#neurocardiogenicsyncope

[marketingbiotronix]

Biotronix Solution Forever ® Tilt Table Motorized Electrical Hydraulic Tilting 0-90 Degree 

Long durable cushion with 90 mm thickness

Low frictional Castors for mobility

As manufacturers we can customize the product's  specification and descriptions.

Customization will decrease/increase the Product charges.

Pediatric size also available

Electrically Operated Tilt Table with A.D.L activity Tray and foam padded upholstery, table works to standing position with heavy duty Actuator that provides silent and smooth Tilting action with hand-held push button control switches. Range of tilt is adjustable between 0 to 90 degrees. Works on 220V AC.

Motorized Tilt Table

Electrical Hydraulic Tilt Table

0-90 Degree Tilt Range

Clinical Rehabilitation Equipment

Precision Tilt Table

Professional-Grade Tilt Table

User-Friendly Control

Compact and Portable Design

Non-Invasive Recovery Solutions

Adjustable Tilt Table

Therapeutic Tilt Table

Customizable Tilt Table

Motorized Tilt Table for Healthcare

Efficient Rehabilitation Aid

Tilt Table for Physical Therapy

Clinical Tilt Table

Rehabilitation Aid with Tilt Table

Adjustable Tilt Angle Table

Electrical Control Technology

Compact and Portable Design

Hydraulic Tilt Table for Therapy

Efficient Recovery Tilt Table

Professional-Grade Rehabilitation Solution

Digital Control for Tilt Table

Non-Invasive Recovery Equipment

Compact Design for Healthcare Facilities

Precision Tilt Table Technology

User-Friendly Tilt Table Controls

Therapeutic Precision with Tilt Table

Expert Tilt Table for Therapeutic Use

Customizable Tilt Table Features

Motorized Tilt Table for Physiotherapy

Premium Model for Rehabilitation

Compact and Portable Tilt Table Design

Clinical-Grade Tilt Table for Healthcare

Contact us / What's app - 9711991264,9015251243,8076549111,8076205625

Website : www.solutionforever.com

https://lnkd.in/ejdC6Jy7

EMAIL : biotronixcareinternational@gmail.com

ADDRESS : F-400, Sudershan Park ,Moti Nagar ,Near Gopal ji Dairy ,ND-110015

#TiltTable

#TiltTableTesting

#OrthostaticTesting

#SyncopeTesting

#CardiacTiltTable

#AutonomicTesting

#TiltTableTherapy

#NeurocardiogenicSyncope

#OrthostaticIntolerance

#TiltTableProcedure

#Dysautonomia

#SyncopeAwareness

#HeartHealth

#AutonomicDysfunction

#CardiologyCare #physiotherapy #physio #physiotherapist #physiotherapie #bpt #dpt #mpt #rehabilitation #rehab #rehabilitationcenter #rehabtherapy

[biotronixcaresalesteam]

Biotronix Solution Forever ® Tilt Table Motorized Electrical Hydraulic Tilting 0-90 Degree 

Long durable cushion with 90 mm thickness

Low frictional Castors for mobility

As manufacturers we can customize the product's  specification and descriptions.

Customization will decrease/increase the Product charges.

Pediatric size also available

Electrically Operated Tilt Table with A.D.L activity Tray and foam padded upholstery, table works to standing position with heavy duty Actuator that provides silent and smooth Tilting action with hand-held push button control switches. Range of tilt is adjustable between 0 to 90 degrees. Works on 220V AC.

