t see anything yet. She’s chewing on EVERYTHING again. She won’t let me put my finger in her mouth anymore to check on tooth status and with the number of teeth she has, if she doesn’t want my finger in there, she’ll let me know by biting it! Those baby teeth are wicked sharp.
We have some news to report on the therapy front. During the second week in April we had the 6-month review of Anna’s IFSP (Individualized Family Service Plan) through Imagine! Anna’s OT, PT and our service coordinator met at our home to discuss Anna’s progress to date and develop some goals for the next 6-month period. Anna met all the goals we set back in October, and by pretty much any measure she has made excellent progress. Our new goals consist of learning how to walk, clapping hands, and developing a refined pincer grasp. It was also determined that Anna would benefit from weekly PT visits rather than the bi-weekly we had during the previous 6-month period. So we now have PT on Mondays and OT on Thursdays every week.
Yesterday Anna was fitted with a pair of orthotics made by a company called Cascade. They are designed to help Anna regain the arch of her left foot and keep her feet in alignment, which should help her to walk and prevent her from developing some bad walking habits. They are made of a semi-flexible plastic and come up just over her ankle bone. We went shoe shopping yesterday to find a pair of shoes that would fit over the orthotics; that was a challenge. We found a pair of teva-esque sandals and a pair of Converse canvas hi-tops. When she wears the hi-tops, you can’t even tell she’s wearing them (she just looks like she has amazingly fat feet). Right now we are only wearing them for 45 minutes a day. We’ll do that for 3 or 4 days and then gradually increase the amount of time she’s wearing them until we reach 4 hours a day. Once she starts walking she’ll probably wear them for longer.
Anna’s OT is going well. She’s using her left hand to help with more and more bi-manual tasks. We’ve been working on using two hands to pick up a ball and a large cereal box. We’re still wearing the cast on Fridays and Sundays all day and the sock during dinner. I must admit it is getting harder and harder to stick with the regimen. She’s started fighting the cast and I find it difficult to be the “bad guy.” How do you tell a 13 1/2 month old that this is for her own good?
Hope to have some pictures to post soon. I need to download them from my camera.
May 1st, 2007
Anna had her first full-day of casting today, and we’re pleased to say that it went well. She was really pretty bent for the first 30 minutes or so after we put it on this morning, but seemed to adjust well thereafter. Anna was just getting to the stage where she didn’t need constant attention while playing or eating; with the cast it feels like we’ve been transported back several months. She pretty much always needs someone there to help her grasp toys or read books. And mealtimes are a true challenge! She’s independent enough that she wants to feed herself all the time now, but she becomes incredibly frustrated when she isn’t able to do it with her left hand. With a little help from Mom and Dad, she’s able to have some success, however. I’m anxious for her “formal” therapy to begin on Monday. I would like to know what types of activities will have the most impact. I feel a bit like I’m flying blind.
I uploaded a couple of pictures I took today. Anna was eating a biter biscuit with her left hand. I included one that shows what her cast looks like, for those who are interested. It was beautiful weather here in Colorado, and Anna and Dad spent some time outside today (thus the hat).
March 17th, 2007
Today we journeyed down to Children’s Hospital to have Anna’s cast made. It was a tramatic experience for Anna (and for me! She looked at me as if to say, “Why are you letting them do this to me?”). For those of you who do not know, we are casting Anna’s right hand to encourage the use of her left. During the next three weeks we will be doing intensive therapy using her left hand. We’ll be attending therapy at Children’s three days a week and we’ll be continuing our normal therapy sessions here at home. Needless to say it will be a busy time for us.
This weekend will be an adjustment period during which Anna will hopefully become more accustomed to having the cast on. Seeing her with her dominant hand out of the picture today made me realize how far we’ve come, and yet how far we have to go in regards to the functioning of her left hand. It was something of a reality check for me. I think it caught me unawares. Her evaluation at Children’s added to that reality check; the doctors/therapists spelled out what Anna’s issues were in a rather clinical way. It all sounded so negative. As to be expected, they were evaluating her from this point in time, without regard to how far Anna has come in the last 4 months since we started her therapy. For some reason it was hard to hear.
