#the Neurodegenerative Disease

[newsfromstolenland]

There’s a renewed call for a public inquiry into why so many New Brunswickers have come down with neurodegenerative symptoms and illnesses.

When an initial cluster of over 40 people presented with similar symptoms – muscle spasms, atrophy and progressive dementia – it was thought to be Creutzfeldt-Jakob disease, until they tested negative.

That’s when a Moncton-based neurologist thought they could be experiencing an unknown brain disease. The cluster was initially focused in the Moncton and Acadian Peninsula areas of the province.

But after over a year of confusing back-and-forth for patients and their families, the province of New Brunswick halted further investigation by its federal counterparts, saying there was an explanation for each patients’ illness.

This week, New York Times Magazine released an article that calls that into question, citing that neurologist Dr. Alier Marrero believes the number of people seeking help with similar symptoms is now over 400.

It has sparked Green Party MLA Megan Mitton to call for a public inquiry into what happened internally between the province and Ottawa, as well as further testing, including environmental, to try and find patients some answers.

Full article

Tagging: @allthecanadianpolitics

[bougiebutchbinch]

anyway SHOUT OUT to the GP I saw a while ago who gave me a neurological test, noted several concerning abnormalities, and concluded that I Was Just Like That

and when I pointed out that my last neurological test had been completely fine, meaning this was, in fact, a change we should investigate further, especially when combined with my symptoms

because I literally study this shit, work in the industry, and know what I am talking about

he shrugged, said he didn't know then, and suggested that I try supplements

[chicago-geniza]

Oh my fucking Gd they just booked me in for all-day memory testing next week, when it rains it POURS ajsjdjfjjfbff

[laureala]

AMELIA SHEPHERD

— in Grey's Anatomy 20.01 - We've Only Just Begun

You told me to say whatever's in my- I'm sorry! It's making me think that maybe Meredith isn't insane.

[mindblowingscience]

A spectrum of neurodegenerative diseases, including frontotemporal dementia (FTD), progressive supranuclear palsy (PSP), and corticobasal degeneration (CBD) are due to the accumulation of abnormal, misfolded tau proteins in the brain. A team of researchers has found potential ways to interrupt this process by targeting “sticky” sites along the long form of mutated tau, preventing the misfolding and spreading of the neurofibrillary tangles.

Continue Reading.

[swinging-stars-from-satellites]

having a hypochondriac moment pray for me babes

[bpod-bpod]

Indirect Influence

A criminal kingpin might orchestrate a whole network of mischief, but only directly instruct a small circle of trusted henchmen. New research on a protein in the cell cytoskeleton – the structural web within cells – reveals a similar pattern of influence. PFN1 is well known to be involved in the assembly of actin (filaments that play a key structural role in the cytoskeleton), but there were also signs of its involvement in microtubules – another cytoskeleton component. Silencing PFN1 caused changes in microtubule abundance and structure (pink and blue, right) compared to normal (left). Reducing actin activity had similar effects, and if actin was restored the microtubule changes reversed, suggesting that PFN1 is acting on microtubules predominantly via actin, rather than directly. Some of the microtubule changes that arose with PFN1 depleted match characteristics of neurodegenerative conditions such as Alzheimer’s disease, so unpicking the lines of power could present new treatment options.

Written by Anthony Lewis

Image from work by Bruno A. Cisterna and colleagues

Department of Neuroscience and Regenerative Medicine, Medical College of Georgia at Augusta University, Augusta, GA, USA

Image originally published with a Creative Commons Attribution 4.0 International (CC BY 4.0)

Published in Journal of Cell Biology, May 2024

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[dramatic-dolphin]

Age gaps are unattractive to me because I just saw my mom see my dad have dementia and I don’t want to have to deal with that or be that for a partner. We better both be the same age and die at the same time or close to eachother…

incredibly extremely valid. sadly it's also possible for your same-age partner to get dementia late in life while you stay as sharp as ever. which terrifies me ngl. watched my great-aunt go through that when i was a child, i do NOT want it!!

[nightmaretour]

If you're going to call out specific groups of people who aren't allowed to relate to your posts (instead of just, I don't know... ignoring people who don't respond to your posts the way you'd like?), can you at least get your facts straight? ADHD absolutely can cause severe memory issues. Real, actual, severe, debilitating memory problems. You're letting your (understandable!) frustration with certain people who do talk over other people with more severe disabilities turn into actual intracommunity ableism, and it sucks.

