Famous Surgeon Reveals SHOCKING Pulsatile Tinnitus Treatments
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- Опубликовано: 26 фев 2022
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Dr. Ben Thompson and Dr. Athos Patsalides discuss pulsatile tinnitus, its diagnoses, causes, and treatments. If you experience ringing in the ears that sounds like a heartbeat, you may benefit from learning about different ways to manage this condition. Dr. Patsalides is a pulsatile tinnitus expert.
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Dr. Ben Thompson and Dr. Athos Patsalides discuss pulsatile tinnitus, its diagnoses, causes, and treatments. If you experience ringing in the ears that sounds like a heartbeat, you may benefit from learning about different ways to manage this condition. Dr. Patsalides is a pulsatile tinnitus expert.
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Please help me get a hold of this doctor, i have something in right ear , cant stand and now in a bed, unable to hold my balance
@@yolitorres9200 what would it mean is MRA, MRI, CT head are ALL NORMAL but YOU STILL HAVE UNILATERAL PULSATILE TINNITUS?
Dr. Patsalides saved my life. I am not exaggerating. I was told by 6 different doctors to just live with it. It was so loud and debilitating, I was suicidal. I am one of the patients with venous sinus stenosis and a venous aneurysm. I screamed when he told me it was in all of my scans from the last 7 years. He placed stents for me in December. My life is 100% better. Doctors need to do better!
Glad to hear that, Michelle! Thank you for sharing. :)
was it seen on an MRI and MRA?
What test showed the venous aneurysm
@@650tonyd I had an MRI, MRA, MRV, and Cerebral Angiogram. All my doctors said they were normal. Dr. P said he could see the stenosis and aneurysm in all of them.
How many Drs said normal? What type of Drs?
what hurts me is thinking il never hear silence again
I had Pulsatile tinnitus since october, 2020 i had ringing and buzzing left ear and sometimes the right ear too i also had vertigo and hyperacusis my first ENT said there is no treatment or cure for your tinnitus you should live with it. I became more depressed my buzzing and ringing i couldnot able to sleep at nights i was depressed and anxious .
Now i am happy after almost 3 years my pulsitile tinnitus went away and my life is 100 % best Thank AlmightyGod
hi bro Mashallah, how did you treat your PT how did it go away? please help a brother out i’m depressed due to this PT in my right ear
@@user-ni1he8qv6u
1.I did walking exercise 45 Minutes daily
2. I eat beans, grapes, banana, i eat bread but not white bread, drink more water
3. I took Tebonin tablets 120mg
4. I stopped watching bad news ( negative news)
5. I minimized listening negative people
6.i stopped sugar at all no coffee no tea
7.three hours before bed i took my dinner and don't use mobile Phone or watch tv two hours before bed
8. Fasting
Dr. P placed a stent in my left venous transverse vein in Nov 2021. He changed my life! Amazing doctor
How did pulsatile tinnitus start for you?
What was the issue that caused your PT?
TonydlP650 venous sinus stenosis of my left transverse vein! Narrowing of the vein
@@jennalyn3017 did your ear ever feel clogged/full?
I’m seeing a neurologist soon for pulsatile tinnitus and blood flow issues in my spine area. And this was very helpful, Thank you
A very good explanation about pulsatile tinnitus, thank you very much!
ty to you both for having this conversation i have PT left side
Hey tanya, thank you for the comment. We are glad to know that our videos have helped you. Enjoy exploring our other RUclips videos, as well as blog articles on treblehealth.com
Glad I found this - will go to a doctors office armed with knowledge and understanding
Thank you, this symptom has just surfaced this evening. This video was the best thanks again.
Update?
what an amazing doctor ! he seems VERY VERY caring doctor and with FULL confidence
Wow…im literally speechless. Im calling in the morning.
The information in this video is priceless and so educational. Now I am armed with all aspects of PS and have made my notes and will bring to my ENT specialist next week for review to get to the bottom of this very scary debilitating problem. Thank you so much.
