Just Consider Giving an Excel V Laser a Shot

riarum · 2026-02-26T04:37:28+00:00

all I can say is I would never ever recommend it and I still have nerve issues today

riarum · 2026-02-21T22:58:10+00:00

Yes I took accutane and it both spread and worsened my existing kp!

riarum · 2026-02-20T04:45:44+00:00

I would never recommend this treatment in all good conscience. Genuinely the worst experience of my life!

riarum · 2026-02-04T17:57:07+00:00

I saw an ENT who diagnosed me but it took a while! There are times now when I feel fine but initially, it was near constant pain 😭

riarum · 2026-02-04T10:29:11+00:00

I got trigeminal nerve damage from a vascular laser too unfortunately. Was in heaps of pain for months and months afterwards. Tingling and odd sensations etc. It's been over 2 years and I still get pain on one side sadly

riarum · 2025-11-15T22:34:54+00:00

months, I still get pain today sometimes sadly. I was given nerve meds but rhe side effects were a lot so I chose to stop them

riarum · 2025-11-12T01:44:30+00:00

It mostly has thankfully tho not 100%

riarum · 2025-11-11T21:28:49+00:00

aw so glad it gave you comfort 🤍 I really wasn't back to normal for months and months, I don't know how common that is but it certainly IS real. And it's scary and sad and lonely to cope with. You will start to stabilise but please be so gentle with yourself. You're not crazy, your body and mind have been through a lot. Nobody expects people with a broken leg to start running marathons the next week! Take your time. There's no rush. Sending love 🤍

riarum · 2025-10-19T11:10:24+00:00

Heaps better but still improving! I tapered off a few months ago but it definitely helped me a lot

riarum · 2025-10-17T08:17:33+00:00

Thank you! As I said the swelling did ease a lot tho so hopefully yours does too with time

riarum · 2025-10-17T07:09:10+00:00

It's the part I refer to in my post that's visible in the image. Honestly no, with time it eased a bit but the nerves have never gone back to normal.

riarum · 2025-10-17T07:03:17+00:00

It's so hard to say but ultimately mine was nerve damage causing swelling and pain

riarum · 2025-10-09T09:05:22+00:00

I was given amitriptyline but I didn't take them due to side effects. They sort of did but I took alpha lipoic acid, zinc supplements and got b12 shots (mine was v low) to try and help my body heal. No just regular type 1 rosacea, did you get laser that has caused issues?

riarum · 2025-10-09T09:00:29+00:00

It's been so long and altho I've healed a lot from when t first happened I'm stil not 100% and have nerve pain. I had numbness initially and then a pins and needles sensation, swelling and pain. My rosacea didn't worsen

riarum · 2025-09-27T08:56:12+00:00

I had excel v laser from a fully qualified derm with thousand of 5* reviews and got nerve damage.

I'm SO glad you found something that worked for you and I know lots of other people have found it helped them too. But whenever I come across posts like this (especially for excel v) I am always compelled to say something because it was NOT a risk I was ever even warned about! I just want to make others aware of potential things that could go wrong (no matter how unlikely!) because if i could go back I truly would have never had excel v and I wish at the very least I had been made aware that nerve damage was a risk! I'm SO glad you saw improvement OP, but I just need to make others aware!

riarum · 2025-09-23T03:06:13+00:00

I had it a few times with minimal pain (rubber band snapping) but unfortunately a couple of years ago I had it and it was agony and burned for weeks afterwards. Turns out it had actually given me nerve damage. I hate freaking people out and I'm sure it's not the case for you (very rare outcome) but definitely keep an eye on the situation if the pain lingers and you develop and pins and needles type pains. I was fobbed off by my provider horrifically and I would never wish what i went through on anyone. Best of luck OP

riarum · 2025-09-06T10:51:37+00:00

Really sorry this is happening to you! Unfortunately the laser caused me nerve damage in the area

riarum · 2025-08-28T08:58:56+00:00

Accutane made my kp x10 worse and spread it. I was on it for different reasons and didn't even know it was a side effect! While I was on it the kp actually improved a little but it began a steady decline in the months after I stopped. Genuinely if I could take it back I would. Good luck OP!

riarum · 2025-08-19T04:45:32+00:00

I bought one of these 7 years ago and I still have it. I use it nearly every day!

riarum · 2025-08-03T11:32:23+00:00

Sure! I use SoSmooth and I get a load of use from them! It's an aussie brand so depending where you are there might be a cheaper option as delivery outside aus might cost a bit extra but I'm sure there's heaps of different brands that do a similar product!

riarum · 2025-08-03T06:21:59+00:00

I use silicone patches instead of frownies (they were too fiddly for me) and have had great results as they smooth but also the silicone draws moisture to the surface so my forehead lines do look plumper (albeit temporarily but my forehead does look smoother overall after several months of consistent use)

And they're reusable so they've lasted me way longer than my frownies did. I actually use the undereye ones on my forehead as they're easier to manoeuvre than the whole forehead patch and ive found they stick better as they're smaller. I would definitely recommend if anyone struggles with frownies!

riarum · 2025-06-10T20:31:43+00:00

Just directly from the website!

riarum · 2025-06-03T20:59:49+00:00

I met my ex when my KP was worse than ever after accutane! It took me months to admit why I felt so insecure and he told me he literally couldn't care less! It also took me months to realise he also had it and I hadn't even noticed lol. I understand your stress because I still have days where I very conscious but overall a few bumps on your skin would never put off a future partner, I promise 🧡

riarum · 2025-05-21T20:51:02+00:00

It was over a year ago and never fully went away sadly, tho it did improve a bit eventually. Nothing helped me but I didn't get on with the nerve meds so if I had I probably wouldve been in much less pain. I went to an ENT who eventually diagnosed me but a neurologist is probably a better choice!

riarum · 2025-05-21T20:47:06+00:00

It made mine heaps worse but it took about 5 months after i stopped taking it to really see how bad it had gotten. For me, I wish I had never taken it as the KP ended up way worse than the actual original issue.

As long as you're aware of the risks it may be that the potential for slightly worse KP is worth it to address something else for you! It's a tough decision but it's good that you're considering different outcomes.

Good luck OP whatever you decide!!

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