- Joined
- May 25, 2010
- Messages
- 446
Hey everyone. Woke up Friday Morning hugging the toilet, took nausau meds, waited a while, hugged toilet again. You know how much I love my toilet, I hug it so much. I was so ill I couldn't even take my meds. My husband called and said either I call the dr. or he was calling. So, I called my doctor, my husband came home, took me to the doctors office, and he did a direct admin to the hospital. I've had an ultrassound of my gallbladder, which came back negative, I think, they haven't really said anything. Did a CT scan last night without the contrast 'cause I couldn't get the contrastt down. So, this morning, after a night of nausua medicine on a regular schedule, I was able to keep the contrast down and drank every drop like a good girl. They got much better pictures. All the pain and problems seem to be the cancer. Apparently none of this flare from the beginning has been Crohn's. I feel like such a fraud now here. :lol: I've been crying to all of you about this badd Crohn's flare and the whole time it's been cancer. I still have Crohn's, but it's in remissionl. I hope you all forgive me. I am going to keep checking here, but I'm getting ready for chemotherapy andd I think I'm going to try to find a support group for that. I know it won't be as good a group as here, but I think I'm going to need people that have gone through chemo to help get me through this. I'm getting very scared and nervous about this cancer..
Anyway, I'm just now up to typing and wanted to touch base. You are all such wonderful people and I will be in and out, but probably not quite as much. Of course, I say that and then I miss you guys and I'm in here 3 or 4 times a day. So, I guess once a day willl have to do for a while. If anyone here has had to go through chemo and feels like sharing, please let me know. I need all the help I can get right now.
I'll keep ya'll posted on my condition as we go and when I get to go home. More soon. Best to everyonel
Anyway, I'm just now up to typing and wanted to touch base. You are all such wonderful people and I will be in and out, but probably not quite as much. Of course, I say that and then I miss you guys and I'm in here 3 or 4 times a day. So, I guess once a day willl have to do for a while. If anyone here has had to go through chemo and feels like sharing, please let me know. I need all the help I can get right now.
I'll keep ya'll posted on my condition as we go and when I get to go home. More soon. Best to everyonel