2024 Fundraising for cllforum.org

Information about the CLL Forum and Forum rules
User avatar
drmoss_ca
Site Admin
Posts: 347
Joined: Wed Nov 16, 2022 10:03 pm
I am a: Patient
CLL Status: Post Transplant
Cancerversary: 30 Jul 2014
Location: Nova Scotia

2024 Fundraising for cllforum.org

Post by drmoss_ca »

It's time to start the begging!
Each year we have to pay for hosting, registration of the domain, and some add-ons like automated backups and site security. We got an introductory rate at first, which was about one quarter of the normal rate. Sadly, those days are coming to an end!
Hosting: $230/year
Domain registration: $21.03/year
CodeGuard backups: $47.97/year
Domain Privacy and Protection: $15.03/year
Having found myself unable to get the latest three upgrades installed I paid $65.27 today to a very clever person who has repaired all the damage and upgraded us to the latest version of phpBB.
I have just paid for all these.

So we need to pay $379.30 USD this year, which is about a dollar a day for this place to be here and available (if you like, that's a day and a half of zanubrutinib, or ¾ of a day of venetoclax). I assume this will go up in future, but I hope no faster than inflation generally. If you wish to contribute, please use Paypal, and my address there is chris@drmoss.ca (if you use 'friends and family' Paypal does not take a cut).
I shall thank all contributors in this thread, but I won't put amounts in to avoid embarrassing both the stingy and the generous.

Chris
Diagnosed July 2014.
FCR x6 Oct 14 - Mar 15.
Relapse 2019, with new 17p13 deletion.
Started ibrutinib Dec 2019.
Transplant February 17th 2021.
lovesbooks
Posts: 80
Joined: Tue Dec 13, 2022 6:50 pm
I am a: Patient
CLL Status: Falling Out of Remission
Cancerversary: 20 Sep 2014
Location: Oregon

Re: 2024 Fundraising for cllforum.org

Post by lovesbooks »

Thank you sooo much, Chris. I'm sure those of us who have never run a site like this underestimate how much time it takes.

Really appreciate you!

Sending funds to help us stay afloat in an hour or two.

Best,
Anne
User avatar
drmoss_ca
Site Admin
Posts: 347
Joined: Wed Nov 16, 2022 10:03 pm
I am a: Patient
CLL Status: Post Transplant
Cancerversary: 30 Jul 2014
Location: Nova Scotia

Re: 2024 Fundraising for cllforum.org

Post by drmoss_ca »

Thank you, Anne, for your generosity!

C.
Diagnosed July 2014.
FCR x6 Oct 14 - Mar 15.
Relapse 2019, with new 17p13 deletion.
Started ibrutinib Dec 2019.
Transplant February 17th 2021.
User avatar
drmoss_ca
Site Admin
Posts: 347
Joined: Wed Nov 16, 2022 10:03 pm
I am a: Patient
CLL Status: Post Transplant
Cancerversary: 30 Jul 2014
Location: Nova Scotia

Re: 2024 Fundraising for cllforum.org

Post by drmoss_ca »

And thanks to Vicky as well.

C.
Diagnosed July 2014.
FCR x6 Oct 14 - Mar 15.
Relapse 2019, with new 17p13 deletion.
Started ibrutinib Dec 2019.
Transplant February 17th 2021.
User avatar
Gulfportdoc
Posts: 201
Joined: Fri Dec 09, 2022 7:55 pm
I am a: Patient
CLL Status: In Treatment
Cancerversary: 11 Jul 2007
Location: Gulfport, Miss.
Contact:

Re: 2024 Fundraising for cllforum.org

Post by Gulfportdoc »

Chris, is there any way to send a check? I don't have a PayPal account.

If there isn't a way, I'll figure something out...

~Art
CD38 71%, B2M 2.5, del 13q14.3 33%, unmutated [crap!], ZAP-70 pos, occasional bad hair day... Started R+CAL101 7/11/11, only CAL101 from 9/06/11 on. Switched to Ibrutinib 2/03/16, then switched to acalabrutinib 9/26/20.
User avatar
drmoss_ca
Site Admin
Posts: 347
Joined: Wed Nov 16, 2022 10:03 pm
I am a: Patient
CLL Status: Post Transplant
Cancerversary: 30 Jul 2014
Location: Nova Scotia

Re: 2024 Fundraising for cllforum.org

Post by drmoss_ca »

Same issue as for others. I'm in Canada, and it isn't easy to deposit a cheque in USD. Opening a Paypal account is easy, costs nothing, and does not cause spam. But if you cannot, PM me for the mailing address, and I'll spend some hours in the bank arguing.

C.
Diagnosed July 2014.
FCR x6 Oct 14 - Mar 15.
Relapse 2019, with new 17p13 deletion.
Started ibrutinib Dec 2019.
Transplant February 17th 2021.
User avatar
Gulfportdoc
Posts: 201
Joined: Fri Dec 09, 2022 7:55 pm
I am a: Patient
CLL Status: In Treatment
Cancerversary: 11 Jul 2007
Location: Gulfport, Miss.
Contact:

Re: 2024 Fundraising for cllforum.org

Post by Gulfportdoc »

Chris, turns out that my wife has a PayPal account, so will send some bucks north in that way.

Last time, when dear Jen was still with us, I sent her a check, and she forwarded the amount to you.

So this will be more straightforward. As always, thank you for your work.

~Art
CD38 71%, B2M 2.5, del 13q14.3 33%, unmutated [crap!], ZAP-70 pos, occasional bad hair day... Started R+CAL101 7/11/11, only CAL101 from 9/06/11 on. Switched to Ibrutinib 2/03/16, then switched to acalabrutinib 9/26/20.
User avatar
drmoss_ca
Site Admin
Posts: 347
Joined: Wed Nov 16, 2022 10:03 pm
I am a: Patient
CLL Status: Post Transplant
Cancerversary: 30 Jul 2014
Location: Nova Scotia

Re: 2024 Fundraising for cllforum.org

Post by drmoss_ca »

And thank you to Kathryn.

Since I don't usually know member's real names, I'm thanking people by the name used for Paypal. If you want me to change to usernames, PM me with your username if you recognise yourself in the posts above.

We are doing well, more than halfway there for this year!

Chris
Diagnosed July 2014.
FCR x6 Oct 14 - Mar 15.
Relapse 2019, with new 17p13 deletion.
Started ibrutinib Dec 2019.
Transplant February 17th 2021.
User avatar
drmoss_ca
Site Admin
Posts: 347
Joined: Wed Nov 16, 2022 10:03 pm
I am a: Patient
CLL Status: Post Transplant
Cancerversary: 30 Jul 2014
Location: Nova Scotia

Re: 2024 Fundraising for cllforum.org

Post by drmoss_ca »

William - thank you too!

Chris
Diagnosed July 2014.
FCR x6 Oct 14 - Mar 15.
Relapse 2019, with new 17p13 deletion.
Started ibrutinib Dec 2019.
Transplant February 17th 2021.
vickys
Posts: 6
Joined: Sat Dec 17, 2022 7:12 pm
I am a: Patient
Cancerversary: 0- 0-2020

Re: 2024 Fundraising for cllforum.org

Post by vickys »

I am amazed so few people have chosen to support our forum.

Please let me know how fundraising is going. I was hoping to see that the forum would have been fully funded a couple weeks ago.

Vicky
Post Reply