#physiotherapy website

[medibrand]

Physiotherapy Website Design and Development Services by MediBrandox

MediBrandox creates visually appealing, user-friendly, and SEO-optimized physiotherapy websites tailored to your requirements. Our designs include essential features like online appointment scheduling, patient portals, and educational content to enhance patient engagement and streamline practice operations. at MediBrandox, we can improve your online presence, attract more patients, and provide a superior user experience, ultimately boosting your growth and efficiency. Stay ahead of the curve.

[theteaisaddictive]

wix dot com your software is incomprehensible and about as intuitive as microsoft powerpoint, in that i’m sure competent people can make something beautiful but i will simply end up screaming at the computer screen in despair after half an hour

[joes-sha-la-la-la-girl]

As most of you know I have been struggling with my health recently. This is my experience of HSD. Each person with the condition is affected differently and no two people are exactly the same with it. Just as a pre-warning I will be attaching photos at the end of injuries I have had but there is no blood. They are just dislocations and subluxations I’ve had. I also talk about some of the injuries as well. I am not writing this for sympathy but more as an explanation as to why I sort of disappear every so often. 

Hypermobility Spectrum Disorders or HSD is a range of conditions that affect joint hypermobility. Often people are referred to as ‘bendy’, ‘flexible’ or ‘double jointed’. It is fairly common in children and young people but only 20% of people never lose the flexibility in their joints. More information about this condition is on The Ehlers-Danlos Society website.

This is my personal experience with the condition. Some people with HSD will experience these problems and others won’t.

When I was nine I had my first dislocation when my brother accidentally stood on my hand. I was taken to hospital by my parents and they sorted it pretty quickly with no alarms raised. However, when I was fourteen it got progressively worse. I kept having subluxations in my pinky finger on my right hand. A subluxation is an incomplete or partial dislocation of a joint. When I kept going to hospital they told me that it was a result of the injury when I was nine and they taught me how to manipulate it back into place. This happened almost everyday for two years at least.

The next year I dislocated my right thumb. Due to a medical error they missed the dislocation and the fracture on the x-ray and left it a week before noticing their mistake. I went back in to have it relocated a week after the injury. This is when I found out that I am immune to local anaesthetics so I had no pain relief when they did this. Due to a very observant doctor after my thumb dislocated inside of a plaster cast I was diagnosed with Joint Hypermobility Syndrome (the previous name for HSD). 

After this I started having more subluxations and dislocations including in my ankle, both knees, my hip, my shoulder and my first and middle finger on my right hand. 

Earlier this year I went to A&E with a swollen finger and they suspected rheumatoid arthritis. However, when I went to rheumatology I found that I was dislocating my finger in my sleep. That’s when my diagnosis name was changed to HSD. I scored a 6/9 on the Beighton Score. It is a system to measure joint flexibility. 0-3 is normal and 4-9 is when there is potentially a problem. I can hyperextend most of my joints and often I don’t notice when I am doing so.

I have now been receiving occupational therapy and I am on the waiting list for hypermobile physiotherapy. 

My main symptoms include:

Fatigue but unable to sleep

Pain and stiffness in joints

Frequent strains and sprains

Frequent dislocations and subluxations

Poor balance

Bladder and bowel problems

I also suffer from scoliosis which I have had no treatment for and cluster headaches.

HSD is incurable and the only things I can do to help is have pain relief, hot baths, hot water bottles and hand warmers and use heat rub creams. 

This condition affects my life quite severely. I haven’t got the worst symptoms someone can have but I am struggling to do daily tasks and even get out of bed some mornings. I use multiple types of joint supports as well as pen grips and back supports in my chair.

I am open to talking about this and will answer any questions about it.

[concerningwolves]

I've been walking around with this hypermobility diagnosis my entire life, and no medical professional ever told me definitively what it means. My parents can't remember specifically when I was diagnosed or who by – I was a severely premature baby with a rare disorder and a slew of other health issues, and the hypermobility got lost somewhere in there with all the other medical noise. Mostly, I was left to see hypermobility as something that made me super bendy and was fun to pull out at parties when I made all my fingers bend weirdly.

