#Multiple Sclerosis treatment cost

[stemcelltherapyinindia]

Minimum Cost for Multiple Sclerosis Stem Cell Therapy in India

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[telltalebatman]

looking up how much my current meds (ocrevus) cost outside of any medical refund systems and bruh, we need to abolish capitalism asap, this shit costs over 20k dollars per infusion................................

[medacess]

Budget-Friendly Stem Cell Treatment for Multiple Sclerosis in Mumbai, India

Looking for affordable and effective treatment for Multiple Sclerosis? We offers advanced stem cell therapy in India that can help manage symptoms, slow disease progression, and improve quality of life—without breaking the bank!

[rebirthgarments]

TW: Chemical w-rfare, Ab-rtion

Urgent Ask to evacuate Nara, a 🍉 disabled woman with MS who also has pancreatic cancer due to chemical w-rfare.

Support by financially contributing to her @FedUp4Palestine vetted funhnd-raizer (that I personally vetted): givebutter.com/NaraMedicalAid

+ resharing/ reposting this post!

I, Sky Cubacub- a Fed up 4 Palestine team member, have been in direct contact with Nara to get to know her and her story more over the past few days. We have become fast friends due to so many overlapping symptoms of our disabilities. Nara’s story caught my eye because I have post-viral ME/CFS which many times is a precursor to MS. I really want my disability community to show up for her to get this campaign funded that is so close to my heart so that she can continue medical treatment.

We have chatted extensively! During our chats, I found out from Nara that she had not previously had health issues until she was exposed in the white phosphorus attack in 2008. The long lasting damage and effects of phosphorus continue to compound and become more and more disabling to this day, even after 16 years.

Here is her story in her own words (edited for clarity):

“Hi I'm Nara,

I'm a cancer and multiple sclerosis patient. I need treatment, examinations, and follow-up on a regular basis, but the hospitals in which I used to follow up were bombed and the other one was turned into military barracks. All I need now is to leave Gaza for treatment, preserve my life, and live with my family in peace.

We're a family of 4, including my 12 and 7 year old children.

I had been diagnosed with a tumor in the pancreas as a result of inhaling phosphorus in a previous war. A couple years after being exposed to phosphorus, I became pregnant, and the fetus was pressing on the tumor, which drew the doctor’s attention to the cancer. My fetus was emergency aborted, and the spleen, 80% of the pancreas, and part of the small intestine were removed. I complained every now and then of a lot of pain as a result of the removal of part of the pancreas. I was having follow up care in the Turkish Friendship Hospital for hematology and tumors. But since the beginning of October, I have not been able to follow up because the hospital has turned into a military barracks.

The remaining part is talking about multiple sclerosis:

In 2018, I was diagnosed with multiple sclerosis. I had many complications, such as inflammation of the seventh nerve in the eye, the inability to walk with balance, movement with difficulty, and many symptoms. I was then required to take 12 injections every month and many medications and vitamins. I was following up at the Nasser Medical Complex in Khan Yunis, but unfortunately the hospital was out of service due to the war. So for a long time I have not received any injections. MS is truly difficult and it controls my life completely, and the attacks occur in many and varied ways.”

A note about her breathing apparatus:

Because people in displacement have to wait in long queues and pay to use the bathroom, Nara had started to restrict her water intake because of a UTI she never has been able to heal from. This has created a problem with raised levels of potassium, so doctors have placed her on oxygen for fear of the potassium affecting her heart.

Goals

she needs at least $15,000 to evacuate

2 adults at $5,000 each

2 children at $2,500 each

this price is subject to increase due to the cost of registration for evacuation continuing to go up

The other money will go to the cost of treatment and living costs.

Nara chooses to stay anonymous because she has had to mask her disabilities so much that only her family knows about her MS and Cancer, so we have not linked her instagram, but we are in direct contact with her and can verify that she is who she says she is! Because of this, she cannot promote her own fundraiser, so it is our job to collectively do it for her!

[Image Description: a digital illustration by @k8deciccio of Nara, a Pal-eh-stienian woman wearing a black hijab/outfit with purple highlights. She has a breathing apparatus that is bulbous that goes in her nose. Text Reads: Help Narawith Cancer and MS Treatment, She Must Evacuate with her family of 4. $30k goal givebutter.com/NaraMedicalAid . There is a QR code in the bottom right corner that goes to her support link. The @FedUp4Palestine logo is in the top left corner.]

[seventhscorpio]

GAZA FUNDS MASTERPOST

Recently many Palestinians from Gaza have reached out to me for help; I'm donating what I can, but as an unemployed student my resources are limited, and sharing their stories is the second best thing I can do. Each of them *is* a person with a story rather than just another fundraiser link, and right now, each of them is in mortal danger. Please consider donating, even if all you can give is a couple dollars. Any amount WILL make a difference!!!

(Last updated Oct. 15, 2024)

@aseelo680 https://gofund.me/16fe6e48 $52,779/100.000 Aseel's mother is sick and needs expensive treatment, and her father had a stroke. They lost friends, family members, and all their possessions.

@hanaa96yousef https://gofund.me/16482899 £28,330/50,000 Hanaa has a 2yo son Yousef. She is suffering from several diseases due to drinking contaminated water and needs treatment.

@naseer220 https://gofund.me/4be10ad5 £9,397/20,000 Israa is taking care for her 2yo son, 2-month-old daughter, and a bedridden father who has cancer and needs urgent surgery. Her husband went missing 8 months ago.

