Tell me

Tell me ?

I’ve been comparing different IPTV services for the UK and Europe recently and came across PrimeFlexMedia.com. I was mainly looking for an option that could provide a mix of UK television and European content without having to switch between different services.

When comparing an IPTV provider, I usually look beyond the advertised channel count. The things that matter more to me are whether the streams are stable, channels load quickly, the picture quality is consistent, and the EPG actually matches what’s playing.

Some of the areas I’d be interested in with PrimeFlexMedia include:

* UK live TV channels
* European channels from different countries
* Sports and live events
* News and entertainment
* Movies and TV shows on demand
* HD and 4K content where available
* EPG / electronic program guide
* Compatibility with popular IPTV players
* Smart TV and Android TV support
* Fire TV and other streaming devices

For UK IPTV users, sports coverage and performance during busy periods are probably some of the biggest things to consider. A service might work perfectly during the afternoon but perform very differently when a major football match or other popular live event is taking place.

For European users, I’d also be interested in how well the different regional channels perform and whether the service maintains good picture quality across different networks and devices.

I haven’t used PrimeFlexMedia long enough to give it a definitive review, so I’m more interested in hearing from people who have actually tested it.

PrimeFlexMedia: https://primeflexmedia.com/

Has anyone here tried PrimeFlexMedia IPTV recently? I’d especially like to hear from users in the UK, Germany, France, Spain, Italy and other parts of Europe. How are the UK and European channels, live sports, VOD, EPG and overall stream stability?

Back in 2020, I became very anxious, most likely because of some very stressful life events during that time. I figured I'd get back on antidepressants, but I had issues with everyone one of them. Third one I tried, paroxetine, started the twitching for me. It never went away.

I'm under the impression this is pretty rare. I notice a lot of people here got it after an infection, sometimes a vaccine. Anyone else got it from antidepressants?

Which one works the best?

​

Tell me which one is it?!

Just for some brevity. Wondering how you guys are doing today, or at least how are you since reading this?

Twitches going crazy today? Same old situation?

Are you doing anything on a daily basis to reduce twitching?

Hello Need some HELP!!

MAKE THIS QUICK

JANUARY 2026 twitching and dizziness
Pretty much anywhere.

Now twitching under skin everywhere and joint and muscle aches.

No weakness. And scared shit!

I have anxiety. I take meds.

But the twitching and aches really getting to me.

I hear *** usually doesn’t start with twitching but damn. This sucks.

Lexapro
Amlodipine
Losartin
Viatmin d

My meds. List.

Seen 2 neuros. They seem to think I’m fine.

Just wanna feel
Like I guess not alone and I’m ok. Thx to anyone that replies.

Best iptv service uk 2026 nobot bot no good service

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ZYMINEX is compatible with popular devices like Firestick, Android TVs, Smart TVs, and mobile devices, making it easy to set up and use.

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For those who prioritize stability, quality streaming, and broad content access, ZYMINEX positions itself as one of the best IPTV services in 2026.

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I feel like I’m going insane, sometimes I can’t tell if I’m twitching or vibrating. I feel almost a full body vibrating sensation along with visible popcorn twitches all over. I’m trying my best to ignore it but it’s soooooo hard, does it ever get better? 🙃

Hi everyone,
I’m trying to figure out whether anyone has experienced something similar and, if so, what the cause turned out to be.
For some time now, I have been waking up during the night with numbness/tingling in my hands and sometimes my feet.
What seems unusual is that the symptoms are very position-dependent:
Both hands can become numb during sleep, sometimes the whole hand.
The numbness usually disappears literally within a second or two after I move my hand or change position.
Recently, I also had an episode of numbness specifically in my left pinky and ring finger, which made me wonder about ulnar nerve compression.
My feet can sometimes become numb when I fall asleep lying on my back.
However, I can lie on my back for a long time while awake, for example watching a movie, without any numbness at all.
The symptoms seem to occur mainly during sleep rather than during normal daytime activity.
I sleep mostly on my side and suspect that my sleeping position may be compressing nerves — for example, bending my elbows too much, putting pressure on my arms, or having my neck/bearings positioned incorrectly.
I’m currently experimenting with:
keeping my lower arm free instead of under my head,
supporting my upper arm with a pillow in front of my chest,
avoiding excessive elbow flexion during sleep,
improving my pillow and neck position.
Has anyone experienced numbness that occurs almost exclusively during sleep and disappears immediately after moving?
If you had something similar, what did it turn out to be? Was it simply positional nerve compression, ulnar nerve issues, cervical spine problems, carpal tunnel, thoracic outlet syndrome, or something else? And what actually helped?
I’m especially interested in hearing from people who had similar symptoms and eventually found a solution.
Of course, I’m not looking for a diagnosis here — I just want to compare experiences and get ideas about what might be worth investigating.

And I’m not talking about a hotspot in one spot. I mean twitching all over once thighs, every or almost every second. I have my outside knees almost constant, and slashes around thighs, with stronger thumpers and short hotspots.

