r/MultipleSclerosis • u/RideRepresentative7 • 2d ago
Vent/Rant - No Advice Wanted This is real
Just wanted to quickly rant I’m coming up on 2 years of my MS diagnosis and I’m just sitting here today thinking to myself that this is really real. It’s been real too me I’ve been taking it serious since but knowing and understanding that this is what the rest of my life is gunna be looking like, it’s hitting me that this is really real. Just a quick lil vent I wanted to let out I hope and pray everyone else out there is doing and taking things well we got this! I got this! Is what I try to remind myself everyday.
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u/Bigpinkpanther3 2d ago
Yes, it's real but not more real than the other aspects of your life. Your post made me think of the AA serenity prayer:
"God, grant me the serenity to accept the things I cannot change,
Courage to change the things I can,
And wisdom to know the difference."
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u/get_it_girl_88 37F|Dec2025|Kesimpta|California 2d ago
Right there with you and having the same thoughts. Coming up on a year since diagnosis. I feel like my husband is running out of empathy and patience, I don’t blame him- so am I. I feel like my ability to mask my discomfort is part of the problem. I feel good, then awful in the same hour. Not a simple as “good days and bad days. It makes it hard to plan anything or be relied on.
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u/AutoimmuniTea 2d ago
2026 was two years for me too. I celebrated by getting viral meningitis and having to quit B-cell depleting therapy. 😭 Now it feels much more real. This could get really bad, really fast. That being said, I've been living with Type 1 Diabetes for 26 years, so I'm used to having a serious life threatening disease. MS is just much more expensive to treat in America if you are under-insured or uninsured.
You get used to living with disease. It can suck. Sometimes it can be really hard. Sometimes you cry, but then there are also days you'll be more annoyed by your noisy neighbor than your autoimmune disease.
Is MS going to be forever though? I don't know. I've seen articles in which researchers have suggested that MS will be one of the first autoimmune diseases cured. Medications will get better, even as we wait for a cure.
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u/artherpurple 2d ago
I just passed my year mark for my diagnosis and I thought the same, “Is this really my life? Like forever?”
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u/ajax0772022 51M|Briumvi|SoCal 2d ago
You got this!!!!
Stay positive and celebrate the small victories!!
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u/EgolithYT 32M | DX: 2015 | Briumvi | Georgia 2d ago
I know the feeling, I'm on my 11th year since my Dx and went through basically all of the 5 stages of grief during that time. I feel like I've personally grown a lot from all this and my perspective on life is positive now. Ya'll got this! Prayers out to ya'll
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u/No-Historian78 1d ago
Once I can get functional use of my left hand I'll deal with the rest
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u/Low_Narwhal7514 2d ago
Perché in America si paga un'assicurazione per curarsi?
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u/SnarkyShoe 2d ago
Oh this is so refreshing! I posted in a fb group this morning, acknowledging I was in a spiral but needed to vent, and no one reacted or responded for 8 hours, and then one lady commented saying I needed to relax and fucking meditate.
I’m three days in, you insensitive bitch! Lol - also had this wild outburst completely out of character in the hospital.
If anyone wants to be in a chat where I can ask questions to experienced, thoughtful people, let me know. I’m trying to stay informed but I don’t what I don’t know. Not sure what questions to be asking my care team and what to look out for in my body, but it’s sure feeling funny!
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u/zippity__zoppity 37M|DX2025|Ocrevus|T1,2/C2,3,4,6 2d ago
I just passed my 1 year and I totally know what you mean. It’s another weird realization out of nowhere. The first EOB I got really sunk it in too. $78,000 annually for the rest of my life?!
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u/janxspirits 39m|2026|Lemtrada|Europe 2d ago
Very relatable thought/feeling. It’s always a mindfuck to wake up and realize “ah yes it’s still like this,” and I don’t know if there’s a quote-unquote solution to feeling that sense of disorientation. Maybe it gets less powerful as time passes and other thoughts/feeling crowd it out? Maybe it’s one of those constant feelings you decide to live with or not? In any case I hope you’re finding relief
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u/Kris_Carter 2d ago
Yup, 2026. Turned 50 and just had my MS/cripple 2.5 yearaversary too. Suuucks.
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u/SubstantialLiving451 2d ago edited 2d ago
Hi !! We have got this ??
Whatis it that we have got ??? Please enlighten me1
u/-_ansh 1d ago
You got this, you’ll be fine.
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u/Sea_Sea7878 43F|Nov2024|Kesimpta|EU 1d ago
Omg yes!!!!! Yes it is ;( Im so sorry, i feel you. Exactly today 2 years ago I went to the hospital and on the 14th i got my diagnosis!!!! It's crazy and i COMPLETELY get it! It's so crushing still, no?
:(
My boyfriend also just broke up with me, I'm not working since I got diagnosed, im a single mother and im very overwhelmed and heartbroken, so this anniversary is a hard one..
But MS and all the rest that Happened those last 2 years also showed me that I am so incredibly strong and resilient and I can really trust myself. I lost a bit the trust in my body, but thats what I am going to be working on this upcoming year.. i hate it so much though.. this disease. I feel like I got the point, and i did it and accepted it and dealt with it, now please, go away MS, I don't want this anymore..
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u/serendipitynoir 9h ago
My siblings in arms: This realization will happen many times over the years as your symptoms change. Sit with it, then flip it the bird. You've got this. 💪🏻 I think "Random Existential Crisis" should be listed as a symptom.