hi guys, just want to say hi

[Michele]

Hello,

My name in Michele, I'm 30 and I have P. I read a lot of info posted here and I'm glad this support group exists. I'm sure I will find a lot of interesting things around here.

Thank you all for being here for people like me!

PS: My English is not very good, but I will try to do my best. Who knows, maybe it will be improved, having a lot of nice people around     


Have a nice day my new friends!

[Fred]

Hello Michele   to Psoriasis Club.

Don't worry about your English, we have members from all over the world and no one will pull you up for the way you speak. You will find us a friendly bunch, so just dive on in.

Your English is perfect as far as I'm concerned.  

Regards.

Fred.

[jiml]

Hi Michele and a warm welcome    to the club, as you have probably already noticed we are an international club with members from around the world, and your English is good and easy to understand

I hope you enjoy your time with us and you should be able to find lots of information on the various treatments available, I don't know about the healthcare in your country  but most treatments are available across Europe

Yes we are all like you Psoriasis sufferers, so  feel free to ask questions there is usually someone who will help

We also have an active off topic section where you can come and talk about anything you wish. I look forward to hearing more from you

[D Foster]

Hi Michele , welcome to the forum, I think that you will find real benefit from all the information on here and you can draw from the experience of people who have the problem so know what they are talking about as the speak from the heart not from books.
Don't worry about your English as it does not matter at all , we will get to the point one way or the other !!
There is a great general fun section which you need sometimes to help you to look at life from a different aspect , take care and just look after yourself.

Dave

[Michele]

jiml, Fred, thank you for the warm welcome!

About me: I'm 30, I have P from 10, and now I'm covered approx. 3%, but is very annoying because I have it on my palms, a little bit inside my ears, elbows and feet. I'm on Humira since last year, but it doesn't work for me. I would like to try DMF or Cosentyx, but these drugs are not available here for now. I will start taking Methotrexat very soon, I hope it will work for me. I also have access to Remicade and Enbrel and I probably change Humira very soon with one of these two drugs. 

I'm sure that I will spend some quality time here with you guys!

Have a nice day!
M.

[Michele]

Hi Michele , welcome to the forum, I think that you will find real benefit from all the information on here and you can draw from the experience of people who have the problem so know what they are talking about as the speak from the heart not from books.
Don't worry about your English as it does not matter at all , we will get to the point one way or the other !!
There is a great general fun section which you need sometimes to help you to look at life from a different aspect , take care and just look after yourself.

Dave

Hey Dave, looks like we were writing in the same time!

I will definitely check the general fun section!

Cheers!  


Thank you,
M.

[jiml]

jiml, Fred, thank you for the warm welcome!

About me: I'm 30, I have P from 10, and now I'm covered approx. 3%, but is very annoying because I have it on my palms, a little bit inside my ears, elbows and feet. I'm on Humira since last year, but it doesn't work for me. I would like to try DMF or Cosentyx, but these drugs are not available here for now. I will start taking Methotrexat very soon, I hope it will work for me. I also have access to Remicade and Enbrel and I probably change Humira very soon with one of these two drugs. 

I'm sure that I will spend some quality time here with you guys!

Have a nice day!
M.

Hi Michele, it looks as if you have been through those difficult teenage and young adult years with the disease, I know with me at age 17 I found it very difficult to cope with the disease, I wish there had been somewhere lik this when I was younger as talking to others with the disease does help you feel less isolated

I don't know what your health service is like but you are lucky to get Humira, it is a shame it's not working well for you . Methotrexate may work for you but I found it a difficult drug to tolerate, although it did clear my skin.

I'm not sure if you will be able to get Fumaderm or Psorinovo ( which are both DMF drugs) in your country...Cosentyx is a great new drug and if you do get the chance to have it, take it .....it is showing some great results with some of our members

Look forward to hearing more from you and don't forget the off topic section [Group Specific]
A good way if you want to chat about anything not psoriasis related is [Group Specific]

[mataribot]

Hello and welcome. Stelara is a good choice of a bio. Highly recommended.

[Kat]

Glad you found your way here!

[pingu]

Hi Michelle and welcome.

Its a friendly forum where language doesn't count so don't worry. Everyone is here to help.

I am from Liverpool myself so most people here think that English is my second language.