Recent content by shrimp

I just wanted to provide an update in case anyone searches for the effects of Azithromycin on tinnitus in the future. I completed the five-day course, and it had zero effect on my tinnitus—not even a slight increase.

Thanks for the reassuring responses, @annV and @Eloy79. I decided to start taking Azithromycin since my test came back positive for whooping cough today. I’m hopeful it will go smoothly. I’ll keep you updated!

I have been coughing nonstop for the past two weeks, and my husband has been the same. We both have symptoms that doctors believe are typical of whooping cough, especially the characteristic sound. We have been tested, but the results take several days to come back. Two different specialists are...

Just wanted to check in and thank @MindOverMatter and @Nick47 for the tip on trying Magnesium Glycinate instead. I switched from Citrate a few weeks back and my tinnitus has gone way down, so this appears to be working! My tinnitus is still slightly higher than baseline when on no Magnesium at...

Thanks for the tip, I bought some yesterday. I will try it out and hope my spike quiets down. Thanks. I've started taking Glycinate now, let's see how it works for me!

Has anyone whose tinnitus gets severely spiked by Magnesium Citrate found a form of Magnesium that doesn't spike their tinnitus? Which one has worked best while still being effective for calming nerves, relaxing muscle spasms etc.? I need to take Magnesium for other issues but it spikes my...

Was hit with a major life crisis 2 weeks ago, have since been struggling to sleep, eat, exist and obviously T has gone through the roof.

Had to have an mri today. Had them before without issues but this one was WAY louder and a few hours after the mri my T has spiked, freaked.

I have this same problem. I've tested it multiple times, stopping and starting Magnesium, and it never fails. It spikes my tinnitus within 24 hours, and it's no small spike either. I'm in one at the moment since I restarted Magnesium a few days ago again. I really need to take Magnesium for...

Anyone else with peripheral neuropathy? Have you found anything that helps? I'm weary of going on drugs like gabapentin etc.

I didn't actually suffer any hearing loss, most with SCDS have it but not all of us. For me it started with vertigo. I was hit with a bout of vertigo that lasted more than 3 months straight. At first they thought I had BPPV and tried Epley manoeuvres etc. I couldn't walk straight and it was just...

I read your post, thanks for the comforting words.

I have a slight Chiari malformation, however I am not under any more investigations or care for it, it was just visible on an MRI. I do have an inkling myself it's the reason for my frequent neck pains and cervicogenic migraines/headaches I've had my entire life. But I've also got SCDS on both...