As if getting your dominant hand casted were not enough, we had Anna’s 12-month check-up today (and no, I didn’t plan on having both of these events happen on the same day!). Everything about her development looks good. She still doesn’t weigh enough for us to be able to turn her car seat around (darn). In fact, the doctor was still a bit concerned about her weight gain. She’s fallen into the 25th percentile in her weight - 19 lbs. 12 oz. She holding strong to the 90-95th percentile for height, however (31 1/2 inches). Some of her meager weight gain may be due to the fact that she’s had a stomach/intestinal bug this last week. I won’t go into detail…suffice it to say, carseats are not meant to handle vomit. Anna also has developed another ear infection in her right ear. So we’re back on the antibiotics. Silver lining: no shots today because she has an infection.
I posted a ton of pictures from Anna’s birthday party and Granny and Papa Rex’s visit to Colorado. I’ll work on posting some short movies of Anna eating her cake and such.
March 16th, 2007
One year ago today you were born, little one, and what an amazing year it’s been.
You’ve learned so much in these past few months: How to breathe, how to cry, how to nurse, how to burp, how to roll over, how to sit without falling over, how to sleep through the night, how to laugh, how to babble, how to giggle when tickled, how to drink from a bottle, how to say mama and dada, how to make the signs for food, milk, and the cat, how to sit up all by your self, how to crawl, how to stand up, how to make friends, how to play with toys, how to read books, how to grow teeth and just a very little bit of hair, how to snuggle, how to eat grown-up food, how to find your way across the room, how to cruise around the coffee table, how to climb stairs, how to clap, how to pick up things with your left hand, how to wave like a princess, how to blow big smacking kisses across the room, how to give hugs, how to give kisses, and how to light up an entire room with your beautiful smile.
And we’ve learned so much too: How to give birth, how to change diapers, how to give baths, how to dress tiny babies in tiny clothes, how to install car seats and baby gates, how to nurse, how to burp a baby, how to make a little girl smile, how to function on very little sleep, how to make a bottle, how to make breakfast, how to teach a baby to stretch, clap, sit up, eat, crawl, stand, sleep through the night, and climb stairs, how to cope with the fears all parents face, how to sing, how to distract, how to be more organized and not worry about when we aren’t, how to be more patient, how to love each other when we’re under fire, and how to love you, unconditionally, always and forever, for you are the most wonderful and rewarding thing in our lives.
Thank you, Anna, for joining our family and for and teaching us so much. Happy birthday, dearest girl. We love you.
March 15th, 2007
Anna’s Granny and Papa from Kansas are visiting us! Anna’s 1st Birthday party is this weekend and they made the drive out to Colorado to help us celebrate. I can’t believe that the little Miss will be one year old! We’ve said it before, but Neal and I agree that it has been both the longest and shortest year ever. So much has happened since this time last year, yet it seems like only yesterday that she entered this world.
Next Wednesday Anna and I will be making a trip down to Children’s Hospital in Denver to see if she is a good candidate for a special type of therapy. We’re meeting with a rehab doctor and a hand specialist. The therapy regimen is called Constraint-Induced Therapy and involves the casting of her unaffected arm for a period of 2-3 weeks. While her right arm is casted, we’ll be doing intensive therapy with her left hand/arm. This type of therapy has shown great promise in children with some form of hemiparesis, and there are several studies that document this success in the literature. We’ve tried some home-grown constraint therapy using a couple of very thick socks or a ski mitten placed over her right hand/arm; it is amazing what she can and will do with her left hand if her right hand is out of the picture. We’re hoping that this therapy will help Anna realize that her left hand can do things, too!
If Anna is deemed to be a good candidate for this therapy, we’ll probably start on the 19th. This is potentially going to be a tough time for Anna (and for us, too). I’m hoping she tolerates the cast and is still able to do many of the things she does now. I’ll keep you posted on our progress!
March 6th, 2007
Anna is wide awake and ready to start her day an hour and a half early.
The joys of parenthood abound.
February 20th, 2007
A couple of new things to report regarding Ms. Anna. First of all, you may have noticed that Anna is wearing a splint on her left hand in some of her pictures. They call it a Joe Cool strap and it is designed to keep Ann’s thumb out of the palm. Anna generally tucks her thumb under her fingers when she makes a fist and it often stays there even when she opens her hand. This makes it incredibly difficult for her to grab anything. The splint prevents this from happening. She doesn’t seem to mind wearing it and it does what it is supposed to do. In our opinions (and that of her therapist), she is better able to grasp things with her left hand now that her thumb isn’t in the way.
