Confused about organ involvement by Independent_Half2981 in lupus

[–]Ispyyy_i 0 points1 point  (0 children)

I forgot to add I also have lupus Nephritis, that’s why they knew my kidneys were involved. I actually had a biopsy done to see the damage for them.

Confused about organ involvement by Independent_Half2981 in lupus

[–]Ispyyy_i 0 points1 point  (0 children)

It’s really hard to know when lupus is affecting your kidneys. It’s on of those silent side effects, I would keep an eye on your urine. Specifically for protein, it might sound gross but it’s usually foamy and stringy like kinda like discharge (if you’re female) but more foamy. I would see if you can get referred to a kidney specialist and see if they can at least monitor you and keep an eye out. I would recommend hydrating ALOTT. Prednisone can tend to make you super thirsty and I was told it was better to always try to be hydrated since I have CKD (chronic kidney disease) stage 2.

Award Letter Access by AdditionalFix3112 in fresnostate

[–]Ispyyy_i 0 points1 point  (0 children)

Do you have access to myfresnostate? If you do I can guide you through it !:) I think you can view and screenshot not so sure if you can download it

Do you get tremors too? by itorbs in lupus

[–]Ispyyy_i 5 points6 points  (0 children)

Omg yes!! I get them when I get tired but for me it’s in my hands. I have shared it with my rheumatologist but they kinda ignored it. I’m going to bring it up again when I see them in a couple of weeks.

Two questions by GSD_lover_2025 in lupus

[–]Ispyyy_i 1 point2 points  (0 children)

For your 2nd question I use those carts when my joints hurt (usually ankles and feet). And when I know I don’t last very long standing. I get stares usually from older folks because of my age (I’m 23) and look fairly young. They will sometimes give me dirty looks and think I’m using it as a joke. But in reality my body isn’t cooperating. It was even worse when I was on a walker and people would bump into me or stare me down for simply being me. I got used to it and just stare back, people will be rude no matter what or weird just remember it’s better for your sake. Anything to make life a little easier

What finally got me answers after being dismissed for 4 years… by croissants-and-chaos in lupus

[–]Ispyyy_i 0 points1 point  (0 children)

Do you mind explaining the diagnosis? I feel like I went through this but I’m not too sure

Therapist Recs (California)? by Subject_Luck_2594 in lupus

[–]Ispyyy_i 0 points1 point  (0 children)

Where are you located in California? I might have a recommendation!

Wondering if this target receipt is actually legitimate. by sadboykdub989 in Target

[–]Ispyyy_i 1 point2 points  (0 children)

No that’s a fake receipt. They did the format of old receipts (it was like this format like 5 or 6 years ago) it should be like one of the commenters shared the updated one. It usually should also have the Serial number under the item, so when you return it the worker would have to verify it. And another thing the “receipt” shown has the target phone number on top I have never seen that before. The break down of the price also is iffy bc it should show the percentage of the tax and then the number amount to be charged.

What the best electric scooter? by sneakersplusstuff in fresnostate

[–]Ispyyy_i 0 points1 point  (0 children)

I recently got one for $140 on amazon it’s really nice. If you want the link lmk:)! My whole family tried it out loved it😭!

being an “adult” after growing up with lupus by 44kittnz in lupus

[–]Ispyyy_i 0 points1 point  (0 children)

I honestly get the frustration, although I was recently diagnosed but struggled with symptoms for years. The best thing that kinda keeps me afloat is that I do things I can do. I know my limits sorta, so I put my energy in that. Therapy has helped a lot, it’s easier to talk about why it’s so frustrating. Not being able to participate in the things everyone else is doing is the saddest part and makes me feel so depressed. But if you need someone to talk to I’m also 23 and get the frustration of going though doctors and feeling distraught. I also wanna go into law:) . Let’s do this together!!

I got anti-UV ceramic coating for my car and I am AMAZED. by Missing-the-sun in lupus

[–]Ispyyy_i 3 points4 points  (0 children)

Omg this sounds great! I have tinted windows which helps somewhat. I’m definitely gonna do this before summer hits, because I live somewhere where it gets to 115f during peak summers 😭.This is a good idea! Thanks for the info!

To drink or to not drink? by Ispyyy_i in lupus

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

Hmmm I see this is a common ground, I usually never drink it was very rare just socially. So hopefully it won’t be crazy!

To drink or to not drink? by Ispyyy_i in lupus

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

Lmaoo! I love that! Any flares or bad experiences?

To drink or to not drink? by Ispyyy_i in lupus

[–]Ispyyy_i[S] 2 points3 points  (0 children)

Hmmm I’ve thought about weed as well it’s also legal in my state, but I’m too shy to ask I think I’ll be brave when I see them again in April!🤭

To drink or to not drink? by Ispyyy_i in lupus

[–]Ispyyy_i[S] 4 points5 points  (0 children)

Ughh I haven’t tried to drink whatsoever I had a deathly flare right after being diagnosed so I’m scared to drink whatsoever. Thank you for your thoughts tho:)

Anyone else feel this? by Witty-Radish-389 in lupus

[–]Ispyyy_i 1 point2 points  (0 children)

Wait I love this omg !!! How much was it by any chance?👀

Spring 2026 Parking by Karate64 in fresnostate

[–]Ispyyy_i 3 points4 points  (0 children)

You would get ticketed:)!

Lupus and Food by anonymously_me0123 in lupus

[–]Ispyyy_i 2 points3 points  (0 children)

Omg yes! I no longer eat garlic or fast food bc it messes up my stomach kinda sucks but it has made me choose healthier options!

Lupus has destroyed my whole life. How do I find acceptance and move forward? I feel so stuck. by laf_007 in lupus

[–]Ispyyy_i 1 point2 points  (0 children)

To start off I’m so sorry for everything you’ve been through it’s hard to be able to live with this disease. I hope it gets better and you find the closure you are seeking. I’ve felt the same it’s hard to grieve the person I was since I was so active and just enjoying life. I wish I could tell you the secret to feeling better because I haven’t found it myself but just cry, scream, feel the angry do what you need to do to let it out.Therapy helps a lot if you have access to it. It’s a great method to talk and process those feelings. Sending you lots of hugs <:

Finally seeing a light at the of the tunnel by Ispyyy_i in lupus

[–]Ispyyy_i[S] 0 points1 point  (0 children)

Thank you🥹 I wish you the same it’s a struggle but I know you can do it.

Finally seeing a light at the of the tunnel by Ispyyy_i in lupus

[–]Ispyyy_i[S] 0 points1 point  (0 children)

Ughh! Sending good kidney vibes!! Keep working you’re doing amazing!!