another journey
well today is a better day,got my 18 treatment so far today,and not feeling to bad, 2nd bone marrow transplant cancelled,until i finish 14 more …
I am 48 I am living with muntiple myeloma now for 3 years.I have a beautiful daughter 27 that live in ontario.Me and my husband separted after 30 years,9 month ago.I had a bone marrow transplant 2 years now and is still in remission.I work 3 days a week it is very hard but it keeps me sane.My job is a cook and i enjoy it.We do not have any support close to my home for my type of cancer. i am 6 hrs away..if anyone would like to share there time and advise i would be glad to hear from you thanks
I am 48 I am living with muntiple myeloma now for 3 years.I have a beautiful daughter 27 that live in ontario.Me and my husband separted after 30 years,9 month ago.I had a bone marrow transplant 2 years now and is still in remission.I work 3 days a week it is very hard but it keeps me sane.My job is a cook and i enjoy it.We do not have any support close to my home for my type of cancer. i am 6 hrs away..if anyone would like to share there time and advise i would be glad to hear from you thanks
well today is a better day,got my 18 treatment so far today,and not feeling to bad, 2nd bone marrow transplant cancelled,until i finish 14 more …
hey how is everybody doing,i don;t get on line much but wanted to say hello to everyone,i am back at my treatments again,i relasped back in nov after …
hey everyone,just wanted to say i miss use all...my dad is having a hard time he had his foot amputed, he;s been the hosptail for 7 weeks now, …
hello everyone just wanted to say happy easter hope use all have a great one
hello everyone it been quite a while since i wrote ..had alot going on lately. but thing are getting better...how is everybody doin fine i fine ..i …
Coming through like a true champion! Yeeeehaaawww!
Thank you !
hope your feeling better
I will pray for you.
i was diganoise when i was 45, i had a bone marrow transplant 2 years ago and in remission..there is no support groups for as far as 6 hr.i have monthly visted with my ongologist.I get aderia every month...looking to talk and share info with people living with illness that is hard to deal with.. thank you