Mine is really mild but my son is still struggling so I am going to give it a whirl and see what happens. I'm doing 1 tsp twice a day. It's kinda gross but not too bad. I am sure I stink and just can't smell it but a girl's gotta do what she's gotta do.
I'm only two days in. I thought it subsided totally for awhile yesterday but not 100 percent sure. Went into a quiet room and couldn't hear it at all. Came back. But that was the first break in the constant really mild buzzing in my left ear that I have had for months. I will keep you all posted.
Any updates on your progress Dolly
Didn't seem to do much to stop the tinnitus but may have kept symptoms in his case at bay. Mine is so mild it was hard to tell. After he saw me taking he was unafraid and did it for awhile while he was staying with me.
He kind of tapered off and tried this and that - so many things on the internet and word of mouth. His situation has not really improved at all with any of it. He is going to have to get very disciplined with the trial and error and essentially be his own doctor. The medical establishment really has no answers for catastrophic tinnitus so they just send you home.
Hi Dolly, thank you for the update. I’m sorry it did not make you and your son’s tinnitus noticeably better. Did it improve any other conditions or aches and pains that you may have? How long did you take it, or are you still taking it?
I am not still taking, but I talked my friend with bad arthritis into combining it with castor oil and using it topically. It has reduced his symptoms dramatically and more than anything else he has taken, including prescription drugs for pain and inflammation like Celebrex. Also, he is sleeping for the first time in years. I think that might be the castor oil.
Thank you for the update. I’m still trying to decide whether or not to give it a shot.
Thanks for the update. I just started it for cuts/burns/bites. I'm testing it on a scar I picked up when I was a kid. Bought it off amazon, 30% aloe.
Sorry for the delay life's been crazy for me this year. I stopped because it wasn't doing much. He was taking it when he was staying with me briefly and same. I have since read that some people that have had nerve damage repair saw results after taking DMSO regularly for a year or so. His is getting worse now and he is really not "buying" the alternative route ideas I come up with, which is frustrating.