Thank you so much for doing this work and interviews. They’re so useful because normal located doctors don’t have time, no appointments or they don’t take one very serious. It’s so good though listening to professionals like you that take their time to give a profound round up of the topic. Keep going with your great work 😊
You're welcome. 😊
Thank you for this video. I will see my ENT doctor on dec, 27th and i will tell the doctor what i got from this video. thank you so much
I'm going to demand my doctor to watch this video, I'm so so tired of her saying there's nothing to be done but I have mostly pulsatile tinnitus which has been debilitating but she never takes me seriously, even asked for an MRI once to have the veins checked but they didn't check the veins it was just a normal MRI. Had years of abuse against my head which I believe caused damage and now I'm done with these so called doctors. Thank you so much! Finally!
Hey Rain, thank you for the comment. We are glad to know that our videos have helped you. Enjoy exploring our other RUclips videos, as well as blog articles on treblehealth.com
Find a new doctor.
OMG!!! Thank you so much. Just the minimal information provided has enlightened me regarding the source of my pusatile Tinnitus. Now to determine if there is any treatment
This video is 10mos ago, I was lucky to come into this video, was diagnosed a month ago with pulsatile tinnitus. I had this for almost 2 years not knowing its pulsatile tinnitus, became worst in 2022. My doctor said to just ignore it. Thank you so much for the information. I have pending ENT appointment hoping I can get the tests you suggested. Thank you💕💕💕
Hi Estela, thank you for the comment. We are glad to know that our videos have helped you. Enjoy exploring our other RUclips videos, as well as blog articles on our Treble Health website.
hi Estela, how r ur symptoms now of pulsatile tinnitus?
Thank you for this cast pod and spesielt to doctor Patsalides. Now I understanding better about PT and what I must to do. Thank you a lot 🙏😊❤️
You're very welcome! I'm glad the podcast has provided you with a better understanding on what steps to take. Wishing you continued clarity and well-being on your journey! 🙏😊
Thank you for this video. 20 yrs ago I started having vertigo attacks that was coupled with significant tinnitus and hearing loss in right ear. The symptoms subsided except for hearing loss. Now I’m going through the same with left year, but feel more in tune with what I’m experiencing this time. I hear a pulsing sound on top of static. I just so happened to notice the pulsing sped up and slowed down upon taking a deep breath. This made me think it was paired up to my heart rate and that led me to find these helpful videos ❤ I have regular episodes of sinus pain on right side of face and all this together, makes wonder about narrowing of passages preventing proper drainage. Ménière’s disease is another possible cause that came up 20 years ago and i will revisit that when I see the ENT soon. My childhood was full of ear infections and throat infections. I hope that at 48, something can finally be identified and treated to help make the 2nd half of my life more comfortable.
You're welcome, Diana! Be well. :)
Sounds like some Upper Cervical chiropractors can help. Reach out to Blair technique practitioner
Thank you for making this video exactly what I needed to hear. Great information that will help me considerably!
Hey Marina, thank you for the comment. We are glad to know that our videos have helped you. Enjoy exploring our other RUclips videos, as well as blog articles on treblehealth.com
Was that pun intended?
thank you for this video! It has gave me some peace of mind and some good advice for how to handle my upcoming ENT appointment in October.
You're welcome, Tiffany! Glad it helped. :)
Wonderful information,,thank you.
You're welcome. 😊
Thank you for sharing this video. It was very helpful.
You are so welcome! Glad it helped, Sharon! Be well. :)
Very informative. Thank you
Very welcome. e are glad to know that our videos have helped you. Enjoy exploring our other RUclips videos, as well as blog articles on treblehealth.com
Such a helpful video! Thanks so much for sharing.
You are so welcome, Juliet! We are glad to know that our videos have helped you. Enjoy exploring our other RUclips videos, as well as blog articles on our Treble Health website.😊
Thank you for this video. I hope to find an appointment with this doctor.
Hi Sharon, thank you for the comment. We are glad to know that our videos have helped you. Enjoy exploring our other RUclips videos, as well as blog articles on our Treble Health website.
