Hey there I just was wondering how many other epilepsy warriors out in the world overcame their disability or curse as I call it and still pursued their love for owning, training, and riding horses.
I’d love to hear your story what type of epilepsy you have if you were able to show rodeo please share anything you feel I’ll share my story for ya’ll.
I was diagnosed with epilepsy when I was 10 but I had been riding horses since 7 I’m 28 now. My mother objected to me riding after I was diagnosed but I still rode because I loved it. I have seizure activity throughout my entire brain I have what they call tonic clonic (grand mal in other states/countries) and partial onset (petty mal in other states/countries) I’ve been on at least 20 different medications to stop my seizures at this current time I have to take 3 different medications to keep my seizures at bay before I was having a tonic clonic at least twice a week and a partial onset every 30 seconds now I can go around 3 months without having a TC and the PO are gone.
Getting back to riding I was never able to get to showing or rodeo I did do a small amount of training for barrels but other then that I have just stuck to riding in the pasture, trails, or along ditch banks.
I’ve enjoyed riding and training for many many years any have had many people warn me about it not being a good idea to be doing what I love to do but to be honest I have never had a seizure around a horse the door latch and table corner were more dangerous I had to get 5 stiches over my eyebrow because I went into a seizure and hit the corner of a table. I had to get 3 staples in my head because I was folding laundry in my bedroom went into a seizure and hit the door latch of all things. Now my husband is paranoid and he took the door latches off all the doors haha!
Anyway ya’ll know my story I’d love to hear yours! I hope you enjoy!