Guys to say you cant cure tinnitus and maneates disease is old school. I took liam bohms advice. you litetally need to cut all thinks inflamatory, exercise, eat meat, no sugars , carbs. put the body in autophagy state. It took me alot ofhatd work, will power, hope and it went away. Just to let everyone know if ypu have the same symptoms you can totally cure it

Just saw this video, omg i can relate, i had tinnitus and exactly same diagnosis. i hated life, and seeing others enjoy life made me try to find cure. Its gone now and when i see Ryan i can tell you can cure it

MD isn’t really a “disease” it’s a series of symptoms. Address the specific symptoms and you will find most people resolve the worst of the problems. Nerve damage is best treated with a hearing aid one or both ears. It washes out the tinnitus and will resolve that “fullness” sensation. Also hearing aids stimulate the nerve and in many cases people actually improve their hearing over some frequencies. A low inflammation diet seems to dramatically improve symptoms. Low sugar low salt.

🙏🏾💪🏾

Hi Ryan, my Hyperacusis experience is the same as yours. I faced it head on and tortured myself with cutlery, dishes etc and after 10 months It improved. I've still got it but it's better. Try not to fear it or be startled. Each day if different. Yes kids are the worst (sounds). Light switches caused me pain too.

Spot on 100%. I'm the same.

Hang in there bro. It will go down. Take a couple years. Don’t let it bother you to much. It’s hard I know. It will get better

Thanks for sharing your experience. Age 42 I developed it during severe stress and trauma on 29th March 2023. 1.3 years now with Tinnitus and Hyperacusis sound sensitivity. No hearing loss or near perfect hearing upto 8000hz. Blood pressure okay. The fridge, freezer, cistern, all somehow exacerbate it. Quiet rooms are horrid. Some days I'm suicidal. Others i can ignore it. Alcohol/beer helps. Sound therapy at nights. What sound therapy do you use? I don't play loud music. Paranoid it'll get worse or something. The Hyperacusis is also evil. Cutlery sounds etc. Thanks

It's an alien implant. That's what I've concluded at this point. It doesn't matter how valid my theory is, because it's just as valid as anything these worthless doctors have come up with. So I'm satisfied with alien implant until a better theory presents itself.

More updates pls sir ryan

I had tinnitus since i was 22 in 1997. Im almost 49. It got wirsexadter covid. I micro dose too. I love the focus & insights

How are you doing now?

Good to hear from you Ryan! You are a model of resilience ! Please make more updates! 20:33i hope you are feeling better +

Thank you Ryan…super powerful and important share from you

Thanks for your videos im 19 from uk and had t for month. Definitely came from all the gaming and listening to Metallica all the time 😂.I admire your mindset and you give me hope to habituate. Praying for a better future and when that happens we’ll all come together for a f….. good time 🤘

Wait so did u get tinnitus from MD? Or noise induced

What’s your talking about is sudden brief unilateral tapering tinnitus ! Everyone gets it apparently but people with chronic tinnitus gets them more. Don’t worry it scared me to but I got used to it

Hey Ryan I got into a really bad acute acoustic trauma 12-01-2023. Shot around 700 rounds without ear protection. Instantly lost hearing and had very loud tinnitus. I have noise sensitivity and I feel like I get dizzy sometimes. I’m 6 months in. I think I’ll be like this forever???? I think maybe I have manieres disease too

@11:57 welcome to my world lol 😂people are mad fake! Do you get help from Traditional Chinese Medicine?

Have you looked into Julian Cowan Hill? His videos help a lot❤ hope that helps! Also have you tried massages and cold showers?

Hey dude. So how are you coping. You doing well With tinnitus ??

My T started 3 1/2 years ago now. I started with vertigo and they thought i had Meniere's initially. I understand the violent vertigo and nystagmus ( eye movements) id have residual dizziness afternoon. My vertigo went after 3 months so they think its more a neuritis ( virus attack vestibular nerve) . Ive been doing low dose ketamine and having the effects like you with my depression and t a little better.

Hey Ryan, in this case is it possible to have menieres if I don’t have vertigo, if I find that all my other symptoms are present

It’s good to see you posting again!

Thank you for posting an update Ryan. Having noise induced Tinnitus brings lots of guilt and depression, especially after making it worse by continuing to live my previous lifestyle. Took too long to realize the seriousness and accept it. You are right, when i go outside/spend time with my kids i cope with it a lot better. Hopefully the Susan Shore Device brings some relief.

Still here with you bro ! Ive had tinnitus for the same amout of time .its brutal but we must endure

Funny.. I have one weird symptom, you know when you stand up to fast from the bed and get dizzy/light headed. My tinnitus disappears completely

Good news it’s better, mate. Have you considered trying the carnivore diet? Some people have had success with it

Hope you are well, please update us.