This video was so helpful. I have not been diagnosed with anything specific yet but have an appointment with an ENT on May 17th and I'm stressing quite a bit about what could be causing the intermittent PT. I sometimes have a headache accompany the PT but no other symptoms, and my brain has assumed everything under the sun. This video has helped me figure out exactly what I need to tell my ENT in order to get the right tests performed. Three doctors in the last month have told me it might be my sinuses which I absolutely do not believe, and it's been frustrating/disappointing. Thank you so much.
I also have a question regarding the more serious causes of PT: Dr. Patsalides mentioned that the most serious category can have potentially life-threatening problems if left untreated. For these potential issues, how long is too long to leave it untreated?
Hey N M, thank you for the comment. We are glad to know that our videos have helped you. Enjoy exploring our other RUclips videos, as well as blog articles on treblehealth.com
How WasYour ENT Appointment ?
@@NM-nc2nh Good question that I am wondering about. I also have vertigo,
Thank you! You may have saved my life, I’m calling to schedule with this doctor asap.
Glad I could help! Be well, Rose!
@@treblehealth thank you Ben I cannot tell you how it is to never have a moment of silence, I have an appt with the doctor on October 19th. I pray for even a little help.
Very informative Thank you !
Hey Santy, thank you for the comment. We are glad to know that our videos have helped you. Enjoy exploring our other RUclips videos, as well as blog articles on treblehealth.com
Very very helpful. Thank you!
You're welcome! Glad it helps. 😊
Thank you this helps. I do wish there were more doctors in south africa confident with stenting as I've approached 2 now who say it is very high risk and wont do it. So I'm living with PT.
This doctor is amazing. My ENT never talked about such things and did not order a MRI for my pulsitile tinnitus.
Thanks for your comment. S B. Be well.
Thank you for this video!
You are so welcome! Be well. 😊
I thank the doctor for being interviewed. I believe I might have read some articles he has written. I am also on Long Island.
I was diagnosed with pulsatile tinnitus in July of 1989. I was sitting on the bed and thought the cat was purring near my ear and I've heard every heartbeat ever since.
Got worked up back then but I doubt I got an MRA and yes, it can be fully blocked by pressing on my neck. So hopefully I'm in the venous category.
In the past 10 years when my blood pressure has been up it's gotten really loud. A few years ago I went to emergency because it was so loud I was going out of my mind. And it turns out my blood pressure was very high.
When I went to an ENT several years ago he had said that it would go away if my blood pressure went down, this is not true, I've had this damn thing for just about 35 years, again, every heartbeat, it's not intermittent, it never went away once it started. I noticed way back when, certain medications and alcohol would make it worse and of course raised blood pressure as I already mentioned.
One good thing about it, it is about the only good thing I can say is I think it may have saved my life because since blood pressure is the silent killer and I hear all my heartbeats, I know when my pressure is up. As well, I had dangerous arrhythmias from low potassium and I could hear that in my ear as well.
Whether I'm rationalizing or
not, I'd swear that having it has let me know about things going on with my heart that I wouldn't have otherwise known.
I have both pulsatile tinnitus and I have ringing in both ears, it's positional; if I move my jaw in a certain way it gets a lot louder if I turn my head it gets louder. Currently it's starting to really bother me at a high pitch in the same year with the pulsatle tinnitus. Though I have some teeth issues going on.
I wrote on Dr. Ben's other video that the massaging and scalp is helping with the ringing tinnitus.
It would be helpful to know what are the percentages of the three categories the doctor sees. I know the first category is very dangerous, but it would be very helpful to know the evidence-based findings. I know he said category 1 with is rare, but he didn't give any numbers.
It would also be helpful to know when someone like me has had it for so long, what the odds are it is of a certain cause.
To anyone suffering from this or ringing tinnitus, I think the number one advice I could give you since let's face it, I'm certainly an expert in living with it is to simply ignore it. But I would say that if it gets really loud definitely check your blood pressure. Always know when mine's low when it's near quiet and of course I always know when it is high.
Getting exercise and a low salt diet really helps this situation as well.
