Great news....I have nothing new to report!

Yep...it feels great to have nothing new to fill everyone in on. Livvie is doing great. We went back to her endocrinologist...and not much has changed since the last time. He kept all her meds the same and ordered a few new labs...but other than that, he was very happy with Olivia's progress. He was quite amused by her new silly personality. She was literally bouncing off the walls. =)

I guess this means we can take a little break from doctors for awhile. She doesn't have to go back to him for 2 1/2 months. Although she will be seen by Dr Davis, her neurologist, in October. I'll let ya know how that goes.

So, like I said....no news if good news, right! Liv amazes us everyday with her improvements. She really is a happy little girl now! We have been waiting too long for that!

"Aunt" Dr Belton

For all of you that have never met Livvie's wonderful pediatrician, here she is. This is Dr Belton. Sad to say, but I can pretty much guarantee that she has seen her Dr more than most of our friends and family. In 2006 alone she saw Dr Belton and average of once a week. 51 times in all!!!

Dr Belton has been through it all with us. Starting from when Olivia was newborn and jaundice. Pretty much as soon as that cleared up, we were jumping in head first into this non stop medical hell that we have endured for the last 3 years. At first, it was almost like a joke, she would walk in and give us the "you have got to be kidding me" look. Somewhere within the last 2 years and 7 specialist, it became a look of horror and disbelief. I could feel the frustration that she felt in not being able to put her finger on what was going on, even with the help of every "ologist" she could think of. She said she often looked over Olivia's chart during lunch breaks and after hours, scratching her head and pondering what it could be. During Liv's hospital stays she would call from her home and check on us, asking for all the details and trying to play "quarterback" for us. She decoded tons of medical mumbo jumbo that was thrown at us by countless Dr's and I can honestly say that without her, we would be lost. We could not have asked for a better Doctor. She has been a God send.

Liv's 3 year WELL visit to the doctors!

Well, Livvie had her first WELL visit ever yesterday. Yep, that's right...her first in 3 years. lol Sad huh! Every time before, we were always in for some illness or recheck and they always wind up doing all the well visit things during those visits.

Sooo...this is how it went...Livvie is now 40 inches (95%) and 35 lbs. They tested her vision and unlike me, she seems to have perfect vision. Her blood pressure was great, 84/52 ( good news since we will have to keep an eye on it because of the Florinef, salt pill.) And a little added bonus...no co-pays for well visits! Yay!

Dr. Belton was happy to see Livvie in a great mood, which is a huge change from the old Livvie. She asked if it would be ok to share Olivia's story with the guest at a pediatric conference coming up. Of course, we agreed...if just one doctor has an "ah ha" moment and is able to diagnosis a child with Addison's...it will be well worth it. =) Liv's endocrinologist also asked permission to discuss Livvie at a national endo conference. He wanted before and after pics of her tongue and tan. What can I say...we always knew Liv was one of a kind...but apparently she is sparking quite an interest in the medical community.

Some other great news...I found a really great message board online that is for moms with children suffering from adrenal insufficiency. I have gotten tons of great advise, and about what to expect. It is a small group of about 10 moms, so they are all pretty close and all know each others stories. I am settling in nicely and it is so nice to hear from others with stories like ours.

Ok, so keep your fingers crossed...Dr Belton said she doesn't want to see us for a whole year! Other than Addison's related illnesses. We are really going to try to make it to our next well visit.

EEG...Not fun!

Well, I took Livvie to have an EEG today. Boy...that was not fun! It has been about a year since her last one, the infamous 24 hour one. This one only lasted about an hour, including the 15 minutes it took for me to get her calmed down enough to sit still while they placed the electrodes on her head. About 20 in all! They use this disgusting paste/gel to stick them to her head. We spent 3 minutes blowing a windmill, followed by about 4 minutes of strobe lights. =) After all that, they said, "ok, she can go to sleep now". lol Ok...a lot easier said than done. After about 20 minutes, she fell asleep. ( I did too) lol Ten minutes later...she said, "ok, we're done". She just had to take all the electrodes off her head. The paste left her hair a wreck!

Anyway, we survived another EEG and are waiting for the results. We are hopeful that this one will come back normal. If so, she will have to have a 24 hour one. If that one is normal, than we should be able to start weening her off her seizure meds. Yay! Keep your fingers crossed!

Ahhh....new mold!!!

Well, as if things weren't complicated enough with Liv's health...we found more mold last night. This time it is through the drywall and paint in our room. The carpet was wet under both windows. We are waiting to see what our insurance will do about it. Hopefully this won't bring on any new illnesses. Keep your fingers crossed.