Guest guest Posted November 26, 2008 Report Share Posted November 26, 2008 Hi Sharon, I'm also a patient of Dr. Shah's and go through the same routine as your son. Labs first, then appointment with Dr. Shah. I have a PCR every three months and as far as I know, it takes about a week for the results to come back. B from California Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 26, 2008 Report Share Posted November 26, 2008 Sharon T.... Prayers are going out to you and your son for a calming and wonderful doc visit tomorrow. We are there with you. The smiles of the strangers in the room are reflecting ours. Be strong and hopeful. Peace, Rhonda Sent from my Verizon Wireless BlackBerry [ ] Happy Thanksgiving w/update on my son Hi everyone, it's SharonT (ie's mom - 18 yr old diagnosed with CML Aug 2008. Just wanted to say Happy Thanksgiving to everyone and that I'm a little scared and hoping for good news for Thanksgiving. ie has been doing ok on the Sprycel, better than the Gleevec, his blood counts have been succesfully dropping. At diagnosis his WBC was 58,000, in September it was 5,100 and in October it was 4,700 little low, but so far so good. His hemoglobin has been low and they are watching that closely. I wouldn't be surprised if it's still low tomorrow if he starts some sort of supplments for that. Tomorrow is his appointment with Dr. Shah and he's having his first PCR done since diagnosis. Anyone know if those results will be as quick as the blood counts? Usually at clinic we do labs and then appointment an hour later with results reviewed with doctor. Is PCR result that way in terms of how quick they get the results? I'm so hoping for some good Thanksgiving news about a log reduction for ie. I've been doing a ton of research still trying to educate myself about CML and have learned alot just by reading everyones posts here. I'm still a little shy here but felt the need to thank all of you today for educating me since my son's CML diagnosis and for all the support I received when I do reach out. ie's doing really well at Cal Berkeley, loves it there and the excitment in his voice on election night (we spoke about 5 times that night as the results were coming in) and oh how I wish I could have seen the look on his face that went with the tone of excitment in his voice while he was rejoicing with the students at Cal, you should have heard the cheers in the background, I had goosebumps that night all night. I told him " baby, you worked hard to get there and you go ahead and enjoy every minute of the experience, get off the phone with me " . He truly is loving the Berkeley experience. Last week he was just as excited with Cal beating Stanford and getting that axe back LOL. I'm looking forward to having him home for both Thanksgiving and his Christmas break, I get him for a whole month. I miss my son so much and even though he's not that far away from home home and I have a 3 year old and 13 year old still at home, my home just seems so empty without him in it. I'm doing better accepting and trying not to be so hard on myself. ie has both CML and cystic fibrosis so as a mom it's a double wammy in 21 months for me as he was diagnosed with CF at 16 years old. He's getting he best care possible I know and he's very private and he's being really strong and brave as always and is focused on his education. I think he refuses to let this burden him and sway him from his goals. He's more determined than ever and that's so nice to see that this hasn't crushed him as it has me. He always says " Mom, please don't worry about me, I promise if there's something you need to worry about I will tell you, but take care of yourself " so much easier said than done and hence why I go with him to his oncology appointments. It's the only way I find out how he's really doing because he's honest with Dr. Shah and tells him things that he won't tell me because I'm not suppose to worry LOL. As a Mother, I want to take all this from him and constantly ask why, he's such a good son and he's my pride and joy and he's suppose to be enjoying his college years and experience instead of adding cancer to CF. I keep telling myself there has to be a reason for all this, why he was chosen. I've learned alot about bravery and strength from my sweet son and it's been a humbling journey. I still cry alot of tears in silence about all this, mainly because the fear is still so fresh and real and until I know for sure he's going to be ok I don't know if I'll ever sleep right again to be honest but I've been doing better at taking care of me and not focusing on all the unknown right now. ie tells me to take the pressure off myself, I didn't do this to him, especially the cancer and that I can't feel guilty anymore about giving him these illnesses, but it's still hard bitter pill to swallow most days to be honest. Tomorrow is an important appointment. They will tell us if he's headed in the right direction towards a major molecular remission right and I know I'm suppose to ask about how much of a log reduction he hopefully has achieved. I'm praying so hard that we hear those words tomorrow, all I want for Thanksgiving is some good news about his Leukemia. Anyway, Happy Thanksgiving everyone. I will update ie's PCR as soon as I know. Thanks for letting me share and talk about my fear. Quote Link to comment Share on other sites More sharing options...
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