very encouraging

I need NeNe Leasks surgeon is this in Atlanta Ga

Can this causes cough syncope type of episodes? My dad has recently been suffering from 15-20+ episodes where he suddenly starts coughing and then faints for 10-20 seconds, sometimes upto 2 min. It can also occur when sleeping, talking or just sitting watching TV. The doctors suspect Nervous system disorder & have determined it’s not epilepsy or seizures. He’s working on a referral to Mayo Clinic now. And I’m researching as much as I can to try to find an answer.

Dr. Shah is a great resource for people who have been struggling with these conditions . I know that because I am a patient that can attest his ability to do amazing work.

I had a near life ending accident which involved a multilevel fusion T3-T8. Severely fractured sternum and multiple broken ribs and a mediastinal Haematoma. This was 3 1/2 years ago. I complained of shortness of breath and it has been gradually getting worse. I have now been diagnosed with both Phrenic nerves severed approximately around the level of my heart. I live in Australia and I cannot find anyone that does this repair. I am very concerned as the atrophy is getting worse and where I will end up breathing wise.

Dr. shah did this surgery on me and I’m 10000% better because of it

I reversed the pain and numbness of peripheral neuropathy with zinc 14 mg per day in 14 days.

what were the symptoms what was the procedure what do you experience now

I'd love to have a surgery to get rid of my pelvic pain...

i have those eyes since... forever. Its been my biggest insecurity since childhood but it is a family thing and I don't have any medical problems with that.

My injury happened in april 2018. Had nerve transfer surgery within time. Pain is still there however its less severe. I got part of my arm working.

What the hell is a plastic surgeon doing operating n this nerve? My perineum doesn’t need a facelift

My lil bro's back head started hurting randomly from 4 days ago. And it hurts in random times like if move very fast or shake. Please help me...

I was just diagnosed with this issue on my right lung. The doctors where I went told me there is nothing that can be done. My diaphragm does not move all, up or down. I was surprised to find there is a pacemaker for this. Has anyone had that procedure done?

Hi I’ve been watching a lot of your videos I’m from Los Angeles California do you guys recommend anyone that may be able to help me I’ve had foot drop for a long time now i damaged my peroneal nerve and got a nerve graft from my sensory nerve and I haven’t been able to do anything nothing happened I just gave up but every time I watch your video I get hope you guys might get me back to running ❤

Aside from pain from sitting did you have terrible pain after bowel activity? Thank you very much for your testimonial.

🤡

here it is june 2024 i'm suffering every day from this. i been begging the drs to help me. such a long process to get help. burlington vermont is where my dr is.

How could I get help for the bad headache cause I got many sleepless nights

That's not gender affirming, it's gender DENIAL! And no, she didn't transition to a man, she just mutilated herself.

I'm going though this right now in Alaska.

I’m so happy you finally found someone t9 help you. I’m in Perth Australia.. not one doctor wants to do surgery on me. They tell me it’s not operable. For what reason I don’t know? Still mystery to me.

Is the surgery invasive? Do you have to shave away hair? Where is the Dr. In this video located and is insurance an option... I'd love to know this before calling

What surgery is this?

Ive been offered cryoablation, before trying to get my Kaiser insurance to pay for pudendal nerve decompression surgery. I've had two 100% successful nerve blocks done at the ischial spine. He wants to do a block at the Alcock's Canal, then treat there. But that's distal to my previous blocks AND to the most common entrapment location for that nerve - the spot where the sacrospinus and sacrotuberous ligaments cross. Apparently all ablation types for treating pudendal neuralgia get done this way. This doesn't make sense to me, and I can't talk to this doctor until the day I fly there for the block. What am I missing? I'm an Electrical Engineer who spent my career in Silicon Valley developing novel medical devices, including implantable defibrillators and RF generators for performing ablation procedures - which is what i was expecting to be offerred. BUT - if that block doesn't help, wouldn't that verify my nerve issue is proximal to the canal and is likely trapped between the ligaments? Pain started during a six month time period where I had to use a knee cart for a right leg injury. I tried the DRG stimulator, and have had my genitofemoral nerve and the perineal branch of my left pudendal nerve cut.

I feel like this is what i have but doesnt someone need to confirm this before i make any appointment?

