#spasticity treatment

[drchristophedelongsblog]

Spasticity

Let's start by clearly defining spasticity:

Spasticity is a neuromuscular disorder characterized by increased muscle tone, stiff, involuntary movements and exaggerated reflexes. It is often associated with lesions of the central nervous system, such as those caused by stroke, multiple sclerosis or spinal cord injury.

Causes of spasticity:

* Cerebral lesions: stroke, head trauma, brain tumors.

* Spinal cord injuries: road accidents, sports injuries, degenerative diseases.

* Neurodegenerative diseases: multiple sclerosis, amyotrophic lateral sclerosis (ALS).

* Other: encephalitis, meningitis, certain infections.

 Symptoms of spasticity:

* Increased muscle tone: muscles stiff and difficult to move.

* Involuntary movements: spasms, muscle contractions.

* Exaggerated reflexes: excessive muscular reactions to a stimulus.

* Walking difficulties: stiff gait, leg spasms.

* Pain: muscle contractures, joint pain.

Diagnosis of spasticity :

* Clinical examination: assessment of reflexes, muscle tone, muscle strength.

* Medical imaging: MRI, CT scan to identify underlying cause.

* Electromyography: measurement of muscle electrical activity.

Treatments for spasticity :

* Medication: muscle relaxants, baclofen.

* Physical therapy: stretching, muscle-strengthening exercises.

* Orthoses: splints to support joints and improve function.

* Botox: injections of botulinum toxin to reduce muscle spasms.

* Surgery: in the most severe cases, to correct deformities or contractures.

Living with spasticity:

* Adapting to everyday life: technical aids, home improvements.

* Psychological support: to cope with difficulties and improve quality of life.

* Patient associations: to exchange ideas and find support.

Advice for caregivers:

* Training: to understand spasticity and its consequences.

* Get informed: about treatments and available aids.

* Take care of yourself: to avoid exhaustion.

Go further

[dilfsisko]

The history of Botox is so funny. ‘I am going to put one of the most dangerous neurotoxins in the world in your face to see if it stops your eyes from fucking up. Holy shit where did your crows feet go’

[cripvideoproductions]

Talk to teaching students about stroke in adults and toddlers

On November 21 I spoke to another  class of Carol Carielli’s students learning to be teachers who had seen “A Stroke Of Endurance”. One student asked if the real professor who “A Stroke Of Endurance” is based on had his stroke in class, and I told them he had the stroke on campus but not during our class. I explained to the student the character in the film and the real professor did have side effects of the stroke that made him dizzy which led to a discussion of other different types of strokes, emergency treatments to stop a stroke, and individuals who had mini strokes and concussions which led to questions about institutional developmental delay, early intervention, Cerebral Palsy and my science essays https://medium.com/@dylanrothbein/how-does-mammal-fetal-development-relate-to-developmental-disability-guest-post-by-margot-8d52475fdaec  on Cerebral Palsy like The Moro Reflex https://medium.com/@dylanrothbein/the-moro-reflex-guest-post-by-margot-3d9ccc4758b2  and how the Moro Reflex and gag reflex effect children with Cerebral Palsy and Autism and how some children have both Cerebral Palsy and Autism at the same time. We discussed how teachers must also accommodate parents who have disabilities who have to meet with teachers and access the school buildings. 

This post is posted with permission of Professor Carol Carielli.  

[shreyajainblogs]

Pediatric physiotherapy plays a vital role in the effective management of cerebral palsy, helping children improve their mobility, strength, and overall quality of life. At the Kids Neuro Clinic, expert therapists collaborate with a leading pediatric neurologist in Dubai to create personalized treatment plans tailored to each child's unique needs. Combining advanced therapeutic techniques with compassionate care, the clinic ensures that children achieve their developmental milestones. Families seeking comprehensive cerebral palsy treatment in Dubai can rely on the clinic's multidisciplinary approach, which focuses on enhancing physical abilities and promoting independence for children with cerebral palsy.

[drpushpvardhanmandlecha]

Choosing the right specialist for chronic osteomyelitis treatment

Chronic osteomyelitis is a persistent and challenging bone infection that requires specialized care. Choosing the right specialist for chronic osteomyelitis treatment is crucial for effective management and recovery. This article will guide you through the essential factors to consider when selecting a specialist and highlight the importance of seeking treatment in Indore, a city known for its advanced medical facilities.

