#multiple sclerosis relapse

[adamslilith]

In July of 2022 I was diagnosed with Multiple Sclerosis and on New Year's eve the same year I ALREADY had my second flare up. On YT I talk about this, the symptoms, the denial.. the treatment, and what this might mean for my future.. here's a sneak peek..

And here's the full video ⬇️

[u2hearts]

A UTI I Should Have Known

Good morning everyone. So, looks like my latest stretch of the last few weeks of suffering might be due to a UTI. Even though we are still waiting on the lab results, my doctor prescribed me antibiotics yesterday. However, when the culture does come back, we might have to change antibiotics based on the strain. I should’ve known. I can’t feel that area anymore yet my aide has said my urine has…

[adamslilith-msart]

Find out more in the video below 🧡

[kindajd]

[irresponsible-masochist]

Today is the third anniversary of me being officially diagnosed with MS.

It’s kind of a fucked up thing to keep track of, I guess, but…it feels like it hasn’t been that long, but at the same time, it feels like it’s been much longer.

It’s a weird thing to live with, MS. I feel like I just got to a point where I can accept that I have it. I still mourn the days before-life before I had infusions and medical debt and a fucked up immune system that makes it hard to fight off even a simple ear infection. I hope it will get easier with time, but who knows?

3 damn years I’ve been putting up with MS. 3 years my wife has been putting up with me having MS. I can say that as scary as it is, I’m glad that I’ve always had her. Her love and support have never wavered. Even on my bad days, my hard days, my worst days, she’s been there to love me through it and I have no idea how she’s done it.

3 years of MS Living. I’ll be on this fucked up ride for the rest of my life. At least I’m what they call “stable.” No new lesions, no PML, I’m doing as well as a person with MS can be, and I’ve learned to accept that.

I just hope that I can continue to be “stable.”

[jamiesonwolf]

A Dance with the Waves

A neighbour gave me a gentle telling off today. For the past three weeks, I’ve been going through a multiple sclerosis flare up. I thought I was just tired at first and suffering from burn out. Then that tiredness became exhaustion. I booked a couple of days off work and was looking forward to getting some much-needed rest. When I woke up on the next day, the fatigue has increased. I had slept…

[arrozaurus]

ms changed my worldview because it meant that my future was unpredictability and things that i take for granted today, like my mobility, my senses or my cognitive abilities, may fail me in the long term. i dont know if ill lose them or to what degree. i just cannot make any plans because every plan will backfire no matter what.

idk somehow i just figured that what i have now i would enjoy it to the max. im going to love going up the stairs, im going to love touching the dirt, or im going to do that thing ive always wanted to do but i never dared to because i thought maybe it was not for me. im going up mountains and seeing plants and animals no one ever bothers to pay attention to. im going to love balancing my weight on rocks that are not fixed to the ground just to see if i can.

and because of this my life is probably more enriched that has ever been? sensorially, mentally and physically. and maaan... i could not recommend this enough to someone in the same situation as me

[sparrow-prophecy]

I have relapsing remitting multiple sclerosis. I filmed this to spread awareness about MS. It hits me hard a few times a week, but most of the time I'm perfectly ok. This was on October 25th (two weeks ago). It's not normal for me to talk like this when I'm having a flare up, but severe movement issues, including speech issues and difficulty breathing are normal for me.

[reportwire]

Lessons From My Journey With Relapsing-Remitting MS

By Darbi Haynes-Lawrence, PhD, as told to Evan Starkman It’s been 13 years since my neurologist diagnosed me with relapsing-remitting MS, and I still forget that I’m disabled a lot. I’m 47, but in my brain I’m still a college track athlete who ran marathons on the weekends. I’ve always been a big goal-oriented person. I got my doctorate by the time I was 30, and my dream has always been to be a…

[oliviawebsite]

disabled struggling trans girl in need of help again to stay housed, fed, and medicated

im really sorry for this. last month, out of pure desperation, i took a job that looked promising but ended up being a horrible experience that was way more physical demanding than i was prepared for to the point i agitated my already-existing symptoms and dysfunctions and was forced into resigning because i got to a point where i could no longer physically perform my duties and literally couldn't even walk for several days. i have multiple sclerosis that relapses and remits and obviously i should be on disability but this too is an incredibly long and tiring process, especially considering i have already been denied for it. between that and trying to find some kind of job that i can actually DO its obviously a bit of a tight spot. i have some funds left from when i was working but i need to make up the gap after my bill payments to pay my rent for the month. right now that comes to a figure of a little more than 600 dollars. this way i can at least pay my rent and feed myself at least until my next round of appointments and/or interviews. please help if u can i really dont wanna lose my place in the condition i'm in and i'm so exhausted from being put thru all this ableist capitalist torture labyrinth bullshit. please help or share. thank you i love you i am sorry i will get there someday if i just keep at it

0/600

you can also buy my music if u want some type of material exchange for ur money:

[kikingback]

This Pride month didn't start exactly how I predicted 😅😂

I'm currently (and just provisionally, don't worry!) on my wheelchair again, due to a bad relapse of my multiple sclerosis, BUT it doesn't mean I don't get to show off my flags ✨✨

It's a good time to make people aware of the huge (both material and cultural!) barriers the disabled LGBTQ+ community has to face everyday. There's so much work to make sure we're not forgotten, and we have the right to feel empowered in our true colors ❤️🌈

Happy Pride month to everyone from your friendly neighbourhood Kiki 🏳️‍🌈🏳️‍⚧️❤️🧡💛💚💙💜🤎🖤

[adamslilith]

Let's talk about paresthesia...

that's the medical term for abnormal sensations of the skin, that is pretty common when you got MS for example..