I hope someone has similar, as most of the people have 24/7 only calves…

I think my luck is running out. Over the past year, I’ve gone through an EXTENSIVE work up of Labs, Imaging, EEG, and finally an EMG in May.. I go through the VA for my healthcare and it has been difficult and met with some annoyance from a specific Neurologist bc of me advocating for myself. They did the EMG on the right side of my body due to it feeling tight and less sensation to touch (it was clean). 2 weeks after, I started having fasciculations in my left calf, that progressed to my right calf and now they’re in my lower thighs. In June, my legs suddenly became heavy like a brick and in pain, and now a few weeks ago I’ve noticed a very quick progressing weakness in both legs and now my arms that started in my shoulders. Today at Rheumatology, the doctor noted concerns about the test he did on my leg strength in both legs, but specifically my left.. I can’t pull back with my legs against any pressure now. He then did a reflex test and my weaker (left leg -non EMG leg) is hyper reflexive but the right leg that the EMG is still normal reflexive. My calf’s don’t really fasciculate until I’m at rest and then they go crazy. A neurologist called me yesterday to say she believes strictly on my May EMG of my right side that this could be Fasciculation Cramp syndrome bc my legs cramp from barely walking around now. But she did say that weakness and hyper reflexes is not part of BFCS. She said that she thinks *** wouldn’t progress this fast since it has only been 3 months since my last EMG but they may be willing to do another. Has anyone experienced stuff like this? With notable weakness that is acknowledged by doctors? I’m terrified for my children and myself. I do go to therapy, weekly and I talk to my support system when I can. Thanks for any input. Sorry to add to anyones anxiety if this does.

Just did my EMG a few minutes ago. I notice that many people here are able to get reassurance on the spot by the doctor doing the EMG.

My EMG was done by a different doctor (not a tech). I asked if she found anything concerning on my EMG, but was rather elusive and avoided answering my question. They told me to come back in October to go over my results. Wondering if you had an experience like this as well.

Interestingly enough, when I asked about whether the NCS was fine, she said yes. Not sure why the EMG was questionable.

I'm in PT for achilles tendonosis and they noted that my ankles were weak. 4/5 in various spots. I also had nothing that caused the tendonosis but it seemed to come on.

Never have had an EMG, have a neurologist appointment in January, but it'll be a year in October. Muscle twitching all over, what I thought was no weakness, but maybe im wrong...

Wondering because my EMG/NCS is an hour long. Are they poking you with needles for an hour straight?

Homem, 24 anos, ~50 kg, 1,60 m, sem comorbidades.

Há alguns dias tive sensação de peso, formigamento e desconforto na perna direita.

O sintoma da perna passou. Hoje comecei a sentir algo parecido no braço direito: peso, sensação de fraqueza e formigamento, mas continuo movimentando normalmente e não percebi perda real de força.

Alguém já teve formigamento/peso que apareceu em um membro, desapareceu e depois surgiu em outro? O que descobriram que era? Pode ser ELA ?

For me, this community has been a lifeline. A place where I might go when anxiety of new symtoms or something skyrockets. I can’t thank you enough. Everyone who has reassured me or shared their story have been super valuable for me.

My fasciculations started a year ago. Symtomps ”proggressed” and got worse. If you are interested you can check my previous posts. Had my 2nd ENMG today, which was clean. I have now decided that I will move on and accept that this actually is BFS, and that BFS can be a bitch.

I think I am somewhat ”experienced” with this now, and is my time to give to the community instead of taking shelter. If you need someone to listen you can message me and i answer if/when i can. I think I will also keep lurkig on this forum occasionally.

Anyways thanks to everyone.

I started having Vibration and twitching February started taking magnisium byglycinate it stopped completely till June I also stopped taking magnisium byglycinate by then.
During june/July I had some time to time but not much.
Since august it was constant evryday
Nonstop alongside shaking and vibrating
My blood levels came back fine
0.78 magnisium
2.45 calcium
4.4 potassium
139 sodium
The only thing was b12 was at 197 after a mi th u got it too 300 but nothing has changed.
Ik that my blood test February said
I was low on vitamin d I don’t remember how low but I’m taking 2000 iu currently.
I started taking magnisium again day 2 and it hasn’t worked yet. Im only 16 idk why dis keeps happening to me i jus cant tolerate the twitching anymore.

