It's Me Sarah!

****look up skype on google and download it. It's so that you can IM or video chat with Sarah while she is home. Once you have skype downloaded add sary1inamillion

***Another note: I have heard from many that they are unable to leave comments. I have now set this blog to accept comments from any visitor:) Just click the comment link left of the little yellow pencil below any update and leave a comment!!!:) you can leave an anonymous comment and then just leave your name in the comment.

Hey everyone, this is Sarah writing! I am home now and feel great to be out of that hospital. Don't get me wrong I am so grateful for everything that all my doctors, Dr. peterson, Dr. Ash and Dr. ford have done for me and also the wonderful Nurses at L.D.S. hospital. They saved my life! But it was so hard going through everything that I can't even explain it. I see this disease as a blessing in my life also because it has brought so much good and positive things in to not only my life but others as well. I just want to thank all of you for being so loving and supportive! I have had so much love to get me through this hard journey. I just posted some new pictures of my home coming and my new wigs, I hope you will enjoy! I am doing a lot better and hope I wont have any set backs to where I have to go back to the hospital. I still have to where my mask for at least another 3 months and be very very careful not to get sick but I cant explain how happy I am to be home! I can deal with all of that just to be home! My twin sis is doing good, she left to oregon with my father last night to go see my grandfather. My grandfather isn't doing so well so they are going to see him.  I wont be all the way better for about another year, but hope to See a lot of you soon! Thank you all again! Love and Light Always! 

~*SaRaH*~