I’m one of those people who woke up one day and developed pulsatile tinnitus. I hear it mainly in my right ear but sometimes my left. I’ve had every test out there done, including a CT scan of the temporal bone with and without contrast and they found nothing. Mine does overlap with ringing and when I yawn I can get it to stop. It comes and goes. Sucks but I fall into that third category he was referring too. They couldn’t find anything on me to do surgery for.
Great information! Not only do I have pulsatile tinnitus in my left ear, my tinnitus changes frequency and intensity with every stride of walking, and also gets louder when I press anywhere on the left side of my head/scalp. ENT and audiology look at me with a blank stare when I tell them this.
Somatic and pulsatile tinnitus both
I'm having pulsatile tinitus from last 6 months....i visited 3 drs (prof) and they said no need for scans ...advised me to use anti allergics and ear drops etc... But now i ll follow the instructions of dr patsalides...
Sorry for you! Mine was torture, but easily treated intravenously under sedation.
Thank you so much for sharing this video! Excellent medical information.
Hey Carmine, thank you for the comment. We are glad to know that our videos have helped you. Enjoy exploring our other RUclips videos, as well as blog articles on treblehealth.com
Thank you so much for the video
You are so welcome!
Great video thanks. It explains pulsatile tinnitus perfectly
Hey Julie, thank you for the comment. We are glad to know that our videos have helped you. Enjoy exploring our other RUclips videos, as well as blog articles on treblehealth.com
Was recently diagnosed after a 3 year battle to get more tests done, until finally an MRA and a radiologist who knew what to look for got it right. Had been suffering of pulsatile tinnitus in my right ear especially throughout the years, but always assumed that it was because of stress, exhaustion, etc. The past 2 years however, it's gotten so bad, I am plagued with side effects of vertigo, severe headaches, nausea, hearing and visual problems because of it... and it's NEVER EVER quiet anymore. The only thing is that I now have a diagnosis: an AICA loop compression (right ear) which surrounds and overrides the right cochlear and facial nerve complex. Something I've been born with apparently, and apparently is extremely rare (?) , but have not had any symptoms until now in my 30s. No matter where I searched I can't find substantial medical reports on the condition or suggested remedies' success rates, but I am aware there is surgery than could help. While I am trying to decide the next best step, my hearing seems to have started getting affected lately, which I was warned about that it could happen if the artery begins damaging the nerve. At this stage, i can't watch even concentrate at work at times when it gets very loud. Can't do the things I liked to do because if I exercise more or do any activity I used to enjoy before, the tinnitus gets so bad it knocks me into bed. I always need to be careful, and while white noise helps to an extend, it's not a possible thing to have 24/7. Not sure of which decision would be best next, so it's still a struggle to do anything regularly, even sleep.
These same symptoms are happening with my mother ...
What should I do ??plzz help
My ENT doctor told me I had tinnitus (but not pulsating). I had a CAT scan done because I have a pacer and can’t have any magnetic imaging tests. It came back clear. Since the test almost a year ago, I have not heard from their office inquiring about my condition. I’m trying to work through this by myself. Needless to say, I’ll be calling them soon to voice my discontent over their lack of interest.
You will never know the underlying reason for Tinnitus; that's why they did not call back. Pulsatile tinnitus is completely different from tinnitus.
pulsatile is very easily distinguishable. It is a whooshing or heartbeat in your ear. When I had my hearing test the Audiologist actually said she could hear it. It's nice to know you aren't crazy because someone else hears it too!
@@juliannarathmell that's true. Its awesome someone validated your problems
Can you hear this sort of tinnitus all the time? I noticed it a bit last night and woke up with it really loud this morning, and now I’m freaking out that it’s something really serious. When I gently press on the right side of my neck, it almost stops got a moment…
I rang 111 and my GP will call tomorrow. I truly hope they investigate 🔬
Some people do hear pulsatile tinnitus all the time while others only hear it in certain positions. Oftentimes, there is no underlying reason for concern. We are glad you made an appointment with your GP to discuss further. Wishing you all the best and please know that we are here to support you when you are ready.
Thank you for this video, your approach, and both of your demeanors.
Will a CT scan show the vessels as well as an MRA?
No, CT scans are best to show bone definition. MRA is best to show blood vessels.