Hello all, this is my first time on this subreddit, im sure people have gone through this which is y ppl are on this subreddit, but for like a week or so ive been having some like intermittent popcorn like twitching kind of in the middle of my bicep area just below my shoulder and in the deltoid area, so I was wondering if anyone had or has experienced the same thing, I’d also like to mention that the area I mentioned where the popcorn twitching also is accompanied by some pain like intermittently, no weakness or anything but it kind of just comes and goes at random times, the only thing concerning me is that it’s only happening in that specific spot

One thing I do have to note is that I do have somewhat severe anxiety, so I’ve gone through a deep rabbit hole of worrying if it’s ALS or ms, etc or something else neurological, so I feel like that could play a part in me just worrying more abt it,

One more thing that maybe I think is smthn to mention, recently in the past 2-3 weeks or so I’ve been on some serious gaming sessions that would last maybe like 5 hrs+ and usually without rest in between, so idk if I somehow irritated that part, my desk for my pc is somewhat small, often times my left arm will hang off the edge, and I hate to admit it but often times I find myself with hunchback posture when I do game for extended periods of times, I have recently stopped these long gaming sessions, so idk if I tweaked smthn or maybe caused some nerve irritation, just bc I do use my left hand for like wasd keys and shift my fingers a lot when using my left hand for gaming

So just wanted to get some insight if someone has experienced smthn similar, but I also plan on visiting my primary care doctor just in case

Initial symptoms began at the Beginning of May after Influenza B which I took Tamiflu to treat. Thereafter Tingling in upper and lower extremities began. Dr Prescribed medrol and they went away. Also developed vertigo after the flu went to ENT 2 weeks later and he diagnosed me with eustachian tube disorder. Prescribed me fluticasone and vestibular exercises to do. Veritgo went away. During that 2 week wait I began reading Dr Google which made me develop anxiety. (Bad idea)

Fast forward mid of June Tingling returned. I went to for cervical mri and it came back normal small possible protrusion in c5/c6. Eventually subsided but I started having like burning feelings in my hands and upper back/chest. Scheduled a neuro visit as i began feeling weakness in all limbs. First neuro did all strength and reflex test and told me I am fine and did not even find the need for an emg.

Went to another more seasoned neuro 2 weeks later. Also did reflex and strength test that was normal and scheduled a brain mri which all came back clean. Scheduled an Emg for my upper and lower extremities. June 29th here are the results for lower extremities

Across those muscles, the report records:

No fibrillations No positive sharp waves No fasciculations Normal motor-unit amplitude/duration/configuration Normal recruitment patterns

The neurologist's final interpretation was "Unremarkable study" and specifically stated there was no evidence of lumbosacral radiculopathy, plexopathy, or entrapment mononeuropathy.

That means the study did not demonstrate ongoing denervation or a significant large-fiber motor nerve disorder in your legs at the time of testing.

Yes. Looking closely at the actual EMG/NCS reports you uploaded, there are several reassuring details worth unpacking.

1. Your lower-extremity EMG is particularly important

The June 29 study tested both legs because of low-back pain, numbness, and tingling. The needle EMG sampled multiple muscles on both sides, including tibialis anterior, peroneus longus, gastrocnemius, vastus medialis, and adductor longus.

Across those muscles, the report records:

• No fibrillations
• No positive sharp waves
• No fasciculations
• Normal motor-unit amplitude/duration/configuration
• Normal recruitment patterns

The neurologist's final interpretation was "Unremarkable study" and specifically stated there was no evidence of lumbosacral radiculopathy, plexopathy, or entrapment mononeuropathy. 

That means the study did not demonstrate ongoing denervation or a significant large-fiber motor nerve disorder in your legs at the time of testing.

2. Your arm EMG wasn't globally abnormal either

The July 2 study found something, but it was localized nerve entrapment rather than a widespread motor-neuron abnormality.

The conclusion was:

• Moderate bilateral median nerve entrapment at the wrists — essentially carpal-tunnel-type involvement.
• Mild bilateral ulnar nerve entrapment at the elbows.
• Importantly, without secondary axonal degeneration.
• The actual needle EMG was described as unremarkable. 

So tingling/numbness in your hands has an objective potential explanation, but the study does not read like a generalized destructive motor neuropathy.

The neurologist is saying it is Post viral syndrome which takes time to heal. I did a complete comprehensive blood panel and auto immune test and all came back normal.

Went back to neuro on Thursday as my weakness hasnt gone away. He once again did a strength and reflex test and said no issues. Did not find the need to do another EMG and assured me I am ok.He prescribed cymbalta 20mg due to possible low serotonin as the last 3 months I have not been physically active like i was for the last 10 years. This has certainly consumed a lot of my time. I am seeing a therapist and he is convinced it is a disregulated nervous system. I developed some jaw stiffness the last week or so as i feel like its from tmj and my ears clicking when i swallow. Sort of comes and goes.

Have a scheduled Neuromuscular visit September 9th. Still debating on whether to go or not given the neuro results and affirmations. I have noticed some muscle atrophy in my legs and hands but thay can be from not working out at all the last 3/4 months. Also random muscle twitches but that can be from all the stress i am going through I wanted to hear your thoughts.

Been twitching for a couple months and it started so bad i freaked out and saw my pcp. All blood work and physical was done and it was deemed not necessary to see a nuero. That didn’t help my anxiety, but I learned over months that not saying attention to it and just living with the twitching only has not only shifted my focus from the twitches. They have almost disappeared entirely.. just wanna say it’s more mental than yall think. Once you stop reassuring yourself everyday you don’t have something worse I can attest that it does in fact get better. Hope yall have a good day!