Motorized Tilt Table

Electrical Hydraulic Tilt Table

0-90 Degree Tilt Range

Clinical Rehabilitation Equipment

Precision Tilt Table

Professional-Grade Tilt Table

User-Friendly Control

Compact and Portable Design

Non-Invasive Recovery Solutions

Adjustable Tilt Table

Therapeutic Tilt Table

Customizable Tilt Table

Motorized Tilt Table for Healthcare

Efficient Rehabilitation Aid

Tilt Table for Physical Therapy

Clinical Tilt Table

Rehabilitation Aid with Tilt Table

Adjustable Tilt Angle Table

Electrical Control Technology

Compact and Portable Design

Hydraulic Tilt Table for Therapy

Efficient Recovery Tilt Table

Professional-Grade Rehabilitation Solution

Digital Control for Tilt Table

Non-Invasive Recovery Equipment

Compact Design for Healthcare Facilities

Precision Tilt Table Technology

User-Friendly Tilt Table Controls

Therapeutic Precision with Tilt Table

Expert Tilt Table for Therapeutic Use

Customizable Tilt Table Features

Motorized Tilt Table for Physiotherapy

Premium Model for Rehabilitation

Compact and Portable Tilt Table Design

Clinical-Grade Tilt Table for Healthcare

Contact us / What's app - 9711991264,9015251243,8076549111,8076205625

Website : www.solutionforever.com

https://lnkd.in/ejdC6Jy7

EMAIL : biotronixcareinternational@gmail.com

ADDRESS : F-400, Sudershan Park ,Moti Nagar ,Near Gopal ji Dairy ,ND-110015

#TiltTable

#TiltTableTesting

#OrthostaticTesting

#SyncopeTesting

#CardiacTiltTable

#AutonomicTesting

#TiltTableTherapy

#NeurocardiogenicSyncope

#OrthostaticIntolerance

#TiltTableProcedure

#Dysautonomia

#SyncopeAwareness

#HeartHealth

#AutonomicDysfunction

#CardiologyCare #physiotherapy #physio #physiotherapist #physiotherapie #bpt #dpt #mpt #rehabilitation #rehab #rehabilitationcenter #rehabtherapy

[subtleshenanigans]

Story time about me discovering that hey, maybe I’m chronically ill?

Nothing too intensive but I’ll put it all below the cut!

So, I’m about 15, at home, trying to go to sleep. Aside from having chronic migraines and insomnia, I figured I was fairly healthy. Just the kid who would prefer to read than play.

I’m trying to sleep, when I notice it: I can’t feel my heartbeat. Now, I’ve been through severe trauma, and had a lot going on at the time, so I start sobbing, terrified I’m dying or something.

I don’t remember if I called for help or not, but my parent (I’m keeping vague for reasons) takes me to the ER, let’s cousins know, and off we go.

Turns out, I just have a super low Blood pressure and heart rate (I probably noticed because of my severe anxiety at the time). We’re talking when I sleep my BP is usually 48, and up and moving about between 60-70. They say it’s no worry, it’s just an athletes heart, and try not to get up too fast.

But the thing is, I’m not active, never really have been. Probably because I fatigue easy, which I assumed was normal.

(We would have to do the mile every Friday in PE, and grade was based on the time you finished. I usually got a C or B, so I finished in under 8/7 minutes. But I’d be gasping and feeling like passing out, so uh, something was obviously going on.)

Now, I’ve always had presyncope - you know how you stand up too fast and dark encroaches on your vision like you’re gonna faint? I experienced that almost every time I stood up, even at school. Figured it was normal, happens to everyone right? (It does not, in fact, happen to everyone all the time.)

Passed out a few times between ages 12 to now, but figured it was other things. Oh, I didn’t eat enough, or I was sick, etc.

Until one time I ‘passed out’ as my sis did my makeup, and I was just sitting there and had been for awhile. (We’re still not sure if I passed out or had a seizure - the ER doc was super unprofessional and brushed us off, just gave me an EKG - and with NCS you can have non-epileptic seizures.)

So we go, “okay this isn’t normal”.

Finally a rhuemetologist says, “oh you have Dysautonomia.” (I went to see about my fibromyalgia because apparently base level pain is a 0 and not a 3.)

A cardiologist gave me a two week heart monitor, and shoved meds on me. Didn’t expound on what type I had, and refused the tilt table test.

(I eventually started the meds after fainting in the middle of the night - I had used the restroom and luckily I had pulled my pants up and angled myself to the carpeted hallway. Somehow, no one woke up to the thud and i laid there and silently cried.) I had side affects from meds but I’m still on them, and I’ve only had one accidental faint since (I still have presyncope episodes but we tried upping the dosage and I actually got worse, so I’m stuck on this one dose that kinda helps.)

