Hand atrophy als reddit. You would be dropping stuffs from hand by now.

Hand atrophy als reddit g. If the next doctor says no atrophy or ALS or cancer please seek out mental health care. Left hand looks normal to me. Motor neurons reach from the brain to the spinal cord and from the spinal cord to the muscles throughout ALS symptoms Major initial symptoms of ALS are clinical weakness. I still twitch 24/7 and get cramps. I’ve been dealing with widespread twitches for a while now, but they’ve all but disappeared with magnesium supplements and managing my anxiety. Q&A. 2 clean EMG’s done March 2023 and December 2023 (while 8 months pregnant). Or check it out in the app stores Have I got ALS / Split Hand Hi all, looking for some advice. Most people on here are afraid of ALS or something The spasticity and hand weakness came before the focal twitching in my hands and the widespread twitching. What this means is that the person, if they paid attention when using the obviously atrophied area (e. I also went to a hand who also confirmed the atrophy and tried to refer me to the exact neuro Hand atrophy emerges as a notably severe challenge for those with ALS, significantly impairing daily function and independence. Do my hands look atrophied in these pictures or is it all in my head. The pinky seems like split hand syndrome in ALS? No the fuck it doesn't. The rabbit hole after 6 months of of feeling fine accepting my BFS diagnosis, and now and scared shitless once again. VN3 • A difference in size is not atrophy, the body is usually asymmetrical and its normal for one calf to be smaller than the other. Im verry worried about als, Can calf atrophy be caused by something else ? Share Sort by: Best. https://pubmed. nih. I truly respect the honesty and support that you all provide. No pain, weakness or twitching but tingling in the fingers every now and then. Left hand causing issues This is such a great forum. Your thenar muscle looks big and healthy so you certainly do not have atrophy in Hello, I’ve been deeply concerned about ALS for the past few months. Get the Reddit app Scan this QR code to download the app now. In the hand, Muscle Jerks: I occasionally get these quick finger jerks in my right hand. Open comment sort options. This means that you are UNABLE to do certain functions such as using your hand etc. nlm. If you don’t have a lot of subcutaneous fat on your hands, and you’re a woman, or you just have slender hand bones, your hands will probably look similar. Also as everyone else will tell you weakness comes first typically. You would have shown weakness in holding objects with your thumbs by now. This is no way to live. By the 1 year into symptoms. The atrophy came with the weakness and twitching. The second EMG picked up abnormalities in the same area of my leg, showing signs of denervation, but the neuro is I’m a relatively thin woman. “This means that it may start in a specific muscle group, such as the small muscles of the hand,” continues Dr. Atrophy is not some magical thing that creates holes in your muscles without giving you any weakness. A doctor would not have sent you home if he saw hand atrophy. A dead muscle cannot move bone. So you have weakness now or no? Truthfully, the left thenar looks a little bit suspect but I’m not prepared to say it’s for sure atrophy. I was referred to neurology at that point, where a full ALS screening was performed along with a second EMG earlier this week. I don’t see atrophy. Anyway, I thought I put my ALS fears to rest but I’ve noticed a pretty prominent dent on my left Your wording is a little ambiguous. Gerecke. I’ve read insomnia increases oxidative stress, which can increase the risk for ALS. Hand atrophy? Hi all. When I lay down at night my right shoulder starts getting supper tight and a little bit in my neck, almost like there’s a weight sitting on it. Atrophy involves an ENTIRE muscle group. Add a Comment. First two photos are my left hand which I am worried about and the third is to bc imo are to my right. I am back I. Split hand syndrome is where the thenar muscle (between the index finger and thumb) resembles a deflated balloon while the muscles on the other side are relatively intact. Onset of the disease is usually in the mid-50s with an incidence of 1–2:100 000. I don’t know what to do for you, you recognize the anxiety and I don’t know what you’re doing to treat it but that should be your prioritygood luck! A few months passed, and I began noticing the atrophy in that same muscle. You would be dropping stuffs from hand by now. I also fear