tag:blogger.com,1999:blog-7822945577422872838.post6660235176886932243..comments2015-07-22T03:47:12.103-04:00Comments on Sisters With Addison's Disease: Dr Belton and Dr Desrosiers appointments...Mommy Of Miracleshttp://www.blogger.com/profile/15486112808251080010noreply@blogger.comBlogger4125tag:blogger.com,1999:blog-7822945577422872838.post-81282541305271826882015-07-22T03:47:12.103-04:002015-07-22T03:47:12.103-04:00This is a really quality post.I find this informat...This is a really quality post.I find this information through Google. Great job <br /><br /><a href="http://www.unisonbiomed.com/index.php?route=product/product&product_id=272&search=TOSHIBA+PVM-375AT" rel="nofollow">TOSHIBA PVM-375AT</a> Anonymoushttps://www.blogger.com/profile/16710131686065196125noreply@blogger.comtag:blogger.com,1999:blog-7822945577422872838.post-41981730869284148562015-01-22T13:12:07.866-05:002015-01-22T13:12:07.866-05:00Hi
I´ve Addisons disease too and started the Swedi...Hi<br />I´ve Addisons disease too and started the Swedish Addison association. How can I Contact you for a question?Anonymoushttps://www.blogger.com/profile/13425667817642783927noreply@blogger.comtag:blogger.com,1999:blog-7822945577422872838.post-82675992333112185062011-12-14T20:22:18.587-05:002011-12-14T20:22:18.587-05:00Hi I was just reading your blog and I am so sorry ...Hi I was just reading your blog and I am so sorry that your girls have this horrible disease. I too have Addison's. I was diagnosed July 2009. I was in complete organ failure when they finally diagnosed me. My endo says that there has been alot of damage done to my body and organs from going undiagnosed for almost 4 years. I wanted to tell you that I recently have started a foundation for more Addison's Disease research. You can look at my website www.addisonsdiseasefoundation.com. I would love for you to be a part of the foundation. My modo is I may not save my life or help me with my disease but I will help many others with this horrible disease. I will keep you and your beautiful daughters in my prayers and hopefully my foundation will help your daughters to have better meds and a better life with Addisons. The Barbara Davis Center at the University of Colorado has agreed to perform the research for my foundation and I am very greatful. We have to do the best we can with what God gave us. I believe he gave me Addisons to start this foundation and help other with this disease. Your girls have a reason for having this disease. They are strong and special and they will do great things in the future. Best Wishes and God Bless you!Joanna Thanthanavongnoreply@blogger.comtag:blogger.com,1999:blog-7822945577422872838.post-43191092126935225062011-02-28T15:59:04.392-05:002011-02-28T15:59:04.392-05:00I wish the girls didn't have this disease, but...I wish the girls didn't have this disease, but I am so thankful they have a diagnosis and a mommy who does her best to stay on top of it all. Thanks for sharing.<br />Lana C. www.findinglana.blogspot.comLana Chttp://www.findinglana.blogspot.comnoreply@blogger.com