@monis-family2 https://gofund.me/dcee6396 $4,203/41.300 Monis has cancer and his wife is sick with polio. They need medicine that costs $100 every three days, and they have no chance of treatment in Gaza.

@omarmohammed2 https://gofund.me/8796dd9f €1,164/25,000 Omar lost his family in the war save for his brother Mohammed, who suffers from multiple sclerosis and needs treatment. They also need basic necessities to survive the winter.

@karemanfamilye https://gofund.me/59d321bd $11,033/20,000 Kareman lives in a tent with her husband Ayman and their baby son Hamound. Due to contaminated food and water, Hamound constantly gets sick, and the conditions the family lives in are unbearable.

@sfaamq10 https://gofund.me/9955bd5a $22,058/75,000 Before the war, Safaa was studying to be a lawyer. She lost her home and relatives, and had to give birth to her son Amir in difficult conditions. Her father had a stroke, and her mother suffers from diabetes and her condition is getting worse.

@lendaabdalhadi https://gofund.me/34901cf7 €646/30.000 Linda got separated from her husband when the war started. She was pregnant, but due to the lack of food and medicine she suffered a miscarriage, and last April she also lost her beloved older brother.

@ahmed-al-saidi-11 https://gofund.me/9da4f51b £1,812/30,000 Ahmed's family is living in inhuman conditions, without food, electricity or running water. His son Qusay is after a difficult throat surgery but doesn't have access to medical care; both his parents are elderly people with heart diseases.

@mhammedmosa37 https://gofund.me/66f6d9fd $4,350/20,000 Muhammad has a baby son who was born during the war in difficult circumstances. Their family needs food, diapers and milk, and is collecting funds to escape gaza.

@fidaa-family2 https://gofund.me/94b9dfe0 $55,900/75,000 Fidaa gave birth two months ago in horrific conditions. She needs food and medication for her 2yo daughter Sila and infant son Muhammad Ahr.

@ahlamramadan1 https://gofund.me/61f1dd1f €2,230/30,00. Ahlam suffers from kidney failure and needs dialysis 3 times a week. She is in dire need of treatment.

@tahrir12 https://gofund.me/2119998c $11,888/65,000 A large family in a critical condition, including children with severe injuries: toddler Ameer with a broken pelivs, and Khamees, who is after surgery and needs appropriate medication.

@free-gaza2 https://gofund.me/9e4024a3 $7,071/12,000 Doaa escaped Gaza and is collecting funds to buy a sewing machine and restart her business so she could continue to support her family and autistic son. Her husband is still in Gaza.

@hashem19798 https://gofund.me/0dfe3470 $4,020/60,000 Hashem's family of six is trapped in Gaza in dire need of shelter, and Hashem herself has been injured.

@malakalmughrabi https://gofund.me/f4eac6d9 €766,/25,000 Malak, her husband and 3yo son are homeless after their house was destroyed in a bombing.

@khawla-gfm2 https://gofund.me/5050ded3 $13,445/20,000 Khawla's son contracted hepatitis from drinking contaminated water. They have no food or medicine, not even milk for her youngest baby.

@hyamshehabb https://gofund.me/3e0c4580 €13,814/25,000 A family of 6, including two children and two elderly people who are sick and in need of treatment.

@wafaaresh6 https://gofund.me/4ae11497 $46,495/50,000 Wafa's mother has a chronic illness and needs urgent surgery.

@asmmma-family https://gofund.me/791dc07f $7,504/20,000 Asmaa's family lost their newly-built house and are now living without food, water, and shelter. The funds will be used to evacuate them from Gaza.

@falestine-yousef https://gofund.me/77ca82d7 $7,504/20,000 Palestine gave birth to her son Yousef during the war. They live in unsanitary conditions and need medicine, food and diapers for the baby.

"I am strong when you help me and stand by my side." - @monis-family2

[p0tat0-g0ddess]

Please help my best friend's family afford a new car and medical bills

UPDATE 7/15/24: We've raised 15% of our goal!! Thank you so much to everyone who has donated!

G has been having additional struggles since I made this post. Testing revealed that she has warning signs for Multiple Sclerosis, which one of her sisters has. Their family also had a sewage pipe burst and contaminate one of her brothers' bedrooms. She's still in a lot of pain, and struggling mentally and emotionally as well. Thank you all so much for your prayers and shares.

UPDATE 8/28/24: G's family had to move out of their home temporarily due to black mold growing following the sewage pipe bursting, but they are back in their home now. G is in so much pain that she is looked into getting a wheelchair, and is currently working on getting surgery scheduled for her spine. They are still struggling, but they are surviving.

__

Hiya y'all. I wanna tell you a little bit about my best friend.

She's very private online, so I'm not going to share her name, especially since she doesn't know that I'm making this fundraiser, so we're gonna call her G. G is the hardest working person I've ever known. She's in her young 20s and is the oldest of seven children in her family, supported by their hardworking mother. She's been working for her family's sake for her entire life, throughout custody battles, a plethora of genetic health issues, and the financial burden that being a single mother of seven brings on. She is an incredible artist and writer, and is an art teacher as well as running a YouTube channel. She's funny, intelligent, and is one of my favorite people in the world.

About three weeks ago, G and her mother were rammed from behind while driving on the highway at night.

Their minivan was totaled, leaving them with two sedans in the family, and G has a spinal injury. She is in severe pain all the time, and is bedridden as she risks paralysis of her lower body. She will be unable to work for at least the summer, and it's unlikely that she'll be able to work during the fall semester either. While she is receiving medical treatment that is paid for by the offending driver's insurance, her progress is slow to nonexistent.

