Since the last update on March 22, little happened with regard to Jenelle's progress until very recently. Shortly after that last update, we meet Dr. Steenari and the RNS team on April 4. At that time, they adjusted Jenelle's RNS very slightly - think of that .25 I mentioned in the previous update, this adjustment went to .5. Remember, the RNS is programed to send electronic stimulation when it sees a specific pattern that is programed for it to see ... not in "response" to other indicators like the VNS. So for this adjustment, they kept the electric current the same, but for it to go for a longer duration when triggered. Baby steps. As a result, we saw very little improvement seizure wise. Jenelle was still having at least 1 to 2 or more grand mal (tonic clonic) seizures a day at this setting. Brett and I were really frustrated, and felt maybe the RNS surgery was a mistake.
During this time, I kept uploading the data and eventually called Dr. Steenari's Care Team to see if we could get in sooner. Instead of an earlier appointment, we decided to add a very small dose of Depakote to Jenelle's medications to see if that helped. And it did help, but just a little. We were seeing at least 1 grand mal a day, which was better than more than 1 a day. Still, very slow, very frustrating.
School ended in late May, and Jenelle continued for ESY (Extended School Year) during the month of June. During that time, big brother Jack graduated from the University of La Verne and the family spent a weekend in La Quinta, CA celebrating. Jenelle was stable, but that still consisted of daily drop seizures and grand mal seizures.
On Wednesday, August 14, we had our next RNS follow up with Dr. Steenari and team. Dr. Steenari was out on vacation, so her colleague Dr. Donald Phillips met with us to explain their plan for the next step. After reviewing hours and hours of data from the RNS (and specifically, one of Jenelle's grand mal seizures that went over 5 minutes) the team decided to "significantly" change the settings on the RNS. This meant increasing the electronic stimulation. In layman's terms, we went up three steps from a .5 to a 1.5, and we were told we will either see improvement, or immediately see more seizures. We left feeling hopeful.
The next day, things were definitely different. Jenelle didn't sleep well that night, and had been awake since 4:00 a.m. for school. But no seizures. She had a similar sleep pattern that night, and no seizures again the next day. I keep a Ring camera in Jenelle's room, and we were getting up to 70 notifications of movement in her room during the night. She was not sleeping well at all. That Friday, I increased her Melatonin as sleep deprivation can also bring on seizures. She slept somewhat better, and finally had 1 grand mal seizure that Saturday. BUT, the exciting news - Jenelle went 3 full days without any seizures! Since the significant adjustment, we continue to see better seizure control - in fact, maybe 8 grand mal seizures total. We are extremely encouraged and everyone, including her teacher and aides at school, are noticing an improvement in her demeanor and overall happiness. Brett and I finally feel like we made the right decision.
Jenelle also started back to school for her last semester on August 14. We recently had her IEP and everyone was encouraged by the increased seizure control. Next month is Jenelle's 22nd birthday. We hope to see continued improvement as she finishes her last semester. That is all for now - as always, I will keep you posted.
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