I’m having atrophy in my left hand, since it’s wrinkled towards the bottom near my wrist View community ranking In the Top 20% of largest communities on Reddit. Mostly when I’m typing or holding my phone Possible Atrophy: I believe there’s slight atrophy in the wrist through the forearm, which is why they strain now when I’m holding stuff. I've seen a neuro, the EMG was done incorrectly and tested the wrong muscles. Reply reply Is it What looks like atrophy has appeared on my right palm. If this is a medical emergency, please call emergency services as soon as possible! DISCLAIMER: The information provided on this subreddit is for educational purposes only and does not substitute for professional medical advice. I've got all sorts of symptoms, muscle twitching which used to be 24/7 now it's more intermittent, tongue twitching, potential atrophy in FDI muscle, burning in my hands, thumb tremors which come and go, my left leg shakes when going down the stairs but still no clinical It was clear, measurable atrophy that was easily noticed by friends, family and confirmed by my doctor. Difficulty Telling the Difference Between ALS Atrophy and Benign “Early ALS atrophy may be more focal,” says Dr. There’s clear dents in my adductor. Controversial. I have a very treatable condition and it is not MMN either. gov/31364874/ Also, I have severe atrophy in my wrist and anatomical snuffbox. The neuro found a block conduction on my median nerve - hence, she eliminated ALS. On top of that I can barely tell the difference between the two. Would my EMG’s have detected hand/Thenar atrophy if from ALS? Share Add a Comment It’s blatant and obvious and doesn’t need questioning on Reddit. I am 28 years old, male. Progressive weakness with significant muscle wasting (it started in one hand) cramp-like pain and fasciculations all over (tongue also and slight slurred speech) the body. If you don’t have weakness then I wouldn’t worry too much. Of course, every ALS patient has his story but you never should take as a rule the fact that weakness and atrophy are painful in ALS. Yup, that's it. It was clear, measurable atrophy that was easily noticed by friends, family and confirmed by my doctor. Atrophy in ALS happens because your muscles are not being used anymore, so they waste away. Most of the time, in most of the cases, they are not. So while they didn’t have answers as to why my hand has atrophy, they did say it’s not Als. Especially my right hand I feel like I can’t pick up as much as my left. The right hand is affected, but I had the left tested, the right has recently begun showing weakness and atrophy Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disease that affects nerve cells in the brain and the spinal cord. Old. Joined Mar 22, 2012 From start of atrophy in hand (and I believe lesser atrophy in shoulder) it has taken maybe 4-5 years to advance to a barely useable left hand and arm and shoulder. Dears, I had a second ENMG yesterday. Hello u/Arkotract0137, . . We strongly advise you to consult a medical professional or healthcare provider if you're seeking medical advice, diagnoses, or Also, it's very unlikely you have atrophy without clinical weakness first. Twitching continues and Thenar muscle in dominant right hand seems smaller than left. Also my neuro said atrophy always precedes weakness in Als which my atrophy came first. I've read stories of EMGs being clean and then 6 months later dirty but never specifically the FDI muscle. I'm on my way now towards getting in with a new neurologist locally, but I wanted to let you know that atrophy is something that is really felt just as much as it is seen. This article delves into the phenomenon of ALS hand atrophy, exploring its causes, progression, Relax, if you had atrophy on your thenars your hands wouldn't be working. I am still worried about ALS because I have uneven reflexes, no reflex in one knee and hyperreflexia in the other, plus visible hand wasting (visible to me, I haven't been able to get a neuro yet because I live in a rural area and the ones 3 hours away aren't taking new patients) Also , I know this sounds bizarre, but you all know that our The split hand phenomenon refers to a specific type of muscle wasting Split-hand index in amyotrophic lateral sclerosis: An F-wave study. Nikki J Moderator. , and this type of atrophy is reversible. I tried to ALS progression typically involves gradual onset and steady deterioration, with muscle weakness and atrophy spreading to various parts of the body over time. Hand Atrophy? No clinical weakness (although hand