Understanding chronic osteomyelitis

Osteomyelitis is an infection in the bone, typically caused by bacteria. When the infection becomes chronic, it can lead to severe complications such as bone destruction, impaired function, and systemic illness. Chronic osteomyelitis often requires prolonged treatment, including antibiotics and sometimes surgical intervention.

Importance of a specialist

Treating chronic osteomyelitis is complex and requires a multidisciplinary approach. A specialist in this field has the expertise and experience to manage the condition effectively. Here are some key factors to consider when choosing a specialist for chronic osteomyelitis treatment

Multidisciplinary approach

Chronic osteomyelitis often requires a team of healthcare professionals, including infectious disease specialists, orthopedic surgeons, radiologists, and physical therapists. Choose a specialist who works within a multidisciplinary team to provide comprehensive care.

Advanced diagnostic tools

Accurate diagnosis is the cornerstone of effective treatment. The specialist should have access to advanced diagnostic tools such as MRI, CT scans, and bone biopsies. These tools are crucial for determining the extent of the infection and planning appropriate treatment.

Customized treatment plans

Every patient is unique, and so is their condition. The specialist should develop a customized treatment plan tailored to your specific needs. This plan may include a combination of antibiotics, surgical procedures, and physical therapy to ensure the best possible outcome.

Rehabilitation and follow-up care

Recovery from chronic osteomyelitis can be a long process. The right specialist will not only focus on treating the infection but also on rehabilitation and follow-up care. Regular monitoring and adjustments to the treatment plan are essential to prevent recurrence and ensure full recovery.

Chronic osteomyelitis treatment 

Indore has emerged as a hub for advanced medical treatments, including chronic osteomyelitis. The city is home to several renowned healthcare institutions and specialists who offer state of the art care. Here are some reasons why you should consider seeking chronic osteomyelitis treatment in Indore 

Advanced medical facilities

Indore boasts world-class medical facilities equipped with the latest technology and equipment. These facilities ensure accurate diagnosis and effective treatment for chronic osteomyelitis.

Expert specialists Indore has a pool of highly qualified and experienced specialists in the field of infectious diseases and orthopedics. These experts have a proven track record of successfully treating chronic osteomyelitis.

Comprehensive care Healthcare institutions in Indore provide a multidisciplinary approach to chronic osteomyelitis treatment. Patients benefit from the collaboration of various specialists, ensuring comprehensive and holistic care.Affordable treatment

Compared to other major cities, the cost of chronic osteomyelitis treatment in Indore is relatively affordable. Patients can access high-quality care without the financial burden often associated with complex medical treatments.

Clubfoot treatment 

In addition to chronic osteomyelitis treatment, Indore is also known for its expertise in treating other orthopedic conditions, such as clubfoot. Clubfoot is a congenital deformity that affects the feet and can lead to mobility issues if left untreated. The city offers specialized clubfoot treatment in Indore with advanced techniques and experienced orthopedic surgeons dedicated to correcting this condition and improving patients' quality of life. Choosing the right specialist for chronic osteomyelitis treatment is essential for effective management and recovery. By considering factors such as qualifications, experience, a multidisciplinary approach, advanced diagnostic tools, customized treatment plans, and comprehensive care, you can make an informed decision. Indore stands out as a premier destination for chronic osteomyelitis treatment and clubfoot treatment, offering advanced medical facilities, expert specialists, and affordable care. Prioritize your health by seeking the best possible treatment in this renowned medical hub.

[physiotherapy-clinic]

Spasticity, often associated with neurological conditions such as cerebral palsy, stroke, and traumatic brain injuries, is a condition that can significantly impact an individual’s quality of life. In this article, we’ll delve into the essential role that physical therapy plays in managing spasticity and improving the lives of those affected.

[edsonjnovaes]

a pioneering medical #cannabis patient

50th anniversary of my brother Danny’s death — a pioneering medical #cannabis patient in early 1970s. My parents bought weed illegally as Nixon started War on Cannabis; it vastly transformed Danny’s quality of life on chemo toward end during his unsuccessful fight with leukemia. Peter Grinspoon, M.D. – @Peter_Grinspoon. Jan 13, 2023 Medical cannabis has a long history dating back thousands of…

[afeelgoodblog]

The Best News of Last Week

⚡ - Charging Towards a More Electrifying Future

1. The Kissimmee River has been brought back to life—and wildlife is thriving

The Kissimmee River in Florida was straightened in the 1960s, causing a sharp decline in wildlife and ecological problems. But in the 1990s, a $1 billion restoration project was initiated to restore the river's natural state.

