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Post Accutane/Minocycline Facial Flushing


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#681 soul78

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Posted 12 October 2009 - 06:49 PM

QUOTE (lamarr1986 @ Oct 12 2009, 03:30 PM) <{POST_SNAPBACK}>
Xan tan gives a very natural appearance.... I started using it around the same time as starting the mepa as i wanted to prevent anyone from noticing the yellowing if i was to suffer from it... Remember the old articles saying a suntan covers up the yellowing? well that was my reasoning...


Lamarr,

Cool man, thanks a lot. I am not familiar with the old articles, any chance you have links to them for me to read?

Also, sorry for the questions, but how often do you apply the tanner, everyday or do you do you go 3 times per week etc. to maintain a light tan to cover the yellow and not go super dark etc.

Were you using the tanner when you posted that pic in the scar thread, because your complexion looked great there?

I will try the Xen tan product and also thinking of trying this one, a lot of good reviews. It is derived from natural essential oils but I would like to hear you opinon on the ingredients and if anything looks like a red flag given my sensitive rosacea skin.

Aroma Sun Self Tanning Milk SPF 8 4.2 fl oz.

Octinoxate (ethylhexyl methoxycinnamate): 7.5%, Oxybenzone (Benzophenone-3): 5%, Avobenzone (butyl methoxydibenzoylmethane): 2% Water, glycerin, dihydroxyacetone, hydrogenated polydecene, sorbitan stearate, propylene glycol myristate, cyclopentasiloxane, polymethyl methacrylamide, cetyl alcohol, fragrance, pelargonium graveolens oil, anthemis nobilis flower oil, rosa damascena flower oil, jasminum officinale (jasmine) extract, cucumis melo (melon) fruit extract, eclipta prostrata extract, luffa cylindrica seed oil, C13-14 isoparaffin, erythrulose, oleoyl tyrosine, benzyl salicylate, laureth-7, tocopheryl acetate, oleic acid, linalool, tetrasodium EDTA, hydroxyisohexyl 3-cyclohexene carboxaldehyde, geraniol, citronelol, hydroxycitronellal, citral, eugenol, alpha-isomethyl ionone, D-limonene, coumarin, benzyl alcohol, evernia prunastri (oakmoss) extract, phenoxyethanol ((0.36%), methylparaben (0.08%), ethylparaben (0.02%), butylparaben (0.05%), isobutylparaben (0.01%), propylparaben (0.01%).

Cheers mate!

Edited by soul78, 12 October 2009 - 06:50 PM.


#682 halfpipe101

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Posted 13 October 2009 - 05:13 AM

guys what do you think about this


http://rosaceacare.com/products/zinco.html

Thinking of getting it

but it would not be tinted in the way of brown tanned tinted would it? its like a white tinted to shield the redness right

thats what i was looking for plus the spf is great

and the zinc oxide which is 14.5 is one of the highest you can get on the market

and zinc oxide is great for seb derm..flakes and so on

Im most likely going on doxy this week though to get rid of my seb derm/mild acne/roughness

my flushing has greatly reduced but i just gotta get rid of my skin problems too

then i hopefully can maintain good skin by being on 5 months of doxy = red/yellow light therapy= gentle skin cleanser = ddf sulfur mask once a week

Edited by halfpipe101, 13 October 2009 - 05:38 AM.


#683 jordan1234

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Posted 13 October 2009 - 07:10 AM

Halfpipe, how much has your flushing improved since you've been on the mepa?

#684 soul78

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Posted 13 October 2009 - 09:24 AM

QUOTE (halfpipe101 @ Oct 13 2009, 06:13 AM) <{POST_SNAPBACK}>
guys what do you think about this


http://rosaceacare.com/products/zinco.html

Thinking of getting it

but it would not be tinted in the way of brown tanned tinted would it? its like a white tinted to shield the redness right

thats what i was looking for plus the spf is great

and the zinc oxide which is 14.5 is one of the highest you can get on the market

and zinc oxide is great for seb derm..flakes and so on

Im most likely going on doxy this week though to get rid of my seb derm/mild acne/roughness

my flushing has greatly reduced but i just gotta get rid of my skin problems too

then i hopefully can maintain good skin by being on 5 months of doxy = red/yellow light therapy= gentle skin cleanser = ddf sulfur mask once a week


It's tinted and a flesh colour - so a gamble in my opinion. It may blend well with your skin, it may not, depends on your skin type/colour. It's not a tanner but more somewhat of a concealer but for men as well. You could try it, it says good for concealing redness.

