Yeah, I have positive experiences with cannabis. My tinnitus is constant and difficult.I think I might try an edible and microdose next weekend with a friend. I just don't want to let tinnitus stop me from these things that I love.
Is there ANYONE who has a positive or neutral experience using marijuana with tinnitus??
This was so wonderful and positive. Thank you so much! I think I'm going to try and get high with my friend this weekend and see how it goes. I want to reclaim things that I love. And yes, weed is one of those things lol.Yeah, I have positive experiences with cannabis. My tinnitus is constant and difficult.
When I use the herb, at this point I ingest it, I macro dose. I take enough to leave my body and ride the waves.
Sounds like you miss the herb and really enjoyed it. Smoke kicks off our reptilian mind so people get scared.
You will find your balance. Bad tinnitus leaves most of us with PTSD, so we are easily scared for good reason - our worlds get turned upside down and we are super fragile to further damage.
I've just cleaned myself out and have been on the sober train. Tomorrow I will cook up a batch of infused coconut oil and will lunch into the cosmos in a day or 2. I usually give my family a heads up because it is strong and it shows.
Good luck Shelbynn... You got this.
I hope you can regain the things you love and discover new ones to love as well.
Peace.
Are these studies based on "pure" cannabis smoking?Not really, compared to a lot of other shit in the environment like huffing down diesel fumes on my motorcycle.
Cannabis smoking and lung cancer risk: Pooled analysis in the International Lung Cancer Consortium:
Cannabis Smoking and Risk of Lung Cancer in Men: A Pooled Analysis of Three Studies in Maghreb:
Effects of smoking cannabis on lung function:
More or less some studies find a minor association with long term heavy use, but it's not nearly as dramatic as tobacco, and so far we don't have long term data on vaping flower / oil but there's reason to think it's not nearly as detrimental since the main thing that makes pot smoke carcinogenic is post-combustion carbon products (unlike commercial tobacco which is chock full of heavy metals and carcinogenic flame retardants and god knows what else).
* goes back to 3am oil rips of Trainwreck to fall back asleep
That is, really weird. Still getting high off eddies?I use cannabis at least 3 or 4 times a week. Smoking seems to increase the volume of my tinnitus, likely due to allergies/sinus issues; recently switched to edibles, which have no effect as far as I can tell.
I use THC/CBD capsules, which are legal in my country (Canada).That is, really weird. Still getting high off eddies?
Yeah buddy! LolWhen I use the herb, at this point I ingest it, I macro dose. I take enough to leave my body and ride the waves.
Sometimes it's just a matter of finding the right strain. I do get paranoid too, but I try to vape right before bed so it just knocks me out.Weed makes my tinnitus worse initially, but then goes back to normal after 15 to 20 minutes. It also makes me paranoid. May end up quitting.
Hi @Gemini Crickets -- My own take is that tinnitus appears to be quite reactive in the initial months following tinnitus onset, and gradually becomes less reactive over time. I don't know if that indicates a certain amount of healing, but that seems plausible to me. State of mind is always important, but it seems there are likely other factors involved as well.I think the spike comes from your state of mind, and if you're not worried or anxious it probably doesn't affect anything. Weird, right?
Hope you are right about this. The constant reactivity is killing me. If I only had the ability to mask or distract myself with other things I'd be able to deal with this. The reactivity competes with every single sound including my own voice. 2 months in and no change.Hi @Gemini Crickets -- My own take is that tinnitus appears to be quite reactive in the initial months following tinnitus onset, and gradually becomes less reactive over time. I don't know if that indicates a certain amount of healing, but that seems plausible to me. State of mind is always important, but it seems there are likely other factors involved as well.
Hi @IntotheBlue03 -- That's the way it was for me the first few months after my tinnitus onset. It then started very gradually improving after that, and now four years on, I very seldom notice a reactive tinnitus reaction.The reactivity competes with every single sound
Hi @Lane,Hi @IntotheBlue03 -- That's the way it was for me the first few months after my tinnitus onset. It then started very gradually improving after that, and now four years on, I very seldom notice a reactive tinnitus reaction.
Thanks @Guywithapug. I have hyperacusis (sound sensitivity only) mixed in with the reactive tinnitus so I'm hoping there's still time to improve at 2 months in. I have no hearing loss except past 16 kHz but my tinnitus is reactive to every single sound, making it impossible to mask and driving me crazy especially since it's in my head and not my ears.@IntotheBlue03, I have reactive tinnitus in my left ear which started when I lost hearing in that ear. It reacts with certain frequencies, the ones that I'm deficient in. I'm about a year and a half in with no change but have gotten used to it.
There are theories that reactive tinnitus doesn't even exist, and that it is a subset of hyperacusis. The other is that it's loudness recruitment in frequencies your deficient in.
Personally, I believe it's the auditory cortex turning up the "gain" to hear frequencies that there is an issue with, specifically for those with hearing loss. For those without measurable hearing loss, it could be that part of the brain turning it up for other middle an inner ear pathologies or auditory cortex malfunction. Just my 2 cents.
Just to clarify, my "reactive" tinnitus is barely noticeable these days, but my "non-reactive" tinnitus is still with me, four years after my onset on Feb. 4, 2018. That said, my non-reactive tinnitus is better, though it took a long time for that to happen.I'm sure you barely notice the tinnitus now but can you recall as to when you could first, for example, listen to music or watch TV without significant reactivity?
Thanks for clarifying and I'm happy that the poppy seeds are helping. That's interesting that the reactivity improved but habituation for the regular tinnitus in general was more challenging? I know it's early for me but I've been forced to listen to my tinnitus and only my tinnitus since onset so I'm hoping that means something in the way of neuroplasticity/habituation. I guess I will have to see what month to month brings.Just to clarify, my "reactive" tinnitus is barely noticeable these days, but my "non-reactive" tinnitus is still with me, four years after my onset on Feb. 4, 2018. That said, my non-reactive tinnitus is better, though it took a long time for that to happen.
I recall that I thought I might be doing better as I approached my 2-year anniversary, and even thought I might write a bit about it in the "success stories" section. But it then got worse again, and my tinnitus was barely better at 2 years than it was when it first started. It has gotten better in the past few months however, especially the past several weeks, when I started eating poppy seeds before going to bed.
That single thing took it down from an average intensity of 7-8, to around 6-7. May not seem like much, but it did allow me to awaken in the middle of the night, notice the tinnitus, and treat it with a degree of indifference. And I hold out hope it will get better going forward.
Thankfully, sleep is not an issue for me these days, while in the beginning I could barely sleep at all. Things have definitely gotten better for me, but these things can take a long time. Others on this forum that improve usually do so much earlier than I did.
Best I can recall is that I used "as needed". I think a typical day was 1-2x.Curious if you recall what your treatment protocol was?