Her family managed to get a new minivan, but it cost them $20,000 that they didn't have. Today, her brother's sedan burst into flames in a parking lot, harming no one but torching the car and everything inside. G is distraught and struggling heavily with her mental health as well as physical.

I wish I could help support them financially, but being unemployed myself I have very little that I can give, so I'm making this fundraiser instead. I've asked her several times to consider making a gofundme, but she's been hesitant, so I'm making one in her stead. Please consider donating, I know it's a bit of a cliche but every dollar helps, and if you can't donate please consider sharing. Thank you for reading.

[covid-safer-hotties]

Also preserved in our archive

The cost is set to go far beyond human suffering, yet almost five years into the pandemic, not only are there still no treatments for long Covid, there aren’t even any diagnostic tools – and we don’t seem overly interested in finding them.

The jig is up. People are catching on that “mild” Covid-19 may not be so mild, and that the mysterious lingering symptoms they’ve experienced after catching the virus, such as fatigue and brain fog, may just be connected. For others, this will be the first time that they put two and two together. I hate to be the bearer of bad news, but strap in for what comes next.

Recently, RNZ ran a piece outlining the estimated $2bn per year economic cost of long Covid in New Zealand and signalling that further research would be needed to determine a more precise figure. The average reader would assume that this research is under way or has at least been planned and funded. Human suffering aside, such a hit to productivity would surely raise alarm bells across the political spectrum!

I say this solemnly: yeah… nah.

Almost five years into the pandemic, not only are there still no treatments for long Covid, there also aren’t even any diagnostic tools – and we don’t seem overly interested in finding them.

At present, a long Covid diagnosis relies on a patient finding a doctor with up-to-date knowledge, who will believe their symptoms, and who will spend time investigating further to rule out other possibilities. This mythical trifecta is out of reach for most people, particularly women, who are affected by immune conditions at far higher rates, but have their symptoms written off as hysteria; and Māori and Pasifika, who face barriers to healthcare, and have their symptoms written off as laziness. Obtaining accurate data on prevalence under these circumstances is simply impossible.

In this way, and several others, long Covid mirrors ME/CFS (myalgic encephalomyelitis), a brutally debilitating biophysical condition, though the oft misused term “chronic fatigue” doesn’t quite convey that. Around half of long Covid sufferers meet the criteria for ME/CFS, which by the World Health Organization’s scale has a worse disease burden than HIV/Aids, multiple sclerosis (MS), and many forms of cancer. But again, there are no treatments.

I suffer from ME/CFS myself. My illness predates Covid-19 and came on after an infection with cytomegalovirus (CMV). I went from a fit and active young man to debilitatingly sick and fatigued, with several unexplained symptoms.

Pre-pandemic there was estimated to be more than 25,000 people in New Zealand suffering from ME/CFS, and only one specialist in the country, working one day a week, who has since retired (well earned, bless her). For years I had been praying for any sort of diagnosis, even if it was bad, so that I could get on the path to recovery. I got the diagnosis – but for a disease with no path to recovery.

As the pandemic unfolded, patients and advocates in the ME/CFS community warned that a tsunami of disability was approaching. They were of course ignored, as they have been for decades, and are now joined by masses of long Covid sufferers facing the reality that the medical profession has no answers for them, except perhaps euthanasia.

Frustrated with my lack of options, I connected with cellular immunologist Dr Anna Brooks, who had become a leading expert on long Covid, so I assumed that her biomedical research would be well supported. Alas, she detailed the uphill grind that it’s been to gain traction compared to other countries, and that generous donations, usually from patients themselves, had been the driving force of funding.

Together we founded DysImmune Research Aotearoa, with the goal of developing diagnostic tools leading to treatment for post-viral illnesses like long Covid and ME/CFS. In layman’s terms, we collect blood samples, analyse differences in cells, and put together an immune profile. My priority is ensuring that Māori and Pasifika patients and researchers are at the table and taking action into our own hands.

We’ve made a small start, and we have some incredible collaborations lined up, with far-reaching implications for community health. We’re in the process of seeking partnerships to take things forward. The expertise exists, it’s here in New Zealand. Still, the barrier to progress across the research space is the urgency for resourcing. It is dire to say the least.

Without some long-term project certainty, it’s difficult to pull the necessary teams together. While study after study illuminates more horrifying long-term effects of Covid infections, and prevention has been completely abandoned, research and development for treatments for long Covid is tanking. The private sector is at the whim of the quarterly financial report, and with no guaranteed short-term profit in treating us, it has very little incentive to take the risk.

So, barring some philanthropic miracle, only government can fill this gap. Yet where Australia had set aside A$50m specifically for long Covid research, and the US Senate considers a billion-dollar long Covid “moonshot” bill, New Zealand has allocated nothing. We’re fast asleep at the wheel. No other country can determine how many of our people are impacted by post-viral illnesses. No other country can address our specific needs.

Since this government is focused on ambition, productivity and fast-tracking, I assume they’d want to be world leaders in research, warp-speed some projects, and get long Covid sufferers back into work, no? This is what we are calling for. Not surveys. Not “talk” therapy and positive thinking. Biomedical research.

Put the money down and commit to this. Seize this opportunity to right decades of neglect. There are tens of thousands of us fighting for our lives, and millions more around the world. You think it won’t be you, then after your next inevitable Covid-19 reinfection, it is, and you’re left to wonder why nobody stepped up.