Today, nearly half of the river has been restored, wetlands have been reestablished and rehydrated, and wildlife has returned, including rare and threatened species. Already the biological impact of the project has become clear. As the wetlands have come back, so have the birds.

2. Plastic wrap made from seaweed withstands heat and is compostable

A cling film made from an invasive seaweed can withstand high temperatures yet is still easily compostable. The material could eventually become a sustainable choice for food packaging.

Scientists started with a brown seaweed called sargassum. Sargassum contains long, chain-like molecules similar to those that make up conventional plastic, which made it a good raw material. The researchers mixed it with some acids and salts to get a solution full of these molecules, then blended in chemicals that thickened it and made it more flexible and pliable.

3. An Eagle Who Adopted a Rock Becomes a Real Dad to Orphaned Eaglet

Murphy, a bald eagle that had been showing fatherly instincts, has been sharing an enclosure with an eaglet that survived a fall from a tree during a storm in Ste. Genevieve. Murphy, his rock gone by then, took his role as foster parent seriously. He soon began responding to the chick’s peeps, and protecting it.

And when, as a test, the keepers placed two plates of food in front of the birds — one containing food cut into pieces that the chick could eat by itself, and another with a whole fish that only Murphy could handle — the older bird tore up the fish and fed it to the eaglet.

4. World's largest battery maker announces major breakthrough in energy density

In one of the most significant battery breakthroughs in recent years, the world’s largest battery manufacturer CATL has announced a new “condensed” battery with 500 Wh/kg which it says will go into mass production this year.

“The launch of condensed batteries will usher in an era of universal electrification of sea, land and air transportation, open up more possibilities of the development of the industry, and promote the achieving of the global carbon neutrality goals at an earlier date,” the company said in a presentation at Auto Shanghai on Thursday.

This could be huge. Electric jets and cargo ships become very possible at this point.

5. Cat with '100% fatal' feline coronavirus saved by human Covid-19 medicine

A beloved household cat has made an “astonishing” recovery from a usually fatal illness, thanks to a drug made to treat Covid-19 in humans – and a quick-thinking vet.

Anya​, the 7-year-old birman cat, was suffering from feline infectious peritonitis (FIP), a “100% fatal” viral infection caused by feline coronavirus. That was, until Auckland vet Dr Habin Choi​ intervened, giving Anya an antiviral used to treat Covid-19 called molnupiravir.

6. Kelp forests capture nearly 5 million tonnes of CO2 annually

Kelp forests provide an estimated value of $500 billion to the world and capture 4.5 million tonnes of carbon dioxide from seawater each year. Most of kelp’s economic benefits come from creating habitat for fish and by sequestering nitrogen and phosphorus.

7. Medical Marijuana Improved Parkinson’s Disease Symptoms in 87% of Patients

Medical cannabis (MC) has recently garnered interest as a potential treatment for neurologic diseases, including Parkinson's disease (PD). 87% of patients were noted to exhibit an improvement in any PD symptom after starting medical cannabis. Symptoms with the highest incidence of improvement included cramping/dystonia, pain, spasticity, lack of appetite, dyskinesia, and tremor.

----

That's it for this week :)

This newsletter will always be free. If you liked this post you can support me with a small kofi donation:

Buy me a coffee ❤️

Also don’t forget to reblog

[figs-and-cigs]

Saw a post recently that said if you're not a good communicator you shouldn't be in a poly relationship. My first thought was, "right communication is an absolute MUST!" But thinking about it some more, I think there needs to be more nuance to the idea. What makes good communication? And who's to say who should and shouldn't do polyamory?

I'm an easily overwhelmed, agoraphobic, introvert - and at times communication IS hard. I often seek alone time with very little interaction with the outside world.

I had a girlfriend who HATED texting and wanted lots of in person face to face time. That relationship slowly unravelled and disappeared - without communication. I'm a texter and couldn't fit my schedule or find the spoons to spend more time with her - and she never texted.

