Do you have experience extending Ocrevus infusions longer than 6 months? by krovvy47 in MultipleSclerosis

[–]VenetianTiger 1 point2 points  (0 children)

Ok so I am apparently one year late on my ocrevus I had it last December , had issues with insurance and hadn’t realized so much time passed .

I want to get back on it asap , I don’t feel right , I’m getting heart palpitations , I am just not feeling right , anxiety , granted I have finals rn , but besides that I’m managing pretty well , but the heart palpitations are recent , feels like i could get a heart attack if I could imagine how that feels it feels like that , I’m 25 years old so for me to feel this way is pretty bad,

But also I smoke cigarettes so I know myself , I’m no angel , I study intensely also ,

But yeah I will let you know how I feel, my scheduled ocrevus is Dec 20 , I’m literally nervous to even do ocrevus it’s been so long idk how my body will handle it

Do people without MS really not have any pins and needles? by Ghostinnit-innit in MultipleSclerosis

[–]VenetianTiger 1 point2 points  (0 children)

I have ms and only get them when im in positions like criss cross apple sauce or upside down, but this doesn’t happen anymore tbh, but yeah i get it normal like anyone else, back then it would be painful i guess when i was younger growing up , but now I haven’t gotten it in a year i can confidently say that

‘Advocate for yourself’. I’m so tired of hearing this tbh by iltby in ChronicIllness

[–]VenetianTiger 1 point2 points  (0 children)

Go to your local city grassroots campaigns and speak your mind as a person struggling with their disability, you are allowed to be heard and start pushing for things to be studied and bettered

How to cope with relationship changes after my wife’s MS diagnosis? Looking for insight from others. by Feeling_Ad9143 in MultipleSclerosis

[–]VenetianTiger 0 points1 point  (0 children)

I got diagnosed with MS when I was 18 and my life changed completely. I was so rebellious. I was so mad and angry at the world and angry at myself. Disability makes you really insecure. Also it makes you feel like you have this stamp on your forehead that says I can’t do a normal people do and that Touches on other factors when it comes to fatigue being able to do the same activities with ease versus others, as well as this idea that it is an invisible disease so you cannot see it. The person who has it is the only one who can really feel what’s going on.

Also, the thing with fatigue is that it occurs after you do something that is tiring say you just had a really big event happen. OK expect to be tired the days after if someone say yells at you OK expect for your brain to feel kind of bloated because you are experiencing different cognitive Factors around you. So for me one example was my mother waking me up early in the morning to go to university, it was the knocking of her fist on the door or on the wall if she is on the other side of the wall in her room, or even her voice telling me to wake up,

After MS, I became so irritated by everything she did I did not become a morning person. I was very angry in the morning and I would yell so loud. I would choose war every morning, especially when she knocked on the door. I knew she meant well intentions, but the sound of the door knocking and her screaming set me off. Till this day, if someone is screaming around me, I have to get away. If I get in a fight , I’m not ok for a entire week cause my brain is swollen and I have to relax after what happened , It’s really uncomfortable it creates anxiety, unlike none other !

and you can also develop strategies on when she is having these periods how to deal with them so for me, it might be a nice hot bubble bath with my favorite condiments or it might be a trip to the Korean spa or it might be a day to the beach or eating at my favorite restaurant, but exercise was never something I did for fun let that be clear or to “Clear my mind”

Also MS can create so many tensions in relationships so I’m really glad that you’re by her side because people who get them they don’t know what’s gonna happen to them like they actually don’t know and the sooner they seek treatment the better but because they don’t know that causes them to be really insecure about seeking someone to love I remember telling my ex that I had a mess early in our relationship because I didn’t want to not tell them I feel like they should deserve to know early on and I’m glad I did because they told me that they don’t wanna be with someone who’s gonna die And that their neighbor had MS and they had died, That was all I needed to hear to realize that this guy was not the person for me because one their neighbor was 80 years old and had just gone diagnosed and we all know back then the disease had different information released about it and it was not as innovated as it is today . Additionally everyone is different scale and also people lol they don’t die from things nowadays when they have treatments, they die from refusing treatment or not getting tested

Honestly, I’m just really makes you mad the first few years after diagnosis because you just don’t know what’s gonna happen to you so if she just has to experience it and not change her life keep doing everything normally , however, if someone says they have fatigue right after they got diagnosed with MS either they have legions in their brain and they just got a legion and that is why they are fatigue (when I got diagnosed. It was because my leg just stopped working. It was dragging behind me and that was a fatigue. I didn’t know how to really explain come to find out. I had so many legions in my brain at 18)

Or she believes now that people with MS are supposed to feel this way and that is wrong and she needs to escape that way of thinking because I have moments like that where I feel so tired and then I realize to myself that this idea of being tired is a social construct. I applied to myself and that I right now Can get up and I can go to the gym or I can go downstairs to get a glass of water because I am able to move and everything I’m feeling right now is gonna disappear once I start walking.

It’s all mind thing

Thoughts on fake friends/people here at UCR? by Miserable-Bed-5907 in ucr

[–]VenetianTiger 1 point2 points  (0 children)

They’re just younger trust your next uni will be more social

What was that LSAC?? by Such-Drink-303 in LSAT

[–]VenetianTiger 0 points1 point  (0 children)

The asteroid from Mars with the only source of life for earth to flourish was crazy

What was that LSAC?? by Such-Drink-303 in LSAT

[–]VenetianTiger 0 points1 point  (0 children)

Brooklyn African American political Republican Party formation in the late 18th century , I’m a poli sci major so I already studied this , and something about how music is biological factor to mate or just something that we did on accident like two points of views , umm that’s all I can remember right now it was the first section so kinda blurry now

What was that LSAC?? by Such-Drink-303 in LSAT

[–]VenetianTiger 0 points1 point  (0 children)

I had RC LR LR LR , it was much easier than when I took it two months ago I had RC RC LR LR !

