A list of puns related to "Lateral pectoral nerve"
Any assistance or advise is appreciated. Is this normal? I had an internal mesh βbraβ inserted to aid the implants and maybe thatβs effecting then nerve? My doctor says it will resolve in a week or two. Hopefully.
In the diagrams and images I'm seeing most do not label if the diagram is of the left eye or the right.
Iβve finally gotten my life set at 37 years old. I have a good career and done with the whole school crap. Now, I feel I have to βrushβ and find someone, so I can get married and finally have kids.
Iβm sitting on a clock thatβs getting louder by each tick informing me that βIf I want to have babies, I need to nowβ.
Also, having that conversation with the guy I match with⦠Are they going to be okay to want to be with someone like me who is in her late 30s and feeling as if I am rushing them. Are they even going to want me at that age?? I feel so stuck and I hate it.
Itβs so uncomfortable bringing those things up 1. Are you okay with my age? 2. How soon do you want to get married and have kids? I feel sick to my stomach each time waiting for their response, since I tend to get matched with guys who are a little younger than me. But these are things I need to know up front.
Has anyone ever gone through this and what did you do? How did it go? Am I too late in the game?
Idk⦠I just feel very ugly being in this situation.
****Let me clarify since Iβve noticed some comments about βI would scare the men awayβ. : I donβt ask them right away if my age is okay, clearly it is okay since these guys put forth in conversations. I am speaking to someone now and he is wanting to get married and have children. BUT he did mention that since my birthday is literally next week and that indicated Iβll be 38 makes it seemed rushed. THAT is when I asked him if he is okay with it because if heβs not I want to cut tiesβ¦ I just donβt want to down the line be faced with a guy who up and changes their mind because they figured out theyβre not ready for that after saying they are.
^ this is the part of the dating experiences for me thatβs difficult.
***For those with harsh responses on me being βhell bent on wanting kids even though every aspect of my life is going wellβ just because someone is doing well in life does not mean he/she does NOT want children. Thatβs a dumbest feedback Iβve ever read on here so far.
****I personally WANT them, so I can share that βWell lifeβ with them
... keep reading on reddit β‘So, while we were on holiday, my 3 year old managed to fall and break her lateral incisor. We immidiately took her to a local dentist who told us that it would most likely need to be extracted, but it could wait until we returned to our home city.
After returning, we first went to one dentist (she didnt do an xray) who likewise told us that it was impossible to save it and that it would have to be removed. She then recommended another dentist to us to do the extraction. We went there today, she also took one look at it and said it had to be removed (again no xray) then she applied local anesthesia with 2 shots to the gums and pulled it out.
The problem is that my wife is now wracked with guilt, she is certain that if she had gone to a dentist in her home country (japan) they could have saved the tooth. She has a pretty dim view of the local dentists already, but I have told her repeatedly that two separate dentists recommended it be removed and that the lack of a tooth is only cosmetic.
Can someone here confirm or deny whether it would have been possible to save it?
Thanks.
I learned this from Andrew Huberman, Ph.D., a professor at Stanford who studies how vision and our brains are interconnected.
For some history here, I first noticed this during my freshman year in college. Honestly, I just thought I was sleep deprived. It didn't bother me or stick around long enough to make me look far into it. Just a few Google searches, where I then realized I couldn't find anything. I'm a white, 20 yo male, 5'9" 148 lbs. I have dust and some pollen/grass allergies as well as migraines, but not taking any medication besides ibuprofen/zyrtec as needed. Near sighted, contacts and glasses. Otherwise pretty healthy. This has been going on for over a week.
Basically, whenever I move my eyes laterally, I feel this sort of dizzy feeling on my left side. It's sort of under/behind my left ear, sort of where your mastoid muscles meet your skull. Sometimes I feel the sensation down to my arms or chest/neck area. Interestingly, I can also feel a sort of twinge of the muscle in that area whenever I move the eyes, again, where I think my mastoid is/behind my ear. The sensation is much greater when I move my eyes to the left rather than the right. As far as I can tell right now, I don't feel it on the right side of my head, but I recall feeling it down my right side similar to the left in the past.
The sensation doesn't hurt, but it's really starting to aggravate me. Interestingly, it began happening during a more stressful time, just like it did during college (I just started a co-op for my degree, changed my sleep schedule, started working out more frequently).
If anyone has any thoughts, please share. Thanks!
Haven't been able to understand this question. I answered contralateral (answer is ipsilateral) because I assumed all corticospinal fibers decussate at the lower medulla.
I've had pain on the top of my foot (midfoot) for going on three years now. It's accompanied by pain in my outer (lateral) leg starting about 3" above my ankle to about halfway up towards my knee. When I tap on the area above my ankle I get shocks down into my toes. Sometimes the foot and leg area feel numb, sometimes it burns, sometimes it's just painful. Sometimes it hurts while running, sometimes after. Sometimes just later that night while I'm laying in bed. It's capable of keeping me up at night. The pain is hard to describe.
One year ago I posted this:https://www.reddit.com/r/ultrarunning/comments/7f5612/my_ultra_running_injury_has_several_doctors/
The pain came on suddenly in a 50k in 2016 and it's never went away. Photo of my swollen foot the day after the race here: https://imgur.com/a/fhAbB Where the swelling was I now have a bony protrusion. Here is a photo of the marked protrusion location over two years after the injury: https://imgur.com/a/MSxGO59
A previous poster suggested it could be an exostosis. A doctor suggested removing it through surgery but I declined at the time. I've seen three doctors, had Xrays, done PT, taken time off, no progress. A PT said it appears to be my superficial peroneal nerve. At the time I was running about 60 - 80 miles a week. Now I can manage 15 but the pain will keep me awake if I run more than an hour during the day.
