I was wondering if you'd like to share your journals on www.mymedworld.com
its a new site that allows people to write about personal experiences so that it can help others. hope you check it out as the site has a lot more reach and your blog can really help people!
I really hope you post on Mymedworld, so many people can learn from your journey!
My name's Sophia Ahn and I'm an editor and writer for Myeloma Beacon, a site that offers news and information about multiple myeloma to patients and family members. I was wondering if I can interview you about your experiences with the disease. Please email me back on sophia.ahn@light-kr.com about your availability. Thank you.
Thanks for keeping your blog up and running. I just read through EVERY post and now have tears in my eyes. My dad was just diagnosed in May 2009 with Lightchain MM - it's quite advanced and he is currently debating about the SCT. His 2nd opinion - Dr. Berenson in Los Angeles advises against it. We're going for a 3rd opinion at Mayo in AZ shortly.
So much in our lives has changed...everything really. I'm researching like crazy and the more I learn, the more I realize I don't know about MM. Your blog has been a big help - I added lots of links to my favorites. Thank you. I pray my dad can hang on as long as Richard did. Is it sad that I don't want to be nieve and hope that they may even find a "cure" during his time...I guess it's just one day at a time.
Thanks for following our unfolding story. I took my first trip to KC in 1991 when my cousin was playing for the Royals. I got to meet Wally Joyner in the locker room after the game :) George Brett was at a funeral and miss the game :(
I'm writing this story to help others diagnosed with this relatively rare cancer. I'm a family nurse practitioner, working in a hospital. My husband Richard was a fifth grade teacher. He retired on disability in 2005 after thirty years of teaching. He was diagnosed with multiple myeloma in April of 1999, one week after his 49th birthday.
He died February 28, 2009. The blog will stay for awhile. Hopefully our experiences can help others.
5 comments:
hi Teresa
I was wondering if you'd like to share your journals on www.mymedworld.com
its a new site that allows people to write about personal experiences so that it can help others. hope you check it out as the site has a lot more reach and your blog can really help people!
I really hope you post on Mymedworld, so many people can learn from your journey!
Viv
Hey Teresa,
My name's Sophia Ahn and I'm an editor and writer for Myeloma Beacon, a site that offers news and information about multiple myeloma to patients and family members. I was wondering if I can interview you about your experiences with the disease. Please email me back on sophia.ahn@light-kr.com about your availability. Thank you.
Thanks for keeping your blog up and running. I just read through EVERY post and now have tears in my eyes. My dad was just diagnosed in May 2009 with Lightchain MM - it's quite advanced and he is currently debating about the SCT. His 2nd opinion - Dr. Berenson in Los Angeles advises against it. We're going for a 3rd opinion at Mayo in AZ shortly.
So much in our lives has changed...everything really. I'm researching like crazy and the more I learn, the more I realize I don't know about MM. Your blog has been a big help - I added lots of links to my favorites. Thank you. I pray my dad can hang on as long as Richard did. Is it sad that I don't want to be nieve and hope that they may even find a "cure" during his time...I guess it's just one day at a time.
Thanks for your blog.
Jill
Thanks for following our unfolding story. I took my first trip to KC in 1991 when my cousin was playing for the Royals. I got to meet Wally Joyner in the locker room after the game :) George Brett was at a funeral and miss the game :(
God Bless, Phil
Nice to meet you.
I was going to paste the link without permission because I had very felt the interest for your blog.
Please link me with the blog if it is good.
URL:http://hiro-anniversary.blogspot.com/
E-mail:h-mori@ibs-office.com
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