Are you trying to cover redness or yellowness? If you flushing has stopped then the redness will fade in time so looks like you are looking for something to cover it up in the mean time.

How is your yellowing and what is your current mepacrine dose?

I am on 100mg per day about a month with some yellowing so am going to try a tanner to help mask it and also going to pick up some B-vitamins (read a study where it lessened the toxicity effects of mepacrine when taken with at the same time) and also going to pick up some Yellow Dock Root or Milk Thistle to help support the liver and purify the blood, detox the skin. Hopefully with all these things it will work out with lesenning the yellow.






#685 Seattle JT

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Posted 14 October 2009 - 06:01 PM

QUOTE (oli girl @ Oct 12 2009, 12:04 PM) <{POST_SNAPBACK}>
Seattle- Have you been taking the Vit D? If so how long? Have you noticed any improvement in the joint clicking? I think that is one thing Vit D has helped with the clicking of the bones and joints.


Yes. I took the 50,000 IU mega dose of D2 for eight weeks and for 3-4 weeks now have been taking 2,000 IU D3 daily so about three months in total. I have been waiting to get my blood test results back for about two weeks now. Prior to starting my level was 19 so we'll see what it was two weeks ago in a couple of days (hopefully). To answer your question though I haven't noticed any change in anything. Still clicking as much as usual and in the same areas. But then again maybe my level is still low so I won't know for sure what's up until I get my latest test results. I'll let you know what my level is whenever I find out. If my levels are still low it definitely has to do with me not synthesizing vitamin d properly because I have been pretty methodical about making sure that I get enough calcium/magnesium so no excuses there.

Did you PM me about that O'Donnell fellow? I haven't received any PMs so I wanted to double check to see if you had sent it yet. If you haven't don't rush, but I just want to make sure that I haven't missed it.

#686 halfpipe101

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Posted 17 October 2009 - 03:12 AM

Seattle ive been having good results with sulfacetamide 10% sulfur 5% lotion

U must use klaron or sulfacet-r im guessing but in canada they have none so i get mine compounded and ive only been using it for 2 nights and it has helped already without giving redness or anything



#687 Seattle JT

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Posted 17 October 2009 - 09:56 PM

QUOTE (halfpipe101 @ Oct 17 2009, 02:12 AM) <{POST_SNAPBACK}>
Seattle ive been having good results with sulfacetamide 10% sulfur 5% lotion

U must use klaron or sulfacet-r im guessing but in canada they have none so i get mine compounded and ive only been using it for 2 nights and it has helped already without giving redness or anything


Hey man. I'm glad to hear that it has been working. I use the generic klaron (sodium sulfacetamide 10% lotion). I would be surprised if it gave you redness as it is sometimes used for rosacea and is said to have an anti inflammatory effect. I have been using it for over two years now and it really helps me stay clear in my problem areas without having a negative effect on my flushing or dryness. I really couldn't be any happier with it.

#688 A new start :)

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Posted 02 November 2009 - 04:13 PM

Hey guys! Some of you might remember that i wrote her some months ago. I am now 2weeks post tane, and cant wait until the side effects fades away. My lips are already better, but the redness and flushing are of course still a bit annoying. Unlike you, I have no "long" flushes, it is only due to embarrassment, which is a bit worse in hotter environments, and its lasts for a few seconds. The flushes are not as intense as they used to be, and hopefully that is a good sign. I am aware of that the only thing which heals this is time, but my question too you are; Is there anything i can do to speed up the process, or lessen the chance of it becoming permanent?

Peace out.