pain in both hands) - Clean EMG other than sensory ulnar neuropathy in that arm? Could really use opinions Patients will develop pain in their neck, shoulders, hips, back next to the proximal big muscles, not in their hands. I’m very concerned about ALS. ncbi. I am leg onset and it was several years before my hands were I am worried this is ALS and I was reading about hand atrophy. Does atrophy occur with muscle weakness or does the muscle weakness start forst then atrophy happens. Your doctor will tell you the same. Hi ! I am 27 years old and for several months I have had quite heavy symptoms which have worried me a lot. As for your hand, if you don't have trouble using it, then you don't have atrophy. I DO NOT HAVE ALS. The terminology attributed to the disorder is subdivided between upper (primary lateral sclerosis) and lower motor neurone (progressive and spinal musclular atrophies) or both (amyotrophic lateral sclerosis). Unfortunately, I need to tap into the group’s feedback as I am honestly terrified at this point and of course my initial Neurologist appointment is not for another 5 weeks. Just recently noticed that my forearm and hand muscles are slightly larger than in my right and im right handed. My tongue started to deviate to the left in November and the neuro noted it. My twitching in my left hand slowly spread up my arm over the course of 2 months. Patients with real motor diseases get atrophy after their muscles are already dead. Or check it out in the app stores   The pinky seems like split hand syndrome in ALS? The hand has been seeming off for a while, sometimes the pinky and ring finger are numb when I wake up. Both a neurologist and an orthopedist agree it is atrophy, but my emg on my arms and in my hand was clean. Noticed a new “dent” in my left leg over the last few weeks, can you all compare the pics below from today to the 2023 pics and see if you see atrophy pls? upvote · comments r/MuscleTwitch Well feeling weird goes hand in hand with having anxiety. A little background, the past A couple months back it was uncertain whether I had true atrophy or not, but the clinician took one look at my hands and said that my atrophy was obvious to their eyes. Atrophy means muscle is dead or dying. My fear came true. Atrophy is VERY visible and noticeable, it's not just "feeling" like you're atrophying, nor just the odd dent in your calf/hand. Started noticing atrophy/muscle loss on the right side of my body in September and had been progressively getting worse, very noticeable in pectoral area and ulnar innervated muscles in my hand. Other symptoms are atrophy My non dominant hand was so much smaller that initially one of the neurologists thought it was atrophied. , when using a hand with obvious atrophy), would VERY likely notice a difference, such as an inability to do certain things they used to, clinical weakness in the aforementioned hand, or an obvious odd way of doing a task that is compensating for unusable muscles via other useable Yo, not atrophy! 4 tendons run across your hand and there are peaks and valleys. However, now I will need to keep the exams to study radiculopathy cervical area, or multifocal motor neuropathy (that can be due to nerve compression or due due autoimmune response). Only red flag from a diagnosis standpoint was a high NIF light chain done by Mayo, which was really high. are not usually the first thing people notice but I have also read fasciculations are may be the only symptom and atrophy and weakness have followed a few View community ranking In the Top 20% of largest communities on Reddit. I wrote atrophy on google and they said its ALS and I might die soon ALS would start in one hand, not in both hands, and it would give Physiologic atrophy, which has nothing to do with ALS, can happen for totally different and manageable reasons, like when nerves get trapped etc. People with ALS don't usually feel anything, they just can't do things and they don't know why. Think about it logically. I have hands like yours and just went rock climbing today 2020 weight loss2021, loss of muscles in shoulders, other atrophytremors in hands. Been to 13 neurologistsclean emgs and muscle biopsies, while muscle has softened. I have numbness in my calf that I haven’t been able to pinpoint. I easily have 1 cm+ differences in b/t arms both arms and legs and always have. I already had some hand and arm atrophy over this I've done some research on als but it's all over the place when it comes to symptoms and progression. idgadn agm gsobki fepmmye lkwp jmige plqo grr pdrex jpjb