Everything I have been told about hypermobility came to me piecemeal, usually by happenstance. A nurse who said that the hypermobility explained why it was always difficult to draw my blood. A GP who mentioned that hypermobility was likely why my ankle hadn't broken, but had instead subluxated and then been left to heal incorrectly because it'd been misdiagnosed as a sprain. A rheumatologist who I was only seeing because of a colossal fuckup, who explained that hypermobility makes you far more prone to bruising. Everything else, I had to find out under my own steam, trawling websites repeatedly over the years and watching as the body of information grew.

When I went to my paediatrician with joint pain, she told me it was growing pains on multiple occasions. I've been to physiotherapy three times and multiple OTs when I was younger and none of them noticed that my knees' resting position was hyperextended. (It took 22 years and the aforementioned colossal fuckup that landed me back at rheumatology instead of seeing the chronic pain specialist nurse for someone to tell me that that wasn't normal.) PE teachers and gymnastics instructors made me feel lazy and inadequate and work-shy instead of thinking hey, this child has told us he's hypermobile, maybe we should pay attention to that. For a little while I got to use a portable slanted desk in middle school which was meant to make writing easier for me in lessons (it didn't). In high school I got to use an AlphaSmart – not because anyone listened when I explained that writing caused me serious hand pain, but because I was writing too slowly to keep up in lessons (and I was still told repeatedly by teachers that they were surprised I needed the AlphaSmart because my handwriting was so neat, as if that had anything to do with anything). It wasn't until my GCSEs that I first got serious accommodations in exams.

Did all those doctors I saw about my pain just think I was, I don't know, too young to be sick? I was born sick. It was there in my records! They knew, and they either decided I was some other speciality's problem or they straight up did not care.

Children can be ill and disabled. More than that, they deserve to be given all the information they might need and be offered necessary accommodations. They should be listened to! Parents shouldn't have to fight and claw for something as simple as a crappy plastic slanted desk. If I could trawl my brain to extract everything I'm feeling right now and inject it into the minds of every doctor who failed me, I would.

[milkywayagere]

Request from @swagscottpilgrim (My first request!! Tysm!)

Title: Crayons + Best Friend = Perfect Play Date

Summary: Jimmy and Timmy have a little play date involving crayons.

Characters: Jimmy Valmer and Timmy Burch

(Jimmy’s parents too ig)

Word count: 820 words

(Sorry if it’s a little short, I really struggled with this for some reason. I guess I need to interact with more Jimmy & Timmy content)

__________________________________

As much as Jimmy never let his disability stop him from doing what he wanted, he knew that logically sometimes it was better to listen to his body rather than his mind. Especially after a tough physiotherapy session, it was better to take it easy for a while.

What better way to take it easy than a fun time with his best friend?

He sent a quick text to Timmy, speaking aloud as he typed and including each and every stutter - his stutter was a part of him, so why leave it out of his text messages?

________________________________

Jimmy: ‘H-Hey TimTim! W-W-Wanna com-come over? I pr-printed off s-s-some new coloring pa-pa-pages.’

Timmy: ‘Timmy! 👍’

Timmy: ‘🦃?’

Jimmy: ‘Yeah TimTim I print-printed off some t-turkeys for y-you.’

Timmy: ‘Timmy!! 🤩’

__________________________________

Jimmy smiled to himself as he put his phone down on his bedside table, grimacing with effort as he pulled himself up of the bed and to his feet, gripping onto his crutches like his life depended on it - which it technically did if he didn’t want to eat shit and fall on his face.

He kept his complaints to himself, too tired to force them to be uttered aloud, as he slowly moved around his room and gathered everything they’d need. Jimmy kept a collection of big crayons as well as the regular kind, the big ones were easier for Timmy to grip.

Once he’d gathered all the things necessary for a fun few hours of coloring, he got them and himself down the stairs to the dining room table. He sat at the table, rolling a blue crayon back and forth as he waited for Timmy to arrive.

It didn’t take long, Timmy was quite fast on those wheels after all. Jimmy’s mom answered the door and invited the boy inside, smiling at both of the boys as they greeted one another.

