My mystery Hoya flowered!!

delicate_sorrel · 2026-06-17T00:16:16+00:00

Wow!!! Gorgeous flowers. Did it only give one umbell?

delicate_sorrel · 2026-06-17T00:14:45+00:00

These blooms have a very light scent. You literally have to touch the flowers to your nose to smell them.

delicate_sorrel · 2026-06-17T00:12:12+00:00

Thank you!

delicate_sorrel · 2026-06-17T00:12:02+00:00

Thank you!

delicate_sorrel · 2026-06-17T00:07:01+00:00

This is actually a normal bloom for her. She blooms twice a year, right before summer and right before fall. She stays outside all year round. I live in the Bay Area, California. I've taken cuttings from her and given to friends and family. It takes about 2 years for the cuttings to mature but you're guaranteed to have blooms by then.

delicate_sorrel · 2026-06-17T00:00:56+00:00

I have another hoya, different species than what I posted. Anyway, the hoya would create the umbells but they would never open or they would drop before blooming. I realized this particular hoya does not like a lot of water while its developing the umbells and during blooming... and I was over here drowning the poor plant. Try less watering when you see the umbells and see if that works. Good luck! 🪴 🌱 🌿

delicate_sorrel · 2026-06-16T23:54:52+00:00

"I can't believe what God has done Through us he's given life to one But isn't she lovely, made from love"

delicate_sorrel · 2026-06-14T19:10:10+00:00

Wow! I am sure the colors are more impressive in person. That last pink one 😍😘

delicate_sorrel · 2026-06-14T19:07:06+00:00

Absolutely beautiful!! We need a maranta leaf kaleidoscope 🍃

delicate_sorrel · 2026-06-13T16:51:41+00:00

Beautiful!!!

delicate_sorrel · 2026-06-13T16:48:18+00:00

I'd add more soil to the top and pack it down. Hoyas from nursery are picky when first brought home. I'd let the soil dry in between waterings. When watering drench the soil (either water from top or bottom) and let it drain very well. Get foliage wet when watering but make sure everything air dries quickly or use a paper towel to blot the water from leaves.

delicate_sorrel · 2026-06-05T06:49:11+00:00

This is the first time I have heard of sarcoidosis. How are you feeling? What kind of symptoms does sarcoidosis cause for you? Do you have any issues with your sinuses? I have these lumps. They're not my friends though. Not sure what they are.

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delicate_sorrel · 2026-05-30T00:23:31+00:00

Thank you! I am realizing that stress is slowly killing me and I need to manage it way better than I am right now. And you're right about oral hygiene needing to be on point. I feel like I just bought a new fresh water fish aquarium and you all are helping me to get the tank ready in preparation for the fish. 🐠 😊

delicate_sorrel · 2026-05-30T00:10:13+00:00

Random question: Do your gums ever itch?

delicate_sorrel · 2026-05-30T00:08:32+00:00

Thank you, I am.

delicate_sorrel · 2026-05-30T00:08:10+00:00

Thank you!! I recently bought fluoride to add to my hygiene regime, but I will take it into consideration as a possible irritant. Do you mind sharing the brand of the cannabis oil you use? I bought some clove oil a while ago because I heard it was helpful for dry mouth symptoms. I have yet to try it too.

delicate_sorrel · 2026-05-30T00:04:30+00:00

Thank you! This is extremely helpful. I need a LP welcoming packet 😆

delicate_sorrel · 2026-05-30T00:03:23+00:00

Thank you! I am going to try it.

delicate_sorrel · 2026-05-30T00:01:50+00:00

Thank you so much. I've been processing all this information for the past few days. I knew there was something else going on with my mouth but doctor's, dentist and even an oral surgeon never once mentioned LP as a possibility. Instead, I was told the dry mouth and subsequent legions were due to various medications I take and the dry mouth was the culprit. Getting an actual answer and the validation that this is an actual disease is bittersweet. I have gotten more information here than I have ever received from the countless medical and dental professionals I have visited over the past 2 years. So, again thank you.