Government, iwi and whānau ora groups, health organisations, philanthropists – reach out. Let’s work.

Rohan Botica (Te Ātihaunui-a-Pāpārangi, Ngāti Tūwharetoa) is a lived-experience researcher and co-founder of DysImmune Research Aotearoa.

[racheldenugent]

As some of you may know, my husband has had Multiple Sclerosis for 25 years or so. Over that time, certain treatments and more than a few accidents caused by falling over or into things, most of his teeth have been damaged to the stage that our dentist has given him a dental plate to wear.

Unfortunately he has a severe gag reflex when wearing it and his weight has dropped drastically because of the difficulty he has in eating with or without the plate. This is causing real concern for me and those close to us.

It has also had an impact on his (and thereby my) mental health. He avoids speaking with people, socialising and only leaves the house when he absolutely has to.

Our dentist tells us that in his opinion, because of the damage done, the only viable solution would be dental implants. The cost of this procedure is way beyond our means with our income, and we find ourselves in the embarrassing position of seeking help.

Between his disability income and what I make, we will save as much as we can, but it would take years to reach the target. We are not asking for the full cost of the procedure but a portion of it. We will also do our part and cut corners and make hard decisions where necessary - To this end we have set up a GoFundMe page which was a heart wrenching and humiliating decision to make but we can't do this without the kindness and generosity of others.

Please share this far and wide, even if you can't contribute. Any contribution, be it pennies or pounds will be gratefully received with thanks from the bottom of our hearts. I want to see him smile again.

[sassypotatoe1]

A comprehensive list of things chiropractors can treat or cure by clicking your back, according to old lady gossip circle:

Multiple sclerosis

Diabetes

Asthma

Cardiovascular disease

Ibs

Chrons disease

Immunocompromization

Your fight or flight response

Anxiety

Depression

Neurological conditions like tourettes

Lymph node drainage

Infertility

Endometriosis

Pcos

Virtigo

Chronic pain caused by "inflammation" which is not actual inflammation but refers to conditions like arthritis and osteoporosis

Chronic pain in general

Tuberculosis by way of lung massages that put more air in the muscles and makes breathing easier

Difficult pregnancy

It has to be noted that chiropractors can treat exactly 0 of these conditions, and chiropractic "treatments" can not even provide relief for most of these. Chiropractors can massage and stretch you, providing temporary relief for pain caused by injury, muscle tension or cramps. They can not even address the underlying cause of these issues. They do not require a medical degree to practice, and they aren't covered by most medical insurance FOR A REASON. you can get the same effect from your hairdresser giving you a neck massage while shampooing you and that does not cost an arm and a leg.

Chiropractors are exploitative quacks who make bold claims and use big words to make money off your suffering. If you want to treat an injury go to a physical therapist who has a medical degree or sport science doctorate at least, or ideally a biokineticist. If you want to treat ANY OF THE REST OF THESE go to your GP, get a referral to a specialist with a PhD in their selected medical field that they got from medical school, and treat it with clinical evidence based intervention.

For the love of God if you want your back clicked pay a chiropractor a fuck ton of money but don't expect a cure to come for your chronic illness from theatrics and some stretching.

[ammg-old2]

Chronic illness is well hidden from society.

Before I had a name for what ailed my body, I thought of myself as dehydrated and out of shape. I believed that the physical discomfort I’d experienced for years — numbness, pain, tingling and pins-and-needles sensations throughout my body — must be traceable to a cause of my own making. At that time, I looked at chronic illness as an outsider. It was a thing that happened to others, not to me.

That changed on Christmas Eve 2014, when a neurologist at NewYork-Presbyterian Hospital read my M.R.I. and confirmed that I had relapsing-remitting multiple sclerosis. This form of the disease, as the name implies, is characterized by unexpected flare-ups and periods of remission.

I was 26. I realized right then that my dream of being an artist, and the unconventional lifestyle I expected along with it, was over before it began. Four months after my diagnosis, I received my first infusion of high-dose intravenous steroids. In the fall of 2015, under the care of a neurologist, I began a monthly intravenous treatment of medication that blocks immune cells from entering the brain and spinal cord. I travel 65 miles to a site in the Hudson Valley for the infusion therapy.

Treatment has been successful, and I have remained in a state of remission while taking it as recommended — every 28 days, indefinitely. But even today, nine years into managing the illness, I struggle with the chronic nature of my condition. I am always aware that if lose my access to regular treatment, I’ll be at risk of severe disability.

Though I don’t like to admit it, every choice I make is determined by my need to maintain uninterrupted access to medical care. This has made my illness the truest navigational force of my life. Rather than orient myself to the cycle of the moon, I orient myself to the cycle of infusion. And it has become a system in my creative work. My body is a clock.

Every 28 days, I point the camera toward myself to document my illness and care. I have used my time as a patient in the infusion suite, a place where I sometimes feel powerless, to reclaim my autonomy as an artist and photographer.

In the infusion suite, both my body and my mind become containers for information. My body holds the new intelligence of the medical drip. As the fluid flows through my body and into my bloodstream, my mind is usually inundated with information from the staff.

Since my diagnosis I’ve thought often of my aunt, who has lived with progressive multiple sclerosis for years. Without health insurance, she did not have access to advanced imaging, diagnostic testing, medication or lifestyle guidance until her disease was very advanced. Instead, she found ways to self-medicate. Now in her early 60s, she is immobile, hardly able to speak and unable to navigate the social programs for which she is eligible.