I have had 3 bouts with whatever this is. I was ill with some kind of bad cold last week. Then, like you, I knew this was coming. I had fullness with slight hearing loss in the left ear. Over the past couple days I have been slowly developing diplacusis disharmonic again. It doesn't seem AS bad as the first two times, but it could also still be progressing. I'm taking prednisone right now, not sure if it helped or not the last couple times. Both of the times before this that I had it it corrected in about a week or so. Hoping this also heals. Not sure how I could deal with having this permanently.

tinnitus treatment report check it out

Hi Ryan thanks for the update sorry to hear thing’s haven’t changed much regarding you tinnitus that a shame as we are all routing for you and hopefully in the not so distant future you will find so relief. Until then the tinnitus treatment report are constantly updated the outcome of the research for a possible cure and it’s looking very positive so check it out and subscribe they send you updates daily/weekly via email which helps me at least my tinnitus is still there constantly almost 4 years now until next time buddy keep fight the good fight

I got hyperacusis after recovering from having fluid in my ears. It’s very frustrating some sounds affect me more than others. Lately the sound I’m hearing the most is like a low hum, but it’s worse when I’m in my house or a building. Then it triggers anxiety, and it’s been a rough couple of months. I guess I’m just in the expectance phase. I feel bad for my husband he tries so hard to understand. I have faith that once I get my body out of the hyper stimulated state from the anxiety this has caused things will get better. Thank you for sharing your story.

Hi Ryan, so the HBTO didn't really help. I wouldn't suggest it unless you have the cash to spend. BUT my tinnitus is definitely settling with time. There's some nights where it's almost silent now. I found what helped was trying to sleep with as little noise possible. I seem to have reactive tinnitus (which is temporary) - This is combined with hyperacusis. So when I have a loud day my tinnitus seems worse, and on chilled days my tinnitus isnt as loud. It's been around almost a year through recovery. Studies suggest it might take 2 for everything to settle. They say once with hyperacusis goes away the tinnitus will also subside. I went for an OAE test and hair cells seems normal. So luckily no inner ear hair cell damage. How are you holding up dude? Will keep you updated

❤ love from india a sufferer of age 18 😢

Hey man, does your tinnitus ever go crazy from driving and showers? That shit seems to spike mine like crazy

How are you ryan

Anyone else have a problem with seeing after images after getting tinnitus? If im reading black bold text and look away ill see a negative image of the text. Vertical lines are also a big trigger when i look away. Any words that appear on Tv ill see the words on the wall if i move my eyes. Been to the eye doctor already and everything was fine. Cant find much info about this condition.

What a great message! Thanks ! Looking forward to your next one! I hope you are now doing better!

Have you looked in to the upper cervical causes of your T? I took mine from a 5 or a 6 to usually a 0 to a 2 at worst. As you are sitting i notice your lower neck is too far forward. Your shoulders are also folding in a bit and your neck structure looks rather straight. All of those things lead to your jugular being compressed and also the venous drainage system of your brain possibly being backed up. This puts pressure on the cerebellum and ears and can for some people causes T. If you have not been to a highly reviewed nucca, Blair or AO upper cervical chiropractor I highly recommend it, they need to do scans and or x rays to see if losing the curve in your neck and your forward head posture is placing waaay to much pressure on your jugular and drainage system. Also your c1 and c2 could possibly be rotated pinching the system, and mrv scan can show that best. mri have a hard time detecting that and doctors don't know what to look for. Posture exercises, neck curve traction and restorative exercises along with rotating my atlas and c2 in place is what stopped my T. I am convinced tinnitus is caused more from structure problems then direct ear issues and the ent doctors can only help the 30ish percent or so that have tinnitus from anxiety or hearing damage, the rest of us need to regain proper csf flowl spine alignment and remove tension from the neck. Good luck.

Love your videos If possible, make a new vid on your current tinnitus! Is it getting better, any changes etc. Thanks!!

Have u tried lenire? :((( pleas keep us updated

I’m with you every step of the way. Injections injections injections of drugs in my ears.Did not work

Hey mate, been following your channel for a while. If you have the morse code tinnitus along with visual snow and all this other bullshit. Please get yourself tested for Mycotoxins - CIRs (otherwise mold illness). I got all this from a concussion made worse by exposure to mold (this has been th e underlying cause of the neuro-inflammation). Sounds absolute quack shit but, but you can put yourself into remission with binders if you are confirmed for CIRs.

😢 have you done cranial sacral therapy? There’s so many things to try don’t give up

Every day these conditions drive me in to the ground. But listening To you really makes me smile. thanks for the good vibes.

I’m with you on this. 30 years dealing with it but the last three years it’s gone supersonic. 53 now,went totally deaf. Apart from the noise in the head

I’m with you on this condition. And you’re not losing your mind it is the condition. At this level it does this to you.

I want to share this video with the ENT I saw. This makes more sense to me why when he said I have low frequency hearing loss - but it is only when women talk at high pitches that I hear them at an even higher pitch in my bad ear. This started 2 weeks ago and he is saying "possible Mineires" because of the low frequency loss. But when I explain to him my only symptom is this weird sound of women and high pitched men in my left ear he looks confused as if I'm the first person to come to him for this problem. And BTW when I left his office after the hearing test now I have a new problem which is that fan like noise constant- always in that ear. Loudest in the morning. When I wake up.

you really helped me at the beginning of my struggles thanks a lot