I had to explain to a new person I'm dating that I'm not good at asking a lot of questions - which can look like a lack of interest and a failure in gathering information for a good match. The reality is I figure others will tell me what they want me to know over time as they get comfortable, and if it's important it'll come up. Meanwhile, I'm an open book. I communicate with lengthy paragraphs and stories to paint a picture of my world. Which often gets others to share similarly - through text, and more importantly get to know me on a deep level. In person I'm spastic mess, I get emotional about everything and excitement or frustration can jumble words into an incoherent rant.

When I'm upset, I cry... And trying to help someone see my point of view doesn't work well between frustrated sobs I can't control. With my husband we make an effort to take a pause with intense discussions and let me write/text it out. And while he can be a stoic type during emotional discussions - giving him time to process is important. But my anxious attachment will precieve it as if I'm doing all the communication and he's got nothing!

I also unintentionally go into circles and rants as I process which can be overwhelming to the other party. I've been in relationships where we'd talk and talk and talk and talk until we'd exhaust each other and that talking might turn into yelling or unhealthy silent treatments. Neither of us could understand each other or find common ground.

To prevent this with my husband we set timers. 5/5/10. We each get 5 minutes to share our thoughts, and then we'll have 10 minutes to collaborate on a solution - or to bond or support each other.

I have a FWB who I rarely hear from. Maybe every few months when he's in town and able to set a date to meet. He's not the talkative type unless we're alone in a room together - and I realized I'm ok with this. I don't need constant contact to enjoy my time with him.

I think a huge part of healthy relationships is meeting people where they're at and accepting each other exactly as we are. The good, the bad, the messy, and perfectly whole. And it's beautiful and wonderful! But it's also complicated and hard. Not every relationship is going to last. But the experiences together are valuable nonetheless.

When our communication styles and skills are different, what do we do!? Ironically, we communicate about it, and even a "bad communicator" can find work arounds. I think it comes down to boundaries and trying to understand each other. And if it doesn't work out between both of you - it doesn't mean we can't find someone else who it can't work with.

And while we can find total acceptance of each other one would hope each of us is working on personal progress and improvements in areas that we struggle.

Just like there's no one right perfect way to be poly, I don't think there's only one right perfect way to communicate. We each need to find what works best for us and our individual relationships. And it's going to vary and be different almost every single time.

The end.

[stevenbasic]

Growing into the Job, Post 412: Back to Her Stinkbugs

“You’re…y-you’re Adriennne Aleppo, aren’t you?” the young woman said, standing nervously in the aisle of Flight 4433, headed to LAX, “I’m sorry to disturb you…I’m just such a big fan.”

“Awww, yes, thank you,” replied the bosomy red-haired woman, who immediately was silently cursing this stupid airline for letting coach passengers the unfettered ability to just stroll on up into first class and bother its patrons. “That’s nice of you to say.”

“I loved you in ‘All Tomorrow’s Yesterdays’ and ‘Uplight’ and of course now I watch every episode of ‘Stinkers!’  - Tuesday nights at nine! - with my girlfriends,” the woman continued. Her voice had the spastic, unmistakable cadence of a starstruck admirer. There were more of those every day. “You’re so, so beautiful. I can’t believe I’m seeing you here, on the same plane as me, in person!”

“That’s sweet,” she replied, doing her best to smile up at the plain, underdressed young woman who was now leaning in towards her.  Adrienne Aleppo, Product Study #F8-042-AA and daughter of immigrant Portuguese bakers, was a growing celebrity, slowly becoming jaded to the fame she was acquiring, but still a sucker for adoring praise. She figured she could indulge this obviously over-enthusiastic fan a little, at least for a moment or two. “But soon you won’t have to wait ‘til Tuesdays. There’s going to be a new episode every Saturday night now, too. ‘Stinkers After Dark!’”

“Omigod really!?”

“Yeah it starts next week,” Adrienne Aleppo added. The new show was going to be the network's chance to get a little more risqué, capitalize on its rising star’s captivating figure and how exactly she’d been using it to more-or-less take over the house.

“Omigod im so excited. I love ‘Stinkers!’. I’m glad they picked such short guys, I’m glad you’re on it! The show is becoming so popular! Everyone loves it!”

Of course it is, and of course they do. The camera spends the whole show in my cleavage. “Oh thank you,” the starlet replied. She was happy, of course, that the show was now enjoying such huge viewership. It wasn’t really much more than your typical reality show where young, beautiful but otherwise unlikeable people were thrown in to live together and backstab one another. They were basically halfway through its planned run and the producers were tickled pink by how exponential its growth had been…with no illusions that it mirrored that of its now main attraction. A main attraction who was now a little annoyed by the woman standing in the plane aisle over her. How can I get rid of this person?  “Would you like an autograph?”

