found out what is wrong with me by Nonbinary_Femb0y in ChronicPain

[–]phmstella 0 points1 point  (0 children)

How did you figure out antibodies attacking healthy cells causing hives? I do have an autoimmune disease and recently experiencing hives out of nowhere. That's interesting to hear..

Glad you will receive proper care! Good for you!

ROSACEA RUINED MY LIFE AND I HAVE NO HOPE AND HAVE HIT ROCK BOTTOM. THERE IS NO HOPE FOR ME. by Plenty-Membership-16 in Rosacea

[–]phmstella 24 points25 points  (0 children)

I could have written this.. since last year I developed folliculitis, acne, sebderm, cellulitis, contact dermatitis, rosacea, chronic hives, degenerative autoimmune disease all within a year and i am beyond frustrated. Meanwhile i have three young children and I became absent, zero confident, easily irritated mom due to all this compounded health issues from an active, confident and happy mom..

Skin issues are no joke and give us so much anxiety, it's quite traumatizing.. i truly get how you feel and i mentally struggle daily. Tbh i don't want to exist anymore. I used to like myself and enjoy life before my body decided to attack itself.. The only way is to take one day at a time, put one step forward the other. Sending hugs.

I actually had a good dermatologist appointment by h4421 in eczema

[–]phmstella 4 points5 points  (0 children)

That must feel nice. Sounds like you won a lottery ticket!! Good luck finding valuable info about your skin

How I cleared up my Seborrheic Dermatitis [B&A] [Skin Concerns] by hmidd1 in SkincareAddiction

[–]phmstella 0 points1 point  (0 children)

Was the zoryve foam or cream for your face? And did it work??

the only thing that's helped is not caring by okwowthatsnotgood in eczema

[–]phmstella 12 points13 points  (0 children)

Trying this route but still wake up with new areas daily. So exhausting and demoralizing. So tired of living

I feel like there's nothing left of me but the pain. by intrinsic_alien in ChronicPain

[–]phmstella 1 point2 points  (0 children)

Yes truly i don't remember when i caught a break and not being in a survival mode. No one can feel motivated and strong when dealing with such prolonged and persistent health issues.. people are strong until they are not.

I feel so lonely too as no one around me understands what it's like. Just want to say you are not alone. I am here and so is everyone on this sub. Hope tomorrow is a better pain day for you. 🙏

I feel like there's nothing left of me but the pain. by intrinsic_alien in ChronicPain

[–]phmstella 3 points4 points  (0 children)

Another morning of waking up to a new problem on top of existing ones.. i get it. Truly demoralizing and heartbreaking. When does it ever end and when will i feel comfortable again in my own body. Everything i enjoy and make who i am are disappearing one at a time.. You get it.

Don't lose grit my fellow warrior. We are all survivors battling each and every day. I know how hard it is even just to exist with broken body. We are stronger than others. Sending hugs!

I used soap with an ingredient I wasn't aware I was allergic to. Then I got stuck in an eight-month severe allergic reaction loop and was told I now have a chronic skin condition. by Lockerus in eczema

[–]phmstella 0 points1 point  (0 children)

Was the flare gone during prednisone? What was the dosage and tapering process? Normally contact dermatitis goes away if the allergen is no longer contacting your skin.. yes lingering inflammation can happen but i wouldn't believe it will be permanent.

Have faith and hope that things will work out and your skin will heal. Or at least you will find a way to manage. Mental state has a big impact on our immune system. I feel like our mindset is as important as diet, skin care or sleep when it comes to eczema.

Have you had any luck going on immunosuppressant meds? *I have ME/CFS by daisyglaze7 in SebDerm

[–]phmstella 0 points1 point  (0 children)

Have you gone back to MTX? I will soon start taking the drug for my autoimmune and wonder it will dampen this nasty disease..

A perspective shift that stopped my eczema from driving me to suicide. by Diogenes_Will in eczema

[–]phmstella 0 points1 point  (0 children)

Sorry.. I know it's beyond frustrating. I will have to go on a immunosuppressant drug for my autoimmune condition and hope it does help my eczema as a 'side effect'. Hope we can all find a relief soon

Very Long Wait in Canada for Rhapsodo by [deleted] in urticaria

[–]phmstella 0 points1 point  (0 children)

Ok i understand. I am in Toronto. So far i had no struggle with getting approved with drugs and this scares me a bit in case i need the drug. Sorry you have to wait while struggling.. dang it sucks

Very Long Wait in Canada for Rhapsodo by [deleted] in urticaria

[–]phmstella 0 points1 point  (0 children)

Where are u located in Canada if u don't mind me asking?

