Thymoma
Support Group
more than just info on a website
updated:2007.3.29
more than just info on a website
updated:2007.3.29
|
Thymoma
Support Group
more than just info on a website updated:2007.3.29 |
|
Due to the high demand on personalized information we
offer now something to help you better.
The Thymoma Support Group. |
| visitor | Thymoma Support Group Member | |
| use of all regular websites at thymoma.de | yes | yes |
| use of the forum | yes | yes |
| use of the chat | yes | yes |
| Moderated chat with Eva or Joe if requested | no | yes |
| E-mail support from thymoma.de We might not be able to answer your mails if you are not a Support Group Member! |
no | yes |
| My own free of charge
e-mail address: my name@thymoma.de Please send us an e-mail with the name and the password you want to use. |
no | yes |
| Can I call Eva or Joe? | no | yes |
| Will you do some research for me and / or help me with my search? | no | yes |
| Will you take the time and tell me what are my chances, options or simple the truth? | no | yes, but you have to understand, that we are no healthcare professionals, our opinion comes just from experience. |
| Will you accompany me during my illness | no | If it is possible for us to do so, yes. But please understand, our time is limited, and for just a one year fee nobody is able to do very much. |
| Cost | free |
5$ or 5 Euro per months or whatever you can afford |
Are you ready? then go here
