My husband was recently diagnosed with LAS after an ANOXIC/HYPOXIC BRAIN INJURY due to cardiac arrest/ cardiopulmonary arrest all from a stupid asthma attack. He was in a coma and on a vent for over a month and woke up blind. Unable to speak or move much. He is now speaking slowly but understandably, he can walk with a walker and gait belt and assistance in case the shakes knock him off his feet ..but he still can't see and that is the hardest part. It complicates what is already a really tough situation with the brain injury and LAS shaking and then not being able to see just....it sucks so much. I'm so thankful he is alive but as I sit here in bed with him feeling his body involuntarily shake as he rests and occasionally starts jerking heavily when he tries to move, it makes me so sad for him. Brain injuries are so hard to deal with. I feel like this whole medical crisis we had just stole our future, stole our current life and left us with a shell of what we had. Now he can't work again, I lost my nursing job because I've been with him non stop in the hospital and rehab facility and now home. There's no one else to help us and no one to step in and help care for him so it all is on me. I don't mind helping at all I am just sad for him. It hurts to see him hurting and not be able to fix it.
@NEUROLOGYMADEINTERESTING26 күн бұрын
We’re sorry to hear about your husband’s struggle with locked-in syndrome. It must have been incredibly challenging for both of you. Your strength and dedication as a caregiver are truly inspiring.
@dr.nishantsharma5415Ай бұрын
Patients are the best teachers. Thanks to this gentleman. Hope is doing fine now.
@phualeon1941Ай бұрын
I got it, but I'm slowly recovering..
@hashiaktar9501Ай бұрын
এই রোগের কি ওষুধ নাই
@lewflwefkmkm2 ай бұрын
Thank u
@NEUROLOGYMADEINTERESTINGАй бұрын
Welcome
@uwemichaelsteidel77662 ай бұрын
Ich habe diese Krankheit seit ca 12 Jahren lance Adams Syndrom und das ist nicht angenehm
@PetterNe2 ай бұрын
My body twitches A LOT all over at night, but far less so during the day. I have some sense of weakness but after one year of symptoms I am stronger than ever at the gym and also weigh more than ever. At 178 cm I weigh 103 kg and can bench press 150 kg. Does this rule out ALS despite me having a weird sensation of my throat collapsing and constant twitches at night in different muscles at the same time? (Even inside my ear)
@srinivasaraosirasapalli51042 ай бұрын
So nice,but whats the relationship of Marfa syndrome to syncope
@NEUROLOGYMADEINTERESTING2 ай бұрын
People with Marfan’s syndrome are prone to develop spontaneous pneumothorax.
@srinivasaraosirasapalli51042 ай бұрын
@@NEUROLOGYMADEINTERESTING ok got it.thank you doctor
@sunitadogra18622 ай бұрын
Same problem ha ky Karu pls bataye
@faxm90612 ай бұрын
As a resident neurologist i give my depest gratitude sir.
@mktech20423 ай бұрын
Plz try biotin tablet my Father suffering from dystonia seens 20 years and my fathers friend suggested biotin tablets.He was completely fine in one day. plzz plzz try it
@NgaNguyen-pz4pm2 ай бұрын
Where can you buy the biotin? Ty
@mktech20423 ай бұрын
Plz try biotin tablet my Father suffering from dystonia seens 20 years and my fathers friend suggested biotin tablets.He was completely fine in one day. plzz plzz try it
@NazimAli-ug3bo3 ай бұрын
Doctor, Bell's palsy ke bad hone wala HFS curable hai...plz reply
@aparnaappu55224 ай бұрын
Treatment?
@bramvanstraten88374 ай бұрын
Fascinating that this works
@NenehAgan4 ай бұрын
Thankyou!
@dranshumansahu61144 ай бұрын
Maza aa gaya sir
@user-tw9ts4yp5h5 ай бұрын
You should expect(in case of ALS) weakness in that part of body which have twiching or it isn't any corelation?
@tsegatesfamariam55945 ай бұрын
I have the same syndrome . How can i get people with the same conditions
@isakisak66895 ай бұрын
Thanks a lot 👍👍 have u Instagram?
@sitialimahtunsodiahchaniag40855 ай бұрын
diagnosis sir ?
@hozanziyad76735 ай бұрын
I think it’s right UMNL
@cmcampana75 ай бұрын
AMAZING !! THANKS !!
@lovelydia216 ай бұрын
Big difference with “twitching” and these. These almost look like waves or like a huge worm is inside squiggling around.
@23dfmahghd6 ай бұрын
This is stage 2 myoclonus and dementia
@23dfmahghd6 ай бұрын
Sign of LMNL
@alfarouqelboom84657 ай бұрын
Thanks for sharing! appreciated
@kanwalmushtaqahmad37067 ай бұрын
❤❤
@instareel42217 ай бұрын
I am also facing same twitching but when i get nervous
@sheldonmurphy60317 ай бұрын
You are very pretty ma'am! It says this video is 8 years ago, and im pretty sure lots of guys have loved staring into your eyes, not even caring if there is a twitch or not. I only say my words that way because a lot of girls can feel very self conscious over this, and thats absolutely unnecessary! 😊 2 Thumbs Up From The States Ma'am! 👍👍
@breakupshood77477 ай бұрын
Is it serious issue or not..
@sajin28215 ай бұрын
Yes , it's the serious issue . It needed to be cure in the starting stage
@breakupshood77475 ай бұрын
@@sajin2821Muze Aisa kabhi kabhi hota hai...1-2 mahine me 1 ya 2 bar...to ye serious hai ki nahi....
@redrosees5 ай бұрын
I have this problem from last 3 years@@sajin2821
@PethraEsienhower7 ай бұрын
Nohnkenourwm do do v😮😅
@bharatbabu74927 ай бұрын
Jaldi se acchi ho jao☹️
@user-gx4nk6ob7y7 ай бұрын
Thank you
@NEUROLOGYMADEINTERESTING2 ай бұрын
You're welcome
@gamaltaher97147 ай бұрын
Thanks
@NEUROLOGYMADEINTERESTING2 ай бұрын
Welcome
@Magictrip6787 ай бұрын
Very helpful . Thank you
@user-vy6tb7ot6x8 ай бұрын
i have this 12 years and train and live bullshit there must be anotyher symptoms not only this
@biprajitdas45848 ай бұрын
Left sided lmn
@RahulMeena-zt1py9 ай бұрын
Can eye ball able to move of affected side?
@NEUROLOGYMADEINTERESTING2 ай бұрын
Yes
@RahulMeena-zt1py9 ай бұрын
Sir please dont disable comments onyour shorts because there is important discussion.
@user-jv8nx8th3f9 ай бұрын
I have benign cramp Faciculation syndrome. I have twitches in calf’s and thight but fire Randomly all over body. They come and go sometimes Constant sometimes not. 1 year in no weakness. Als is not twitching alone ! Twitches are harmless and if als would appear after weakness and atrophy as a response to dying motor neurons . If u twitch and can still walk talk grip then carry on with you life And crack on life is to short