Timmy parked his chair in front of the table and Jimmy slid over the printed coloring pages of turkeys and the big crayons. He’d found a gold mine of turkey-centric activities on a website meant for teachers to use for their students at thanksgiving. It may not have been thanksgiving just yet, and Jimmy certainly wasn’t a teacher, but the website had been perfect.

Jimmy moved so he could be sat right beside Timmy, just incase his friend needed any help. Timmy was happily coloring away, muttering and mumbling to himself in a sing-songy way.

Jimmy enjoyed talking to people, but he had to admit, he did also enjoy just sitting in a comfortable silence with his friends while they did something together.

It wasn’t long until he found himself regressing. Physiotherapy really had been exhausting that morning, physically and mentally, so it wasn’t exactly a surprise to him. His grip on the regular sized crayons faltered more often as his mind became fuzzier and fuzzier, switching to the big ones to continue his messy scribbling on the page, ignoring the lines.

Timmy noticed his friend slipping into a younger state of mind and was sure to share the crayons with him. It was the least he could do, Jimmy had printed off all of these coloring pages for them both after all. Timmy soon regressed too, being in the presence of another regressor had that effect, and they continued to color for another hour or so before Jimmy’s mom came in to give them some snacks.

“Th-Thank’oo.” Jimmy uttered quietly, glancing up briefly from his current coloring page to see what exactly his mom had served them.

His mom smiled at him, immediately picking up on the change in cadence of her sons speech, “No problem sweetie, can’t have you boys being all creative on empty tummys now, can we?”

Jimmy shook his head in agreement, blindly reaching to the tray of snacks with his free hand, handing some goldfish crackers to Timmy before getting a handful of his own.

Once every single coloring page has been sufficiently colored, the snacks devoured, the boys moved over to the living room to watch some tv. They’d only gotten through a couple episodes of SpongeBob before Jimmy fell asleep, the earlier exertion of therapy catching up to him. Timmy became aware after he hadn’t heard Jimmy giggling at the jokes playing out on the screen, turning his head to see his best friend completely knocked out on the sofa.

Timmy wheeled himself over to the kitchen as quietly as he could, breaking his aac device for the first time since coming over - he never did have to use it when talking to Jimmy, they were that good of friends that Jimmy could practically read his mind - alerting Jimmy’s parents to his current state. Jimmy’s dad picked the sleeping boy up and took him up to his room as Timmy prepared to go home.

“JimJim.” Timmy uttered with a smile, wishing his friend sweet dreams before he left.

[no-schedule-crepescule]

Hello, I'm from Gaza, my little daughter Nour has hydrocephalus and seizures, we are now in a tent in very bad conditions, and every thing destroyed our house, hospitals and physiotherapy centers 😔 I'm waiting your reply hope you will support Nour as she's a palestinian child needs your urgent help because the seizures attacks have increased, and hospitals don't receive her because of the huge number of injuries and martyrs. She must see a neurosurgeon soon to adjust the doses of the antiseizure medications. Also she needs CT scan and MRI to ensure that the shunt is working well. She also needs to continue Physiotherapy ASAP and Occupational therapy sessions to enable her to stand and take her first steps. Please support my campaign because Nour needs special care out of Gaza war, GOAL $1350

hey yeah, in case anybody else is still confused about things like this. It is a scam.

Usual steps to check for me includes going through the blog to see if it's only recently created, and also copy and pasting the entire text into the tumblr search bar to find if there are multiple other accounts saying the exact same thing.

Anyways, if you want to, here's a link to a website that provides you with a lot of the links for actual donations:

stay safe!

[disabled-dragoon]

You don't have to answer this ask if you don't want to but I kinda need advice and I do not know where to start.

This is going to be a long vent I am so sorry.

I'm a minor and I have chronic pain. When I was young I was always told I had hyper mobility because my dad has it (that was a lie). I was also told that it was untreatable, incurable and I could do nothing but live my life in pain (again a lie).

A few years ago I started spiraling down disability/mobility aid youtube, because I was in so much pain and I could barely walk. Which made me have to stop ballet, and that made some of it better.

Anyways, a few months ago I went to my physiotherapist and mentioned my hyper mobility. She said I didn't have it, and did the exam on me. She also said that my chronic pain came from not sporting enough (i stopped sporting because of my pain.)

