My Myoclonic jerks started around 12-13, of course I just called them twitches until I know what Myoclonic jerks are
I'm currently 28 and the Myoclonic jerks are progressively becoming more frequent with some being a little more intense than others. I cannot do really any task without a jerk happening. I can have like 4-10 in the space of a minute
The essential tremor is relatively new, only the past 5 years but has significantly got worse. If I am standing for more than 5 minutes or maybe Its a hot day and I am attempting chores, my entire body will be shaking
I had an MRI a few years back with nothing showing apparently but I don't have a Neurology appointment until April 2024 and because I'm undiagnosed I never know where to turn
I have various other health issues too including craniosynostosis and a cervical spine issue also undiagnosed
My daughter had her first visibly recognizable seizure 15 years ago this month (April 15, 2004), it was extremely tough to watch my child go from blank stares that I could not get her to break from to a completely stiff body then full body, uncontrollable jerks. We thought this may have been cause by an illness, a fever until it happened again, and different instances of stares, some quick moments of the jerking. I can’t remember the date when she was officially diagnosed with a seizure disorder/epilepsy but, I know she’s had a long history of mixed seizure types; Grand mal, generalized tonic-clonic (with clusters), myoclonic (jerking), dialectic (staring), nocturnal. All of that lead her neurologist diagnosing her with Intractable& catamenial epilepsy. On March 12th, she was implanted with the Cyberonics SenTiva for VNS therapy to help her with intractable . Intractable are seizures that fail to come under control easily with medication. VNS- vagus nerve stimulation is supposed to help reduce the frequency and intensity of seizures. It’s been 6 weeks/42 days since “implantable parts” have been placed with hopes of helping with her fight against seizures, how is it going? Have the seizures stopped? • Things are going well! I’m thankful we decided to get the VNS. The seizures have not completely stopped. However, they have NOT grown in rapid intensity like they used to before VNS. In the past, I have watched Kerstin start having small seizures that may start with a stare, then the face twitches increasing to the jerking and the only thing that could be done was staying close to her, reassuring her that I was there, hoping it would soon stop. Sometimes they would, a lot of times they would not, causing a need for Diastat or at really bad seizures she would need 2. The aftermath; she would be so groggy, sleeping for hours and hours. Since VNS placement, when a seizure is spotted, a swipe is given, sends pulses thru the nerve to her brain to slow the activity. We journey on! 💚 💜 #VNS#Epilepsy#SeizureDisorder#Seizures#IntractableEpilepsy #Myoclonic #Dialeptic #NocturnalSeizures #CatamenialSeizures #DandyWalkerSyndrome #SpasticQuadriparesis #DevelopmentalDelay
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