@@treblehealth thank you for your response. I have bilat IOLs, wondering if I am not a candidate for an MRA.
I’m shocked intracranial hypertension is not mentioned 😮
He mentioned it.
Do you think that because the pressure in the head is high, the hypertension, that you can hear the pulsing worse because of pressure on the ear and veins?
I have pseudotumor cerebri, and I have almost gone into remission from that, which in turn has lowered the pulsing sound. It’s not gone, but it’s definitely not as low lid now that I can tell my pressure is down.
I have that now . 😞
I have been dealing with this for 10 years or more, but the last year it has been incredibly difficult, I had an mri scan 6 or 7 years ago, came back normal, my balance has been terrible lately. I have no hearing in my right ear that completely went in 2014. I wasn’t born deaf but did have measles and had I think a bacterial infection aged 2 and was put in some kind of bubble, family were told I might not make it, thankfully I did. I recently had an infection and had antibiotics. Plus I have had pinna perichronditis, I don’t wear the hearing aid no more, as that really aggravates the ear pain, I’m currently suffering with. I have moderate loss in my only working ear, plus the pulsatile tinnitus prevents me from hearing properly. I’m going to see the doctor to have an examination. Thank you for this.
Hey Janette, thank you for the comment. We are glad to know that our videos have helped you. Enjoy exploring our other RUclips videos, as well as blog articles on treblehealth.com
My mri showed that I had empty sella with chronic remodeling of the bony sella tuccia.
I went through all the ct scans I had done previously I’ve had empty sella since 2019 but I was never told and I never had any symptoms until a few months ago
howz is ur PT now?
Thank to you both the dr.
You're welcome, N J. Enjoy exploring our other RUclips videos, as well as blog articles on treblehealth.com
Dr. Patsalides was a life saver for me. My Pulsatile Tinnitus was so loud that my wife could here it when she put her ear near my ear. I had a very bad Durel Fistula. All my local ENT and radiologists told me to live with it. They didn't even detect the very bad fistula condition. It is 95% better now and I don't even hear it as I am so used to the faint noise. Before I was contemplating on rupturing my eardrum so I don't hear it.
2021 July swooshing began and increased greatly and constantly until 2021 September when I suffered a stroke causing paralysis on my right side, the same side of swooshing. The stroke was deep in brain on its left side. After the strike, the swooshing disappeared.
did you get any imaging like a CT, MRI, MRA etc before the stroke happened?
At what time did this ever happened to you. Mine would be in the middle of the night. Sounds like a pulsating tapping sound. I'm trying to match it to my pulse but they don't seem related. I suffer from severe gerd and bloating. I noticed I had been eating breads during those episodes
I have sigmoid sinus dehiscence. I experience pulsatile tinnitus, blurred/darken vision, vertigo, and headaches. I’m taking gabapentin but they don’t know why I have the headaches.
I had this for 1 week and was going crazy, i don't know what happened but it went way when i did some neck exercises.
Excellent!!!!
Many thanks!
Since 2006 I have had Tinnitus. A continuing high pitched sound all the time in both "ears" and recently I also have the pulsatile Tinnitus in my left ear. This one is directly in tune with my heart rate and is more difficult to deal with. The original Tinnitus becomes " white noise " ,for me, most of the time while doing my daily routines but in the morning and bed time is when it's the hardest to deal with.
Have you seen a doc? Xx
What should I do if I am having pulsutile tinnitus from a venous cause? Help me. 🙏
Thank you!
You're welcome, Rebecca! Be well. :)
Thank you very helpful
You're welcome! Glad it helped! 😊
I’m having both mostly without but when both increases in noise .just left ear but right ear is now ringing on and off yuk .
I just left Kaiser and I know for a fact my symptoms align more with Pulsatile tinnitus. The doctor said it’s EUSTACHIAN TUBEN DYSFUNCTION because I have a stuffy nose. It’s hard to go to work with these symptoms of throbbing, heartbeat, whooshing in my right ear.
hi
i’ve got the same symptoms and it all started with ETD. did your Pulsatile tinnitus ever get better?