“Yes sure of course!” the woman gushed, as Adrienne Aleppo was already pulling a pen and pad from her bag. She kept these in her purse exclusively for this purpose.

“I’m headed back to the ‘Stinkers!’ house right now-“ she began, as she swiftly scribbled the swirly scrawl that constituted her celebrity signature.

“‘Gotta keep your little stinkbugs in line’!” the girl interjected.

“….yeah, that,” the busty redhead said. The girl was quoting her directly from last week's episode, when she was commenting to the camera on her new strategies concerning her housemates. “Anyway, I think the fasten seatbelt sign just went on……”

The fan looked up in confusion just as - soon after Adrienne spoke -  the ding of the sign came to life and the captain got on the mic telling people to get to their seats. The fan stammered a few words of thanks and admiration, and left.

The bosomy young beauty took the chance to relax again, gaze out the window, and plan. She had another several hours before she’d be back on the ground and swooped up, driven to and sequestered in the Hollywood megamansion that doubled as a reality show set. The only one allowed out of the house, and only for these weekly treatments at that rink-dink little Midwestern clinic, Adrienne Aleppo knew that she was in perfect position to not only come away from ‘Stinkers!’ as the game’s victor, but with new assets to insure a meteoric rise in fame. She was already in talks with her agent about a new show, one centered entirely around her, and there were rumors of imminent movie offers. She knew how things worked, though, and that she should still take the opportunity and spend the last two months of ‘Stinkers!’ run building her cult of personality.

In fact, something the girl in the aisle said earlier - ‘I’m glad they picked such short guys’ - rang back into Adrienne’s head. It got her thinking about the clip she’d seen, shown to her by one of the pretty girls at the clinic, of the Kathy O’Connor show. She’d already made her male housemates more submissive. What could it do for my ratings if was able to…?

Images came to her, images not of stinkbugs, but rather of a houseful of men the size of rats, scurrying around her feet.

=========================

[homo-taylorsversion]

The fact my entire life could be a whole fucking lie... Kinda hurts...

At 3, I was diagnosed with spastic cerebral palsy. And that means (quick google search): Spastic CP is caused by brain damage that affects muscle control, coordination, and movement, mainly in the arms and legs. This damage can occur before birth, during childbirth, or later in life.

But I had to go every 2-6 years for an MRI because of some noncancerous cyst or whatever the fuck it was on my spine. to make sure it wasn't getting worse.

(First red flag! That's how I got diagnosed. The cyst, NOT brain damage. And my dad even pushed it because he didn't want to accept my autism diagnosis)

However, my most recent MRI (in a completely different state) shows none of that. (Aside from minor things, IG?) However, it showed signs of multiple scoliosis. They couldn't go forward on the testing because they had none of my childhood MRI's.

After MONTHS of fighting my og hospital in the state I grew up, I just got my MRI's.

Guess what? NO mention of cerebral palsy. Just spine/nerve damage. Just the "cyst". But also guess what? ALL DIFFERENT "DIAGNOSIS"

Also, apparently CP and MS have A BUNCH of overlapping symptoms. And honestly, the MS symptoms make SO MUCH more sense than the CP ones.

Also, you're supposed to get reassessed for CP if it's mild to make sure it's not misdiagnosed. Never happened for me. Or some surgery for leg/walking issues? No, I didn't get that either.

Did you know, cp can't get worse, only better. MS fluctuates and has lapsing/varying symptoms. It can happen at ANY age.

Oh! Auto immune disorder runs in my family! Almost everyone has ONE!

And, moving to this new state, I came aware of these other issues that I just thought were cerebral palsy related. Because that's what everyone did. Any symptom? Nah, just cp. They completely overlooked any and all symptoms! Now, the doctors here are listening. They're doing TESTS instead of "it's cp, stop complaining and being dramatic" And I'm getting the help, the actual listening and understanding. The right diagnosis. The TREATMENT! Not JUST "Alright, back to physical therapy for you." that never seemed to work. Aside from learning to walk and talk. And yet, it barely got better.

It's just that, my entire life... Nobody cared, nobody listened. I was restricted from SO much because of this. I practically lost my childhood. Nothing I wanted to do was allowed. And it hurts, because I was so medically neglected because my doctors just glossed over everything because ONE possibly wrong diagnosis.