We took Anna in for an RSV follow up and weigh in on Friday. Fortunately, her ears have cleared up and she looks to be in good health. The other good news is Anna’s weight gain. She gained over 1 lb. in a little less than a month! Anna has turned into a heavy-hitter when it comes to eating. I’m amazed at how much that little body can put away.
And lastly…a little rant on my part. I hate insurance companies. My employer is switching one of our insurance plans (the one Anna and I are on) to a vastly reduced plan with very very few doctors in our area. We’re now supposed to drive to Aurora (southeast Denver metro area) for Anna’s therapy and to visit a hospital. In its stead they are offering a crapppy plan with a high deductible. Grrr…. And we’re also having to jump through several hoops to get some of Anna’s therapy approved by our current insurance plan. Universal healthcare…I’ll vote for it in a heartbeat. You shouldn’t have to look at your finances to determine whether or not you can give your family the care they deserve/need.
I’m hoping to post a few pics soon…Anna had some spaghetti today. It was a mess, but she certainly had a good time.
February 11th, 2007
As I’ve mentioned in past posts, we’re working on getting Anna to sit up from being on her tummy. Yesterday morning I put Anna in her crib for a nap. About an hour later I went in to get her because I could hear her playing and chatting away. I walked in and was pleasantly surprised to see Ms. Anna sitting up in her crib waving at me! Now that she knows she CAN do it, I’m hoping we’ll be seeing more and more of her sitting up.
I took this opportunity to work on a little child-proofing. Since I KNOW Anna can pull herself to standing if she’s in a sitting position I thought it would be a good idea to lower the mattress in her crib. I’ve also been installing covers on all the electrical outlets. She’s very interested in drawers and cabinets lately, so I’m going to be installing some of those cabinet/drawer lock-thingies soon.
January 23rd, 2007
It is absolutely amazing how quickly time flies these days. We’ve been quite busy, as usual. Granny Debbie returned home to Kansas yesterday after a week-long visit. We miss her already! I hope she had a nice time visiting her grandbabies, because I know we certainly enjoyed her visit. Neal and I went out on our very first date since Anna was born. Granny Debbie watched Anna while we went out to eat. Of course, we spent about 50% of our time away talking about Anna and wondering if she was giving my Mom a hard time! It was really nice to have some time to ourselves, though.
On Sunday we celebrated Henry’s 1st birthday! Speaking of time flying, I can’t believe that it was one year ago that we rushed to the hospital to be with my Sister at Henry’s birth. It literally seems like yesterday. Henry seemed to enjoy himself at his party. He was a little confused when everyone sang to him, but enjoyed the attention as he made a total mess of himself and his cake. Happy Birthday H-man!
Last week we heard from the doctor’s at Children’s Hospital regarding Anna’s blood work. Anna does not have a clotting or bleeding disorder that caused her stroke. From what it sounds like, this was an isolated incident. This is all very good news because it means she is not necessarily at increased risk for additional strokes.
I realized I haven’t given any reports on Anna’s occupational therapy appointments. So far we’ve had two session and we’ll have another one this afternoon. Thursday is shaping up to be a busy day for us. Anna has physical therapy every other week and occupational therapy every week on Thursdays: one in the morning, one in the afternoon. Our first OT appointment didn’t go so well, as Anna was cranky and very skeptical of Kathy. Last week’s session went much much better. I made sure she’d had a nap and a snack before the session started.
Kathy was quite impressed with Anna’s progress. Anna has been relaxing her hand more these days, which is a great thing. If she’s having a good Bob-day, she fists her hand only slightly and most of the time it is open. Of course, there are those days when it seems like her hand is clenched very tightly and no amount of stretching will make it relax. I’ve tried to correlate it to something - lack of sleep, hunger, stress, not enough stretching - but I haven’t nailed down a definite cause yet. I doubt it is any one thing that causes her to tense up. Overall, Kathy told us to continue doing what we are doing: a little constraint therapy, sensory work on her left side, stretches, etc. We’ve been trying to strengthen Anna’s left arm by doing lots of weight bearing exercises: baby push-ups, leaning and propping. I can really see a difference in how long she can hold herself up using her left arm.
I believe Anna tries very hard to please us and works exceptionally hard at the tasks we give her. I don’t mean to be sappy, but it often brings tears to my eyes when I see how hard she is working to do something. I remind myself constantly that what she is going is very hard work. I know that I couldn’t do many of the things that I’m asking her to do! And yet, she furrows her brow, grunts a little, and pushes herself a farther. What a trooper.
