Anyone else with SCA-6

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Just wondering if there was anyone else here who struggles with this. I was diagnosed with Spinocerebellar ataxia type-6 when i was 17. I knew that i had the disease since i was a teenager. It doesnt have a huge impact on my day to day life, but it does have certain annoying effects. If there is anyone else out there with sca-6 id love to hear from you, maybe swap stories and ideas for dealing with daily living.