We provide the thymoma website since spring 1997
First it was thought to connect to other patients to share information,
but we were the only ones who provided information what we gathered on
the web through very time intensitive research. It was not easy to get
all the personal information you find today on our website. The majority
of web users is not in giving information but only in getting information.
We provided countless help via email personal chat and even via telephone
and fax and where often working until late night, since when you are in
Germany there is a 6 to 8 hour time difference to the USA.
Sue and I (Joe) did all the work and payed for everything. Now comes the time when you can do your share to keep this service alive. We do not get any funding, so it is up to the thymoma comunity to care for the website. With just $5 to $10 a months you can make a difference. You can send us money, a check, a money order, or use your credit card over the web to support thymoma.de Tell your friends and family about us and if they do not know what to do for you, this is a way to help you direct by making thymoma.de stronger to help and serve you better. I will post on the bottom of the "you can help thymoma.de" page the ammount how much money we got so far.
Over the time and with lots of hours of hard work and
enthusiasm it has grown to the web largest and most informative thymoma
web site.
We often had the question: "how can we help thymoma.de?",
and now you can.
This website was scheduled to close, when Sue's 5 years
are over. That would be in summmer 2001
Since we are getting several new thymomas each months we think this
site should be on the net for longer.
Here we need your help.
If you find this website and the help we provide useful for you, please
support thymoma.de with a donation.
- You can use Paypal.com
and send money to thymoma.de
Use your credit card or checking account. It is fast, secure and there are no fees for you.
Just click on the link above and sign up for free.
We use it for transactions since 10 years without a problem.
You can send money to everybody with an email address.
In case we should get more money than we need to pay for keeping the site online, the additional money will be donated to Dr. Patrick Loehrer and his thymoma research fund.
Wir starteten
diese Webseite um andere Menschen mit einem Thymom zu finden und um Informationen
über diese sehr seltene Krankheit auszutauschen.Es entwickelte sich daraus die weltgrösste Thymoma Seite.
Oft wurden wir gefragt: "Wie kann ich thymoma.de helfen?" und jetzt gibt es eine Möglichkeit sich zu engagieren.
Diese Webseite sollte, wenn Sue's 5 Jahre um sind, im
Sommer 2001 vom Netz genommen werden.
Nachdem sich jedoch mehrere neue Thymoma Fälle pro Monat bei uns
melden, denken wir thymoma.de sollte permanent zur Verfügung stehen.
Hierzu benötigen wir deine Hilfe.
Wenn du thymoma.de nützlich und hilfreich für dich findest,
kannst du thymoma.de mit einer Spende helfen.
- Inlands Überweisungen bitte an:
Rudolph
Netbank Hamburg
Konto: 7007396
Blz: 20090500
Kommentar: für thymoma.de - Endlich keine hohen Bankgebühren mehr
für Überweisungen aus dem Ausland. Unsere Internationale
Kontonr ist:
01805-638226 IBAN
Sollten wir mehr Geld bekommen als wir für thymoma.de benötigen, so wird dies Dr. Patrick Loehrer und seinem Thymoma Forschungs Fundus zur Verfügung gestellt.
