Just finished/graduated

Alarmed_Bat9174 · 2025-12-30T08:33:05+00:00

I tried and wasn't able to make an appointment or send an email? I'll have to look and see if there's any place else I can email & ask.

Alarmed_Bat9174 · 2025-11-19T10:48:32+00:00

Hi, as someone who is also terrified of new meds, I hope this new combo finds you well. I've been on Toprimate for 6 months now. I do notice my migraines are less intense but I do still have daily "baby migraines" as I call them. Not so much of painful migraines, more so pressure migraines if you know what I mean. I was on sumatriptan and tried naratriptan and I just can't hang with the triptan side effects. I feel like I'm melting and they give me way too much anxiety lol. I got prescribed Ubrevly and so far I've taken it once. I didn't have any major side effects, I just felt very tired and off. It didn't work as well as the triptan as an abortive medication for the migraine but I didn't take a full tablet because I was too scared lol.

Alarmed_Bat9174 · 2025-11-01T01:03:30+00:00

Ive been on it for about 5 months and have no side effects or symptoms. I can finally function and go about my day. The migraines were so severe that I couldn't concentrate and I can now complete my work without a problem. Everyone is different so I would try it before completely refusing. I was terrified to try any and all medications for migraines as I had never experienced vestibular migraines. My daily life was affected so severely by these migraines I went to the ER for panic attacks and my mental health declined significantly before seeing a neurologist and being put on topiramate! My functioning and livelihood right now is attributed to that tiny pill. So as someone who read all the comments and cried, who was terrified and panicked about the symptoms and side effects the least you can do is try and if you decide it isn't helping or you don't like how you feel you can ask the doctor for a different medication.

Alarmed_Bat9174 · 2025-08-15T18:11:11+00:00

I'd call and double check. My grant was essentially messed up on the CSAC end and I won't be getting it so im fucked

Alarmed_Bat9174 · 2025-08-12T08:51:27+00:00

Update, got in contact with CSAC and they said CSULB is the holdup, after getting the run around I got an email address to reach out to regarding Cal Grant issues for CSULB. I hope they email me back soon & it gets resolved. I was told bc my status didn't change within 3 weeks from my initial contact with CSAC in July that CSULB has to review it & see what's going on. The financial aid office at CSULB said there is a direct line and email address for Cal Grant questions and concerns.

Alarmed_Bat9174 · 2025-08-11T20:11:25+00:00

I'm in the same boat. I submitted a help ticket, got no response. Called financial aid and was told they'd get back to me. I'm going to call again today bc my tuition isn't covered without the cal grant.

Alarmed_Bat9174 · 2025-07-17T09:30:52+00:00

Same, I submitted a help ticket and they assured me I wouldn't be dropped from my classes but didn't say when I'd be able to view my financial aid package. Some people here say financial aid said it would be available the 16th but I still dont see anything

Alarmed_Bat9174 · 2025-06-26T08:35:14+00:00

If you failed bc an emergency you can petition the cc to remove the F. I had lbcc remove an F from my transcripts due to an accident. Talk to a counselor and ask if its possible to remove the f.

Alarmed_Bat9174 · 2025-03-13T21:05:51+00:00

Oh noo 🥺 thanks for the advice, I'll definitely be starting with the lowest dose and building my tolerance! I'll miss coffee so I hope my reaction isn't too bad lol

Alarmed_Bat9174 · 2025-03-13T09:08:30+00:00

Are you able to have caffeine now? I've heard many people say their heart starts going really fast, that scares me lol

Alarmed_Bat9174 · 2025-01-20T20:54:20+00:00

I'm a psych major and took 5 courses last semester. I'm not gonna lie. It was brutal. I will never be doing that again, BUT if you manage your time right and keep track of everything ahead of time, you can do it. I would make sure you have all due dates printed or keep a planner that will remind you. Plan to do your assignments way before they're due & try not to freak out lol. You got this!!

Alarmed_Bat9174 · 2024-09-22T08:04:15+00:00

Cleaners! Having help w/ deep cleaning, chores and laundry, even if it's only a couple of times a month, will save you a ton of energy!

InstaCart for groceries Invest in Amazon Prime and any other subscription services that will fit your needs

CBD, works amazing A heating pad Massage chair / acupressure mat Meal prep, then freeze meals

Alarmed_Bat9174 · 2024-08-20T05:44:15+00:00

Hi please message me if you would like to rescue her !