And to learn that none of that would have happened if they listened and kept trying figure things out...

[shychick-52]

My physical disability (long post)

Given that it's Disability Pride Month, I wanted to share a bit of my own experience.

After experiencing HORRIBLE back pain for weeks in late 2016 (the doctor didn't send me for an MRI or any deeper scan after the x-ray didn't show anything), I woke up one morning in January 2017 with literally ZERO balance. Like, I could move my legs, but I still couldn't walk. It was the most terrifying sensation.

Called the ambulance, they took me to the hospital where I had the proper scan done, and it turned out to be a massive tumor pressing on my spine and crushing the nerves. Because it had been growing for months, everyone agreed it was a miracle I wasn't totally paralyzed. (The tumor turned out to be cancerous, and I had several more tumors in other places too, including my stomach, ovaries, liver, and kidneys). After it was removed, I still had zero balance.

Well, the entire five months I was in the hospital getting treatment wasn't fun, made even worse by my destroyed mobility. During my stay, I switched back and forth between a wheelchair and a walker. I was so depressed, terrified I'd never walk properly again and convinced my life was over. Even after I was discharged from the hospital, and still continued to use a wheelchair and walker, I can't count how many times I freaking bawled. I had very poor control of my legs, and had to look down at them at all times to know what they were doing so I didn't trip.

And for the first time in my life, I was met with challenges that able-bodied people don't have to worry about (the worst of which were stairs). I could finally appreciate how frustrating it is when able-boded people selfishly use the handicapped stall in the washroom (when the other ones are perfectly available) when you have to go!

Not long after I got out of the hospital, I started attending physical therapy. I worked for months and months, and graduated from a walker to two canes to just one cane. I practiced walking in the pool by my place (with aqua-therapy, I didn't have to worry about injuring myself if I fell in the water, and I fell plenty at first). I gradually got better, but it was HARD.

Shortly after my very first visit to physical therapy, my therapist diagnosed me with spasticity in my legs and feet. That's a condition caused by a spinal cord injury; the injury to the nerves in the spine cause the signals between the nervous system and the legs/feet to be thrown completely out-of-whack and fail to communicate properly (which was why I couldn't sense what my feet were doing unless I looked at them), forcing the leg muscles to be in a permanent state of horrible stiffness and constant spasms. It's a horrible feeling.

Finally, in the later part of 2019, I no longer needed a cane. I could walk just fine on my own (for the most part), and I haven't had to rely on walking aids since then, and I don't have to watch my feet to know how they're moving when I walk. But the spasticity- which is permanent- remains. I manage it with medication, which helps the stiffness a bit. And my biggest challenge remains stairs; I absolutely cannot go up and down stairs (especially up) without a banister. But because of how generally stiff my muscles are, my balance will never be perfect. And I can't really run, although I can walk just as fast as I used to.

Cold weather, rain, and atmospheric pressure all make the spasticity worse.

[dozing-marshmallow]

Hii I was wondering if I could request a fluff about Chris x fem!reader that has Spasticity (abnormal increase in muscle tone or stiffness of muscle, which might interfere with movement) i haven’t seen anyone write anything with this disability before because it’s not as brought up. If not that’s totally fine🫶

Ohh but it wouldn’t be! It’s important to address disabilities and keep people educated! This was a delightful request and I’m thankful you submitted it, apologies it took long! I hope everyone’s been having a great day and enjoying the last few days of 2023 :))

CHRIS MCLEAN X FEMALE! READER WITH SPASTICITY FLUFF

Even though your stiff muscles had limited a lot of what you could do, you were still bubbly and motivated by life.

And Chris adored that.

He wasn’t embarrassed to be seen with you as you thought he would be.

Anywhere like now, he would push your wheelchair for you.

You were going shopping together.

He’s witnessed only a handful of those who stared, made offensive comments or tried to touch you.

Like some strange specimen that could be stared at.

So, he became your number one security guard.

You felt guilty that he had to go through the trouble of having to stand up for you until you see his face as he does it. 

Looks like misinformed people bothered him as much as they did you.

Throughout your shopping trip, he gave you massages to soothe the tightness in your muscles and even allowing you temporary movement.

Your spasticity made it difficult for you to speak, which was no problem for Chris.

