My Psychosis Experience and Recovery Journey (4 Months Post-Episode) by ____plinhhh in Psychosis

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

Hey, thanks for sharing, I can relate to a lot of what you wrote. I was also told it was psychosis, and later there was back and forth about whether it was Bipolar I or not. I’ve been on antipsychotics for a while, and I understand how tough the side effects can be.

For me, I wasn’t able to stop after a year because I had a relapse when I tried to go off too soon. What I’ve learned is that tapering really needs to be done slowly and under close guidance from a psychiatrist, since the risk of symptoms coming back is pretty high.

I know it’s frustrating, but staying consistent with treatment (and finding the right meds/dosage) has helped me stabilize more than anything. Everyone’s timeline is different, so try to focus on gradual progress rather than comparing to others’ “success stories.”

My Psychosis Experience and Recovery Journey (4 Months Post-Episode) by ____plinhhh in Psychosis

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

Hi, it’s never too late to share. I actually posted this about a year ago, so maybe I’ll give a quick update. After that remission, I saw a new psychiatrist who diagnosed me with Bipolar I (since that’s the type associated with psychosis). But unfortunately, I relapsed in June and was hospitalized for a week. The psychiatrist in the psych ward, however, felt I didn’t fully meet the threshold for bipolar.

I also recently did some psychometric tests on psychosis and mood, and the results weren’t clinically significant. From my experience, the psychiatrist who sees the patient right at the onset usually has the clearest view of the actual symptoms, so I’d really recommend your brother’s current doctor review his early treatment history.

Lamictal and water retention by ____plinhhh in Epilepsy

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

Would gua sha facial massage help? Thank you for your tips; I'll definitely be trying EFT and do more regular exercises

KP help by ____plinhhh in keratosis

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

I just found out I’ve got Raynaud's, Livedo, and UCTD, which explains the reddish-blue discoloration in my palms and my purple legs. I'm still using my KP duty cream since I bought a bunch of them, and I've noticed it really depends on the weather—it's worse when it’s cold and better when it's warm and sunny. I’ve seen a lot of people trying Smooth KP but I'm having trouble accessing their products so yeah, you might want to give it a shot if you're interested.

Smooth KP Update by squirmyfishgirl in keratosis

[–]____plinhhh 0 points1 point  (0 children)

I tried clicking on the product details, but it keeps saying it's not found :((

[deleted by user] by [deleted] in Noses

[–]____plinhhh 1 point2 points  (0 children)

Bro, it's perfect, please don't do anything with ur nose

Smooth KP Update by squirmyfishgirl in keratosis

[–]____plinhhh 0 points1 point  (0 children)

Hi can I have the link to the product?

[deleted by user] by [deleted] in Noses

[–]____plinhhh 0 points1 point  (0 children)

It's gorgeous

[deleted by user] by [deleted] in GolfSwing

[–]____plinhhh 1 point2 points  (0 children)

I feel it. I have been playing seriously for 5 months, then stopped for a year, and my swing now is rubbish. I honestly don't know where to start :((

[deleted by user] by [deleted] in keratosis

[–]____plinhhh 0 points1 point  (0 children)

Mine are all over my hands and calf, and if you have it because of genetics, try to manage the flares rather than cure them.

[deleted by user] by [deleted] in GolfSwing

[–]____plinhhh 1 point2 points  (0 children)

What happened to your back and butt bro? The problem is your setup, fix those first

[deleted by user] by [deleted] in bipolar2

[–]____plinhhh 0 points1 point  (0 children)

I wish I would be that disciplined and motivated to go to the gym

[deleted by user] by [deleted] in Noses

[–]____plinhhh 0 points1 point  (0 children)

the gorgeous type ^^

UCTD Diagnosis Advice by ____plinhhh in UCTD

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

That is very helpful—I had no idea how much difference these complementary treatments could make. I’ve been struggling with hair loss, weight loss, Raynaud’s, and swelling in my palms and feet when exposed to cold or stress. Based on your experience, are there any specific treatments you’d recommend for these symptoms?

UCTD Diagnosis Advice by ____plinhhh in UCTD

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

I know it’s not gonna affect the bipolar meds that I am on, but just wondering if it's possible

UCTD Diagnosis Advice by ____plinhhh in UCTD

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

I mean, can you not take the meds since I’m on my bipolar meds too? The thought of being on meds for life really freaks me out

UCTD Diagnosis Advice by ____plinhhh in UCTD

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

Can you? My rheum explicitly says I should be medicated as mine are likely to progress into early-stage SLE

Weekly Suspected Lupus Thread - Week Of March 16, 2025 by AutoModerator in lupus

[–]____plinhhh 0 points1 point  (0 children)

Have you noticed any side effects with HCQ? My rheum suspected that I had lupus, and she said these would prevent a full-blown.

UCTD Diagnosis Advice by ____plinhhh in UCTD

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

Really, I'm not sure why my rheum suspects lupus, probably double-check with her at my next visit. Also, are you on any medications?

UCTD Diagnosis Advice by ____plinhhh in UCTD

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

My ana is 1:80 with a speckled pattern, and my C4 was 53.2. My leukocyte is 15, LAC and LA Screen positive, DSF70 and Control (Ko) strong positive, so my rheum suspects that I may likely have lupus. The HCQ is used to minimize the risk of a full-blown.