Either way that kinda broke me, because there was no explanation for anything and I was still in pain. So I went to my local doctor and she said I probably have fibromyalgia and she said I should go to a special physiotherapy (I have school and exams and I said I'll do it after I finish high school, she thought that was a good plan).

But yeah, I am still in pain right now. And I kinda want mobility aids because there are days I can barely walk. I discussed this with my mum, and she kinda doesn't know what to do with it. I just want to go to the doctor and ask them, but I don't know how to convince her.

My dad is apparently anti-mobility aids, and he also said he lied about being hyper mobile. He says he has this unnamed thing going on, and that I should do the thing his physiotherapist told him to do, like 30 years ago. For a disorder that didn't exist back then and he doesn't know anything about. As in, he doesn't even know -what- condition he has.

Oh his advice btw was to not try to find external help, but fixing it myself because that's the only way to get rid of the pain.

I'm so pissed off about it, but I know talking to him wouldn't help (he's kinda bad dad like that).

I just feel sick because of the pain and I don't know what to do. It really sucks it really really sucks.

I don't know if you can give any advice or anything at all, but anything would be appreciated.

- 💚

I don't know if there is much advice that I can give you in this situation, unfortunately. My fear is possibly making the situation worse for you, and I do not wish to do that.

I'm so sorry you've had to go through all of this. It sounds awful, but it's good to see that you are trying to take steps to make things better, however difficult they may be at the moment.

That first physiotherapist was ridiculous, good on you for getting a second opinion. Waiting for physiotherapy isn't ideal, but I'm glad you have the option for the future and I really hope it helps you. You should never do exercise beyond your comfort levels, however, if you want to look into some light physio-like exercises while you're waiting to see if helps at all, I have some links here that may be useful to check out:

Justin Agustin: A fitness influencer who does a lot of videos on "beginner workouts" and gentle exercises to help with mobility. Actually, all of the exercises in this video are exercises that I have done in my own physio at some point.

Alycia Klein: This woman has the same condition that I do- Hereditary Spastic Paraplegia- and posts videos about exercises and stretches to help with muscle spasticity and pain. I know it is not the same, but it could be of some use to browse. She is actually mentioned on the official Spastic Paraplegia Foundation website as a reputable resource.

Gentle Chair Yoga: Yes we're all sick of the "have you tried yoga" comments, but hear me out on this! Chair exercise can be incredibly beneficial for those of us who simply cannot stand long enough for much else. And this video, though 9 years old, is created by the Canadian LEAP service.

None of these resources are substitutes for actual medical advice, of course, and you should never try and push yourself beyond your limits if you do try them, but I am putting them here in case you decide to look into them.

In terms of mobility aids, other than sitting your mother down and discussing it with her, I do not have much advice here. I would recommend doing some research into exactly what type of mobility aid may be best for you, and, if possible, having a trusted adult and/or acquaintance in the room with you while you talk to her. It can make the discussion easier, should you choose to do it. Also, sometimes it can be easier if a professional- such as a teacher- brings the issue up with them first so you don't have to be the one to broach the subject first.

You're going through a difficult time and it's easy to start to feel like no one is listening to you. But that's not true, and you always have a space here to vent or seek advice if you ever need it.

Take care, anon.

[sparklecryptid]

I’m sorry but can we talk about how some websites when it comes to POTs and some other stuff like Chronic pain are like “this person may not be able to do much exercising because of this condition” and later it’s “exercising is recommended to fix the issue!” LIKE HUH.

i agree with the sentiment that exercising is often cited to disabled people as the answer to everything and by god does it get annoying. like exercise? thank you! it's not like im in pain 24/7 and have time to fit exercise into my routine when i'm busy trying to do the fucking dishes. like ooooh i havent thought of that before! thank you random website! I totally never thought of this before!

there are certain things that exercise does actually help but the 'exercise' that helps with pain in a lot of cases is actually physiotherapy! and while physiotherapy is exercise it's not what most people think of when they say exercise. so by referring to physiotherapy just as 'exercise' can give people the idea that they should be out running or lifting weights when that is not what is going to help them the most in the long term and might actually make things worse depending on what you have/what is causing the pain.

but yeah. mood.

