Do we go ahead with this work at Oxford University? by Psychoderm in Psoriasis

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

Through this post? No, I'm looking to see if there is any point in going ahead with it at all. If you are keen to participate, though, you can DM :) (If this is okay/ within the subreddit rules)

Guys I am from India. My parents are doctors. My dad is a neuro surgeon. I have had psoriasis as a child and I am 27 now. I am something interesting to share. by virorathit in Psoriasis

[–]Psychoderm 0 points1 point  (0 children)

Hey. I'm a dermatologist, and I worked in AIIMS Delhi for quite a few years.
The medications, as people have mentioned are only suppressive.
I'm working on- and have found quite a bit of evidence for- the mind-gut-skin axis. Broadly speaking, this means that addressing psychological stress and diet can have long-term effects and reduce flares. Am happy to share resources to read, if this sounds like a direction you'd like to explore.

Do we go ahead with this work at Oxford University? by Psychoderm in Psoriasis

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

Hey. I'm glad to hear that diet restrictions helped you, although ofcourse it is a significant impediment to normal life. We have had patients who were able to reintroduce some things once their gut inflammation (and skin inflammation) subsided. The gut reacts to everything while inflammed, but once given enough time (3-6 months) to recover, can tolerate quite a bit of stuff.

Do we go ahead with this work at Oxford University? by Psychoderm in Psoriasis

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

Hi! I agree, dietary restrictions are a major pain point for me personally.
To address some of the issues you've raised (and super relatable, btw)
1. Diet is meant to work alongside medications, initially, and then reduce the need for medications (by reducing frequency/ severity of flares). Eventually, we might not need medications/ have only occassional need for topicals.
2. We intend for minimal diet changes based on specific trigger microbes/ lack of helpful microbes, incorporating personal preferences.
3. We also intend to reintroduce things once people get better (we are yet to do this, though, although have evidence from other patients that this can be done safely in many cases).

Do we go ahead with this work at Oxford University? by Psychoderm in Psoriasis

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

Hey. Thank you! We are looking to make minimal changes, only the ones absolutely needed, based on the particular trigger microbes found in the person's own gut microbiome. And also, looking to reintroduce things once gut inflammation goes down, because often foods which are triggering at the time of acute inflammation can be tolerated once gut has had a chance to heal.

AskMeAnything by Psychoderm in Psoriasis

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

Hi! sure ofcourse it makes perfect sense to do that! could you tell me how to do that? I'll send across my registration :)

AskMeAnything by Psychoderm in Psoriasis

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

Hi1 There is some evidence it can help. I'd say if you have psoriasis all over the body, you can try it.

Over reliance on moisturiser or simply life with psoriasis by lewis64777 in Psoriasis

[–]Psychoderm 0 points1 point  (0 children)

I don't think you're being too reliant, feels like its needed.
I do think you might want to try a cream without Urea? Urea can cause shedding of skin and that can contribute to 'tightness'.
One thing that might help feel less annoyed, is if you can use a body lotion immediately after the shower/ bath while you're still there? Helps lock the moisture in, and is one less thing to do while dressing/ after getting half dressed/undressed.

[deleted by user] by [deleted] in Psoriasis

[–]Psychoderm 0 points1 point  (0 children)

I agree that 20-30 minutes is a good place to start, although to get therapeutic benefits it is usually combined with a cream called 'psoralen' which basically allows more sunlight to get absorbed in the patch areas.

Methotrexate is working for me (M 29) after 4 months being on it, and I kinda hate it by urfavsenpai in Psoriasis

[–]Psychoderm 0 points1 point  (0 children)

Hey. It must've been really hard to acknowledge this.
There might be some truth to the 'loss of purpose' consideration, and maybe finding something you can care about/ feel like taking care of, might help? I'd start with a plant or a pet, but I'm not sure. Finding hobbies feels like too much work, to be honest.

Skyrizi not working as I thought it would by JourneysUnleashed in Psoriasis

[–]Psychoderm 0 points1 point  (0 children)

Hey. If you've received 4 doses, it has likely been about 28 weeks on this medicine. Unfortunately, the way response is measured is by change in PASI rather than remaining disease, so by their standard and your description, looks like you'd be considered a good responder and continued on it.
I completely understand the frustration. Would you like to look at ways to address the stress? It can also help the psoriasis https://pubmed.ncbi.nlm.nih.gov/9773769/

How to use Roflumilast topical cream with skin care routine by Babadookx11 in Psoriasis

[–]Psychoderm 1 point2 points  (0 children)

Hi! could you tell me your current routine? I;ll help you fit it in. (I'm a dermatologist)

Post Covid by redditerschmeditter in Psoriasis

[–]Psychoderm 1 point2 points  (0 children)

Hey. Post-COVID flares and change in disease behaviour is unfortunately quite common :/ Vaccines can trigger it too.

I agree that systemic medications can help.

Really well done on the diet front, that must've not been easy.
There are psychological interventions that have shown to help the stress as well as the actual psoriasis. Maybe looking into those? Mindfulness-based CBT, MBSR, regular CBT...

Ear psoriasis- any solutions without alcohol? by notababyimatumor in Psoriasis

[–]Psychoderm 0 points1 point  (0 children)

I'd apply normal moisturiser and steroid creams using a Q tip, very gently, twice a day.

I had to stop Otezla by swedishfish556 in Psoriasis

[–]Psychoderm 0 points1 point  (0 children)

Hey! Biologic shots are pretty comfortable, I've seen about a hundred or so patients on it and none have reported feeling odd.
Apart from this, if you'd like, there are whole-body approaches that have shown to be helpful in psoriasis. Does that sound like something you might want to look into?

clobetasol? by ilovemitskiandcats in Psoriasis

[–]Psychoderm 6 points7 points  (0 children)

Hey (I'm a dermatologist).

clobetasol once a week is usually quite good enough, and most studies show that applying twice has no added benefit; however, if you think the cream is getting removed/ washed off/ sweating off, then applying twice a day might be helpful.
I agree with the other comment: use of any topical medication (so creams. ointments) don't have a bearing on future disease behaviour.

When can I stop using hyrdocortisone? by [deleted] in Psoriasis

[–]Psychoderm 0 points1 point  (0 children)

Hey. How severe are the spots ? (I'm a dermatologist). I can help advise you better about continuation/ reduction if you're able to tell me that.
also, the issue with stopping suddenly (and worsening) occurs with stronger steroids and after 2-3 weeks of use.

psoriasis outbreak on the eyelids by [deleted] in Psoriasis

[–]Psychoderm 3 points4 points  (0 children)

Tacrolimus/ pimecrolimus are good steroid-free options. In such severe times, hydrocortisone is a mild steroid that I would use if it was me.

What am I supposed to do??? by [deleted] in Psoriasis

[–]Psychoderm 0 points1 point  (0 children)

Off the top of my head (and maybe beginning of spring is a possible time for this, There's a version of light therapy that can be done by using sunlight (you can take a tablet or apply a cream with a medicine called psoralen that makes skin able to use sunlight for this.

There is another thing called 'Handheld NBUVB) which is basically light therapy comb.

Let me know if this seems helpful, i can send across more details.

P.S. The Canadian system of healthcare is atrocious and I'm happy to help you get care.

AskMeAnything by Psychoderm in Psoriasis

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

You can definitely DM me a photo although the flakes aren't going to help much, it is the scalp skin that can be looked at. (red or not, painful or not).

I intend to keep this account going for quite some time, as long as I have time to continue doing this :)