One more question- Are brief nighttime headaches (that wake you up) associated with a vascular cause of PT? Thanks.
I experienced sudden hearing loss in my left ear then it came back. However, it is very sensitive and not as good as it was. I developed vertigo and i been dealing with it for the past month. Could this all be related to a neck adjustnent i got. It was the first time i got neck adjustments in my life. I also had ear infection two half minths ago whuch was treated
thank you for educational information. i have this kinds ear problem . what shall i do . it has been more then 8th month but nothing is change besides that i have balance program going with tinnitus , fullness of ear and reduced hearing.
You're welcome, Abi. Regarding your question, feel free to contact our team via email and we can do our best to help you. Our email is contact@treblehealth.com
Thank you so much
You're most welcome! 😊
Iam having unilateral tinnitus in my left ear for past 10 years and I visited ent specialist then they told that my ears were perfect. I still having ringing in my left year.
I have Fybromuscular dysplasia in my bilateral internal carotid arteries, is there any cure to dim the noise? It’s hard to fall asleep, so need meds to sleep. It gets loud at times and it alarms me.
Ok so im waiting to go take my mra and mrv... if i have vascular pulsating tinitus is it fixable? And if so do you just go in and clean out the artery?
What about MEM - middle ear myoclonus? Is it completely different than pulsatile tinnitus?
What about Mentures Disease and that effect? I had tinnitus, then balance issues, then hearing loss in my best ear.
I feel like I have this but also have symptoms of Occipital neuralgia. Could this be a possibility one related to the other?
Thank you
You're welcome! Be well. :)
Thank you so much doctor very well said cause i have tinitus more power and GOD BLESS
You're most welcome Be well.
any medical students/healthcare professionals with tinnitus, how you manage it and if it impacts your everyday practice?
When I was young, I had a chronic otitis media both ears. My doctor referred me for an operation to help me with hearing. But the surgeon refused to do it for a reason that I was still young. Now I am 33 and I am experiencing Pulsatile Tinnitus on my right ear. My hearing level is not consistent. Sometimes the sound is too low and sometimes it’s great. When I blow my ears while covering my nose (like scuba divers do), it makes my hearing better but not all the time it is effective. So I am confused about this hearing issues. I also suspect having an allergic rhinitis.
I had Pulsatile Tinnitis present about 3 years ago. I saw an ENT and an Audiologist. The ENT had me do an MRA and it showed that I had a high jugular bulb on the right side. He told me this was the cause and didn't look any further into it. Well here we are 3 years later and its back. This time I had a cough and was coughing so hard that my right ear plugged up. The PT is back and i'm concerned. I want another MRA to see if it is something else. My BP spiked for some reason during the cough and I feel it my be part of the reason why this is happening. My Dr said my eardrum looks swollen and she can see fluid behind it so maybe the swelling is just pushing against the jugular bulb. IDK i'm just over the sound as its literally driving me INSANE
I had the same thing my ent look my ear said he didnt see swollen but he notice my ear is kimd a wet. But this time before i heard this thumping i need to go my pcp again. Also my BP is elevated that day when i started hearing this thumping aound in my left ear. Its kind a scary i would ask for MRI or MrA to make sure its not dangerous.
hi how r u doing now with your PT?
Thank u for this! I had double jaw surgery a couple weeks back and developed this whooshing sound on my left ear when i came back to the rented apartment (i first thought someone’s vacuuming downstairs until i laid on a pillow and noticed that the whoosh goes the same rate as my pulse). My surgeon says to monitor for now since i’m still healing. So hopefully it resolves once my jaws and veins and muscles around it are back to normal.
You're welcome, Cesiaj. Be well. :)
is the problem solved now ???
@@Sahouma2020 It still comes and goes, but at least it's no longer loud whooshing 24/7 like during the first few months post-op. Perhaps i just learned to tune it out. I count myself fortunate that it's not the high-pitch ringing type of tinnitus, so it's easier to manage.
Thank you for this, just diagnosed from a scan in March (this is June) that I have benign acoustic neuroma. Since March two bouts of what I though was labyrinthitis and in the second bout, last week, have now got pulsatile tinnitus. Can’t get anyone to speak to me, waiting for doctor to call and consultant who wrote to me with mri results hasn’t called me now going private but this is a week later and I’m so worried. It’s awful.
