Showing posts with label Dr visits. Show all posts
Showing posts with label Dr visits. Show all posts

Friday, July 23, 2010

Kids say the darndest things...

at the darndest times!

Well, in our case, Jayden shows us just how great his communication skills have grown at the craziest moments! Take this morning for instance... Yesterday Jayden took a spill at summer camp and bust his lip pretty bad and also pushed his tooth back. On the drive home I was asking him about his boo boo. He is very echolaic (repeats the last word anyone says), so we hardly ever can get him to appropriately answer a question. So the conversation went like this:

Me: Jayden do you have a boo boo?
Jayden :A boo boo (points to his lip)
Me: Aw...does it hurt?
Jayden: Hurt.
Me: Did you fall down?
Jayden: Down.
Me: Did you cry?
Jayden: Cry.
Me: Aww, baby I'm sorry!
Jayden: Sowwy
But since I knew he could answer this one...
Me:Are you ok?
Jayden: I fine!

So anyway, the dentist wanted us to bring him in for x rays of his front teeth to check for fractures or any damage to the permanent teeth. The dentist came in the room and Jayden (who had made himself at home in the chair and even took off his shoes!!) was ready to show the Dr his boo boo. So here's their conversation...

Dentist: Hi Jayden, how are you?
Jayden: I fine.
Dentist: Do you have a boo boo?
Jayden: A boo boo. (points to his mouth)
Dentist: How did you get that boo boo?
Jayden: AT SCHOOL!
Me and Mike: {JAW DROPS!!}

Yeah. So we just looked at each other and I'm pretty sure I said aloud, "WOW!" Judging from the convo he held above, I bet the dentists didn't even have a clue that Jayden has a speech delay! Now this doesn't happen often and many times people ask him questions that he doesn't understand so he gets echolaic and they look to us with question mark faces. But there are moments like these where he surprises us! It gives me so much hope for his future :)

P.S. His x rays turned out fine. There was no damage to the baby tooth and none to the permanent teeth (they look like they will be HUGE though, lol!). He'll go back in 3 weeks for a cleaning and I am going to talk to his neurologist about the increase in falling and coordination. He walked into the wall at the dentist's office this morning!

Saturday, June 26, 2010

Bad Blogger

Sigh. My goal was to update this blog a few times each week, if not everyday. Mainly because I use this as a journal to keep track of the things Jayden does to amaze me EVERYDAY. There are things that I never want to forget. There are also things that I would love to forget, yet because it is so significant (like the 60+ seizures he had in 2 days)I want to remember it. But, as usual, life got in the way. This month has been SUPER busy for us. Every week of June, either Jayden or myself has had a Drs appt or two (or three!). I tried to squeeze in swimming, gym time, my at home business, my photography, and even playgroup time (yeah that didn't work out so well when I read the dates wrong on the calendar and Jayden and I were the only ones at Chuck E Cheese at 9am!!). The entire month was just like a run on sentence. No end in sight. Also, I had the big 30th birthday. Party and all. It was lots of fun! A nice break from the hustle and bustle that is life. But after the party was over, it was time to head back into reality.

Jayden had a developmental followup the week before my birthday. It was a wonderful followup. The Dr recorded that Jayden has shown significant improvement in all areas of his development. Eye contact is perfect and his social anxiety seems to be a thing of the past. He interacted with the Dr and the resident. His attention span is still terribly short so that caused him to score quite low on the cognitive level and his speech scored at a 23 month old level, but he has improved so much that the Dr feels that the autism diagnosis is no longer warranted. She feels that his delays are largely due to the chromosome deletion which is known to cause global developmental delays, along with a host of other problems, which he does present with. She feels that with continued therapy services, and the care of a good neurologist and GI for his Epilepsy and Celiac, he will be just fine!

On this past Tuesday, he had a followup with his GI Dr. Just to show you how jam packed our month was, I had NO IDEA he had a followup with his GI this month. When I got the recorded message that he had an appt, I had to call back and ask them WHO he had an appt with! Unfortunately, this appt didn't go as well as the appt the week before had gone. As you know, when Jayden was hospitalized in April for his seizures, he'd lost 6lbs. He went from 35lbs to 29lbs and this was in the beginning of April. The GI doc was very concerned with this b/c of his celiac and b/c he does not have the best appetite at all. By the time we went to see her for a followup in May and to see the dietitian, he was up to 33lbs, but she still was not happy with that so the dietitian had us to start giving him pediasure and gave me a list of fatty foods to feed him. He's been drinking the pediasure just fine and I've been adding chocolate syrup to it. However, his appetite is still just not there. Getting him to take more than 3 bites of baked beans in a 24 hour period is a struggle. So when he went in on Tuesday (6 week followup), he still weighed in at 33lbs. The Dr said he had only gained an ounce and there's the possibility that he actually lost some weight depending on what he was wearing. She was expecting him to at least be back at 35lbs after the 6 weeks of increased calories (and I have been pushing and counting calories). He was also in tears and bent over, crying in pain during the appt, so she's concerned about his stomach. He will be having an EGD w/ biopsy done soon. She wants to check the condition of his intestines and his esophagus. Jayden is NOT underweight. The concern lies in the fact that he has lost a significant amount of weight and he cannot gain it back. Celiac Disease and weight loss (in a toddler) is not a good thing, so she just needs to have a closer look. I hate to have him put under anesthesia again, as I can still clearly remember how hard it was for me to watch him struggle until he went under the last time :( But, like every other mother, I hate to see him suffer everyday. I want him to know what it's like to have a tummy that does not hurt everyday. He deserves it.