Whether or not we’re aware of it, we all live in fragile bodies that require tremendous care and attention to function. Each and every one of us exists on a spectrum of illness, often dipping in and out of it. And yet, we also exist in a culture where it is taboo to talk about being sick, and the taboo can allow shame to fester among those who are chronically ill.

Still, I choose not to dwell on the scarier moments of managing the disease — the psychological burden and angst caused by my symptoms as well as the precarity and inhumanity of health care access and costs in the United States. The sophisticated treatments that exist today make this the best time in history to live with multiple sclerosis — if you can get access to care. The politics of this cannot be avoided. To be sick is political.

Maintaining all the pieces to continue to receive care in the current system is exhausting and stressful to navigate. Patient education and advocacy have been critical to my health care experience.

I came of age and of illness after the Obama-era Affordable Care Act established protections for people with pre-existing and chronic conditions. Yet even with this framework and my participation in private insurance, now supplemented by my employer, the recurring thought of losing my coverage and being denied my medication causes me much distress.

We are not prepared for problems that cannot be solved, and living with that reality is part of being chronically ill. There is no practical end. How do we break the silence to begin to discuss pain, loss, a broken health insurance economy, overworked nurses and the precarity of care?

With the coming 2024 presidential election, there will surely be renewed calls to repeal and replace Obamacare. The threat and fear of losing access to care will loom for millions. Even with the recent and ongoing events of the Covid pandemic, an adequate and sustainable system remains out of reach. Hundreds of thousands of Americans have already lost and are still losing access to care as Medicaid pandemic protections expire.

Political responses to this crisis of care matter. But so do personal and artistic ones. What if chronic illness, long concealed and misrepresented by popular culture, was made more visible? What if it was more often a subject for art?

[is-the-post-reliable]

requested by @caecilians

RATING: MOSTLY RELIABLE

The statistic on Canada's cost threshold is outdated, as the threshold has since been increased to $24,057 per year. The information may be somewhat over simplified, but is generally correct.

Australia and New Zealand both deny visas on the basis of potential medical costs, including for autism.

Source: 'People seeking long-term visas for either country must undergo rigorous medical screening. Those who may pose a significant cost to the taxpayer over a period of five years — measured at about $45,000 in New Zealand and about $32,000 in Australia — or who have medical conditions considered especially costly have their visa applications denied. Having private health insurance makes no difference, and being born in either country does not confer automatic citizenship.

Across both countries, over 1,600 people are affected by the policies each year. People have been turned away with conditions as varied as autism, obesity, intellectual disability, lupus and multiple sclerosis.'

The US can deny visas on the basis of a mental or physical disorder only if there is 'harmful behaviour' associated with the disoder.

Source: 'Applicants who have physical or mental disorders and harmful behavior associated with those disorders are inadmissible. [2] The inadmissibility ground is divided into two subcategories:

Current physical or mental disorders, with associated harmful behavior. 

Past physical or mental disorders, with associated harmful behavior that is likely to recur or lead to other harmful behavior.'

In the UK, anyone staying for more than 6 months require a medical examination, and can be denied for health issues that may prevent them from supporting themselves or require major treatment.

Source: 'The objective of the medical examination and recommendation is to prevent the entry of, or bring to notice, persons who if admitted to the UK might:

endanger the health of other persons in the UK; or

be unable for medical reasons to support themselves and or dependants in the UK; or

require major medical treatment (for which an entry clearance application has not been made).'

Canada changed their immigration laws in 2017, increasing the support needs threshold to $20,000, as stated in the video. The threshold has since been increased to $24,057 per year.

Source: 'As currently written, the law allows the government to deny residency to an entire family if even one person in the group has a disability or medical condition that could place “excessive demand” on Canada’s publicly funded health and social service systems – meaning it will cost more than $6,655 a year to care for them, a figure the government says was the average, per-capita health and social service spending in Canada in 2016.

But after Monday’s announcement, Canada will no longer consider certain costs when deciding if someone can come to Canada – such as special education costs for children with intellectual disabilities. The government said it will also triple the cost threshold for denying someone based on medical conditions to nearly $20,000 a year.'

It is difficult to provide any statistics on how many people disclose their autism during a visa application, so I cannot speak to the accuracy of this statement.

This is exactly what I mean when I say the society even more “progressive” societies are inherently ableist

[darrelhickman]

Your Guide to Pain Relief and Recovery

Physiotherapy is a vital component of healthcare, helping individuals recover from injuries, manage chronic pain, and improve mobility. If you’re searching for the best physiotherapy in Calgary, you’ve come to the right place. This guide will explore what physiotherapy entails, the top clinics in Calgary, how to choose the right physiotherapist, and what to expect during treatment.

What is Physiotherapy?

Physiotherapy is a healthcare discipline that focuses on restoring movement and function to individuals affected by injury, illness, or disability. Physiotherapists use a combination of hands-on techniques, exercise programs, and patient education to facilitate healing and enhance physical well-being.

Benefits of Physiotherapy

Pain Relief: Effective for back pain, neck pain, joint pain, and sports injuries.

Rehabilitation: Helps in post-surgical recovery and injury rehabilitation.

Improved Mobility: Beneficial for individuals with mobility issues due to age, injury, or medical conditions.

Sports Performance: Supports athletes in preventing injuries and improving performance.

