So, many of you have called to check on Rollins, so I wanted to let everyone know what is going on. We went to the doctor last Wednesday just to make sure everything was ok and that this was just a freak thing. Dr. Boggess said he believed she passed out from a lack of oxygen because she was crying. However, I did share something with him that I hadn't really discussed with anyone til now. Rollins has this thing she does where she will be playing and all of a sudden go in this daze. I can say her name, and she doesn't respond. I can wave my hand in front of her eyes and she doesn't blink. Then after 10 to 30 seconds, she loosens up and starts laughing. I had always thought she was doing this on purpose to be funny. She sometimes does it multiple times a day. Dr. Boggess has another theory, though. He said it sounds like typical
petit mal seizures, and asked how long she had been having them. It's been going on so long, that I honestly have no idea. He said he wanted to get her to a pediatric neurologist because this can really affect her ability to concentrate when she starts school. I told him how Brother has been saying he thought she had ADHD because she can't concentrate and looses focus very easily. If this diagnosis is correct, this could explain her lack of concentration.
Of course as soon as I got home, I got on google. I found out that many times these seizures go undetected for months and these type seizures don't have that "confusion" phase that happens after most seizures. Rollins is able to go right back to what she was doing before it happened and has no remembrance of what happened during the seizure. In most cases, they outgrow them by their teenage years and even though they can't be prevented, medication can be taken to help lower the frequency.
I have to be honest, I am not upset about this at all. I know we have been through a lot with Rollins, and this just seems like another bump in the road. It could be so much worse--I had friends that would have grand mal seizures--that would absolutely terrify me. I know God isn't going to give us more than we can handle. He has already done wonderful things with her Gastritis, and she is a healthy 34 pounds (25th percentile) 3 year old. Grady, too, is getting much better, and is now 27 pounds (25th percentile) and will be 2 in two weeks. We are even planning a trip to Disney World in the next couple months. I am very anxious to see how this goes since neither Rollins or Grady have been away from home since last Fall when we went to Auburn. For those of you that don't know, their
Gastritis and
Esophagitis is much worse when we travel. They also will not even spend the night with my parents. It's really sad when your 3 year old says she doesn't want to stay in a hotel because it makes her throw up. I am keeping my fingers crossed that all the excitement of Disney will trump these disorders!
Anyway, I will keep you all posted on Rollins appointment with the neurologist. She is such a special little girl with a heart of gold. I am so blessed to have her!