And I will end this post with some really good news! You know the language explosion that many moms say happens around 18-20 months of age? Well it looks like it finally found it's way to our residence! We've been waiting nearly 2 yrs for this moment! A few weeks ago, Jayden was in his booster seat and was ready to get down, so he started to yell "DOWN DOWN!" like he usually does. Before I could get to him he closed his eyes tight, as if to concentrate, and then he opened them and said "Mommeeeee, I want...to...GET DOWN!!" Mike and I just looked at each other. And the phrases have been coming ever since, out of nowhere. Last week we were driving to my aunts house and we stopped at a red light and Jayden said "Mommeeee, I want to watch a movie." Again, Mike and I just looked at each other. The other day at the hotel, Jayden got off the elevator and there was a lady waiting to get on and Jayden looked up at her and said "How you do-eeen?" and the lady replied "I'm fine sweetie!" OMG. Other things he has said to shock us..."Mommy, I hot!" "I don't want to do it!" "What you do-een?" "Where we go-een?" and this one we really couldn't believe "Mommy, I hungry!!" Don't get me wrong, the phrases are little gems that he presents us with rarely, but everyday which is BIG for him. He still does ALOT of meaningFUL (it means alot to me!) gibberish, but he is trying. Every mom I've come across who knows about Jayden's speech delay would tell me "Don't rush it because once he starts talking you will want him to be quiet." I know it's just their way of making me feel okay about the situation, but I am happy to kindly say that they were WRONG! In fact, when Jayden talks, I drop whatever it is that I am doing and I answer his questions over and over and I encourage him to continue. The fact of the matter is that when my baby talks, I never want it to end :)

Friday, May 14, 2010

Immunologist

We took Jayden in to see the immunologist today. He explained to us that the immunoglobulin levels can go up and down and there's always that chance that Jayden's test results could be normal now. He tjhinks this *may* be the case with Jayden b/c his long bout of back to back illnesses just recently started in March and we just moved into a new house in January, so it could have been his immune system readjusting. Jayden never had a history of recurrent infections. He does get sick alot, but it was never as often as it has been since March. He's been on antibiotics off and on since March! So he had some more bloodwork done (6 vials of blood!!) and the Dr is going to just evaluate Jayden's entire immune system to see if there is truly a cause for concern. Also, his GI Dr wanted to repeat some blood tests. So they were vampires today. We go back in 2 weeks for results and I'm optimistic about it! We have a VERY busy weekend planned so I'm off to bed to prepare. Hope you all have a great weekend as well!

Wednesday, May 12, 2010

New Post! New Look!

First of all, I know my usual readers were surprised to see the new look! Ever since I calibrated my monitor over a year ago (color correction), I've hated the colors of the old blog. Besides, the lollipop picture of Jayden was so cute, but he's grown up so much since then! So you get a fresh new banner and a new color scheme that I hope is better on your eyes like it is on mine :)

Well, this blog will be filled with updates b/c alot has gone on here since the last post. Mother's Day turned out to be a good day, despite it being a day of mourning for my family and then receiving a call that my younger brother was in a bad car accident and nearly causing a deja vu. We still cried a good bit, but I know God kept us all strong and being together helped us to keep our mind on better things. My parents did the Mother's Day BBQ in their backyard and the weather was nice. It was a beautiful day.

Monday morning, Jayden's GI dr called me. She had done bloodwork on him the week before and she was calling me with the results so I knew it couldn't be great news. She checked his levels to see if he had gluten in his system, which would then tell us that we needed to re evaluate what it was we were feeding him. I expected the test to come back showing gluten b/c sometimes I just don't feel like we are doing everything right. And not to mention that he still has very grainy poop and the seizures are not stopping. Well, much to my surprise, his levels for that were normal. I had to pat myself on the back! However, the Dr was calling me b/c she tested all of his immunoglobulin levels, IgA, IgG, IgE, and IgM, and all of them are abnormally low. So she wanted him to get in to see the immunologist asap for more bloodwork. He goes on Friday afternoon, and until then I am forcing myself not to google what all of this information may mean for Jayden. I am very thankful for the group of Drs who have been working together to help Jayden and I'm sure that he will be better soon!

Finally, I'm so excited to share that I've been blessed with a wonderful work from home opportunity! I've just started, but the opportunities ahead of me are so exciting and I am so thrilled to know that I can actually be at home with Jayden and earn a steady income at the same time! God always answers our prayers!