Anj also said that the doctors did an MRI scan, which reportedly determined abnormal activity. The little girl was diagnosed with absence and petit mal seizures.

As scary as this was to hear, we at least knew what was wrong and how to help her. She was given seizure medication to combat the seizures and we thought she was on the mend.

Bur, unfortunately, the little girl continued to have what they thought were seizures. But they were lasting longer than the few seconds we were told they would last. READ FULL STORY HERE>>>CLICK HERE TO CONTINUE READING>>>

Her neurologist at the time continued to up her meds or give us a new one to try, but the seizures never stopped. Unfortunately, they seemed to be getting worse.

In a short period of time, Madie was given about 4 seizure medications to try. The side effects in some of the medications were horrible. She was allergic to one of them and another brought on awful side effects.

She had follow up EEG’s that now showed normal brain activity, however she was now have up to 15 episodes a day. When Anj and Madie visited Dr. Coffman, he did several tests and then looked at the video Anj brought.

It took him just a few moments of watching the video to tell us he knew what was wrong with Madie. Paroxysmal nonkinesigenic dyskinesia, or PNKD. At her next appointment, the doctor told them that if the genetic testing came back positive, Madie’s immediate family would have to be tested.

At that appointment it was explained that some kids stop having issues around puberty, but with others, it can get worse. Madie’s life was constantly being disrupted. At the end of her 7^th grade year, the family celebrated a milestone they weren’t sure they would ever see. Madie made it through her entire 7^th grade year without a spell! The family’s visits to the children’s hospital will now be every few years instead of every year just to monitor everything as she gets older.