November 16th, 2006
Our neurologist called yesterday evening and gave us the results of Anna’s MRI. The MRI confirmed the initial diagnosis - Anna did indeed have a small stroke on the right side of her brain. We have been referred to the stroke clinic at Children’s. Hopefully, after our appointment with them we will know a bit more about what may have caused the stroke and the full extent of the damage to Anna’s brain. We’re waiting for them to call us to set up an appointment.
Meanwhile, we’ve been working with the folks at Imagine!. Imagine! is a local, private, non-profit organization established in 1963 that provides support services to people with cognitive disabilities (including epilepsy, cerebral palsy, Down syndrome, and autism). We’ve been assigned a social worker (she’s wonderful — caring, engaged, efficient, knowledgeable) who is helping us navigate the various national, state, and county-wide support systems for kids with CP. So far this has been a fantastic experience, and we’re amazed at how fast all this is moving. Since our initial diagnosis on September 12, we’ve met with our case worker at our house to our many options. To get the process moving we took Anna for an “interview” with a physical therapist (gross motor), an occupational therapist (fine motor), and a school district nurse (hearing, vision) with the folks at ChildFind on Monday morning. (ChildFind is a national screening and evaluation program “designed to locate, identify, and refer as early as possible all young children with disabilities and their families who are in need of Early Intervention Program (Part C) or Preschool Special Education (Part B/619) services of the Individuals with Disabilities Education Act (IDEA)“). After her interview we were told that Anna’s been approved for both PT and OT, and that the next step would be to locate physical and occupational therapists to work with Anna.
Well, last night (just a day later!) we learned that our Imagine! social worker sent us an email:
I have located therapists that have availability through an agency called Tiny Tim Therapeutic Outreach. This is a program in Longmont that serves children birth to three and beyond. They have a developmental preschool program as well. I have several families using their services and have been very happy. I am planning to get all the information to them by this Friday so they can hopefully be ready to start the week of [October] 16th.
We couldn’t be happier. Tara had already heard about Tiny Tim from the director of our daycare (Sunset Academy). Tiny Tim is located literally around the corner from Sunset, and there are kids from Sunset who spend afternoons at Tiny Tim. And so it turns out that the directors of both facilities are good friends who’ve worked together for years. We’re hoping that Anna will be able to enroll in the Tiny Tim daycare when she gets to be about three years old if she still needs help at that point.
All in all we think this is great news. The MRI confirmed the initial diagnosis, and while there’s more to learn on that front it’s still good to know what we’re dealing with. Meanwhile, with the help of the folks at Imagine! we’ve been able to start to navigate the support systems available to Anna, and to get moving on the path of therapy.
Therapy, we feel, is the key. Even just working with Anna ourselves we’ve seen such enormous improvement in her motor skills over the past few weeks and months, and we’re eager to get her paired up with some professionals who can show us how to do this right.
Moreover, it’s been great to get confirmation from our doctors, our social worker, and the therapists at ChildFind that Anna is developmentally “on track” in all other areas (and even ahead of the game in some areas like social skills). At a time like this it’s been important to get some confirmation of what we, as parents, already believe: That despite some relatively minor problems with her left side, she’s a healthy, happy, bright, curious, active, engaging, wonderful little girl.
October 4th, 2006
Anna had her MRI today, and we’re happy and relieved that it is over! We weren’t allowed to watch the procedure or be there when they put her under, but maybe that was for the best. I guess they had a very hard time finding a vein for her IV. She has stick marks on each of her hands and feet and a couple on her arms (thank goodness she was already mildly sedated with gas while they were sticking her!). The MRI went well except that she woke up half-way through! The doctor and technician noticed she was moving her feet…and then all of the sudden she was waving her arm around. They had to give her a bit more medicine to keep her under during the rest of the scan. When they called us back to her recovery room she was pretty limp and uncoordinated. Within 1/2 hour she was mostly back to normal. She was rather grumpy and very hungry. Understandable, considering she hadn’t eaten anything for over 6 hours at that point.
What a stressful day. My body feels like I’ve been excercising heavily or something…must be due to the fact that I’ve been tensing my muscles all day long. I’m ready for some sleep. I think Neal is too.
Incidentally, we won’t know the results of the MRI for some time. We have an appointment with the neurologist for late October (her first available appointment). We’re going to see if we can move that date up some, but that’ll more than likely be possible only if someone else cancels. We’ll see what we can do.
For now…sleep. Good Night.
September 28th, 2006
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