Lmao clearly you don't understand what "severe" means. Your ADHD does not cause you memory issues on par with anterograde amnesia from a moderate-severe brain injury. It does not cause you memory issues on par with dementia. You assume you can relate because you think you're the most disabledest ever and nobody can possibly suffer more than you, but you really can't. Some people are more disabled than you, that isn't an attack on you personally. It isn't ableism to tell you that something isn't about you, which it isn't.

I wouldn't have to add things like that to posts if people just like you didn't CONSTANTLY insist on making posts by people with more severe disabilities than you all about yourselves and derailing them because you find more severely disabled people invalidating. THAT'S ableism. You try dealing with that on almost every single post you make, no, every time you try to talk about your experiences, then you can talk to me about "just ignoring it". Sometimes things just aren't about you, learn to deal with it and respect other disabled people's boundaries, or leave the rest of us the fuck alone.

[evolve-rat]

We’ve moved past people misusing the word twink and people are now calling old Daniel Malloy a bear. Day ruined

[bougiebutchbinch]

ONE WEEK UNTIL THEY CAN (hopefully) TELL ME I DON'T HAVE ALS

I'm fully expecting that it won't be that - I'm just gonna need the big scoli surgery at this point because ummmmm it's developing rapidly. And I have fully lost my appetite along with 80% of strength in the fail-arm. And that is. Concerning. But as long as it ain't gonna keep getting worse and literally kill me, I can deal lolololololololol

[chicago-geniza]

Did you know. Even if you stop drinking alcohol. You can still drink so much non-alcoholic beer you throw up from acid reflux. Anyway I'm too old to kin fictional characters but some part of me...some part of me does admittedly feel a deep and abiding kinship with Daniel Molloy

[neatrogenous]

we're in this phase III trial of this thing that is soooooooo cool and i want to talk about it sooooo bad but 1. no. 2. no one will understand me if i do. 3. no.

but its so wild to watch disease processes go from totally untreatable to like. one time novel solution. in half of a lifetime. like from "not only do we not know why this is happening or how to stop it but i can tell you that you're just going to go blind," to "well if you come in and get this done every x weeks actually you will preserve most of your vision" to "actually maybe we can just do this one procedure and the thing that robbed 25% of your family of the ability to read by age 75 will simply not be a problem for you"

[lornteeleaf]

Loosing a parent to a neurodegenerative disorder feels like watching them die over months and years.

We're almost 7 years in at this point. I'm still shocked every time there is a noticeable loss of function. I should be used to it by now but I'm not.

I still get frustrated and angry. With the situation, not with them. But at the end it's my parent I lash out against.

I'm still so sad and lost. It's been almost a year in therapy, I found my ways to grieve now and have plans how to grieve after they're gone. But I still cry myself to sleep sometimes.

[bpod-bpod]

Seen Two Ways

Genes and proteins are two sides of the same coin. Genes are sections of DNA that contain the instructions for producing proteins, which themselves play countless fundamental roles in the body – including regulating DNA expression. Researchers have techniques to measure gene expression or protein levels within cells and tissues, but a new approach marries the two to show a more rounded picture of a single specimen, such as the mouse embryo pictured. Clusters of gene expression patterns (top left) can be compared with the location and amounts of proteins (bottom, with colours indicating different proteins). Connecting gene activity and the precise location of protein function provides a level of insight that could answer important questions about health and disease, such as why some regions of tumours express genes differently, how protein imbalances in the brain are linked to neurodegenerative disorders, or how immune cells interact with tissues during inflammation.

Written by Anthony Lewis

Image from work by Archibald Enninful and Zhaojun Zhang, and colleagues

Department of Biomedical Engineering, Yale University, New Haven, CT, USA

Image contributed by the authors under a Creative Commons Attribution 4.0 International (CC BY 4.0) licence

Published in bioRxiv, February 2024 (not peer reviewed)

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[devybobevy]

I hate that I spent my entire childhood promising that I'd never be anything like my mother just to find out that she is the way she is because of Huntington's disease and that whether or not I end up like her is in the hands of a genetic coin toss that happened at my conception