Now, what I've experienced is ... kind of specific and maybe a little weird, watch the video to find out more and please let me know if you've ever experienced something similar 🤔 

[u2hearts]

Happy 25th Anniversary with Multiple Sclerosis

It started 25 years ago today. The beginning of my major attack that brought about my diagnosis. I still remember the story all too clearly. Valentine’s Day weekend, 25 years ago, I was moving into the house my ex-husband and I bought. We spent a few months sleeping at my mother’s house while updates were being completed. We were ready to move in and be alone in our new home. It was supposed to…

[thornfield987-blog]

I know this has been done before but here’s my headcanons for LU Chronic illness/Disability boys:

Legend(he/they): Hypermobile type Ehlers Danlos syndrome. Frequently dislocates joints and doesn’t see why the others make such a big deal about it, it happens all the time! Primarily suffers from widespread join pain, instability and chronic fatigue. Has as many different mobility aids as they have magical artifacts.

Time(he/him?): Early onset osteoarthritis and partially blind. All of the time travel and shifting forms was not kind to his joints, so the connective tissue was damaged and BOOM. Arthritis. The old man jokes are becoming less and less of a joke every day. Also experiences debilitating migraines.

Hyrule(they/he): Sensory Processing Disorder (often associated with autism but can be caused by other conditions). Their magic sensitivity can often cause overstimulation in their other senses, and they are very sensitive to light, sound, smell and touch. They are semi-verbal because even his own voice can overstimulate him sometimes, but they don’t know sign very well. Also has anemia.

Wild(genderfluid he/she/they): hypertrophic contractural scarring, partially deaf, semi-verbal because of vocal cord scarring. Also prosthetic arm(set after TOTK). She switches between sign and speaking, whichever is easiest for him that day. They have to perform daily stretches and apply scar lotion to be functional, but they aren’t very good at remembering to do so. Often blows out his voice because he gets excited, but can’t tell how loud he is speaking.

Four(plural they/them): Dissociative Identity Disorder(but not really because of magical reasons), damaged growth plates because of Minish magic. They have very similar symptoms to DID, but there are slight differences because it was caused magically and traumatically, not like in the real world. They sometimes struggle to walk correctly because their growth plates are damaged, causing their legs to be slightly different lengths. They wear adaptive shoes to correct this.

Sky(he/him): POTS(Postural Orthostatic Tachycardia Syndrome), chronic fatigue. He struggles to breathe the denser air on the Surface, but he struggled with it on Skyloft as well. He has a chronically higher heart rate that causes dizziness and (rarely) passing out when moving from sitting to standing, after eating, and after adrenaline rushes. This causes his stamina to be fairly low, and also causes chronic fatigue.

Twilight(he/him): RRMS(Relapse/Remission Multiple Sclerosis). This is caused magically by the Twilight curse eating away at his body’s nerves, but is kept mostly under control by his shadow crystal. Occasionally, he goes through relapses and experiences anything from tingling and numbness in a limb to temporary loss of vision in one or both eyes, balance issues, vertigo and slurred speech. These flares are almost always debilitating, but thankfully they only happen every couple of months and last from a few days to about a week.

Wind(he/him?): A little cliche, but he has a peg leg. He likes to tell outlandish stories about it getting bit off by a kraken or eaten by a cannibal, but the truth is that he got an infection, couldn’t treat it in time and had to amputate. This happened sometime after his quests had finished, and he’s still a little ashamed of the actual circumstances, so he doesn’t open up often.

(edit) I FORGOT WARRIORS

Warriors(he/him): Speaking Disfluency (Stutter). Often repeats sounds, such as “G-g-g-guys”, or extends sounds; “Llllllll-Iove you”. He grew up poor, so he was never able to get treatment for it, so he communicates using sign while Proxi translates verbally, though this isn’t as necessary with the Chain since most of them know sign.

[kindajd]

[mindblowingscience]

A simple sugar, N-acetylglucosamine, reduces several inflammation and neurodegeneration markers in people with multiple sclerosis, suggest study results. In addition, the researchers also report that this dietary supplement improved neurological function in 30% of patients. The study appears in the Journal of Neuroinflammation. According to the World Health Organization, MS affects more than 1.8 million people, and while there are treatments to prevent relapses and improve quality of life, there is no cure.

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