Home Home Contact Us Help Registering and Participating Disclaimer Please Note: THIS FORUM IS PATIENT MODERATED AND IS NOT CONNECTED TO ANY CLINIC OR DOCTOR. IF YOU WISH TO CONTACT A CERTAIN DOCTOR OR CLINIC, PLEASE LOOK IN THE ASK THE DOCTOR SECTION FOR DOCTOR OR CLINIC PHONE NUMBERS AND EMAIL ADDRESSES.

                       Home || Contact Us || Help Registering and Participating || Disclaimer

Unlock Secrets in Your Own DNA with 23andMe.com

Nutri-Health Products

 Buy 1 Get 1 Free at Puritan's Pride

LivLong – The Ultimate Anti-aging Product

SeaChange Partners with Life Extension Products

 

Barbara and Jeannine's Book

Bea Luis Memorial

 

Join the ICMS


Go Back   Stem Cell Pioneers > Meeting Hall > Caregivers
Register Blogs FAQ Members List Social Groups Calendar Search Today's Posts Mark Forums Read

Reply
 
Thread Tools Search this Thread Display Modes
  #1  
Old 09-13-2010, 09:04 PM
kygal kygal is offline
Member
 
Join Date: Jun 2007
Location: Vineland Station, Ontario, Canada
Posts: 36
Thumbs up New forum for caregivers

I wanted to let everyone there is a new forum for caregivers of COPD patients. It is only a site for caregivers, to give them a place to go and talk to others, share ideas, and learn from each other. The new site is http://copdhelpmates.proboards.com/index.cgi and you have to register to be a user.

I am the moderator/administrator for the group and I'm a widow of a COPD patient. My husband lost his battle with this disease in 2007. I started this, with some help, to provide a place for caregivers to go to have a place to talk, share, vent and even whine. There were no such groups when I was going through this and believe me, I looked everywhere for help. I discovered there were support groups for everything in the world, even for hangnails but nothing for people dealing with COPD. But, this was also at the time that both the U.S. and Canada were advocating to let each country know just what COPD was. I'd love if you want to join us. We're just getting it off the ground and there's only a few members right now, but I know it's the right thing to have in place.

I've been a member of this forum from its inception even though I've not been a very active member over the last few years of my grief. But, I still believe that stem cells is the answer for a cure and I advocate for it every chance I get. I was determined to raise the funds to get my husband the treatment but I didn't get it raised quickly enough. I don't want to see that happen to anyone else.

So, I hope you join us and I look forward to getting to know you as you venture you through this journey.

Take care,

Mary
Reply With Quote
  #2  
Old 03-19-2012, 11:47 AM
ozz ozz is offline
Junior Member
 
Join Date: Mar 2012
Location: Montague nj
Posts: 23
Default Mary

I can not log into your site. There is a piazza hut pop up, coming up all the time.
Reply With Quote
  #3  
Old 03-19-2012, 01:07 PM
Jeannine Jeannine is offline
Pioneer Founding member
 
Join Date: May 2007
Location: New Hampshire
Posts: 1,680
Blog Entries: 1
Default

I can't log in either but we do have a Caregivers section for COPD on our COPDLiving forum if people are interested.

http://www.copdliving.com/index.php?showforum=48
__________________
Still Pioneering
Had UC treatment April 5th, 2007
Had autologous treatment March 19, 2010
Had bone marrow and adipose stem cell treatment (autologous) June 16, 2010
Reply With Quote
  #4  
Old 03-19-2012, 04:43 PM
ozz ozz is offline
Junior Member
 
Join Date: Mar 2012
Location: Montague nj
Posts: 23
Default question on encapsulated mesenchymal SC

Can't targeted MSC's be the alternative to lung stem cells?
Reply With Quote
  #5  
Old 03-21-2012, 03:47 PM
barbara barbara is offline
Pioneer Founding member
 
Join Date: May 2007
Posts: 6,991
Blog Entries: 5
Default

I got a message back about the Caregivers forum. If you would like to contact her, you can do so by private message on this forum. Click on Community, then K, the kygal and send her a message from there.


Kygal
Hi Barb, so good to hear from youl...how are you doing these days? Unfortunately, we closed the forum for the caregivers....several of the gals on there lost their spouses & one gal lost an older lady she was supporting and once that happened, it seemed things just quit being very active. I continued to try and encourage people to chat but you can only do so much without pulling teeth...I know you know that. But I'd be more than happy to chat with anyone...and we're hoping to maybe include something with the COPD Canada site soon.
__________________
First treatment in 2007. Pioneering ever since.

Barbara
Reply With Quote
Reply

Thread Tools Search this Thread
Search this Thread:

Advanced Search
Display Modes

Posting Rules
You may not post new threads
You may not post replies
You may not post attachments
You may not edit your posts

BB code is On
Smilies are On
[IMG] code is On
HTML code is Off

Forum Jump

Copyright 2007 - 2011 Stem Cell Pioneers


All times are GMT -6. The time now is 08:40 PM.


Powered by vBulletin® Version 3.8.7
Copyright ©2000 - 2013, vBulletin Solutions, Inc.
Stem Cell Pioneers