Introducing... Melinda

[williamsMeli]

I have been attempting to load an avatar. Any tips? 
I also have a few articles about LDN and psoriasis that I can share. Should I put them here or in a new thread? 
Hope you are all doing well. I am so very grateful for SPRING!!! Whew. it was a hell of a winter here. 

[Caroline]

I have been attempting to load an avatar. Any tips? 
I also have a few articles about LDN and psoriasis that I can share. Should I put them here or in a new thread? 
Hope you are all doing well. I am so very grateful for SPRING!!! Whew. it was a hell of a winter here. 

Hi Mel,

Yes, spring is great see my pictures in [Group Specific]

Alway interesting, articles, but you have to keep to the rules of this forum.
So no links to articles . 
Best is to write an abstract or describe it in such a way that we can find it if we go search for it. 
Check the posts of Fred, he has a good way of doing that.

O… yes, and on your avatar.
Go to “Control Panel”, is it on the second top menu on the left.
Hitting it you see a personal page and in the menu on the left you see profile picture and avatar.
You can design something, or use a picture that fits your person in any way.

[williamsMeli]

I saw the gorgeous pictures you shared. Love the tulips! 
I will follow the rules and check out Fred's methods for sharing info. 
Thank you ?

[Caroline]

I saw the gorgeous pictures you shared. Love the tulips! 
I will follow the rules and check out Fred's methods for sharing info. 
Thank you ?

You’re welcome. . And thanks for the compliment.

I have expanded my previous answer on how to deal with your avatar. Did you see that?

[Fred]

Hello Mel Caroline is right I do have rules, but I'm always willing to listen. Our rules are not against you or any of our members but Psoriasis Club is about giving peer reviewed or genuine patients experiences, it is after all why I started Psoriasis Club.

All members are welcome to start a thread in [Group Specific] and I will look at it but the buck does stop here as the saying goes, but yes show me the info and I will review them (when I get time) 

Sorry to go on but Psoriasis Club is here to protect people like me, I'm not saying you are wrong but my promise is to protect our members. I have been accused of running a tight ship in the past, and yes I do but that is to protect our members.

Mel I would suggest you use the method I said above or like Caroline said write your own thoughts, I'm all for helping people with psoriasis that is why I and the forum is here but my promise has always been to protect our members and I hope you understand.

Re you avatar, this may help Avatar / Photo in your profile