tag:blogger.com,1999:blog-5185625847334331843.post3108378618245492844..comments2024-03-19T21:57:40.575-07:00Comments on The Sickle Cell Blog: 10 Things Good About Sickle CellVixenhttp://www.blogger.com/profile/14064520755523082756noreply@blogger.comBlogger3125tag:blogger.com,1999:blog-5185625847334331843.post-61917710151771097502021-06-26T00:16:47.179-07:002021-06-26T00:16:47.179-07:00I was diagnosed as HEPATITIS B carrier in 2013 wit...I was diagnosed as HEPATITIS B carrier in 2013 with fibrosis of the<br />liver already present. I started on antiviral medications which<br />reduced the viral load initially. After a couple of years the virus<br />became resistant. I started on HEPATITIS B Herbal treatment from<br />ULTIMATE LIFE CLINIC (www.ultimatelifeclinic.com) in March, 2020. Their<br />treatment totally reversed the virus. I did another blood test after<br />the 6 months long treatment and tested negative to the virus. Amazing<br />treatment! This treatment is a breakthrough for all HBV carriers.MATINAhttps://www.blogger.com/profile/10558912772822043673noreply@blogger.comtag:blogger.com,1999:blog-5185625847334331843.post-85968192552347710012007-12-09T01:16:00.000-08:002007-12-09T01:16:00.000-08:00Tamika, girl you totally rock! Your comment really...Tamika, girl you totally rock! Your comment really did make my day. Sometimes I forget that this is the internet and there are actually people 'reading' my blog! <BR/><BR/>Great news with that article...I'm going to blog about it. <BR/><BR/>Please stop by and leave comments. I hope your hubby is doesn't very well. Look into Pro Arginine, it might be good for him too.Vixenhttps://www.blogger.com/profile/14064520755523082756noreply@blogger.comtag:blogger.com,1999:blog-5185625847334331843.post-23733961973617523862007-12-06T19:57:00.000-08:002007-12-06T19:57:00.000-08:00Hey there...just wanted to tell you I drop in on y...Hey there...just wanted to tell you I drop in on your blog sometimes. I admire you and your honest words about SCD. My husband suffers from sickle thalessemia, a weird hybrid, scaled down version (if you can call it that) of SCD. Less severe as the full blown disease but all the symptoms and daily struggles you speak of. Hospital visits might be once a year or so. <BR/><BR/>Every day I'm keeping my eyes out for a cure, a relief, anything to make his life-- and our lives-- easier. Every day, I watch people overlook how this disease affects the people involved. Every day, we struggle together, living and loving as best we can.<BR/><BR/>Thank you for your strength, courage, even your moments of weakness when you have them. It's nice to know sometimes you're not alone. All the best.<BR/><BR/>PS: I live outside Washington, DC...something I found on the Wash Post tonight...always hope!<BR/><BR/>http://www.washingtonpost.com/wp-dyn/content/article/2007/12/06/AR2007120602444.html?hpid%3Dtopnews&sub=ARAnonymousnoreply@blogger.com