<div><strong>!!!NEW UPDATE!!! 8/2/2026 </strong>
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<div>It's been a while since I've posted an update, but I'm here. I'm alive, still kicking for now despite the heat. Second appeal was denied, which we kind of all knew would happen since the first one already was. So good and bad.
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<div>Bad, because a small part of me thought juuussttt maybe it would go through, despite knowing that's not likely.
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<div>Good, because I'm now one step closer to the finish line. 
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<div>The next step is to see a judge. This is where the vast majority of cases go through. Health is the same. Ever incredibly tired, drained. I've lost a lot of muscle over the past few years and it's gotten even harder to do basic exercises. Not to mention just... taking care of the basics of living.
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<div>We finally got an update on my stomach issues. The diagnosis is BAM (Bile Acid Malabsorption). Bad news, it's not going away. It, like my other disabilities, are chronic.
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<div>However, it is treatable. So while it'll never fully go away, medicine is helping most days. It's still awful and without going into details it's... a pretty rough thing to deal with. I'm going to link some more educational information about this disease down below with the rest of them.
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<div>Nevertheless, I haven't given up hope yet. I'm hoping I won't ever have to. 
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<div>It's weird to think that one day, when this is all over, I'll be signing off of here for good. Just feels like a hallway grows longer every day right now. The door is still there, but the floor has new planks in it every minute.
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<div><strong>As always, thank you all. </strong>
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<div><strong>I wish there were words that existed for how I feel thanks to everyone.</strong>
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<div><strong><em>!!!OLD UPDATE!!! (03/2026)</em></strong>
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<div>So, some news. As is the norm in the US, my disability claim was denied.
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<div>(This happens to a MASSIVE majority of people who apply at first.)
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<div>Unsure if it's automatically looked over and decided via bot/AI/etc, but regardless, now we file the appeal. Lawyer feels confident at least, but it does feel nerve-wracking. Medicaid finally kicked in, so med prices for me went down a ton after a huge hassle and going without a few meds for a little bit. So my monthly expensive shrunk. All in all... I'm trying to stay positive, I am. I'm just hoping and praying it works out.
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<div><strong><em>Thank you all, truly.</em></strong>
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<div><strong>Outdated: *900 is the amount roughly per month I need for bills/meds/health appointments.*</strong>
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<div><strong>New average: Now, thanks to Medicaid helping so much, monthly expenses are probably a lot closer to *700 a month. This is a fantastic update. &lt;3 </strong>
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<div>My name is <strong>Evan Seale</strong>, I'm <strong>29</strong> years old as of this month. I've had <strong>Type One Diabetes</strong> since November of 2015, and I've been diagnosed with <strong>Multiple Sclerosis</strong> since 2024 BUT we believe due to how many lesions that are on the ol' brain of mine, I've probably had it since around 2019.
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<div>If you're seeing this, you've found out that I've gotten to a point where I can no <strong>longer work, maintain my health, and live without help from others.</strong> I'm currently in the process of finally being able to file for disability after the <strong>3rd job I've lost in a row due to medical/health/disabilities. </strong>
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<div>I'm trying to only ask for a little, but at the same time I know it's a lot. I'm hoping with enough people it'll feel like pennies and dollars every month instead of a massive donate. Especially since I don't know how long it's going to take. A little every month will go a long, long way in helping. <strong>&lt;3 Seriously, I can't thank you enough. &lt;3</strong>
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<div>I'm sure for those reading this, you're probably curious just what all impacts me, and honestly I'll try to list them all but I can almost promise as I'm writing this I'll forget one or two.
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<div>I'll break it into 3 parts, and how they impact each other.
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<div><strong>Part one: High blood sugar:</strong>
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<li>Increased thirst and hunger, fatigue, visionary changes, issues with my skin, nerve damage, long term kidney damage, heart damage, pretty much EVERY organ damage (except pancreas since it's literally dead thanks to type 1) The longer someone deals with highs, the more time that is taken from that person's life and it hits down the line. The struggles of a diabetic this year they may not see for 5 years, etc.
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<div><strong>Part two: Low blood sugar:</strong>
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<li>Shakiness (In my case extreme), Sweating (same as before), headaches or migraines, hunger, nausea or upset stomach, fatigue (again with the fatigue) mood swings, brain fog, struggles with balance, dizziness or dizzy spells, numbness in the mouth, and in very extreme cases of lows, just horrible confusion, loss of coordination, slurred speech, blurry vision, seizures, and total loss of consciousness.
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<div><strong>Part three: Multiple Sclerosis:</strong>
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<li>This is going to be a long section because... It's a lot of symptoms.
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<li>MS (Multiple Sclerosis) impacts everyone differently, some people get their first flare up, and instantly need a wheelchair. Some people get a flareup and that's it. I personally have what's called RRMS, which means that it plateaus, comes again and hits, then plateaus again, each time with all the symptoms from before PLUS new ones.