I have been healing from severe inflammation that caused both types of tinnitus and some hearing loss in my right ear. It started with severe vertigo attacks that put me in shock and sent my blood pressure up.
I am 10 months out and just felt called to reply to you. First, try to stay as calm as you can and trust that you will heal. My PT was once so loud, I had to go outside to get my mind off it. I am now using a masking hearing aid and the PT is down to a 1-3 and often I don’t notice it anymore-my brain really has let go of it-ENT thinks mine is related to the TMJ and high stress my system underwent.
Other things that are helping me is worki. G with a Somatic Experiencing trauma therapist to help build capacity in my nervous system. Also, the Quieten AP by Julian Cowan Hill is very helpful for teaching calm and helping your nervous system to heal.
Wishing you well.
Mine only comes on during exercise and is an intense pressure that thumps synced with my heart. What does this mean?
Thank you.. I waiting referral to ENT.. this podcast will help. 😊
You're welcome and best of luck! 😊
I’m having this issue in both of my ears. It started out on the left and now the right. It only stops if I press into my neck. It’s getting louder. I’ve been to three different specialists. I know there’s a connection between my neck and the sound but because they didn’t see anything on the mri they haven’t checked any further. They called today and mentioned intracranial pressure as a possibility and suggested I get a lumbar puncture. The last time I had one it caused back spasms. The first specialist suggested brain surgery although he says he is not sure what the problem is. It’s impacting my hearing but I’m not comfortable with either of these interventions. If anyone has found a tx that works please share
Left ear only. My heart rate is upper 50's low 60's. BP is 127/68. The pulsing in my ear is about 130 BPM on average. Figure that one out.
Dr. Thompson, very inspiring videos and thanks for having honest, insightful conversations about this issue.
I have pulsatile tinnitus, mostly in the right ear. In my case, it comes and goes and is not there 100% of the time. I haven't really been able to determine what the triggers are and I have some lousy days, but also some pretty good days. My question, if anyone has insight, is whether pulsatile tinnitus is typically constant or if it can come and go. If it does come and go, does that help to narrow down what the causes might be?
I went to two ENT's and was told by both that there was nothing that could be done and told to just ignore it. As we know as sufferers of this condition, that's much easier said than done and that makes it even more distressing, as well as expensive.
This video really helped me to get some courage and ask about surgery. Can you share the number of patients who have to replace the stents after surgery? What’s the success rate of stents? Do we need to replace them again and again?
This is a question that would be better suited for the physician doing the surgery. As Audiologists, we are clinical providers rather than medical physicians and we do not complete any surgeries.
Is that dr a ent specialist? Where whould i seek help for this condition thats 5 days new for me? I seen my dr told him my symptoms and he put me on antibiotics. I went to emergency room last night . They ordered a head and neck ct with contrast and labs as well woth ekg for heart . The dr said it all looked and to fallow up with my dr . Just dont nobwhat to do . Please if anyone can give me any suggestions it would be highly appreciated ❤god bless
Going to the neurologist tomorrow for this. I’m 39, dealt with this for years. Did a brain CT and nothing. Did a hearing test, perfect hearing. Feel like it’s getting worse, mostly at night. Going to request an MRI.
Best of luck, DD. 😊
how r u now Dean?
Any supplements you taking
@@treblehealth thanks. All turned out great. I’m also slightly anemic which I found out during my wellness checkout last month. I’m on iron meds and I haven’t had any tinnitus issues like before. It’s practically gone. Thanks! 🙏
Thanks guys!
Hey Jason, thank you for the comment. We are glad to know that our videos have helped you. Enjoy exploring our other RUclips videos, as well as blog articles on treblehealth.com
Mines happening lately like this when I wake no pulstive tinnitus but 2 hours awake up I hear my heartbeat than in the afternoon the sounds changes to a flowing fluid sound.
Hi, I have the same issue. Do you still have this PT or did you find out the main cause of it and got treatment?