New cardiologist finally, and hey, he’ll order a tilt table! Tilt table was positive (almost a negative because I have a severe delayed reaction apparently -_- which explains why when I pass it it’s, like, awkwardly not right after I get up), and I got diagnosed specifically with Neuro Cardiogenic Syncope, or Vasovagal Syncope. (Still curious if I have a form of POTS or not.)

Now, what’s the moral of all this? Mostly I just wanted to share my story. I guess if you find out something in your health isn’t normal like you thought, or it’s interfering with your daily life, get it checked out.

[illitten]

I just found out HyunA has vasovagal syncope????

And like honestly that gives me so much hope for the future??? Like I can barely stand up and walk somewhere now but she's dancing and singing like normal. I know it's probably not easy for her but the fact that she can do it is amazing to me

[chronicforlyfe]

Put a finger down if when you try to have ~normal~ sex for once and get on top but then you have a POTS flare and your HR breaks 160 and you can feel your pulse galloping so you get off but then you plummet and you’re fighting to stay conscious and your bf has no clue what to do and you try to tell him through bradycardic brain fog and he cant understand you so he panics and makes you ramen with cold broth...

[nosympxthy]

[lkira15]

I just want to be normal again

Ever since I was a little kid, I've fainted. It didn't used to be that often as a kid, we'd go out to the park and I'd faint without anyone knowing (back then I didn't even know what fainting was), I'd be running and faint, then at age 16, fainting started to get more common. Woke up, went to the bathroom, fainted and broke a mirror with the fall, managed to open the door only to faint again in my mother's arms, and once more when I came to. Hospital said they couldn't find anything wrong. In school, I was in the process of fainting had it not been for a good friend of mine noticing. She distracred me, talked to me, made sure I didn't stand up and didn't fall over. My vision returned and I thanked her profusely. Senior year I only fainted once, in front of my whole class at a skating rink in Houston. Everyone swarmed me and I was only trying to get them away, as back then I used to throw up every time I fainted.

After that, nothing. In fact, until 2017, I had no more episodes. 2018 comes along and I faint every month. 7 times within 15 minutes. Multiple times at work. Never around people I knew well, though, so luckily I wasn't swarmed when this stuff happened. Mostly it happened when I was on my own. The time I fainted 7 times within 15 minutes, I went to the ER (didn't have any insurance so I hadn't seen a doctor at this time since the year before. I'd turned 19 in August of 2018, after all, and Medicaid doesn't cover kids over 18) and they diagnosed me with Vasovagal Syncope, which has 2 other names [Neurocardiogenic Syncope and Orthostatic Hypertension].

I was told I would just have to live with it. There is no cure, no true treatment, only stopping one's fainting before it happens. As if that's helpful. Without insurance, though, I went about living day to day looking for the signs before fainting, and after a couple more fainting spells, I got pretty good at telling when it would happen, stopping it before it happened. Mostly that entailed inconveniently laying on the floor until my vision went from filled with black to perfectly blurry (as I wear glasses), my hearing came out from inside the tunnel, the pins and needles numbing me receded, and my body was coated in a film of sweat. Inconvenient to say the least and mostly impossible to do in public. Hell, sitting with one's head at their knees usually doesn't fully work as the moment one stands the spell comes back and next thing you know a couple of minutes have passed and you can't remember how you ended up in an awkward position kissing the floor. Sometimes laying down only helps you not fall but you still faint.

I faint, or almost faint, every time I take a shower, every time I'm doing dishes, when I'm outside for too long in the Texas heat, if the air in the room is stagnant (which doesn't help my asthma anyway), if I stand up too quickly, if I lose too much blood due to menstruation, right before starting my period because that totally makes sense, simply walking sometimes causes it. There are no true, definitive triggers. Cold showers. Hot showers. Luke warm showers. It doesn't matter the temperature. I faint when I faint.

And it only recently came to my attention that this is a disability. I can't go out during the day and enjoy it without certain limitations. I can't shower without it taking a long time as I have to stop more than 7 times to let the fainting pass before continuing. A place without AC means a place I can't be as my asthma and fainting will act up. Be alone as then no one will be there to help if I never come to from the fainting spell.