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<li>I personally deal with the fatigue INCREDIBLY bad, on top of the fatigue from highs/low sugar. I have horrible balance these days to the point I've started using a cane JUST in case. I have horrible leg strength now, going up stairs I'm okay, but going down stairs my legs are so shaky if I slow down too much I become unstable/fall. Pins/needles in my feet (not diabetic related, despite my initial concerns.) Random sporadic episodes of neuroglia (half body seizures randomly, usually before bed or when I'm more tired which is yes, almost all the time from fatigue.) Hyper sensitivity/pain. This is mostly just in my thighs/legs. I always describe it as someone pulling my hairs on my legs out with burning tweezers. Insanely awful brain fog; I have never in my life thought I was losing my mind as bad as I have with MS. That feeling of having a word on the tip of your tongue and you just can't quite reach it is an EVERY conversation, or every sentence thing. I have to do my best to think of another word that means the same thing BEFORE I forget where I even started. It happens so much that it's maddening. It's like going into a room and forgetting why you're there with every conversation you have. Vison problems, the main reason I lost my second job. Reading is... doable, but as someone who's always been an amazing reader this feels like a hiker losing a foot, or a surgeon losing half a finger. There are a few more symptoms I won't include just for the sake of my own pride/comfort, but just know that bathrooms are very needed anywhere I go. Heat intolerance to the extreme. I fully can NOT regulate temperature. I have gotten heat exhaustion twice this summer, and I almost NEVER go outside. I stay at home most of my time, and even more due to health issues. Last but not least, 5/6 people with MS suffer from depression and/or anxiety. I can't even blame that one on MS since I already had it, but you better know it go worse with it all.
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<div>First it was what we thought was just extreme burnout and fatigue from Type One, only finding out through doctors later that was the start of my MS fatigue. Then it was on to my second job that I had to start short term, THEN long term disability due to the visionary issues MS gave me. Finally, and most recently, due to complications between MS, Type 1, absences due to what were APPROVED days off due to ADA (with all the paperwork), I'm losing my current position as well.
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<div>The current position was my last hoorah, my last reasonable attempt. My last try at finding ANY job I could do anymore between my illnesses.
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<div>I don't have many more days left with my current job, and while I already have an attorney ready to file disability, once I start, I won't have any form of income.
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<div><strong>Here's what that means for me:</strong>
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<li>The obvious stuff, bills, electric, rent, everything like that.
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<li>It also means no job insurance.
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<li>It ALSO means no income FOR medicine.
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<li>No ability to save money in case of an emergency
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<li>My medical debt will continue to go on unchecked, despite how many calls I get.
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<div><strong>Here how you can help:</strong>
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<div><em>If you're able to, I would INCREDIBLY be grateful if you could help fund and support me during my process of disability. Food is more than welcome, rather that's goods you're not using or money towards this to help with it.</em>
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<div><em>Help with rent, bills, medicine. That's the big one and what the whole GoFundMe is for.</em>
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<div>I never thought in my life I would need to truly do this, but I also never thought in my life I'd have two chronic diseases with no cure.
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<div>One sentence lives with me every day and it kills me to think about: I will never be healthier than I am right now.
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<div>For those close to me you've probably heard me say this a lot, and it's scary to admit. It's not going to magically get better. These diseases only get worse, and while they have a possibility of being managed, I'm not able to manage them, and work any position that supports any form of health/living.
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<div>I hope that if you see this, you can help, even a little bit every month. I figured a monthly thing would help out way more than any up front donations. Especially since the process can sometimes take a little bit. I'm already working with an attorney, therapists, soooooo many doctors that I literally forget one or two when I list them off. Everyone seems to have my back so far, and I hope that in ways I can have yours too.
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<div>I know it's really, really sucky out there right now economically. But I think I can do it, even if it's on leftovers and scraps I'll make it.
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<div>I'm really, <em>really </em>good at being poor.
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<div>Also included in this is several links to videos going over what my illnesses are, what they effect, and how they impact people including myself on a daily basis:
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<li>Here's a video that goes over some of the <a href="https://www.youtube.com/watch?v=pgafmrV5jyY" target="_blank" rel="noreferrer noopener">process and complications of Type One Diabetes</a> .
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<li>Here's a video that goes over some of the <a href="https://www.youtube.com/watch?v=eEGct5EimSs" target="_blank" rel="noreferrer noopener">effects of Multiple Sclerosis</a> .
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<li>And here is a .gov article going over the <a href="https://pmc.ncbi.nlm.nih.gov/articles/PMC9701081" target="_blank" rel="noreferrer noopener">association between T1D and MS</a> .
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<li>Here's an article on BAM from the <a href="https://pmc.ncbi.nlm.nih.gov/articles/PMC8515273/" target="_blank" rel="noreferrer noopener">National Library of Medicine.gov.</a>
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<div>If you don't wish to donate here, you can always donate to my PayPal, or CashApp.
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<div>PayPal: @CSisBS
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<div>Cashapp: $Loafcat
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</div><img alt="" media_type="3" src="https://d2g8igdw686xgo.cloudfront.net/94586669_1757716757221669_r." width="100%" />
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<div>Thank you. I hope I can do this. I have hope.
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<div><strong>I still have hope.</strong>
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Anonymous

Dani Kelly

Plus que $290 !
Apportez votre pierre à l'édifice.

Evan survive during disability process with T1D and MS.

Plus que $290$ ! Apportez votre pierre à l'édifice.

Evan survive during disability process with T1D and MS.

Plus que $290 !
Apportez votre pierre à l'édifice.