“Which one do you like more? This one or this one?” he asked you in the lipstick aisle.

You want the one that’s still on the shelf.

He catches where your eye went, still smiling, pointing right at it,“You want this one?”

You gave the slightest rock of head. He replaces the two samples he had with the one you wanted,“Consider it yours!”

After completing the shopping list, Chris had something to disclose to you,“Listen, I’m not always gonna be there to help you. I’ll have to be away for shooting, hosting. Job stuff.” you heard him explain,“Sooooo when I can’t be there, I’ll have someone come over.”

You whined.

“Ohh come on. I’m everyone’s favourite guy. I can’t be there all the time. I made sure your support worker is good.” he can say that, but how can he be so sure?

There were horror stories of workers putting those who were meant to be in their care through terrible treatment. No amount of high training could convince you that this stranger would be as nice as Chris was. And he wasn’t even getting paid!

To your other whine, he sighed. Sighing... He had other things to do... Not just him... But everyone else in your life. You could never live on your own... You would always need someone... How could you live like that?

“Well! We’ll go over it later.” your beloved declares, sounding not so tired which removes you from your self deprecation,“It’s not like you’ll meet her on the day I’ll be absent. You’ll get to know each other before so you can build up on trusting her.” it’ll be a her? Yeah...if Chris persisted then you’d at least feel safer with a fellow woman,“For now, we should get going. You have that appointment with your physical therapist today.”

Your life is just as important as someone who’s able-bodied. Proven by your heartbeat and him.

[mindorabydisha]

Rj Mitte has Cerebral Palsy? Understanding Cerebral Palsy: A Psychologist's perspective

- Disha Arunagiri

Counselling Psychologist

Yes, RJ Mitte has cerebral palsy

Mitte was diagnosed with cerebral palsy at age three. He wore casts for six months to straighten his feet and used crutches and leg braces for most of his childhood. Mitte has used his platform to advocate for representation of people with disabilities in the media and arts. He has also sought out acting roles that would educate people about his disability.

Understanding Cerebral Palsy: A Psychologist's perspective

This October 6th was considered as World Cerebral Palsy Day, we join hands globally to raise awareness about cerebral palsy.

Cerebral Palsy (CP) is a neurological disorder that affects movement, muscle tone, and posture. It is caused by damage that occurs to the immature brain as it develops, most often before birth. This condition affects individuals differently, with varying degrees of severity. Understanding cerebral palsy is crucial for fostering a more inclusive society where everyone can thrive.

What is Cerebral Palsy?

Cerebral palsy (cp) is a group of disorders that impact a person’s ability to move and maintain balance and posture. The term "cerebral" refers to the brain, and "palsy" refers to weakness or problems with using the muscles. It is the most common motor disability in childhood.

Causes of Cerebral Palsy

Cerebral palsy is often caused by abnormal brain development or damage to the developing brain. The damage can occur before, during, or shortly after birth. Some potential causes include:

1. Prenatal factors: Infections during pregnancy, maternal health issues, and genetic mutations.

2. Perinatal factors: Complications during labor and delivery, such as lack of oxygen to the brain.

3. Postnatal factors: Early childhood infections, brain injury, or events like strokes.

Types of Cerebral Palsy

Cerebral palsy is classified based on the type of movement disorder involved. The main types include:

1. Spastic Cerebral Palsy: The most common type, characterized by stiff muscles and awkward movements. It is further categorized based on which limbs are affected.

2. Dyskinetic Cerebral Palsy: Involves uncontrolled movements, which can be slow and writhing or rapid and jerky.

3. Ataxic Cerebral Palsy: Characterized by problems with balance and coordination.

4. Mixed Cerebral Palsy: Some individuals exhibit symptoms of more than one type of cerebral palsy.

Symptoms and Diagnosis

The symptoms of cerebral palsy vary greatly among individuals. Common signs include:

- Delays in reaching motor skill milestones, such as rolling over, sitting, or walking.

- Abnormal muscle tone, either too stiff or too floppy.

- Poor coordination and balance.

- Involuntary movements or tremors.

- Difficulty with fine motor skills, like writing or buttoning a shirt.

Diagnosing cerebral palsy involves a combination of medical history, physical exams, and various tests such as MRI or CT scans. Early diagnosis and intervention are crucial for managing the condition effectively.

