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Psoriasis Club › HealthHealth Boards › Prescribed Treatments For Psoriasis v
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Neotigason Experiences?

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Neotigason Experiences?
JohnB Offline
I wanted to be an Engineer when I grew up, but was told I could'nt do both

100 + Member I Just Cant Stop !
Posts: 4,725
Threads: 36
Joined: Jan 2016
Gender: Male
Location: Lancashire UK
Psoriasis Score: 10
Psoriatic Arthritis Score: Hmm Maybe
PQOLS: 5
Treatment: Otezla/Apremilast & Enstilar occasionally.
#7
Thu-06-10-2016, 11:13 AM
(Thu-06-10-2016, 09:27 AM)elpuno Wrote: thx @all for the answear :-)

tomorrow week 5 will be ending and at the moment i feel ok. I really love my feet because they look nearly like before the psoriasis and actually the peeling on my feet seems to be ending.

my hands don't look that good but actually just some pustules and a lot of peeling skin there :-) but the skin is very dry so i have to use a lot of cream. I use a cream called "basodexan" with 10% urea. Anybody has some recommendations for me what i could use?

But one thing at the moment does worry me: i am feeling a bit sick and tired like a got a cold. Maybe i got a cold and these are the normal effects? Also my voice sounds like i got a cold...maybe anybdy made the same experiences? Will talk to the doc next week about that issue. Also my bones and muscles start to hurt a little bit which is also a well known side effect and i hope that is going to stop soon.

So i hope that i can maybe reduce the dose from actually 30mg to 20mg or 30 mg every second day or something like that. 

So that was is my update. Greetings from Germany.
Philipp

Good morning Philipp
Well I certainly hope the muscle and bones aches do stop soon. I can't imagine that is very comfortable. As for the peeling hands all I can recommend is the Forums favorite - a good quality virgin coconut oil. Personally I use either that or Dermol but I am fighting a loosing battle on the peeling hands front.
As for altering the dosing regime it may be a little too early to reduce, but it is worth talking to your Dermatologist if the aching is getting you down.
The voice thing could be down to dry nasal passages. Dry mouth nose and eyes are all possible on this stuff.
Hope that helps if not keep on asking the questions, we are all here to help each other.
JohnB
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Messages In This Thread
Neotigason Experiences? - by elpuno - Mon-03-10-2016, 14:22 PM
RE: Neotigason Experiences? - by JohnB - Mon-03-10-2016, 17:22 PM
RE: Neotigason Experiences? - by jiml - Mon-03-10-2016, 19:03 PM
RE: Neotigason Experiences? - by elpuno - Tue-04-10-2016, 12:32 PM
RE: Neotigason Experiences? - by JohnB - Wed-05-10-2016, 20:06 PM
RE: Neotigason Experiences? - by elpuno - Thu-06-10-2016, 09:27 AM
RE: Neotigason Experiences? - by JohnB - Thu-06-10-2016, 11:13 AM
RE: Neotigason Experiences? - by elpuno - Thu-06-10-2016, 16:32 PM
RE: Neotigason Experiences? - by elpuno - Sat-08-10-2016, 17:27 PM
RE: Neotigason Experiences? - by JohnB - Sat-08-10-2016, 19:03 PM
RE: Neotigason Experiences? - by jiml - Sat-08-10-2016, 19:29 PM
RE: Neotigason Experiences? - by elpuno - Sat-15-10-2016, 13:41 PM
RE: Neotigason Experiences? - by jiml - Sat-15-10-2016, 13:51 PM
RE: Neotigason Experiences? - by Fred - Sat-15-10-2016, 13:53 PM
RE: Neotigason Experiences? - by JohnB - Sat-15-10-2016, 16:04 PM
RE: Neotigason Experiences? - by elpuno - Sat-15-10-2016, 16:10 PM
RE: Neotigason Experiences? - by elpuno - Wed-16-11-2016, 19:44 PM
RE: Neotigason Experiences? - by jiml - Wed-16-11-2016, 20:19 PM
RE: Neotigason Experiences? - by JohnB - Wed-16-11-2016, 20:22 PM
RE: Neotigason Experiences? - by elpuno - Wed-16-11-2016, 20:50 PM
RE: Neotigason Experiences? - by JohnB - Wed-16-11-2016, 20:53 PM

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