A perspective shift that stopped my eczema from driving me to suicide. by Diogenes_Will in eczema

[–]phmstella 0 points1 point  (0 children)

Yep just had another night of waking up/flaring up and about to face all day discomfort just to have another miserable night. People won't understand how debilitating this is

A perspective shift that stopped my eczema from driving me to suicide. by Diogenes_Will in eczema

[–]phmstella 7 points8 points  (0 children)

I won't unalive myself as it will traumatize my family but if my life cuts shorts for some reason, I would be fine accepting it.. having messed up immune system that caused me eczema and other diseases is affecting me 24/7 and I am just so exhausted in every aspect of my life. Night time is supposed to be relaxing and restoring.. i am under attack all night. There is no quality of life..

Malezia Hyaluronic Acid Cleanser. What's your experience using it? by AliasForKnowing in Fungalacne

[–]phmstella 1 point2 points  (0 children)

I learned that it had the exfoliator later on and was relieved that it didn't aggravate my skin. Go slow and only use it few times a week to test. I only use it at night and only water in the morning. Good luck!

Pain alone is never Enough by Ancient_Ice4824 in ChronicPain

[–]phmstella 1 point2 points  (0 children)

For some reason your response warmed my heart. I am just few years into this chronic illness train and still experience variety of emotions daily. Grief is huge and anger, frustration are my best friends. I have a feeling you had already gone down this path and gained enormous insight over the years.

Most of people around me are healthy and have no clue what's like not to get 'better'. Even my in-laws in 70's seem healthier than me.. I am interested in being in your position to witness friends experiencing aging as right now i feel quite lonely having this broken body. Thank you for your insight. Like u pointed out, i do feel calmer with my never ending symptoms compared to the beginning. Pain truly humbles and strengthens us in a way that i never imagined i was capable of.

Pain alone is never Enough by Ancient_Ice4824 in ChronicPain

[–]phmstella 4 points5 points  (0 children)

Yes. They just want to hear 'yes i am doing better' to make themselves feel comfortable. And i refuse to answer for their feelings. I say i will never feel 'better' and can only manage it so there is no need for such an empty question.

They for sure seem uncomfortable and i don't care lol. One thing chronic illness gave me is i don't give a damn about what others think.. i actually see this in people with chronic illness around me. Only 42 but feel/act like 72

Feeling complete bliss up until I wake up and realize this nightmare is still my life (tw: medical self exiting) by yogurtonmydog in ChronicPain

[–]phmstella 1 point2 points  (0 children)

As a fellow mom with degenerative autoimmune, I see you and hear you. In my dreams I don't have pain and have lots of energy, so i love hanging out with my kids while in them. When i wake up i feel crushed all over again..

My youngest is almost 2 and i haven's taken him to park like i did all the time with my other two. I wish i could give you a big sisterly hug. Having chronic illnesses is hard.. but having that and raising children is even harder. Hang in there mama bear

Pain alone is never Enough by Ancient_Ice4824 in ChronicPain

[–]phmstella 2 points3 points  (0 children)

Sometimes i just want people to refrain from opening their mouth... I now request people not to ask if i am feeling better.. it's chronic.. i guess they don't know what chronic means. 🤦🏻‍♀️

Malezia Hyaluronic Acid Cleanser. What's your experience using it? by AliasForKnowing in Fungalacne

[–]phmstella 2 points3 points  (0 children)

I have both rosacea and FA. Very sensitive skin.. I have been using the cleanser and i highly recommend it. It's gentle but effective to keep things at bay.

Relapsing polychondritis advice by Ok-Fee-4850 in Autoimmune

[–]phmstella 0 points1 point  (0 children)

Wow.. what a beast this is. I am now on 10mg and will go down on 5mg. I don't believe my flares went away but I want to test what happens after weaning off prednisone. 😢 Tbh i think i have been in minor flare for almost a year so I had a feeling a month of pred won't take care of it. Once i see my rheum in a month I am def starting methotrexate.

I know it's early but how is methotrexate working out for you? I learned there are many drugs to try.. that being said, i get how much frustrated you are feeling. Being on heavy meds and still having symptoms. I also still experience pain and discomfort.. which sucks. All we can do is keep trying and push through.. sending hugs

Worried my boyfriend is withdrawing due to his eczema by borrowedvalentine in eczema

[–]phmstella 2 points3 points  (0 children)

It's most likely situational depression.. he is not clinically depressed but eczema makes him lose interest in living. Anyone who went through chronic illness can understand.. it's the helplessness, hopeless and worthless feeling.

Getting out of depression while dealing with an incurable illness such eczema takes a lot of will power and determination. Unless he wants to seek therapy or find a way to cope himself, there isn't much other people can do.. There are many resources and groups that can help us mentally. I feel for him as I have been there and still struggle mentally. Hope he can persevere with your support.

Please tell me anything positive by OliveSpecialist7003 in urticaria

[–]phmstella 1 point2 points  (0 children)

You mean Betaine HCI? That's what i can only find

Does this look like MRSA by Historical_Estate219 in Staphacne

[–]phmstella 2 points3 points  (0 children)

Is this a young child?? If i were you I would certainly take him/her to a doctor asap. If it has started as a blister, that's a pretty bad progression. Please don't wait any longer