@@jennyfurtado2129 I still have it. Idk if it out diet or what but it comes and goes. One doctor says it's low potassium others clog arteries so idk who to believe
@@rolldog82hi howz ur pulsatile tinnitus symptoms now? i’ve got similar symptoms as yours please update thanks
@@user-ni1he8qv6u what I am seeing is kidneys are connected to our ears and liver to our eyes. Detox both and you will be better I promise you. I am drinking nettle leaf or nettle seed for my ears and you know what it has worked for the most part. Dandelion I see is good for the liver Also. Nettle is good for hair growth too .
Mine was caused by stenosis I had to get a stent put in in my right trans sinus vain so that whooshing noise is now gone but i still have a bit of ringing in my ears
I have tinnitus and I remember when I first got it I worried it’s affect my sleep but you get used to it. This isn’t the same. It’s like someone is beating a drum in my ear. I’m from just north of nyc and I’ll fly back home to see this doc if I can’t get it treated out west because this is intolerable
I been having pulsátiles tinnitus from TMJ for two years now. Had jaw nerve repair in consequence of a bad root canal. Since then, I suffer from náuseas, ringing in one ear, whooshing sound in both ears, and vibration in my head. The pulsing and feeling like I’m in water as soon as my head hits the pillow does not allow me to fall asleep. It is driving me crazy!
The Lord heals u my friend.
is this MRA has to be with contrast ( dye ) ? i don't like to inject this harsh dye into my body ? is the result of MRA without dye can be accurate too ?
According to Independent Imaging, "Newer generations of MRA’s can produce finely detailed images, capturing even minute details of the internal vascular structures without the need for contrast dye. In other words, a non-contrast MRA allows your physician to view tiny blood vessels clearly". Link to article: www.independentimaging.com/non-contrast-mra-used/
Sir iam from India how can I contact you. Is there any branch in India, plz reply
I have pulsatile plus ringing. Going nuts.
I have two tinnitus problem one is pulsatile tinnitus and another one is normal .and what is cost of it
Do ear infections caused the wooshing sound? Does water in the ear which leads to an ear infection/inflammation and pain cause the wooshing/ pulsating or is it two different things?
I've had CTA Brain & Neck and US Carotid Bilateral testing. Will those suffice for the MRA?
Please discuss this with your doctor as this is out of Audiologist's scope of practice.
Can both veins and arteries be seen on 1 MRI test? Dr sending me for MRA, and wondered if no contrast injection? Also wonder what many causes start PT , if possible nutritional deficiency. Noticed when increased vite C and E foods, and magnesium foods, PT has lessened slightly.
Hey 1aliveandwell, you asked some good personalized questions here. My answer depends on more information that I do not yet know about your history. Feel free to contact our team via email and we can do our best to help you. Our email is contact@treblehealth.com
They did a lumbar puncture on me four weeks ago because of a papilledema on one eye and I've had both high pitch tinnitus sounds and what I think is some sort of pulsatile low frequency humming since, it's driving me absolutely insane, I had no problem prior and really need my silence, that's why I moved out to the countryside several years ago...
They don't care and says it probably goes away eventually... I feel handicapped by this. Voices sound metallic as well, and music can sound really weird too, like the speaker is broken, so some sounds come out distorted. I first partially lost hearing in one ear the days following the lumbar puncture, but it came back and the only thing they've done since is an audiogram, which was fine
Does anyone know blood test results? Anyone deficient in anything?
Hi doctors! I have a question 🙃 you guys speak about finding the caused for pulsatile tinnitus, you also mentioned seeing a mostly young women with blood flow related issue causing this. My doctors ran a bunch of test already and found nothing on an MRA and CT Scan. If you want to improve the blood flow in the brain is there a way to do it? Or what would be other causes of PT? If nothing was found on the tests?
Also thank you for the great explanation 🥰
Same here. What I noticed if I am dehydrated or drink coffee too strong it triggers it. And if I take liquid Gingko it improves considerably. Also exercising.
I wonder if manual lymphatic drainage would help to get the blood flowing.
this all started when I wore a headband to bed!