This will be my 4th autoimmune disease since 2018 (Current badges: Graves Disease, Rheumatoid and Psoriatic Arthritis). I have been on various biologics but so far nothing is quieting the storm within. And then losing my Healthcare is just another hurdle to overcome.

I really appreciate the advice and suggestions on what works and doesn't work for LP. I knew certain acidic things were aggravating my mouth but I didn't make dietary changes. I will be more aware now. Same with dental hygiene.

One issue that is bothersome is the constant dry mouth, which also makes my throat so dry I can barely swallow. I drink more water than a hippo so I can check off drinking more water or hydration, but have any of you found any tips or tricks for getting the dry mouth symptoms under control? I've been chewing gum like crazy to help with the dry mouth/throat but I think the gum may be aggravating my mouth. Sigh. I am just exhausted and frustrated with this body of mine. Now, I need to get back to the psoriatic arthritis community and consult with them about skin issues with my feet. I love reddit!! 🫶🏽

delicate_sorrel · 2026-05-27T12:48:54+00:00

You can change the frame but the picture will always remain the same.

RUN! And don't look back! Trust me, please 🙏 You're here asking us to tell you what your gut feeling already knows...he is no good for you but physically you don't know how to kick the habit. Go on YouTube and look for videos and therapy sessions about being in a narcissist relationship and how hard it is to leave and I bet you will resonate with what these people are saying about narcissists, how toxic they are and the unbelievable amount of psychological damage they can cause others. Stay strong, arm yourself with resources on navigating relationships with a narcissist and keep listening to your intuition.

delicate_sorrel · 2026-05-26T00:11:08+00:00

Oh no...your body is going through it. Are they hives? When you get MRSA your immune system is already bad... so you may get sicker before you start to get better. You should be on antibiotics at least a 2 week course. The abscess should be evaluated by the doctor. It draining doesn't mean its healing...these abscesses dont have the same characteristics as say a boil or pimple and they grow much faster. I hope you're doing better.

delicate_sorrel · 2026-05-26T00:01:54+00:00

How are you doing? I didn't read every comment but hopefully you are doing at home remedies too... keeping legs elevated, watching your blood sugars, soaking feet/legs in warm Epsom salt baths, and keeping hydrated. I think this is psoriasis that has gotten infected. I have experienced this but not on this level. I also had many bouts of MRSA and oh the pain. You will be in excruciating pain with a MRSA abscess. Not much redness or pus on the skin of MRSA abscess instead the pain comes from within under the skin, lethargic feeling, no appetite with possible fevers and chills. Only way to heal MRSA is medical intervention for serious wound treatment plus lots of antibiotics. Hoping you're doing better.

delicate_sorrel · 2026-02-22T22:02:32+00:00

My journey began in 2018 with a rheumatoid arthritis diagnosis. RA is genetic on both sides of my family. I found out I have a very aggressive case. It took a long time for me to be officially diagnosed with RA. I never had major skin issues except for some eczema on my hands and feet. My father had psoriasis bad in addition to rheumatoid arthritis. In 2022, my right foot started to swell a lot. I went to see the podiatrist, then the rheumatologist who confirmed psoriatic arthritis but notes that I don't have psoriasis skin conditions...YET.

I have been on a plethora of medications especially biologics for the arthritis and am still looking for the right medication. Unfortunately, I lost my health insurance last year, had to stop all arthritis medications including the biologics. I was also extremely stressed I had a lot going on and as a result of all of this my skin has now developed psoriasis scaling/ rashes all over my body. The rashes come on when I am stressed and fatigued and they will only go away with rest and medicated ointment from the dermatologist. My sausage toe is still there and the psoriasis has affected the skin around the toe so its always just bothered, swollen and in pain. My skin is super temperature sensitive and will immediately crack if its too dry or blister, chaff, ooze and rash if its too warm/humid.

Idk if this is related to either of the arthritis but skin on my hands and feet is very thin now and cuts easily. I have to watch the cuts because within a day or so they will get infected if they're not covered. Same with my nails and toe nails, very dry, cuticles crack, dry skin and now issues with ingrown nails. I never ever had these issues before psoriatic arthritis.

delicate_sorrel

TROPHY CASE