Chronic Condition Management: Helps manage arthritis, multiple sclerosis, and other chronic diseases.

Top Physiotherapy Clinics in Calgary

To help you find the best physiotherapy in Calgary, we have compiled a list of top-rated clinics known for their high-quality care and expert physiotherapists.

1. Momentum Health

Multiple locations across Calgary.

Specializes in sports injuries, chronic pain management, and rehabilitation.

Offers services like acupuncture, massage therapy, and chiropractic care.

Known for personalized treatment plans and patient-focused care.

2. Panther Sports Medicine

10+ locations in Calgary.

Provides physiotherapy for sports injuries, motor vehicle accidents, and workplace injuries.

Offers advanced treatments such as shockwave therapy and dry needling.

Experienced team of physiotherapists with diverse specializations.

3. Lifemark Physiotherapy

Nationwide brand with multiple Calgary locations.

Expertise in post-surgical rehabilitation, neurological conditions, and concussion therapy.

Uses evidence-based techniques, including hydrotherapy and manual therapy.

Comprehensive approach to recovery with additional wellness services.

4. Peak Physical Therapy

Offers state-of-the-art rehabilitation programs.

Focus on evidence-based treatment and patient education.

Specializes in vestibular physiotherapy, TMJ therapy, and pelvic health physiotherapy.

Highly rated for professional and compassionate care.

5. Movement Performance & Health

Emphasizes a holistic approach to physiotherapy.

Uses cutting-edge technology for movement analysis and therapy.

Provides treatment for sports injuries, chronic pain, and postural issues.

Offers tailored recovery programs based on individual needs.

How to Choose the Best Physiotherapy Clinic in Calgary

When selecting a physiotherapy clinic, consider the following factors:

Qualifications & Experience: Ensure the physiotherapists are licensed and have experience in treating your specific condition.

Services Offered: Look for clinics that provide a range of services like manual therapy, acupuncture, and sports therapy.

Reputation & Reviews: Check online reviews and testimonials to gauge patient satisfaction.

Convenience & Accessibility: Consider the location, clinic hours, and availability of appointments.

Insurance Coverage & Costs: Verify if your insurance covers physiotherapy and check for direct billing options.

What to Expect During a Physiotherapy Session

If you’ve never visited a physiotherapist before, here’s what to expect:

Initial Assessment: The physiotherapist will evaluate your medical history, symptoms, and movement limitations.

Diagnosis & Treatment Plan: Based on the assessment, a personalized treatment plan will be developed.

Hands-On Therapy: Techniques such as joint mobilization, soft tissue therapy, and stretching exercises may be used.

Exercise Programs: You will receive guided exercises to enhance mobility and strengthen muscles.

Progress Monitoring: Regular assessments will be conducted to track your improvement and adjust treatment as needed.

Conclusion

Finding the best physiotherapy in Calgary is essential for effective pain relief and recovery. Whether you’re recovering from an injury, managing chronic pain, or looking to improve mobility, Calgary has top-tier physiotherapy clinics that cater to diverse needs. By considering factors like experience, services, and patient reviews, you can choose the right clinic to support your health journey. Don’t let pain hold you back—schedule a physiotherapy session today and take the first step toward better health!

[medlama]

Ocrelizumab Price in India – Affordable Options at Medlama

Ocrelizumab is a revolutionary monoclonal antibody used to treat multiple sclerosis (MS), specifically primary progressive multiple sclerosis (PPMS) and relapsing forms of multiple sclerosis (RMS). This advanced therapy helps slow disease progression and reduces relapses in patients suffering from this debilitating condition.

Finding Ocrelizumab price in India can be challenging, as the cost varies due to multiple factors, including brand availability, dosage, and distribution channels. At Medlama, we ensure that patients get access to this vital medication at competitive rates without compromising on quality.

Understanding Ocrelizumab and Its Uses

Ocrelizumab works by targeting CD20-positive B cells, a key contributor to nerve damage in multiple sclerosis. By depleting these harmful cells, the drug helps slow disease progression, reduce new lesion formation, and improve patients' overall quality of life.

This medication is administered through intravenous infusion under the supervision of healthcare professionals. The treatment typically begins with two doses given two weeks apart, followed by a maintenance dose every six months. Due to its efficacy and long-term benefits, Ocrelizumab is widely recommended for individuals suffering from multiple sclerosis.

Ocrelizumab Price in India: Factors Affecting Cost

The Ocrelizumab price in India can differ based on several factors, including:

1. Brand and Manufacturer

The cost of Ocrelizumab may fluctuate depending on the pharmaceutical company producing it. Original brands and generic alternatives may have varying pricing structures.

2. Dosage and Packaging

Different dosages are available, affecting the overall expense. Higher doses usually cost more, but proper prescription guidance ensures patients receive the correct amount for their condition.

3. Supply Chain and Distribution

Import duties, logistics, and supply chain management influence final pricing. Medlama works closely with trusted suppliers to offer cost-effective solutions.

4. Hospital and Infusion Charges

Since Ocrelizumab is administered via IV infusion, additional hospital or clinic fees can impact the total cost of treatment. Some healthcare centers may include the drug’s price within the total procedure cost.

5. Availability and Demand

Limited stock or increased demand can influence pricing. Medlama ensures a steady supply to help patients receive their medication without delays.

Affordable Options for Ocrelizumab in India at Medlama

Medlama is committed to making essential medications more accessible and affordable. Patients searching for Ocrelizumab price in India will find that Medlama offers competitive rates, ensuring cost-effective treatment without compromising authenticity or quality.

