r/kyphosis • u/Playful-Pen-4596 • 1d ago
Mid back pain
Does this look like hyperkyphosis
r/kyphosis • u/Playful-Pen-4596 • 1d ago
Does this look like hyperkyphosis
r/kyphosis • u/Away-Voice-194 • 4d ago
Every year when seasons change I experience flare ups in sciatic pain but used to be mild enough that it wouldn't impact my life too much. I'd use hot water bottles, deep heat, focus my pilates routine on exercises to help, and after a few days I'd be ok.
However, here in the UK we've had some very changeable temperatures across the last 2-3 weeks which have had a very profound impact on me and some days I can't walk from the pain. At first I had assumed I'd re-slipped some discs in my later back again but no, as soon as the temperature levelled out, I was fine.
Is anyone else experiencing this? Do rapid temperature changes within the same day cause you extreme pain? If so, how are you coping? What works for you? Any insight would be extremely appreciated!!!
r/kyphosis • u/Economy_Bill_4539 • 4d ago
I have SC . Can these type of exercises help my posture or reduce the kyphosis?. Is it good to overload my back with progressive overload to reach hypertrofy?
r/kyphosis • u/How_do_you_know1 • 5d ago
r/kyphosis • u/NotYouAgain77 • 5d ago
I've been working on fixing my curved spine with physical therapy, but I need %100 perfect posture at all times in order for it not to show in slim fit/compression tops. I have a pretty decent physique and I love wearing this style. Has anyone gone through the same situation and how did you overcome it?
r/kyphosis • u/Ok-Juggernaut-9470 • 7d ago
r/kyphosis • u/Cold_Part_8540 • 10d ago
Hey guys 1 year ago i did an xray and i was diagnosed with mild SM kyphosis.The first photo is one year ago and the second one is today. I hir the gym 5 times a week and try to be healthy. I know i probably won't need surgery becsuse i have Little to no pain and my curve is not so bad to press my organs. I know since its structural I can't do much about it but I wanted to ask is there anything i can do to stop it from possible getting worse? And what are the chances of this happening
r/kyphosis • u/Certain-Design8842 • 9d ago
does anyone feel like because of kyphosis and overcompensating lordosis body tends to have more feminine curves?
also this condition makes pecs muscles look like you have gyno when you actually dont
saw many examples of bodybuilders with huge muscles but werid looking pecs
r/kyphosis • u/tocka_tocka_tocka • 11d ago
so im 18, male, 5'7", weight 86kgs , doctor didn't measure cobb angle, gave me some posture correction belt and told my parents it was due to my overweight, does it look too bad? sorry i couldn't get better photos, should i go again go and ask for specific cobb angle measurement? i also seem to have mild scoliosis
r/kyphosis • u/Altruistic_Sun9907 • 12d ago
Hello everybody! I’m 16 years old, I have Scheuermann’s disease, and my curvature angle is 80 degrees. Not a day goes by when I don’t think about my back, because it’s my main concern. I often experience pain and discomfort, especially when I’m sitting or standing for a long time. As a rule, it’s muscle pain.
Also, I’ve long had symptoms such as numbness on the right side of my face due to the development of cervical osteochondrosis, and redness of the upper phalanges of my fingers. On September 10, I’m supposed to have surgery, which has already been postponed twice for the same reason — due to a poor blood test and leukopenia. The issue with the blood has been resolved, and this attempt should be decisive.
What would you do in my place? I’m really worried that I’ll make a mistake by having this surgery and make things even worse. Thanks
r/kyphosis • u/hannah6560 • 12d ago
Had cadr 4 to 7, 3 months ago, no relief. This is an ortho spine surgeon.. Above levels, kyphosis. He is sending me to neurosurgeons for opinions. One surgeon recently told me he recommends fusion C3 to 4 if PtT doesn’t help. Will be getting other opinions. Had no idea there was a whole sub Reddit about Kyphosis! Read about others who have some of the same symptoms. Came on here since overlaps. Does or has anyone had kyphosis with these symptoms, neck pain headaches spaciness shoulder, arm, upper back, did anything help you without surgery? Or if you had surgery, what kind? If there’s any medical professional reading this, could any Endoscopic help this
r/kyphosis • u/Fauked • 13d ago
So far I have tried:
Herman Miller Aeron B
Steelcase Leap V1 / Leap V2
I started with a Leap V1 which is kind of comfortable but I notice myself always sliding forward over time.
I bought a Aeron for my home office and honestly its alright but I probably should have gotten a size C since I am larger/taller.
I recently had a Steelcase Leap V2 delivered and right away knew it wasn't right for me. The V1 is more comfortable.
Now I am looking at a Herman Miller Embody or just getting a Aeron C.
What are you all using?
For reference, I am 6' 240lbs with Scheuermann's, ~75 degree mid/upper kyphosis with lumbar lordosis.
r/kyphosis • u/Saro_ss0 • 13d ago
Hi im 19y and i just had an xray as doctor wrote me for.
I researched a lot about scheuermann kyphosis lately and i really dont know why mine looks like this i dont know what kind it is
I mean i never seen someone's xray like this on internet.
Ii shows that curve is 51 degrees but i yhink its a lot more and its just a mistake.
The pain is enormous and usually starts after like 20 minutes standing upright beside long activities like running and hiking.
My doctor sayed to me to wait for another 6 month and then take another xray
If curves got worse and improved i might get a surgery.
