Guest guest Posted June 7, 2008 Report Share Posted June 7, 2008 thank you so much, that reinsure me , yes i wish my daughter natasha would write on here, but she said her way of dealing with it , is pretending she doesent have it, and doesent want to talk about it, but me in the other hand, behing the mother,, well i cant just sit there not knowing any thing , and wen can she dye, ect,, i have a very hard time with this, i guess i was scared of that word every time i went to see my doctor , because my mom got stomack cancer before and it runs in the family, so i was really worried for miself, but knowing my daughter have cancer,, dam its so hard to breath, i think about it every hour of the day, i can hardly sleep , this is keelling me, and just by reading your letter,, it made me feel so much better,, wow thank you so much, from the bottom of my heart, xoxo sincerely jeanny forest @...: rcd1929@...: Sat, 7 Jun 2008 06:38:22 -0700Subject: Re: [ ] i have another question Jeanny, one of the gentlemen on this list has had cml over 30 years, he is still alive and kicking! When I was dx 13 years ago, they said maybe I had 5 years to live. That was 13 years ago, I am doing great, I'm back in remission on a brand new drug. I live a normal life, I travel, I have a cocktail once in a while, I sit in the sun and get a tan, and unless I am posting on this site, I do not give cml a single thought. Your daughter will do very well on this disease, it is a lot better than a lot of cancers, like bone cancer, or brain cancer, or uterine cancer. This can be lived with, many of the gals and guys have had babies, and they are all fine. The more you learn about cml, the better you will be, and perhaps your daughter would be interested in posting as well? It does help to know there are others out there, young ones too. is getting married soon, and he is a great example of cml and the younger generation. This is a good place to come with yourfears, as there are so many people here that can give you good advice, and if there is something they don't know, they will find it out for you. Please don't worry, I know it is terrible for our children to have a dreadful disease, but your daughter is lucky today, as there are so many new drugs out there to control cml. Blessings, and good luck, Bobby Doylejeanny forest <jeanny-f@...> wrote: hi every one, im sorry i wrote here , but i have no idea how to write a seperate email,, im not a computer wiz , im sorry again , if i make mistake writing in anglish, i am french and to top it all off im blond, lol lol ,, here i go, im jeanny , im sure you saw some of my letters in here, my 19 year old daughter have leukemia, cml, im so so afraid for her , dang, its hard to live knowing my daughter is sick, if it would be me, i would deal with it,, but my daughter,, no , i cant take that , ok for my question now, maybe i cant ask such a question , there is probably no answer to this one, how long can you live on cml, does she have a good chance, to live a long time, does this leukemia can go in remision, could she fite this, can she have a normal life ect, please let me know how you feel about this and what you know, and i hope i havent offend any body thanks for your suport, http://g.msn.ca/ca55/208[Non-text portions of this message have been removed]------------------------------------ Quote Link to comment Share on other sites More sharing options...
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