I'm still not sure what's going on. I was originally misdiagnosed with extensor tendinitis. Although I am beginning to think it's a combination of things. Whatever happened onset suddenly. There was swelling and top of foot pain during the race. Now I have a bony protrusion, along with a lot of nerve pain, from the outside of my lower leg down across the top of my foot. Massage on the lateral area of my leg produces intense pain and shooting nerve sensations into my toes.My foot feels stiffer and less flexible than my other foot. It doesn't feel as strong.
I'm thinking I might have a peroneal neuropathy, possibly due to an exostosis on the top of my foot, or possibly due to pressure in my outer leg. I haven'r ruled out compartment syndrome playing a role. I am not sure where to go from here. Should I see a neurologist? Get a nerve conduction test? Stop running permanently? Get a third round of Xrays? Has anybody dealt with anyt
... keep reading on reddit β‘I'm about 2.5 years post-op (patellar autograft, ACL only), and generally pain free. However, after I run I get a lot of pain in the area to outside of the big patellar scar. It seems to be the same area where the doctor explained the nerves are disrupted/cut so there's no feeling to the touch there. After I run, I get sharp pain when I bend my knee past 90, and also sharp pain to the touch. The longer the run, the worse the pain after, and it usually subsides after an hour or two. I searched a lot for this and couldn't find anything, so I was wondering if anyone has experienced this before or any ideas on if it could be nerve related.
ps also have really bad shin splints in my surgery leg and pain when I press on the tibia.
I have this pain on the lateral elbow when pressing, it's a sharp shooting pain, nerve like feeling, localized, it doesn't radiate or send "electricity" through the arm. It hurts when the elbow is about to be straight but only when the forearm is pronated. It's hard to pinpoint the site, I feel it laterally to the triceps tendon above and posterior to the lateral epicondyle but I also kind of feel it on the anconeus zone...
This may have started some months ago with weighted dips, which I'm not doing anymore, but in hindsight this also kind of started at the time I begun to do reverse wrist curls which I'm still doing. If I warm up the sensation is hampered but later it flares up some. Is this some kind of entrapment or is it inflammation of some tendon of the forearm? I know this is not the place to get a remote diagnosis but to get checked by a professional would take 2 months or so and I would rather take some measures now to prevent further problems.
They get right up my nose.
Not sure what I should be doing day to day. Iβve been out of work for months because I am unable to walk. I get some housework done everyday but am bent over in pain after a short amount of time for the rest of the day. The more I push through and stay active the more pain I am in at night. How much rest should I strive for? Everything I read is bedrest is terrible, but aside for the first 30 minutes of my morning my body refuses to stand straight. No scoliosis here- itβs frustrating when people say well you have to focus on your posture. Thatβs fine but what do I do when my body betrays me? (Reposted from /rbackpain to here after finding this sub.)
Hello everyone,
I wanted to post something online to help others with my condition help to learn for themselves where they stand and what they can do with the site they have left.
I have a condition called "Bi-Lateral Optic Nerve Hypoplasia with Nystagmus being the side effect.
What I have doesn't impact my light perception, but instead impacts my visual acuity as the Nystagmus prevents my eyes from staying on a fixed point.
As a result, I see, but I have no way to capture an object in the center of my eye to see it in higher detail.
The ONH is what causes my Nystagmus. The ONH is also what blocked me for 30 years.
Doctors have said there is nothing they can do because of the ONH as the issues isn't with my eye.
Below is a short explanation of how the optic nerve works from Wikipedia
Link: https://en.wikipedia.org/wiki/Optic_nerve#Function
Function
The optic nerve transmits all visual information including brightness perception, color perception and contrast (visual acuity). It also conducts the visual impulses that are responsible for two important neurological reflexes: the light reflex and the accommodation reflex. The light reflex refers to the constriction of both pupils that occurs when light is shone into either eye; the accommodation reflex refers to the swelling of the lens of eye that occurs when one looks at a near object as in reading (lens adjusts to near vision).[1]
The eye's blind spot is a result of the absence of photo-receptors in the area of the retina where the optic nerve leaves the eye.[1]
I have no issue with light perception, but my eye movement keeps me from seeing in great detail.
It's like trying to pick apart an image that should be in 1080p and instead it's in 240p.
I know I'm not accurate in what I'm saying for everyone, but this is the best way for me to explain where my vision stands.
They ignored me for years until I took steps myself to try and resolve this.
I worked with a doctor to try and look into bioptic driving.
That didn't pan out, but I did learn something.
My vision can be corrected.
I learned that I can use contact lenses to force my eyes to look at the corrected portion and that did help to sharpen the vision.
I then looked into my condition further and that's when I found this.
This is an article on treatments for Nystagmus using medication instead of surgery.
Link: [http://webeye.ophth.uiowa.edu/eyeforum/tutorials/Nystagmus/](h
... keep reading on reddit β‘I had a few studies made and turns out I have olfactory nerve damage from Covid and some neurologists and ENTs told me there's basically nothing for me to do other than wait and pray
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