I wish I was normal. Able to do more things. Rid of this fainting. Rid of this asthma. Rid of this fear of fainting and never waking up. Who's to say death doesn't feel like fainting? I don't know but I don't want to find out anytime soon. So consider yourself lucky, if you don't have this. And if you do, know that I understand your pain and frustrations. I'm sorry if anyone else goes through this

[fluffy-flock]

NCS episode in the showerrrr

Thankfully I didn't pass out, just barely skirted it, and my partner was able to help me rinse off and get somewhere dry and soft. Honestly, dunno what I would do without @im-schrodingers-gay <3

I haven't come that close in quite some time, so I'm still pretty pleased.

[nerdymedzebra]

I'm currently collecting old medical records, and I finally got my Tilt Table Test records from 2011! I feel lucky the hospital still had them as Drs only gave to keep records 6-7 years. It's weird tho bc I DISTINCTLY remember blacking out while the nitrate was still dissolving in my mouth, then waking up on my back. But according to this, it took several minutes for me to faint?! And I was reporting on lightheadedness, etc.. So I remember blacking out but then I was still talking! Whoa, weird. I had no idea.

Look at that heart rate staying steady until the nitrate tho! This was years before POTS was on my radar, but presyncope was already controlling my life I feel like if I had this test done now, almost a decade later, my HR would not be quite so steady, even if I wasn't in a proper POTS flare.

https://www.instagram.com/p/B0i-v0yAskT/?igshid=t5sr5ta2xs7i

[subtleshenanigans]

Dysautonomia is the stupidest condition because IM HAVING PRESYNCOPE SITTING UP.

[illitten]

is it my adhd emotional exhaustion?

or maybe my dysautonomia exhaustion?

or maybe my (undiagnosed) autoimmune disorder exhaustion?

or maybe worldwide pandemic exhaustion?

[autistic-werewoof]

Oh yeah I never updated y’all, I finally (after legit years of waiting and on and off fighting to get a referral) got a tilt table test and surprise surprise to no one yes I was diagnosed with NCS. Though the testing itself was not a fun time I’m glad I finally have written proof that yes these symptoms aren’t normal and there is a legitimate reason they’re happening.

[cripplepunkdesigns]

@bionictilly Time for a power-up 1️⃣️Featuring rad new pullover by @cripplepunkdesigns #HellOnWheels

[ID: @bionictilly is sitting in an infusion chair wearing a black long-sleeved shirt that says “Hell on Wheels” in white across the chest with a bright pink bandage wrapped around her IV site.]

.

Hell on Wheels pullover | t-shirt | hoodie | sticker

[nosympxthy]

[artanissnow]

Dream. ⭐️ My birthday gift from hubby, well one of them. He got me another coffee mug and a beautiful giant crape myrtle tree with beautiful planter. Unfortunately, I am still sick with Covid (round 2) and it has been just as bad as the first time. First time I didn’t have the vomiting or spastic colon. This time…Holy Hera…. I just can’t. I am trying to drink coffee today because my throat hurts from hacking and snoring. I am so tired. So very weak. I can’t walk around much without feeling like I’m going to fall over. My skin even hurts!!! To the touch, clothing touching it, air touching it.. and my four year old needed my comfort last night and it was so unbearable I started to cry. He is still recovering too. Evenings are the worst for him. My cat is better today(he had Covid too) and my oldest is going through the random funk moments as is the husband. I can at least taste and smell. Not that it matters, can’t keep anything in anyways. Emetrol and Dramamine nausea for the win. Dramamine is a great substitute for Zofran (it’s not as strong, but it works) sorry there hasn’t been much fashion content . I will probably be posting pictures of outfits I have worn previously. I am hoping right now my kidneys behave and my heart does not go stupid. And trying to keep the older cat isolated a bit so she doesn’t get it is easy when she is like meh anyways to all of us 😂 #covid #covidround2 #covidbattle #thissucks #coffemug #covidpositive #covidrecovery #stillsick #neurocardiogenicsyncope #kidneyhealth #neuropothy #momlife #mymotherhood #catmom #boymom https://www.instagram.com/p/CfOvjL-AIrS/?igshid=NGJjMDIxMWI=

[saturnaal]

my mom telling me, a 4yo child who just woke up laying down on the side of the road, about the neurocardiogenic delicacy she passed onto me

:(