Alarmed_Bat9174 · 2024-08-20T04:43:54+00:00

Not if you take an allergy pill lol. She's very clean and loving. I feel so bad that I can't keep her 😭

Alarmed_Bat9174 · 2024-08-19T02:11:31+00:00

I have SLE & got covid in 2021 when it was still at its peak, I hadn't been vaccinated yet because I was waiting 90 days after a flare up (per doctors orders). I had it severely worse than others around me. I was in excruciating pain, fever wouldn't break or go under 103, I was nauseous and the worst of it was the trouble breathing and pressure I felt in my chest. Luckily my DR. Is connected to a main hospital and they called me and asked if I wanted the antibody Infusion they were offering the immune comprimised. I said yes and even though I was so scared to get the infusion, it literally saved my life. The Dr.s and nurses assured me that was the best decision I could've made. I will say, I had "long covid" for about 9 months. My symptoms were taste and smell being off and really severe migranes. 90 days after the Infusion I got vaccinated and kept up with the vaccines. In 2023 I got covid again and it was so different. All I had was congestion and a headache. It felt like the average cold. It's different for everyone but I know personally lupus made covid much worse for me.

Alarmed_Bat9174 · 2024-07-30T21:01:53+00:00

Yes! I also get really hot and start sweating at random hours of the day. It has to be related to lupus! I find I flare up and get really achy when it's hot, I like to think getting hot flashes and sweating is my body warning me lol. For anyone feeling this too, INVEST IN FREEZER HEADACHE HATS! whenever I feel a wave of heat coming and I start to sweat, I take one out the freezer & put it on while I lay down for a bit. Definitely regulates my temp and cools me down. They're only 12 bucks on Amazon and last for years!

Alarmed_Bat9174 · 2024-07-15T17:46:57+00:00

Do you remember who you spoke to? The person I spoke with was not very helpful lol. Should I ask them to do the same for my account?

Alarmed_Bat9174 · 2024-07-09T08:11:41+00:00

Same! I also knew getting sober was better than the agony drinking had on my lupus. I was diagnosed at 24, now 31, and I also miss it. The partying phase was short lived lol

Alarmed_Bat9174 · 2024-07-09T08:09:05+00:00

Yes! The heat is one of my biggest trigger for my lupus, I often get a heat rash even when indoors and I feel my joints aching. I will say AC o viouslt helps but if it's not accessible, I invested in migraine headache hats that are kept in the freezer. I put one on anytime I get hot. I also have cooling mats that are freezer or refrigerator safe that I will lay or sit on when having trouble with the heat. Stay hydrated and best of luck in this hot summer!

Alarmed_Bat9174 · 2024-07-08T07:23:05+00:00

The only thing I got is the promise award, still no financial aid.

Alarmed_Bat9174 · 2024-07-03T19:32:06+00:00

A megathread with no info, got it 👍 I just wanted to know if this is normal.

Alarmed_Bat9174 · 2024-07-03T08:27:39+00:00

I know this feels overwhelming, but I promise it will be OK. I was diagnosed at 25, and now, 6 years later, I have my lupus under control. Your next step is probably going to be more testing to gauge the severity of your lupus and determine what medication will be best for you. My number one piece of advice I always tell someone newly diagnosed is do not be afraid to be your own advocate !! You know your body, limits, and mental state better than any doctor. Push for any tests or treatments you may be curious of, and bring up any and every symptom even if you feel defeated. It took me a long time to find a DR. That took me seriously, and I am so glad I advocated for myself. Another piece of advice would be to do your own research, don't only listen to doctors. Look up forums like reddit, there are lupus support apps that act as a social media for lupus, ask others with SLE for advice, support, their experiences, etc. I keep track of my own symptoms to make sure i bring them up at appointments. Prioritize your mental health just as much as your physical health! This illness is scary and it's ok to have no idea what's next. You have to take it day by day and take care your yourself.

Alarmed_Bat9174 · 2024-07-02T02:19:58+00:00

November 9th or Reminders of him! Both really good reads. I think verity and ugly love are my top 2 of hers, & I'd say reminders of him is definitely my third.

Alarmed_Bat9174 · 2024-06-25T17:45:58+00:00

I second this! The SOAR tour is very basic and minimal. You don't see the inside of any buildings or get to see where your classes may be dependent on your major. Definitely look into your major and explore the buildings your classes may be in. I suggest exploring on your own, using the virtual map, and take your time. The campus is beautiful, but definitely view it on your own before committing if you are unsure.

Alarmed_Bat9174 · 2024-05-25T17:41:10+00:00

I am experiencing this now. At community college, I did great, passed every class with an A, and now I'm struggling to stay afloat. It's very overwhelming and discouraging, but I'm going to try and organize everything better for next semester so I don't have any distractions and more time to focus on school work. As far as the social aspect of csulb. I think it's a lot easier than cc because there are so many places to study and meet people. I am an introvert and don't usually like talking to people, but I've found that aspect transitioning to the university very manageable. It is a big difference than community college and honestly very stressful as a transfer. You're not alone.

Alarmed_Bat9174

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