[lalanautism]

Welcome to Lalan Autism Clinic in Ranchi.

Remember, progress is a symphony of small victories. At Lalan Autism Clinic, we celebrate each step forward, knowing that it unlocks a world of possibilities. 🌈���

Services Offered:

Occupational Therapy

Pediatric Physiotherapy

Speech Therapy

Special Education

ABA (Applied Behavior Analysis)

Contact us if :

A child doesn’t respond his name

Feels restlessness/Hyperactivity throughout the day

Having difficulties to mix with peer group

Having poor attention span/ Eye contact

Difficulty in verbal/ Non verbal communication

A child with poor hand-writing skills

For more information or to embark on this healing journey, visit our website: Lalan Autism - Academy of Autism & Child Physiotherapy

🌐https://lalanautism.com 📲+91-9899272246 📩info@lalanautism.com

[elenthyaolyenths]

Asks game

6, 16, 21

Hi @seraphhiim ! Thanks for your ask!❤️‍🩹

6.Do you prefer drawing or writing? 

Aouch, tough one! Let me think about it...🤔

Both are great but can be difficult in their own way - for me, at least. Drawing allows me to express a feeling, a scene, a memory, and if I'm doing it good, anyone might be able to understand with just one glance, even if they don't know my language or how to read. It's kind of... universal? But sometimes it can be less precise or misunderstood.

Writing is my favorite way of expression since 20 years - when I'm not blocked because burn-out or depression. When the words flow in my head, it feels like freedom, everything seems possible. But sadly, I'm not able to write like this in English, only in French.

So... both. Both is good 😁

16. Want any tattoos? What of? 

If I wasn't afraid of needles or changing my mind later - quite common with me - I would have already had one! About an symbol I have created for one of my previous fanfictions because it means so much more to me.

(Other life, other fandom, other website. Search for something called "Foedus Aurorae"...)

Right now, I think I would go for something much personal. One of my own wings, certainly. But not necessarily on my back or my shoulder, because I would like to be able to see it easily. And remind myself that the freedom of creation exists, and that I just need to allow myself to embrace it.

21. How was your day today? 

Honestly? Quiet, but anxious and a little bit sad until now. I miss drawing, but I have to wait 4 weeks more before being able to remove my wrist orthesis. And even then, I'll have to do physiotherapy, so dunno how things will go. But you know what? Writing all of this reminded me that I have other ways to create❤️‍🩹. Let's go to writing! Ooor finally give a try to an abstract painting project I'm thinking about for a while!❤️‍🔥

Thank yoouuuu🥰

Next ask?

[fisiofriend123]

FISIO FRIEND is a leading Physiotherapy Center In Ambala, specializing in personalized treatment plans for neurological injuries, pain relief, and rehabilitation. Founded by Dr. Sharad in 2020, we use advanced technology to help patients regain strength and improve mobility. For more visit our website!

[ioveskye]

Wonder | Leo Fitz x reader Prologue

A/N: Hey everyone, after more than a year I am finally going through with this series that I had planned. Since there is a lack of aos fics out there i wanted to make one myself. On my AO3 there is a version of this fanfic with my OC as well (in case you don’t want to read an x reader, its @ioveskye as well) Please let me know if you like the series and let me know if you want to be on the taglist.

"These are all the files the department could find about the experiments you requested." Lucia, the newly hired intern said to Y/n as she was handed the files she asked for. She smiled at the young girl and thanked her. Lucia made her way back to her own desk and Y/n immediately began to do her research.

Y/n L/n, a well-known detective all around the world. She has solved numerous mysteries and was even the first person to be right about the 'Thor theory'. A recent turn of events has caught the attention of the young detective lately which led her to read all the files that the department could find. Numerous hospitals in the area around Los Angeles all had encounters with patients that died of similar causes. The biggest pattern between these deaths was that the cause of death was never discovered. After some more digging Y/n found out that all the patients had all undergone special treatments at the same medical clinic.

