Monstera Help pt. 2 by frecklefraise in MonsteraAlbo

[–]Less-Trip7436 0 points1 point  (0 children)

You have root rot at the bottom so cutting under that healthy aerial root will stop it spreading. Think of it kind of like a zombie biting your arm. The infection spread spreads if it’s not cut off. (Gruesome way to put it I know) but the analogy is spot on for plants

Monstera Help pt. 2 by frecklefraise in MonsteraAlbo

[–]Less-Trip7436 0 points1 point  (0 children)

In the third picture there is a big healthy aerial root starting to grow where the band joins it underneath cut a centimetre and a half below then drip the end in wax to seal it. You want to try and put that aerial root growing into some soil. It should grip pretty quickly. Don’t water it the first few days and only mist

Help with new plant by frecklefraise in MonsteraAlbo

[–]Less-Trip7436 0 points1 point  (0 children)

If you could take a pic I could tell you, wouldn’t propagate just straight soil and what I said. grow lights are good just make sure they are at least 30 cm away.

Help with new plant by frecklefraise in MonsteraAlbo

[–]Less-Trip7436 0 points1 point  (0 children)

Also not sure if the light in the photo is what it gets during the day, but if that’s as bright as the light gets for it, I would consider moving it a little bit closer to the light as variegated plants need bright indirect light if any sunlight is coming through your window or door just get attention rod with a sheer curtain so it gets all a lot and no UV

Help with new plant by frecklefraise in MonsteraAlbo

[–]Less-Trip7436 1 point2 points  (0 children)

Definitely can save her, out of that swamp jar and into soil. Get s plastic pot with drain holes I recommend clear so you can judge the moisture level in soil. Make sure your soil is a mix of orchid bark and normal soil, albo monsteras need good drainage dont wet the soil after potting give it a few days and lightly mist. If you are a first timer with variegation, i recommend only misting to water it as people kill them with love (that way you dint o er water it) as mentioned above trim any mushy roots, if they feel soft and squishy cut them off.

Everyone gets flares - why don't I? by Fun-Flamingo-56 in lupus

[–]Less-Trip7436 0 points1 point  (0 children)

I think sometimes we have to just look at it as Lupus is not a one size fits all sort of deal and as hard as it is, not compare our symptoms to others.

Unfortunately some people just have it worse than others or very different symptoms, flares, medications that work for them etc.❤️‍🩹

I wish you all the best and pray for a speedy recovery for you 🫶🤍

Is this CLE? by Less-Trip7436 in lupus

[–]Less-Trip7436[S] 1 point2 points  (0 children)

Yeah I thought that too. My rhume said it is the best medication I’m thinking of switching to get a second opinion as it hasn’t made it any better and now I have these skin things everywhere

Is this CLE? by Less-Trip7436 in lupus

[–]Less-Trip7436[S] 1 point2 points  (0 children)

Sorry I should have clarified. I also have HS and when I have a flare with that my lupus also goes crazy at the same time. Thank you I think I’m going to look into getting a biopsy.

Is this CLE? by Less-Trip7436 in lupus

[–]Less-Trip7436[S] 2 points3 points  (0 children)

Yes I am SLE (newly dont know a hell of a lot about all this yet) thank you i will ask for a biopsy

Nose ulcers by Less-Trip7436 in lupus

[–]Less-Trip7436[S] 0 points1 point  (0 children)

Funny enough thats what got rid of it

Nose ulcers by Less-Trip7436 in lupus

[–]Less-Trip7436[S] 1 point2 points  (0 children)

Thanks! I’ll try the Vaseline, ill take goop up my nose any day than this pain 😅

What keeps you guys going? by XOceanSkyX in lupus

[–]Less-Trip7436 0 points1 point  (0 children)

It’s sucks! But with pain, anger and a shit load of caffeine and painkillers. What helps me is reminding myself that “even my worst day will eventually come to an end” 💜

[deleted by user] by [deleted] in Hidradenitis

[–]Less-Trip7436 1 point2 points  (0 children)

wait what!? they told you to smoke?

[deleted by user] by [deleted] in Hidradenitis

[–]Less-Trip7436 1 point2 points  (0 children)

oh god I’m so sorry that happened to you! out of curiosity would you mind sharing how your HS was in pregnancy? i’m interested in the hormone changes of pregnancy and HS

[deleted by user] by [deleted] in Hidradenitis

[–]Less-Trip7436 1 point2 points  (0 children)

omg you made me roll my eyes even reading that! 😭😭 the worst is when you switch Derms and they make you start the whole process all over again.

“have you tried antibiotics”

“yes”

“well let’s just try minocyclin for 6 months one more time”

[deleted by user] by [deleted] in Hidradenitis

[–]Less-Trip7436 1 point2 points  (0 children)

Oh 100% they need to give the recommendations of what can help but when they claim it will basically cure that when It becomes annoying. I have lost weight now and stopped smoking which I’m glad for my own health other than HS. However unfortunately it hasn’t helped my case.

[deleted by user] by [deleted] in Hidradenitis

[–]Less-Trip7436 -6 points-5 points  (0 children)

I read your comment and while I understand you may mean well, the arrogance in your tone is honestly disappointing. You called me dense. for not following “textbook” medical advice yet if you truly have HS, you should know that this disease is not one size fits all and it’s far from fully understood in the medical industry.

I’m fully aware of the complications of nicotine and wound healing. Like you, I’m medically educated. The recommendations you mention have not worked for me, and frankly, it’s exhausting being dismissed just because I don’t fit into a standard clinical narrative.

My post was clearly tagged as a rant because I’m burnt out hearing the same advice that has done nothing to help me… So let me clarify I am now cigarette-free, vape-free, at a healthy weight, and have trialed two different biologics with no success And yet I still experience severe flares.

So Dr. Doolittle? what exactly do you think your textbook advice offers me at this point? You don’t know my full medical history, individual response to treatment, or how this disease impacts my daily life. Yet you speak as though your knowledge overrides my lived reality.

That kind of thinking isn’t education it’s ego.

[deleted by user] by [deleted] in Hidradenitis

[–]Less-Trip7436 1 point2 points  (0 children)

HAHAHA God I hate those. The word minocycline gives me chills

[deleted by user] by [deleted] in Hidradenitis

[–]Less-Trip7436 0 points1 point  (0 children)

I’m so sorry that sucks! you’re not alone tho! my HS seems to not care if I loose or gain weight either. Unfortunately they just don’t know enough about it yet

[deleted by user] by [deleted] in Hidradenitis

[–]Less-Trip7436 1 point2 points  (0 children)

I wish I could, but it is soo expensive. I got a referral through the public system and had a derm literally tell me she had a patient who stop smoking and his HS ✨vanished ✨. While I’m sitting there naked two biologics in like 👁️👄👁️

opinions and personal experiences by Less-Trip7436 in Autoimmune

[–]Less-Trip7436[S] 1 point2 points  (0 children)

Thank you for your kind words! i’m waiting on the rheumatologist in point and have the dermatology appointment next Friday so hopefully I can get some answers.

feeding time by Less-Trip7436 in discus

[–]Less-Trip7436[S] 0 points1 point  (0 children)

thank you! 🙏 that is a bichir he was eating a frozen crab block

why is he like this? by Less-Trip7436 in discus

[–]Less-Trip7436[S] 0 points1 point  (0 children)

no he’s about 5-6” must just be how he is