Treatment and Management

While there is no cure for cerebral palsy, various treatments can help manage symptoms and improve quality of life. Treatment plans are tailored to individual needs and may include:

- Physical Therapy: To improve strength, flexibility, and mobility.

- Occupational Therapy: To assist with daily activities and enhance fine motor skills.

- Speech Therapy: To address communication challenges.

- Medications: To manage muscle spasticity and other symptoms.

- Surgery: In some cases, to correct physical abnormalities and improve function.

Despite these challenges, individuals with CP often lead fulfilling lives with the right support and resources.

As a psychologist, the focus is often on the mental and emotional well-being of individuals with CP, as well as their families. Understanding the psychological impact of CP is crucial in providing comprehensive support and fostering an inclusive society.

Psychological Impact on Individuals with CP

1. Emotional Well-being: Living with CP can sometimes lead to feelings of frustration, isolation, or anxiety, especially if there is a lack of understanding or support from society. It's important to acknowledge these emotions and provide spaces where individuals can express and manage their feelings.

2. Self-esteem and Identity: The visible nature of CP can affect self-esteem, particularly during formative years. Positive reinforcement, inclusive environments, and highlighting strengths and abilities are essential in building a strong sense of self.

3. Social Relationships: Forming and maintaining relationships can be challenging due to physical limitations or societal stigma. Encouraging social interactions and providing inclusive opportunities for engagement can help build meaningful connections.

Supporting Families of Individuals with CP

Families play a crucial role in the lives of individuals with CP. They often face their own set of challenges, including emotional stress, financial strain, and the need for continuous caregiving. Psychological support for families can include:

1. Counseling and Therapy: Professional guidance can help families navigate the emotional landscape of raising a child with CP, providing coping strategies and emotional support.

2. Support Groups: Connecting with other families in similar situations can provide a sense of community and shared understanding. These groups can be a source of practical advice and emotional solidarity.

3. Educational Resources:Providing families with information about CP, available therapies, and adaptive technologies can empower them to make informed decisions and advocate effectively for their loved ones.

Promoting Inclusion and Awareness

On World Cerebral Palsy Day, it’s vital to emphasize the importance of inclusion and awareness. Here are some steps we can take:

1. Education: Educate ourselves and others about CP to dispel myths and reduce stigma. Awareness campaigns and educational programs in schools and workplaces can promote understanding and acceptance.

2. Advocacy: Support policies and initiatives that promote accessibility and inclusion. Advocacy can lead to improved services, better accessibility, and greater recognition of the rights of individuals with CP.

3. Community Involvement: Encourage community activities that are inclusive of individuals with CP. Participation in sports, arts, and social events can provide a sense of belonging and achievement.

Cerebral palsy is just one aspect of a person’s identity. By understanding the psychological impact and providing comprehensive support, we can help individuals with CP lead empowered, fulfilling lives. On this World Cerebral Palsy Day, let’s commit to raising awareness, promoting inclusion, and supporting the mental and emotional well-being of those affected by CP. Together, we can build a world where everyone, regardless of their abilities, can thrive.

I hope this helps everyone to educated about Cerebral Palsy. Thank you for reading.

Disha Arunagiri

Counselling Psychologist

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What is Cerebral Palsy?

Cerebral palsy is a neurological disorder that affects movement, muscle control, and coordination. It is caused by damage to the developing brain, typically before or during birth. This condition can have a significant impact on individuals and their families, requiring specialized care and support.

According to the Centers for Disease Control and Prevention (CDC), cerebral palsy affects approximately 1 in 323 children in the United States. Despite its prevalence, there is often a lack of understanding and awareness about this condition and its different types.

In this article, we will discuss the four main types of cerebral palsy, the causes and risk factors, the process of diagnosis, treatment options, and resources available for individuals and families affected by this condition.

Types of Cerebral Palsy

Cerebral palsy is a neurological disorder that affects movement and muscle coordination. It is the most common childhood motor disability, with about 17 million people worldwide living with this condition. While the cause of cerebral palsy is not fully understood, it is important to understand its different types in order to provide appropriate treatment and support.

Four Main Types of Cerebral Palsy

· Spastic: This is the most common type of cerebral palsy, accounting for 70-80% of cases. It is characterized by stiff and jerky muscle movements, making it difficult to control the limbs.

· Dyskinetic: Also known as athetoid cerebral palsy, this type is characterized by uncontrolled and involuntary movements of the face, trunk, and limbs.

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