Sadly that was as far as she got. An address. It wasn't a well-known clinic and they only specialized in physiotherapy (that's what the website said at least). So she decided to check it out to just 'ask some questions'. The moment she grabbed her gear however she was stopped by the ringing of her phone. It wasn't her work phone so she was very confused about why an anonymous caller was calling her. When she pressed accept she never would've believed to hear the voice of an old friend.

"Y/n L/N, it has been a while since we last spoke hasn't it?" The voice of Phil Coulson said at the other end of the line.

Y/n couldn't help but smirk. Of course, Phil Coulson would call her randomly after three years like it was the most normal thing in the world.

"Well well, Phil Coulson. In what do I owe the pleasure? Does S.H.I.E.L.D. need my help again with something?"

"You could say that. But it isn't just S.H.I.E.L.D. it's also a friend asking for a favor."

She turned to the two co-workers that were waiting for her at the side of her desk. She held her phone to her shoulder so she could talk to the two men. "Guys go back to your other assignments I don't think we'll be heading out for a while."They nodded at her and walked back to their own desks once again while Y/n turned her attention back to her phone.

"So, what kind of favor is this and how do I benefit from it." She asked the man with a smirk knowing damn well it didn't actually matter since she'd always help out.

"I've been setting up a team of S.H.I.E.L.D. agents that are focused on missions with potential 0-8-4's. I think you're familiar with those right?" The line went quiet for a while, Coulson waiting for an affirmation that the young detective still remembered what he meant. When the girl hummed in familiarity the man continued. "Well, I hoped that you would be a part of that team. I know your last team up with S.H.I.E.L.D a few years ago didn't go as planned and that you've decided that working on your own was better but I hoped you could give us another chance. I think you'd be a great asset. If not for S.H.I.E.L.D then just as a consultant. I'd like to hear about your decision soon."

The girl sighed when Coulson didn't say anything else. Of course, she wanted to help Coulson with his team but teamwork wasn't something she was specialized in. The last time she went on a mission with S.H.I.E.L.D it went horribly wrong and she told herself she wouldn't make that mistake again. But now that Coulson asked for her help she couldn't refuse.

"All right, ill do it. But they better pay me for this."

"Don't worry, I've already made sure of that."

[aparnaphysiotherapy]

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[astroismypassion]

hi babe, could u tell me the possible career for NN in Aries in the 3 House. ?

:) <3

Hi there!!

ARIES NORTH NODE IN THE 3RD HOUSE

a writer, an author

researcher

something involving gym, sports, dietetics, nutrition, massages, mental health, pets, plants, physiotherapy

starting your own business or a side hustle

social media, you are really an innovator, especially when it comes to ideas and hacks

you might give great advice so use that in your career

you might be really strategic, methodical as well

you know how to constantly come up with new ideas

you could learn others hacks, how to simplyfy their living

you might start a channel about different careers, jobs, profiles

so you might be a great spokesperson for any profession

marketing, PR, social media influencer

commision work for magazines, newspapers, digital websites

you might write your own book, a poetry book or book about habits, talking, speaking, performing, public speaking

journalism

work in a hotel or a steward

a high school/elementary school teacher

@astroismypassion

[writingquestionsanswered]

Hello, my current project has a protagonist who undergoes a below the knee amputation. I've done a fair bit of research on timelines, recovery, prostheses, and physiotherapy. However, I'm still struggling with more of the day to day nuances of living with the disability. I was wondering if you knew of any resources I could check out? Thanks :)

I'm not aware of any resources specific to day-to-day life living with an amputated leg. However, if you Google "living with an amputated leg" there are some "what to expect at home" resources that look like they might touch on concerns of daily life. There's also a website called "Living with Amplitude" that is geared toward amputees, and this would be a place to look for links to personal stories, blogs, interviews, and articles that will provide a glimpse into life as an amputee. Crutches and Spice is a website and Instagram account run by Imani Barbarin, a writer and Black woman with Cerebral Palsy, which covers issues, information, activism, and resources pertinent to living with disability. That would be another good website to dive into in your research. Finally, go to YouTube and search "living with leg amputation." There are some "what to expect at home" videos as well as videos about amputees and their stories.

I hope that helps with your research!

•••••••••••••••••••••••••••••••••

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[mewaruniversity]

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