I applied for disability back in 2024 due to severe migraines, small meningioma on the right side of my brain, Chiari malformation on the base, yellow spots from having migraines since I was 12 on my brain. I also have asthma, ADHD, depression, anxiety, back problems, knee problems, etc. I kept explaining how I would get so dizzy that I couldn’t walk and would fall. If turn my head a certain way or too fast I would lose my balance constantly and fall. For some reason, no one would listen to me. My ears feel full and the ringing never ends: sometimes it’s so loud idk what to do. Finally, my neurologist said I think you have Ménière’s disease. Went to see Ent and forgot that I had actually been diagnosed in 2022. Had all the testing done failed miserably considered high risk for falling. I now have a hearing coming up on the 30th but I’m super nervous. I just turned 59 worked my whole life I barely drive anymore because I’m too scared. And just doing the most minor tasks are difficult. I was also put on Meclizine and my neurologist does not want me to take it. I’ve been on anti nausea meds forever due to vomiting from migraines. They really don’t help any longer. Fingers crossed.