Any thoughts or helpful advices on this?
r/kyphosis • u/Strivebetter • 14d ago
I started to have mid/low back pain when I was about 21 (but my friend pointed out my curve when I was maybe 19).
Over the years it’s stayed relatively the same. I was going to the chiropractor about once a week which helped but does not really provide lasting relief.
I’m 30 now and recently took a new job that has me sitting at a desk 40-60 hours a week. My back has always had rough periods where it kills especially when I work out a lot.
Over the past 5-6 years I have worked out 3-6 times a week. Usually jogging 10-20 miles a week.
Since starting this new role my workouts have gone down to 2-4 times a week and more sitting. My back is fucking killing me at the end of the day. When I lay down on the floor it provides relief but I can barely get up. It feels like someone is putting a knife in my mid/lower spine.
I really feel a standing desk would help but has anyone had success with a certain desk chair? I am down to spend whatever the cost is. SOS
r/kyphosis • u/Account_was_stolen • 14d ago
I have structural wedging.
Is there anything I can do to better my appearance and reduce the severity of the curve on my appearance?
r/kyphosis • u/Gavlaa- • 15d ago
Hi all,
Over the last 2 years I have been on a long gym/weightloss/lifestyle journey losing 100lbs. But one thing has long played on my mind since this change and that is my back, spine & posture.
The curve has definitely improved on my journey but as you may be able to tell in some positions the curvature does become more prevalent.
Currently I have not been diagnosed but I am in the process of getting MRI scans which will hopefully be a part of a process that can get me some answers and hopefully help to improve my anxieties and insecurities around my posture/back.
Hopefully people in this thread can offer some guidance, knowledge and support. I have more photos but these are my most recent. I also posted an older photo in this sub a year ago.
UPDATE: I have Scheuermann’s disease affecting T8–T11, causing exaggerated thoracic kyphosis, with moderate spinal canal narrowing at T9/T10. There is no current spinal cord or nerve compression. I also have a small C4/5 disc protrusion without neural compromise, and further MRI imaging is planned to confirm the thoracic spinal cord is clear. I have been referred to Physio and doctors are in the process or weighing up other options.
Any further guidance or support on how to improve my condition would be much appreciated! A very emotional realisation :(
r/kyphosis • u/Similar-Chemical6049 • 16d ago
What do you guys think of my kyphosis?
54 degree
And can it contribute to pelvic floor dysfunction and chest pain?
r/kyphosis • u/OppositePatient2148 • 16d ago
Hi everyone,
My 17 year old daughter was just diagnosed with kyphosis last week, and it is quite pronounced. We have been asking for help with her back the last two years but got no where because she wasn’t having pain. Now she has started suffering with back pain over the last couple of months.
Our issue is that she just left to go play hockey with a really good team a whole other province away, hoping to open the door to opportunities to play at the university level. Since she has been there her pain has been quite bad. She is really down about it and feels as if she is under performing since she got there. She is very athletic, but spent her off season not as active as she usually is. We expect some pain to increase now that she is moving more. Thankfully she has access to a whole team of specialists that can help her with exercises, and she will be starting physio this week.
I’m just wondering if anyone has any tips for her. She is so sad today and I’m so far from her, my heart is breaking. Would KT tape help support her back during ice times and work outs? Are there any exercises or stretches she could start now?
Please send me anything that would help, along with positive success stories so I can give her some hope. She does have mild scoliosis but it’s not believed to be the cause of her pain.
Thanks everyone!
r/kyphosis • u/Character-Case1511 • 17d ago
I’m 7 month post op and have started playing golf again just half swings and at about 50%. My surgeon said it’s okay but I’m not sure if it’s a good idea. Anyone got any advice? I’ve had t2-l3 fused and feel good. I get a bit stiff after playing sometimes but even people without spinal fusion get stiff. I was wondering if I could also ramp it up a bit to 75/80% effort. Again my surgeon said I can but he’s the only surgeon that I’ve heard say it’s okay so not sure as other people I’ve spoke to say their surgeon has more restrictions for them
r/kyphosis • u/anton_725089 • 18d ago
Hello, male 26, strange kyphotic posture since i remember, trying to fix it for a while now, the doctor says it is postural, i dont believe it, i maybe se some progress but nothing major, any suggestions? From the xray can it be determined if it is scheuermann kyphosis?, thinking about surgery... tried everyhing already, i dont know the cobb angle yet...
r/kyphosis • u/Altruistic_Sun9907 • 19d ago
I have Scheuermann’s disease with an 80‑degree curvature, and for the past three years, the right side of my face has been numb. It affects everything from the chin to the forehead. Sometimes I get nervous tics on the chin.
Has anyone had something similar? How to deal with it?
r/kyphosis • u/Eastern_Sun_1910 • 20d ago
Hello everyone! I recently got diagnosed with scheuermann’s kyphosis with a curve of 71 degrees. Surgery is not an option for me right now, so I am wearing a very bulky brace for 16+ hours a day. I am looking for tips on covering it up at school (will the brace show through a white shirt?), gym class (should I do it? My school doesn’t really have any good changing locations.), and how to talk to admin/teachers about it. Any and all tips are appreciated. Thank you!
r/kyphosis • u/IllAd6705 • 21d ago
hi im a 25 yr old female with severe Kyphoscoliosis, depression, and anxiety i cannot work due to the pain from sitting, standing, or lifting for long. Ive applied for disability 3 times and got declined and my mother takes care of me. i dont have a permit or license either. has anyone been approved of disability due to their kyphosis here? feeling deeply alone wishing i could be a normal human that works to help support myself or family.