#spinalmuscularatrophy

[comicherovn]

Comic Hero Show: Episode 491

[suramed-health-center]

⚕️Spinal Muscular Atrophy (SMA) is the leading genetic cause of infant mortality. This SMA awareness month, learn more about the rare genetic disorder by clicking this link ➡️ https://www.innow.org/2023/08/30/spinal-muscular-atrophy-awareness-month/

[transorzesolutionstvm]

ICD-10 code G12.9 for Spinal muscular atrophy, unspecified is a medical classification as listed by WHO under the range - Diseases of the nervous system .

For more details:

🌐 www.transorze.com

☎️ 9495833319

[parvathytransorze]

ICD-10 code G12.9 for Spinal muscular atrophy, unspecified is a medical classification as listed by WHO under the range - Diseases of the nervous system .

For more details:

🌐 www.nationalintituteofmedicalcoding.com

☎️ 9495833319

[transorzekochi]

ICD-10 code G12.9 for Spinal muscular atrophy, unspecified is a medical classification as listed by WHO under the range - Diseases of the nervous system .

For more details:

🌐 www.transorze.com

☎️ 9495833319

[darkwhimsycreations]

https://www.votervoice.net/mobile/CureSMA/Campaigns/107567/Respond <---- Petition to go against the income cap for disabled Americans

[saramackenzie1982]

It's August!! This is what this months focuses on. Humanity doesn't stop after the month ends. 💕

#AugustAwareness #ImmunizationWorks #SpinalMuscularatrophy #OverdoseAwareness #Romance #IndieAuthor #WifeAndMother #FellowHumanBeing #OneWorld #NewBritain

[littleredchucks]

View this post on Instagram

A post shared by @littleredchucks

She is Sonic the Hedgehog in her new chair #spinalmuscularatrophy #wheelchairlife https://www.instagram.com/p/CR5eye7ATkE/?utm_medium=tumblr

[globalstemcellcare]

Stem Cell Tests Alleviate Consequences of Spinal Cord Injury'⠀The successful translation of these findings to human subjects may improve the quality of life of chronic Spinal Cord Injury patients

To know more about #SpinalCordInjury visit, www.globalstemcellcare.com

[transorzekochi]

Spinal muscular atrophy is a genetic disorder characterized by weakness and wasting (atrophy ) in muscles used for movement (skeletal muscles). It is caused by a loss of specialized nerve cells, called motor neurons that control muscle movement.

ICD-10 code G12. 9 for Spinal muscular atrophy, unspecified is a medical classification as listed by WHO under the range - Diseases of the nervous system.

www.transorze.com

9495833319

[skywellaquasolutions]

"We must not lose Faith in Humanity. Humanity is an Ocean. If a few drops of Ocean are dirty, the whole Ocean does not become dirty."

[wheellifestories]

Some days are simply meant for playing✨ • • • "Snuck to playground while Josh is at school.. 🤫" - @harryssmamazing • • • Send your pics & videos to @WheelLifeStories or tag #WheelLifeStories for a feature! || Visit our website at WheelLifeStories.com! || #repost #wheelchaircommunity #adaptivecommunity #disabilityawareness #playground #iamadaptive #wheelchairfun #inclusion #wheelchairlife #playtime ⁣#astheworldspins #sma #lifewithsma #spinalmuscularatrophy #smile #abilitynotdisability #nolimits #liveyourlife #wheelchairkid #accessibility #amazingpeople #keeppushing #handicappable #differentlyabled #disABILITY #unstoppable #adaptandconquer #wheelchairmotivation #nevergiveup https://www.instagram.com/p/B4uuAEaJ832/?igshid=if6cdz1ae2vv

[chairpersonchair]

Important petition!! Please read

Hey guys, gals and nb pals, I have a favour to ask! As most of you probably don’t know, I have a disability called Spinal Muscular Atrophy. In simple, more tumblr terms, this means that my muscles are very weak little beans, and are constantly getting weaker over time (you can DM me for a more scientific explanation lmao). This can cause my organs to weaken as well and increase my risk of diseases and could lower my life expectancy. SPINRAZA is a new treatment for my disability that helps to stop my weak ass little bean muscles from getting weaker, and can sometimes even make them a teeny bit stronger! Hell yeah! In Australia (where I currently live) SPINRAZA has been approved for funding and I am now on my 4th dose (the doses are typically every 4-months and will hopefully continue for the rest of my life). Even though I’m only in my first doses, I’ve already seen my tiny little bean muscles grow to slightly larger but still really tiny beans (am a proud mama). While this may not sound like much to ya’ll weightlifters, I can now lift up my hot chocolate cup by myself AND turn on light-switches, which are great steps towards my independence! The problem is that I plan on moving back to New Zealand in two years as I was born in NZ and do not get full funding for my equipment in Aus. SPINRAZA is not yet approved for funding by the NZ government, but many people are fighting for it!! By signing this petition you could not only be helping me continue the treatment, but you’d be helping lots of kids with SMA be much more independent and could increase our life expectancies to normal, how heckin’ cool is that!! I would really appreciate it if you could sign the petition and reblog this post. The petition’s international so anyone can sign it and it only takes a minute of your time! Thanks :)

https://www.parliament.nz/en/pb/petitions/document/PET_84979/petition-of-janine-yeoman-lifesaving-treatment-for-people

[rollinatrophy]

-Turkish writing is on below of English.

-Türkçe yazım İngilizce yazımın altındadır.

🌸🌸🌸🌸🌸🌸🌸🌸🌸🌸🌸🌸🌸🌸🌸🌸

*Hello, Instagram peeps! I'm Seda aka Rollinatrophy. Student. Sketcher and Doctor Who lover. I'm from Turkey and this account is gonna be a blog posting about my life, disability, SMA and things about myself. I created this account to make awareness about disabilities and SMA and i know there's lot of people doing that but in my country there is no one doing this because they're not aware of disability at all unfortunately... But with hope i have and Instagram posts i'm gonna share and soon hopefully with my YouTube channel, something's has to change actually MUST! Because ableism is not alright and unacceptable. We can't normalize that and no one should! So, let's change it together!🌸🌸🌸🌸🌸🌸🌸🌸🌸🌸🌸🌸🌸🌸

*Merhaba, Instagram halkı! Ben Seda -diğer adıyla Rollinatrophy-. Öğrenciyim. Çizim yaparım ve Doctor Who hayranıyım. Türkiye'denim ve bu hesap; hayatım, engel, SMA ve benim hayatımla ilgili şeyler hakkında blog sayfası olacak. Bu hesabı; engeller ve SMA hakkında farkındalık oluşturmak için açtım ve biliyorum ki bunu yapan çok kişi var fakat benim ülkemde bu yok çünkü maalesef ki insanlar engelin farkında değiller... Fakat umudumla, paylaşacağım Instagram durumlarıyla ve umuyorum ki yakında paylaşacağım YouTube kanalımla bir şeyler DEĞİŞMELİ! Çünkü sağlamcılık iyi değil ve kabul edilemez. Bunu normalleştiremeyiz, kimse bunu yapmamalı. Haydi bunu birlikte değiştirelim!

🌸🌸🌸🌸🌸🌸🌸🌸🌸🌸🌸🌸🌸🌸🌸🌸

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