#689 OrionNebula

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Posted 03 November 2009 - 02:16 AM

Wow very well discussed thread, i'll just add my own experiences with accutane so that i can get your opinions on it. I took 4 months of accutane 40-40-80-80 i'm 19 years old, 165lbs Male. I stopped after 4 months because i was getting depressed and couldn't concentrate (these side effects went away almost immediately after stopping my course).

As for flushing, i recall the flushing starting during the 2nd month of treatment, and i'd just flush randomly during the day at school for unknown reasons. My face would feel really hot and i could feel all the blood rushing to my head, then after perhaps a maximum for 20 seconds, it'll subside. I am now 4 months post-tane. Last month i recall flushing while talking to a friend once, but other than that i haven't really experienced the random flushing that i had on accutane. I DO find that my skin is sensitive to hot temperatures, so if i'm in a hot room it does sort of feel like i'm blushing, but definetely not the type of intense flushing sensation that i felt on even 2 months post-tane. I recall about 1 month post-tane i wore a pretty thick shirt to work, where it was really warm, and i felt like i was flushed for the entire time until i was able to unbutton my shirt and let some air in.

Reading through this topic i realize that i have a very mild case of this annoying side effect and i'm grateful for that, but in my case, i noticed that the flushing occurences decreased each month i was off accutane. For those that have scaly and red skin, try piling on the moisturizer at night to help your skin heal (as moist conditions is the best for skin healing itself). If you're not going out, then try to reapply moisturizer as much as you can, it definetely helped me while on accutane.

#690 Seattle JT

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Posted 19 November 2009 - 06:18 PM

Hey guys just have a quick update. It looks like I'm headed towards starting Plaquenil here in the next month or so. At worst it should help with my flushing (which is still quite bad) and at best it will help my muscle/joint issues, but either way I'm pretty excited about it. I'll let you all know what dose I get and more information when I actually get it...

I did have a question though. I'm curious to know what type of facial cleanser you guys use (if you use a cleanser at all)?


#691 lamarr1986

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Posted 20 November 2009 - 05:08 AM

Good luck JT,

I have just been using a salacytic acid shampoo lol. I actually buy it when i go over to america (walgreens own brand salacytic shampoo think its like 4oz). I just foam some up on a wash cloth.

I think i may have to raise the dose of my mepacrin again, been having a bit of flushing. Only on about 200mg a week atm will probabloy go up to 400mg per week.

#692 oli girl

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Posted 23 November 2009 - 08:19 AM

Seattle- That is good to hear...If you do get Plaquenil let me know....and how it is working (esspecially if it helps your joints, my flushing comes and goes) Might need to get the name of your Rhuem for help... Ortho didn't go well though x-rays showed severe arthritis and mri showed Knee damage..(was told there's no help for accutane toxicty)

As for good news the Vit D is obviously processing some, I went from 18 to now 35...Still need to get it up some and I was just advised of a certain type of calcium to take...Will have another bone scan next year to see if any of the Osteopenia reversed...

Hope everyone has a happy holiday biggrin.gif


#693 Seattle JT

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Posted 23 November 2009 - 11:25 PM

Thanks for the replay Lamarr. Haha that's pretty funny about the shampoo from Walgreens. I'm sorry to hear that your current dose isn't keeping you entirely symptom free, but hopefully everything keeps working out at the higher dose.


QUOTE (lamarr1986 @ Nov 20 2009, 04:08 AM) <{POST_SNAPBACK}>
Good luck JT,

I have just been using a salacytic acid shampoo lol. I actually buy it when i go over to america (walgreens own brand salacytic shampoo think its like 4oz). I just foam some up on a wash cloth.

I think i may have to raise the dose of my mepacrin again, been having a bit of flushing. Only on about 200mg a week atm will probabloy go up to 400mg per week.



#694 Seattle JT

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Posted 23 November 2009 - 11:29 PM

The vitamin d result is good news! I'm glad that it has went up so much. Within the next year you should be well within the 50-70 range. The rheum appointment is Wednesday so I'll let you know what the plan is that night or sometime soon after. Sorry to hear that the ortho appointment didn't go well. I hope you have a happy holiday as well!