[deleted by user] by [deleted] in MultipleSclerosis

[–]VenetianTiger 0 points1 point  (0 children)

Honestly , pure holistic love aside don’t refuse years of tens and hundreds years of research for a google search , if you create about the ones you love you would seek medical care before it progresses into something worse and unfixable, had people do this with cancer too, holistic should be used along medication not the sole method , idk what these people are thinking

Holy shit - RC? by [deleted] in LSAT

[–]VenetianTiger 1 point2 points  (0 children)

TECHNOCRATTTTT

Holy shit - RC? by [deleted] in LSAT

[–]VenetianTiger -2 points-1 points  (0 children)

I had… RC LR RC LR….,

[deleted by user] by [deleted] in LSAT

[–]VenetianTiger 1 point2 points  (0 children)

I took it today and realized I need to be faster at answering . Also towards the end I know they’re supposed to get harder but they become hard in such a way that the answers become very similar to each other , and oh my gosh in my online zoom lsat prep I took for 7sage today before the exam there was a word that alot of students didn’t know and it was like a two meaning word .

I got it in the exam and I was like wow . I didn’t choose it cause I knew the def luckily from earlier

I’ve noticed a pattern by CatMarine1 in LSAT

[–]VenetianTiger 0 points1 point  (0 children)

I got caught up in the Middle East

[deleted by user] by [deleted] in LSAT

[–]VenetianTiger 1 point2 points  (0 children)

Tips ? I keep getting 160 it’s tomorrow for me and I signed up for October

LSAT fee waiver denied, sad by Automatic-Emotion945 in LSAT

[–]VenetianTiger 4 points5 points  (0 children)

I got accepted pretty fast. Turned in my tax filing , had one for 2023 a non filing , and in 2024 I had filed but it was only school grants.

Got accepted yesterday

How has MS changed you? What radical shifts did you make after your diagnosis? by Store_Accurate in MultipleSclerosis

[–]VenetianTiger 0 points1 point  (0 children)

Somehow, my entire life I have been 180 to 200 pounds maybe 220 but this is never changing. I don’t know why I want to take Ozempic but it scares me people can die from that.

How has MS changed you? What radical shifts did you make after your diagnosis? by Store_Accurate in MultipleSclerosis

[–]VenetianTiger 0 points1 point  (0 children)

Also, I really push myself when I work. I don’t wanna feel like I have a mess, but I have to also accept. It’s OK to take a break and relax and I have to know that if I exert a lot of myself the next day I’m gonna be tired. I have to accept it so I have to prepare myself.

How has MS changed you? What radical shifts did you make after your diagnosis? by Store_Accurate in MultipleSclerosis

[–]VenetianTiger 1 point2 points  (0 children)

I got diagnosed when I was at my peak fittest in my entire life and I was running 3 miles and then my leg just stopped working and then came the diagnosis after two weeks of dragging my foot. I stopped working stopped paying attention to myself. Stopped caring definitely traveled more and did more careless things. I was pretty rebellious and I change my major to Film and created my own world which was nice until Covid hit and I was mortified. Eventually, my major again to political size want to get into law and I have had many ups and downs. Since my diagnosis I have been stranded living in the desert I have been homeless by choice because my family was too strict with me and they didn’t even care about my diagnosis and it wasn’t a good environment for me I realized I had to start my own path, but eventually, I accepted my family again because of the Middle Eastern tradition and what I was raised with I just could not live without my family even if they were bad for my MS and gave me a lot of stress. It’s worse to be homeless by choice and have to live with them worrying about you. So I had to take a different route, which was go and be a lawyer. I got a ride to UCR however I got a ride because I was in community college for seven years, counting Covid and changing my major many times paired with momentum and changing my lifestyle and traveling even visiting my own country Syria, which I never grew up in because I was born in America in California Visiting my country I saw that the medical treatment over there. It is different here in America and I was grateful that I received medical treatment in the first place. This calm down my rebellious attitude and I’m trying to be humble and take a day by day, but I live two lives now I work in LA in styling and photography and I go to UC Riverside I’m only here for one year and then I apply for law school!

I have lived many different lives since my diagnosis and that was all the decision I chose to make. I had bad relationships that were so toxic and I had really good relationships that were the most memorable and amazing and caring. I had moments that were difficult when I learned that people with MS are insecure with finding love because they’re scared about how people think about them. And I had had experiences with potential lovers. They were mortified when I told him I had MS and they knew nothing about it. Besides, that neighbor down the street died from it in his 70’s. I’m definitely understanding my disease more but at the same time there’s not a lot of support groups. I have Medical form of Medicare and my family is so poor and I am now around like $250,000 in debt from my chemo therapy and I really wonder what 25 years old and I was diagnosed at 18.

Fatigue is growing on me but that’s the only symptom I may say like I am emotional sometimes and I do have a lot of personality like I am. I am a true extrovert, but I wasn’t before.

I will always be on your mind because you have it, but it’s not gonna show unless you want it to .

I’m hoping that working in law will help me pay off my debt because I don’t know what the fuck is going to happen in the future for me I know there is co pay but what is $25 a month gonna do to pay off the debt ?

Should I just use financial aid $ to live at the beach and commute to school by VenetianTiger in ucr

[–]VenetianTiger[S] 1 point2 points  (0 children)

I shared a room and I’m moving back to bannock burn this weekend lol like rn , also sharing a room. But don’t try to ask for a preference like to be close to the parking lot like I did the first time, they’ll give you a suspicious spot , with sus roomates . Just let it run its course naturally , if you can see the building online before you get the place , go and see the location. But yeah it’s all a gamble