Why Choose Medlama for Ocrelizumab?

1. Competitive Pricing

Medlama strives to offer the best possible price for Ocrelizumab injection in India. By collaborating with trusted manufacturers and suppliers, we provide cost-effective options that help patients manage their treatment expenses efficiently.

2. Guaranteed Authenticity

We source directly from authorized pharmaceutical companies, ensuring that every product is 100% genuine and safe for use. Patients can trust Medlama for high-quality medications that meet regulatory standards.

3. Reliable Availability

Ocrelizumab can sometimes be difficult to find due to limited distribution, but Medlama maintains a consistent supply to ensure uninterrupted treatment for patients.

4. Hassle-Free Ordering Process

Patients and healthcare providers can easily place orders through Medlama’s user-friendly platform. Our efficient process ensures timely delivery and smooth transactions.

5. Expert Guidance and Support

Understanding multiple sclerosis treatment can be overwhelming. Medlama provides expert consultation and customer support to guide patients through their medication needs, ensuring they receive the right dosage and instructions for use.

How to Buy Ocrelizumab from Medlama?

Purchasing Ocrelizumab through Medlama is simple and convenient. Follow these steps to get started:

Visit the Medlama Website – Browse our extensive catalog to find Ocrelizumab price in India and check availability.

Submit Your Prescription – Since Ocrelizumab is a prescription-based medication, upload a valid prescription for verification.

Confirm Your Order – Once verified, place your order and proceed with a secure payment option.

Receive Your Medication – Medlama ensures fast and reliable delivery to your doorstep or preferred medical center.

Frequently Asked Questions (FAQs)

1. What is the price of Ocrelizumab in India?

The Ocrelizumab price in India varies depending on dosage, manufacturer, and availability. Medlama offers competitive rates to help patients access affordable treatment.

2. Is Ocrelizumab available in all cities in India?

Yes, Medlama provides nationwide delivery, ensuring that patients across India can access Ocrelizumab without difficulty.

3. Do I need a prescription to buy Ocrelizumab?

Yes, a valid prescription is required to purchase this medication, as it is administered under medical supervision.

4. How often do I need to take Ocrelizumab?

The initial dose consists of two infusions given two weeks apart, followed by a maintenance infusion every six months. Your doctor will determine the best treatment schedule based on your condition.

5. Does Medlama provide discounts on Ocrelizumab?

Medlama frequently offers special pricing and bulk purchase discounts. Contact our support team to inquire about current offers.

Final Thoughts

Multiple sclerosis is a challenging condition, but innovative treatments like Ocrelizumab offer hope for better disease management and improved quality of life. Medlama is dedicated to providing affordable, high-quality medications to patients seeking Ocrelizumab price in India at competitive rates.

With a commitment to authenticity, reliability, and affordability, Medlama ensures that patients receive the best possible care. If you or a loved one requires this medication, trust Medlama for a seamless, cost-effective purchasing experience.

For more details, visit Medlama today and take the first step toward accessible, advanced treatment solutions.

[danishkhan786]

Multiple Sclerosis

Welcome – Help a Veteran with Multiple Sclerosis Live Comfortably

Every day, countless veterans face physical and emotional challenges after serving their country. One of the most debilitating conditions affecting many veterans is Multiple Sclerosis (MS)—a disease that impacts mobility, strength, and overall well-being. Our mission is to provide help for a veteran with Multiple Sclerosis to live comfortably by ensuring access to essential healthcare, home modifications, and life-enhancing treatments.

At GoFundMe, we are raising funds to support a veteran who has bravely served and now battles MS. With your generous donation, you can help provide crucial medical care, additional handrails and safety features for mobility, and even explore stem cell therapy and PTSD treatment for veterans who need support.

What is Multiple Sclerosis (MS)?

Multiple Sclerosis is a chronic autoimmune disease that affects the central nervous system, causing symptoms such as muscle weakness, difficulty walking, fatigue, and cognitive challenges. Veterans with MS often experience worsening symptoms due to the physical demands of military service. Access to the right treatment and support is essential for them to live comfortably and maintain independence.

How Your Support Helps Veterans with MS

Funding for Medical Treatments – Covering the costs of necessary medications and therapies.

Mobility Support – Installing additional handrails and safety modifications to prevent falls and ensure independence.

Access to Advanced Treatments – Supporting promising stem cell therapy to slow disease progression.

Mental Health Support – Providing PTSD treatment for veterans, including therapy and counseling.

Why Do Veterans Need Additional Handrails and Safety Features?

Mobility challenges are one of the most significant issues for veterans with MS. Falls are common, and the lack of proper home modifications can increase the risk of severe injuries. Adding handrails and safety enhancements in homes ensures a safer environment, giving veterans the ability to move freely without fear of falling. These modifications include:

Handrails along staircases and hallways

Grab bars in bathrooms and showers

Wheelchair ramps for easier access

Anti-slip flooring for added stability

By donating, you help cover the costs of these essential home modifications, allowing a veteran to regain confidence and independence in their daily life.

Exploring Stem Cell Therapy for Multiple Sclerosis

Recent advancements in medical research have highlighted stem cell therapy as a promising treatment for Multiple Sclerosis. This innovative approach aims to repair damaged nerve cells and improve neurological function. However, the cost of stem cell therapy remains a significant barrier for many veterans.

Your donations will contribute to funding this cutting-edge treatment, giving a veteran the opportunity to regain strength and improve their quality of life. Every contribution brings hope for better mobility, reduced symptoms, and a brighter future.

