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Hi Dr Arun. I have monostotic fibrous dysplasia on my left proximal femur. Tumor is 4.7cm by 3.1 in the trochanteric region. Many scans and a Benign biopsy but the pain the past 14 months is so bad I can't walk much. My surgeon is "perplexed" she said it shouldn't hurt but... Pain wakes me. MRI next week "Again" Sick of using a crutch. The suggestion to have an op now but I was told the recuperation is tough and might not help the pain. I am 54 and extremely active my whole life without pain until now.

Is this surgery pain full or which is better i mean external fixator is more difficult to carry mange for me plz give us a easy way to get rid of this

Bone graft is full of side effects or not

I was there about two months ago with bilateral club foot with Dr. Dobbs and now I am having but I’ve been with him for about three years and I’ve been in the Paley Institute since I watched three load

First like

Please upload information with the patient's recovery process, 4 months have passed since the operation. Thanks

Such a great video. Sent it to friends and family who keep questioning us as to why we have to go to Florida with our daughter who has MHE. I feel so lucky and grateful for all the “preventive” surgery/care our daughter has received.

Hi Doctor.my daughter had her deformity treat as a baby too but now she complains of pains on the leg and the foot does touch the group completely.her heel is about two inches above the ground. Her case wasn't really a club foot but kind of having a likely shorter anchill tendon that restraint her heel from sitting flat on the ground.what can i do?

My husband has this, pain in his elbows and shoulders. He’s has several surgeries when he was a kid. He has his last surgery on his back of his upper leg, it grew huge and around his sciatic nerve, 4 hour surgery.

can this be done on both parts of the leg for more than 8cm of total gain?

I was born with mine and diagnosed at 25 or so. I'm 41 now. The past four years have really gone down hill. I am cane bound full time. I have grade 2 anterolisthesis which has caused lordosis, degeneration. I am barely walking. The neurosurgeon I saw recommended physical therapy. Yeah, it's probably not going to help.

Sir contact number please

Contact number plz

Gold standard of LL. just too expensive

Thank you so much for the information.

Great sucess from great surgeon

A Great nail in the hands of a Great surgeon.

Am from Ghana

please i need help

Thank you so much ❤

First 👍 and salute to all kind drs🎉🎉

Is it good for a person with MHE play sports

❤❤❤❤

First like, i hope you can notice my goal here for my disabled son. Ineed help to walk for the first time. Help him to walk, please.❤

I also have this so should I must do operation

Not helpful without showing the specific anatomy

All talk without pictures is not helpful. Just saying.

I have Multiple Hereditary Exostosis. My diagnosis was given to my mother when I was 2 years old. I have had over 20 surgeries removing growths . I have "knock Knees". I inherited this disease from my father, who inherited this disease from his mother. I was one of four children, and the only one who inherited this disorder. My right arm is 2 inches shorter than my left arm. My ulna in my right arm is shorter than the radius. When I was 23 years old, I had major surgery on my right wrist to align my hand into a normal position. I have 2 artificial knees. I was lucky as an adult, because I found orthopedic surgeons who believed me when I told him where I was in pain. My childhood orthopedist ignored my complaints. My daughter, an only child, has inherited the disease She has decided that she does not want to have children.. My daughter has normal length in both her arms and legs. I was born in 1956. I was diagnosed with Parkinson's disease in 2004. In September 2020, I suffered a stroke, while taking Eliquis, a blood thinner, morning & night. I am 5' 2" tall, weigh 105 lbs, and through extensive therapy walk with a cane.I suffer from left drop foot. I am thrilled to see that this disorder is getting the attention from orthopedic surgeons that will help children overcome the stigma that was shown to me, from both children and adults, throughout my lifetime.Thank you!

having this in the near future. Whatvques should i ask the surgeon? Is it fair to ask how many of these have they done ? Thx docs

He kind of sucked 14 years ago. I thought he'd be retired by now.

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Awesome video presentation more need to see this. Shared with thanks ❤

Very informative, thank you

he overcharges. it costs $125,000 for paley vs if you go to las vegas its like $85,000 with dr debiparshad

Iam 37 years old..I have 1st grade L4/5 lumbar spondylolisthesis due to L4 pars fracture with mild disc changes and dr recomended surgery Sympthoms are not much yet Do u recommend surgery now Is it the only workable way?!

Where is dr. Paleys institute

Thanks For this video...my son Mateo (10yo) have Escobar Síndrome and we search all the information possible. Regards from Patagonia-Chile 🇨🇱

My son is disabled and my aim is to take him to your hospital. I want to see him to walk for the first time. I hope you will notice my message.

Great Information thanks 😊

Im here again support watching from uk

At 2:20, he said it just took 'half an hour' for a bilateral femur surgery? That's pretty fast

First 👍 Dr, I wish you will notice my goal here. My son is disabled and my dream is to see him walk for the first time. 🙏 🙏

Thank you so much for helping me be able to walk now

0:27

Hi Sir, I'm from Denmark and 45 years old and I have MHE, although here they call it MO (Multiple Osteochondromas). I keep having nervepain shooting down my left leg and inside the hip joint with certain movements. I'm on pregabalin and duloxetin to deal with the nervepain and backpain around the pelvis. But i keep getting told it cannot be the osteochondromas i have in my hip areas. And i'm pretty concerned since i've been told that the risk of osteochondromas growing malignant is higher in hiparea and shoulder area (where i also have 1). My question is, if it's true there's a higher risk in those areas than others and if 1 controlcheck per year is enough?

👍 guys i wish you can help my disabled son who is 16 now , from uk. He is been neglected here. I want dr Mathew dobb to do the operation, unfortunately i haven't find the sponsor to help the fund. I hope you will notice my message here. Many thanks. Annabelle Attwood, im a youtuber too.

Que bendiciones tienen en otros lugares de estados unidos que ayudan para el bien de niños para que salgan a delante mientras en México pobresa desigualdad corrupción niños que tienen malformaciónes padres de bajos recursos sin poder Aser nada tener un gobierno que solo pide y no ayuda que daría por tener una gran fundación y hospital y apoyo de doctores y aportadores para estabilidad emocional de muchos niños con ganas de sobre salir y uno de esos es mi niño que es mui difícil pero no medare por vencida para que el siga adelante felicidades a todos estos grandes doctores en este tema triste

Cure?

Is it correctble at the age above 30 yrs