QUOTE (oli girl @ Nov 23 2009, 07:19 AM) <{POST_SNAPBACK}>
Seattle- That is good to hear...If you do get Plaquenil let me know....and how it is working (esspecially if it helps your joints, my flushing comes and goes) Might need to get the name of your Rhuem for help... Ortho didn't go well though x-rays showed severe arthritis and mri showed Knee damage..(was told there's no help for accutane toxicty)

As for good news the Vit D is obviously processing some, I went from 18 to now 35...Still need to get it up some and I was just advised of a certain type of calcium to take...Will have another bone scan next year to see if any of the Osteopenia reversed...

Hope everyone has a happy holiday biggrin.gif



#695 oli girl

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Posted 24 November 2009 - 08:59 AM

Lamarr- Do you think you will always have to be on the Anti's??? Do you think it might ever get better?
I think I read to a while back in one of your posts that you took L-Cartine for your muscle and mild joint aches. what brand did you take and how much...If I am correct that supplement can cause issues???? I mean my joint and muscle pain is a lot worse but It's worth a shot for now.

Seattle-Thanks let me know too once you get it how it is working after awhile.

Edited by oli girl, 25 November 2009 - 08:04 AM.


#696 lamarr1986

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Posted 26 November 2009 - 10:43 AM

I think it will slowly get better, but how much i don't dare say.

from the hundreds of people i have spoken to, it seems the first 5 years post tane are the worst some people seem to get better after this time period.

The thing we all need to do is try and prevent the damage the systemic inflammation is causing, only way to do that is with anti inflammatories and immunomodulators. If you do this you should prevent permanenet damage and allow yourself a much better chance at some form of recovery.

The trouble with the joint pain, depression, sjorgens etc etc is that if the inflammation is left to run wild for long enough it can cause permanent damage, we want to try and avoid this.

#697 oli girl

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Posted 10 December 2009 - 09:33 AM

Thanks Lammarr....I am going to my 1st Rheum here in Illinois, I've already had been to 3 in Michigan. I guess at least this time I have a xray showing arthritis and I have internist now who understands and believes my issues. So maybe I will try them..

Seattle-were you able to get the Anti's???? If soo how is it working and which one did they give you???

#698 lamarr1986

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Posted 10 December 2009 - 12:46 PM

Good luck with that, hopefulyl you will find some help.... Remember there are things like tnf-a inhibitors which could potentially be of great help with your situation and have a low incidence of side effects!

It's just a matter of doing your research and pushing for the drug you feel you need and which is obviously safe enough...

#699 Office Lase

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Posted 10 December 2009 - 11:25 PM

Hey everyone... I have had a lot of redness (well pinkness, actually) since going on accutane 10 years ago. I flush really bad and my whole face gets really red way too often.

I am going to try the v-beam laser in a couple weeks. I was wondering if anyone here has heard of it.

Also, in short... without reading all the 35 pages on the thread what can I take away from all the advice given here? I see there is some good stuff here, just not sure what to do.

Thank you much.

#700 Seattle JT

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Posted 11 December 2009 - 06:57 PM

QUOTE (oli girl @ Dec 10 2009, 07:33 AM) <{POST_SNAPBACK}>
Thanks Lammarr....I am going to my 1st Rheum here in Illinois, I've already had been to 3 in Michigan. I guess at least this time I have a xray showing arthritis and I have internist now who understands and believes my issues. So maybe I will try them..

Seattle-were you able to get the Anti's???? If soo how is it working and which one did they give you???


Hey Oli Girl,

Sorry for not posting sooner. My rheumatologist appointment didn't really go all that well so I figured that I would wait to post until after I saw my regular doctor today. I thought that I could get the plaquenil today, but my doctor wants second opinions from a physical therapist and physiatrist before she will do anything so I'm quite frustrated. This is really setting me back. I need to call them on Monday to try to get in as soon as possible because I'm quite fed up right now. I'm starting to get the feeling that my doctor is going to decide against giving me plaquenil which would be unfortunate. I would have to start this whole process over with another doctor. I don't view that as very appealing...

In other news though I found out that my vitamin d level was like 45 a couple of months ago so by now I should be in the 50-70 range. Not that it really makes any difference since increasing the levels didn't really help anything.





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