I've been on carnivore diet for 10 weeks now my numbness in feet and toes is about 90 percent gone

Do NOT consent to this ‘treatment’….you will regret it. Search Four Corners Pain Factory on RU-vid

Thank you for this positive hopeful video since my daughter just had a similar surgery after a bad accident and we hope for the best recovery possible.

Im going through the same thing been a little over a year due to being in a a car accident and it sucks this video gives me hope now! Wearing the AFO sucks because foot starts hurting after a while im used to it but sick of it also

Just reading the damn name hurts me.

Will the nerve get compressed again after decompression? Seems like it will since its more of a result of his throwing/exercises.

If the nerve entrapment isnt at the Alcock canal why would the steroid work ??

Yes. So bad

If a sufferer on Medicare, the procedure is likely to be not approved.

Hello sir after vagotomy can reattached vagus nerve I had anterior Vagus nerve vagotomy Now i have only one vagus nerve But after i got many symtoms I think I'm soon die😢😢😢😢

Mine is genetic… inherited from my dad I was born with it, unfortunately mine can’t be fixed, it’s ok I am coping ok with it…

ru-vid.comRIlw2nHtu8Q?si=gfV_q1P9c5h6jx-j At 18, I was diagnosed with AVN, the pain was unbearable. Miraculously, after 2 years, I found relief. Now, my AVN stage is 5 for the left hip and 4 for the right, with stable bone density.

ru-vid.comRIlw2nHtu8Q?si=gfV_q1P9c5h6jx-j At 18, I was diagnosed with AVN, the pain was unbearable. Miraculously, after 2 years, I found relief. Now, my AVN stage is 5 for the left hip and 4 for the right, with stable bone density.

Hello sir I am from India how can we contact you

Anyone who doesn’t understand how someone with pudendal neuralgia can actively wish for death, has never had pudendal neuralgia.

Funny, until recently I hadn't realized that Mario updated his favorite way to tackle ED and it's a relief! Although what he previously suggested was pretty good, it was a real pain to follow... I just go'ogled the latest in Mario's Thunderous Erections, it's so much easier and potent now!

Was the inside vaginal skin on fire? That’s what I’m going through. I had many vaginal infections in the last five years and now constant burning.

I had severe foot drop suddenly after prolonged kneeling and sitting on leg for hours(floor instalation) Initialy i had not lift my foot even one mm After 10 days i restored full range of motion but i noticed there is not full power like before,when i put weights around 10 kg's on foot and try to lift i only can do few reps Will my muscle power restore fully if i keep exercise? Now is 2 weeks when problem started,,range is there but power is not fully restored.

Hey I have occipital neuralgia due to an impact from a soccer ball to the back of the head and neck. I've been doing pt and nerve block, start medications soon for it. I''ve noticed some improvement but haven't made a full recovery yet. Is occipital decompression surgery only for people who are really struggling and can't do anything. I've had this for about 6-7 months now. I just want to make a full recovery and don't know when I will be able to do with my current strategies.

I have diaphragm paralysis from a fall at work. I was approved for L and I in Idaho. My fall was 1 22 24. I need help

I had tendon transfer in my right foot. I was walking to the side of my foot. Also drop foot from peroneal nerve damage right leg. Surgery was Dec 1 2023. Best decision I ever made. No longer have drop foot. Walk flat on my foot. If your considering it, go for it

I’m 22 in the UK and recently started getting this extremely bad. It’s been two weeks now and doesn’t seem to be getting better. It started off with a bad uti and the symptoms continue.. I’m scared I’ll have this forever. I’ve been trying to explain to my doctor I think this is what I have as every symptom I have ticks the boxes, but the doctors won’t do anything. Please help I need advice..

My cause of neuropathy is a TRAUMATIC BRAIN INJURY, and it is awful!! 😢. I find some relief from CBD oil.

Do people with this feel like their diaphram cant expand and heavy pressure. When i try to mediate and do diaphram breathing the pressure is intense when expand and feel like sets off autonmic issues as i feel dizzy and get overheated internal flushes and feels like sets of sympathetic response as panic and flight or fight is constsnt. Its lkke a constant grilping pain from neck to right side chest upper abdomen down mid adbomen. I am looking at surgery for TOs however i am thinking my other issues are related to phrenic nerve.