PTSD Treatment for Veterans – Supporting Mental Well-being

Many veterans diagnosed with Multiple Sclerosis also struggle with Post-Traumatic Stress Disorder (PTSD) due to the emotional and psychological toll of military service. PTSD can lead to depression, anxiety, and severe emotional distress. Access to proper mental health care is critical, but many veterans face long wait times and limited resources.

By supporting this campaign, you are helping fund:

Therapy sessions with PTSD specialists

Access to medication and alternative treatments

Community support programs for veterans

Holistic approaches such as meditation and cognitive therapy

Your generosity ensures that veterans receive the mental health support they need to lead fulfilling lives.

How You Can Make a Difference

Your contribution—no matter how big or small—can change the life of a veteran in need. Here’s how you can help:

Donate Today – Visit GoFundMe to make a direct contribution.

Share the Campaign – Spread the word by sharing this fundraiser with your friends, family, and social media networks.

Sponsor a Treatment – If you’re part of an organization or business, consider sponsoring medical care, home modifications, or therapy sessions.

Raise Awareness – Advocate for veterans' health and support legislative efforts that improve access to MS treatments and mental health care.

[global-research-report]

The Rise of Specialty Generics: Market Analysis, Competitive Landscape, and Future Outlook

The global specialty generics market size is expected to reach USD 148.72 billion by 2030, according to a new report by Grand View Research, Inc. It is expected to expand at a CAGR of 9.9% over the forecast period. The growth in the market is largely driven by increasing product approvals and the rising prevalence of complex chronic diseases, such as multiple sclerosis.

In April 2022, Dr. Reddy’s Laboratories launched a methylprednisolone sodium succinate injection in the U.S. for the treatment of patients with arthritis, blood disorders, and certain rare cancers. Furthermore, in June 2022, Elixir launched copay solutions enhancement program for the management of specialty generic medication prices. Under this program, an eligible patient receives a generic version of specialty medication at zero cost. Thus, the launch of new low-cost generic injectables and the availability of such programs is projected to fuel market growth.

Increased claim settlements and availability of specialty generic drugs increase their prescription rates due to the high safety, efficacy, and tolerability associated with them. According to the Human Resources Benefits Office University of Michigan annual report (2021), around 1,383 claims were settled for specialty generic drugs such as glatiramer acetate (Copaxone/Glatopa), teriflunomide (Aubagio), and fingolimod (Gilenya) in 2021, compared to 1,360 in 2020, with a rise of 1.7% for the treatment of patients with multiple sclerosis.

However, high costs associated with specialty generics may hamper their uptake. The lack of ability to attract patients toward drugs, marketing rights acquired by companies for off-patent drugs with no generic competition, and small target patient pool, subsequently increases the prices of products. According to the University of Michigan Prescription Drug Plan Formulary report, the average cost of specialty generic is over USD 4,500 monthly per person, compared to USD 17 to 22 for a generic prescription.

Specialty Generics Market Report Highlights

Based on type, the injectables segment dominated the market in 2022. It is estimated to maintain its dominance during the forecast period due to its high prescription rate on account of long-term effects, and immediate absorption compared to oral drugs

Based on application, the oncology segment is expected to witness significant growth during the projection period owing to the increasing prevalence of cancer. According to Globocan, the number of new cancer cases is anticipated to reach 28.4 million within the next two decades worldwide

On the basis of end-use, the specialty pharmacy segment dominated the market in 2022 owing to features like timely delivery, optimized patient access, and effective distribution management

Based on region, North America dominated the market in 2022 due to the presence of supportive regulatory policies regarding the approval of new products. The U.S. FDA introduced Generic Drug User Fee Amendments (GDUFA) under the Hatch-Waxman act to quicken the approval of new generic drugs

Specialty Generics Market Segmentation

Grand View Research has segmented the global specialty generics market by type, application, end-use, and region:

Specialty Generics Type Outlook (Revenue, USD Billion, 2018 - 2030)

Injectables

Oral drugs

Others

Specialty Generics Application Outlook (Revenue, USD Billion, 2018 - 2030)

Oncology

Inflammatory conditions

Multiple sclerosis

Hepatitis C

Others

Specialty Generics End Use Outlook (Revenue, USD Billion, 2018 - 2030)

Specialty pharmacy

Retail pharmacy

Hospital pharmacy

Specialty Generics Regional Outlook (Revenue, USD Billion, 2018 - 2030)

North America

US

Canada

Europe

Germany

UK

France

Italy

Spain

Denmark

Sweden

Norway

Asia Pacific

Japan

China

India

Australia

South Korea

Thailand

Latin America

Brazil

Mexico

Argentina

Middle East and Africa (MEA)

South Africa

Saudi Arabia

UAE

Kuwait

Key Players in the Specialty Generics Market

Teva Pharmaceuticals Industries Ltd

Viatris Inc.

Novartis AG (Sandoz International GmbH)

Hikma Pharmaceuticals PLC

Mallinckrodt

Bausch Health Companies Inc. (Valeant Pharmaceuticals International, Inc.)

Reddy’s Laboratories Ltd.

Endo Pharmaceuticals Inc.

Apotex Corp.

Sun Pharmaceutical Industries Ltd

Fresenius Kabi Brasil Ltda

STADA Arzneimittel AG

Order a free sample PDF of the Specialty Generics Market Intelligence Study, published by Grand View Research.