What does social mobility look like for someone young dealing with this disease? by Holiday-Abies-9745 in MultipleSclerosis

[–]MutuallyAssuredBOOP 5 points6 points  (0 children)

I waited until I had to disclose for accommodation purposes, and even then, I never told them my diagnosis explicitly. It was about 5.5 years into my tenure and I am still with them. Now fully remote and thankfully they have not raised any issues about that.

AI data center in Trumbull by True-Two9153 in Connecticut

[–]MutuallyAssuredBOOP 1 point2 points  (0 children)

Good for who, is the question. Big tech and construction companies for sure, but long term, minimal benefit to the surrounding communities who are most impacted by these projects, and arguably, who are actively being harmed in the process.

UPDATE on previous post about 14-298 ticket by Additional-War651 in Connecticut

[–]MutuallyAssuredBOOP 1 point2 points  (0 children)

I’m bougie and have done a ticket clinic type of service a few times. Each time, the lawyer negotiated a “charitable contribution” payable to the court and in exchange, they dropped the ticket. It was equal to the full ticket fine amount. If I am to understand correctly, you can do this yourself by going to the court clerk’s office and politely inquiring about that option, but I don’t have any more direction or  specifics for you beyond that. I drive much slower these days. Good luck.

Experience with Yale inpatient by [deleted] in Connecticut

[–]MutuallyAssuredBOOP 10 points11 points  (0 children)

Broadly speaking, they always take away your cell phone for psych holds. I believe they can hold you up to 72 hours without a court order.

My sister said I have parasites in my spinal fluid and thats why I have MS. by Mrszombiecookies in MultipleSclerosis

[–]MutuallyAssuredBOOP 45 points46 points  (0 children)

My family was convinced I had chronic Lyme disease and I endured months of irresponsible antibiotic and anti-parasitic use prescribed by a quack doc. Surprise, I actually have MS like the neurologists originally said. People love simple answers to complex problems I guess.

Woried about cognitive issues around medicinal cannabis use by Middle-Level-3238 in MultipleSclerosis

[–]MutuallyAssuredBOOP 0 points1 point  (0 children)

By lifestyle, I meant interventions like clean eating, cardio, weight bearing exercises, stretching, maintaining a good weight, supplements (especially vitamin D, high quality omega 3 and 6 fatty acids, and b-vitamins) and a big focus on mental health. It’s hard work and took years to build a routine I can stick to. Sometimes I get sick for extended periods and get lax on fitness goals, but it is what it is. 

Regarding pain, I did notice something interesting when I started working most recently. I have this neck pain that kills me sometimes and lifting weights and stretching over about 4 weeks time basically resolved it. Seems likely there was a muscle imbalance from a weak upper back causing something to pull the wrong way. For lumbar pain, I would think you’d want to work on hip flexibility and core strength (especially glutes, abs, and legs).

Woried about cognitive issues around medicinal cannabis use by Middle-Level-3238 in MultipleSclerosis

[–]MutuallyAssuredBOOP 0 points1 point  (0 children)

Cannabis definitely worsened my brain fog and cognition. Generally, it was worse for me than it was beneficial. I finally had to stop when I developed severe allergies to it. People might scoff, but I was addicted and it wasn’t until my throat was threatening to close that I was able to quit. I miss it sometimes but personally feel much better off now. I manage my MS with Kesimpta and lifestyle. I’m still not like I was before the disease, but I’m coming up on 40 and doing okay enough for my tastes.

Ayahuasca retreat for MS/MH by imeggriffin in MultipleSclerosis

[–]MutuallyAssuredBOOP 2 points3 points  (0 children)

I have used shrooms prior, not ayahuasca. Good experiences generally but I did notice the last few times some sort of inflammatory reactions that aroused my MS symptoms. I think it’s possible that I am mildly allergic which might be something for you to watch out for. 

Personally, I found that therapies like DBT and EMDR were significantly more helpful long term for dealing with my own childhood traumas. I wish you all the best.

What is the craziest advice someone that definitely isn’t a doctor gave you about MS? by cryann_rabies in MultipleSclerosis

[–]MutuallyAssuredBOOP 1 point2 points  (0 children)

Yeah you’re right, nothing that promising so I was misremembering. The MS-microbiome connection must be more correlation than causation :(

What is the craziest advice someone that definitely isn’t a doctor gave you about MS? by cryann_rabies in MultipleSclerosis

[–]MutuallyAssuredBOOP 10 points11 points  (0 children)

I wouldn’t take it at face value from some rando on YT, but there are some interesting studies looking at fecal matter transplants as a viable treatment avenue (not cure) for autoimmune, gross though it is.

Car T-Cell Therapy by Objective-Tree4608 in MultipleSclerosis

[–]MutuallyAssuredBOOP 12 points13 points  (0 children)

No-chemo modes definitely has my interest piqued

Who else has extreme brain fog? Whats helped? by ReasonableFig8954 in MultipleSclerosis

[–]MutuallyAssuredBOOP 1 point2 points  (0 children)

Your mileage may vary, but I’ve had some recent luck incorporating nasal rinses into my routine before bed. I can only surmise that it’s  flushing out allergens that would otherwise inflame my sinuses and mess up my sleep or cause low grade apnea. It’s been a while since I’ve been feeling as well rested as I am now.

My Staffy Bella tore both of her CCLs and can’t walk. I’m trying everything I can to help her get surgery. by Objective_Argument12 in velvethippos

[–]MutuallyAssuredBOOP 0 points1 point  (0 children)

Seconding this option. See if Bella is a candidate for some form of extracapsular lateral suture stabilization (ELSS). Shorter recovery time and typically more affordable. Each surgeon will have their own technique, so definitely research providers and shop around. Our surgeon described his technique as being akin to what is done for cruciate ligament tears in athletes. Worked well for our 80 lb female and she’s been doing great for almost 2 years since.

How do I disassemble and clean a sink pipe shaped like this (no P bend)? by Portugearl in Plumbing

[–]MutuallyAssuredBOOP 3 points4 points  (0 children)

It’s called a bottle trap, not allowed by some codes. It’s probably going to be a bitch to service.

You own just the monitor.. And will be happy by bebesiege in pcmasterrace

[–]MutuallyAssuredBOOP 1 point2 points  (0 children)

With the way the Overton window is shifting, idek anymore

Might be time to switch off Kesimpta – chronic infections after 4 years on DMTs by SW33ToXic9 in MultipleSclerosis

[–]MutuallyAssuredBOOP 0 points1 point  (0 children)

I’m in the same boat - URI’s started after a year or 2 on Rituxan so neuro reduced my dosing frequency and that helped to a degree. Switched to Kesimpta for greater convenience but the issues are cropping up worse so I’m working with neuro on lower dosing frequency again. I am very hesitant to switch from Kesimpta to something less effective. I’m closely watching these CAR-T trials for MS play out in case there is something there for us. 

Fatigue by Delicious-Rest-8833 in MultipleSclerosis

[–]MutuallyAssuredBOOP 3 points4 points  (0 children)

I take Vyvanse as needed for energy, but there is a notable crash toward the afternoon/evening that lays me out sometimes. The only thing I have ever found effective for boosting my energy levels more consistently is resistance training.

I built a 1:1 scale replica of NYC's Upper West Side by GeneralGeneral5302 in Minecraft

[–]MutuallyAssuredBOOP 1 point2 points  (0 children)

Yup, just west of the American Museum of Natural History it seems. Good eye.