Thank you so much for making these positive videos. I have been diagnosed with vestibular migraines. Been dealing with daily symptoms for 14 months. Even though I am not 100% I am way better than I was to begin with. I am so happy to hear how well you are doing.

Really appreciating your videos right now mate. Been in a chronic phase at the age of 18 for time spans of 10 months, and now another chronic phase for 2 months

Thank you for posting these videos. I’ve had VM for almost 4 years now and my symptoms have been up and down. I do feel that vitamins definitely help as well as doing my best to keep a clean diet. I too feel like vestibular rehab and exercises really can only help so much. They seem to help me for a little while, but then slowly loose their effect. It’s very encouraging to hear that you are doing better.

Feeling great, it’s month 6. For myself it’s been a monthly progress. Vitamins have helped tremendously. Started running again, feel great. Glad your feeling better.

Hiya just come across your page, I’m from London! Suffered with VM/PPPD for 7 years, did not want to go down the medication route so suffering 24/7 - it’s been a complete life changer! Glad you are feeling better and it’s great that you are also raising awareness

Great tips, very wise words. I especially agree that you need to give yourself and your body time to heal. Glad to hear you’re getting there!

Hi your posts have been wonderful for me. I started dealing with this in September this year. At first it was constantly spinning. Inability to focus on anything. Now I’m on amitriptyline 40mg I don’t know if it’s that or simply time but I can do everything I normally do albeit it takes more effort. Now it’s like a rocking sensation in my head but it isn’t affecting my visuals. I still have ear fullness from time to time. I’m just praying to heal soon. I also take magnesium citrate.

Glad to hear you're getting better Matthew. Keep us posted on the evolution of your symptoms. Can I ask if you have/had the rocky type of dizziness (where you feel you are in a rough sea or on a plane with turbulence)? That's the symptom I'm most struggling with, it's exhausting. Cheers!

This video has been so helpful. Thank you

Thank you for posting these videos. I'm just stumbling upon them I'm hoping that you've come a long way from then and things are improving. I'm just getting started with this journey. I've been down for a month now. My neurologist wants to try me on topomax. I was wondering if you have tried it. Thanks for the glasses reference. I was just looking at them and wondering if they were legit. I'm dealing with a lot of emotional issues and this very hard to deal with especially thinking about going back to work. I'm scared that things won't improve so your videos are comforting. Thanks 👍

Thanks for inspiring Matt.Im still recovering from Vestibular Neuritis.

So happy your in a good space😄

Thank you for the help

I’m in the early stages. I live in Kansas, I got diagnosed a few weeks ago. I feel like I’m on a boat 24 seven haven’t been able to drive for over a month. I was just wondering if you’re able to drive and they’re being on a boat feeling never goes away?. This video gives me hope I have quite a bit to figure out here but the first drug you mentioned I’m on that have a neurology appointment coming up. I guess the main thing is finding your triggers but yes it’s definitely life-changing go for now you can get your life back because I feel like or felt like there’s no hope. Thank you for your videos!

Hey - your videos are so relatable but also inspiring. I've just started on Amitriptyline. I was wondering how long you took it for and what % would you say you're operating at now? Have you reached the 95%-100% phase? I really hope so.

Did you have trouble looking at phone screens and computer screens? And did you have sound sensitivity?

I think I have this and have started amitriplyne. I’m now at 20 mg. How long did it take you to start feeling your symptoms improving ?

Hi Matt. Just checking this vid out. What made you increase propanolol from 20mg twice a day to 40mg twice a day? Cheers

Hi I was diagnosed vestibular migraine back in November 2021 after having balance problems and dizziness for 2 years I was on propranolol but caused me chest pain so stopped it but found relief on it now I’m on nortriptyline similar to amitriptyline but still ain’t finding relief from it I was wondering if you think my doctor would allow me to take nortriptyline alongside propranolol again

I have many of the same symptoms people with vestibular disorders have... except for 2. I’m so sensitive to motion I can’t even lay down with my eyes closed without feeling somewhat motion sick/nauseated. I can also barely move without feeling very nauseas. Does this seem normal? Did you ever experience anything similar?

Hi im wondering if you can help me i have vestibular migraine also and had depersonalization with it for 3 months now constant! Just started on propranolol but im so fed up of this depersonalization if the vestibular migraine doesn't go away will the depersonalization go away or not? Just the GP isn't giving me any answers i feel so lost so fed up! 😕😔 Would appreciate it if you could help me please, a really can't live like this

Drinking alcohol? What's it like for you?