Hello, this is Denise's husband. The transplant happened yesterday and everything went ok. My sister in law is already talking, she looked swollen but they said that it was expected. She should be able to walk today.
My lady, when I tried to talk to her was going in and out because they had her in strong medicines cause she had very bad nausea. They overdose her and that made her sleepy, they say she should be better today and I would be able to talk to her.
I'm waiting for my sister in law to call us when she's awake so we can go and see them. My lady will write when she's back. I'm not much of a writer. Thank you very much to all the people that have wrote and donated to her. I hope all of you have a great day as it was for me yesterday when I heard the news that both were doing great!!! Take care bloggers!!!
Tuesday, March 17, 2009
Tuesday, March 10, 2009
Pre-Op Day
Silvia arrived on March 4rth, 2009 and will stay with us until the end of the month, Hector is arriving this weekend to take care of Silvia while she is in the hospital. The Pre-Op appointment is Wed. March 11, all morning long. Then I will go to dialysis in the afternoon. The appointments are for a chest x-ray, anesthesia clearance, an EKG, a final blood crossmatch, a final interview for Silvia, and a physical with the surgeons. I also have to do an extra dialysis session on Saturday, in preparation for the surgery on Monday.
Wednesday, February 11, 2009
Transplant Date
March 16th, 2009 is the planned day for my transplant. I hope the transplant surgeons don't cancel because my blood pressure goes over 200/125 almost every day. Maybe it will be under control by then.
Friday, February 6, 2009
Transplant Approved
Silvia received a phone call yesterday to tell her that she is approved by the committee to donate her kidney to me. But we don't have a set date yet because the Donor Coordinator is on vacation. We need her to make the appointment for us. We are so close now! Finally. My blood pressure was 204/125 two days ago and 166/109 this morning. I still get shortness of breath at night from the fluids.
Tuesday, January 27, 2009
Week in the hospital
I went in for the dialysis catheter on Tuesday, January 20th. I fasted since Monday night and they had me wait at the UCD hospital all day. The appointment was at 11 am and my catheter was placed at 5 pm, then I didn't feel like eating until the next morning. The catheter placement was so painful, they barely sedated me, if at all. I felt every needle prick, about 12. The shoving in of the catheter was the most painful. Afterward, they couldn't stop the bleeding, so the nurses took turns pressing their fingers onto the wounds many times for long periods, I wanted to cry. They didn't give me pain medication until my husband requested they give me some after all the pressing. We requested my bloodwork results and they gave them to us later, my platelets were 89 and my hemoglobin 8. They sent me home, still bleeding and told me to go to emergency if it didn't stop. A few hours later, Yarid took me to the Sutter emergency room, where they did some more pressing. An ambulance picked me up and took me to the Woodland Memorial at 1 am. That morning, I had a transfusion and my first dialysis session together. It made me nauseas and dizzy and raised my blood pressure. Afterwards, I couldn't breathe, and I felt like fainting, by the time the nurse believed me, it was night and they found that I only had about 50 % oxygen, instead of 100%. I was rushed to the ICU. They drugged me and placed a breathing mask on me. I woke up toward the end of my second (emergency) dialysis. I would have drowned without it. They told me I had fluid overload. The next morning, I had dialysis again, I had nausea and dizziness, then I almost vomited. My body became very hot and I went deaf for a while. I almost passed out but they stopped that part of the dialysis. Later they told me my heart had stopped beating for 6 seconds twice during th0se 15 seconds, when I almost passed out. Monday, I had another dialysis session, and I became nausea, dizzy and had very strong stomach pains, my session had to be limited. I was discharged and went home with a major headache. The highest my blood pressure went during the week was 240/130. They can't figure out why it's always high. Tomorrow, I'll have a new dialysis session in Dixon. I am afraid.
Labels:
ambulance,
dialysis,
emergency,
hospital,
kidney failure
Sunday, January 18, 2009
All day testing complete and dialysis starts Wed
Silvia finished her initial tests: cat scan, 24 hour urine, chest x-ray, transplant doctor evaluation, EKG, blood work, and interview. We don't have all the results yet though. The coordinator told us that the soonest surgery date that is open is mid-March. My newest symptoms are hot flashes that make me dizzy, and a very sweet taste (like artificial sweeteners) in my mouth. I am always tired, but I can't sleep. My edema is even worse than before. My blood pressure is still very high. I have bruises on my legs that are getting darker instead of healing. I also had a very bad leg cramp when I woke up yesterday, and a painful cramp on my chest today. My creatinine was over 11 last week, GFR 4, and my platelets are decreasing. My neck catheter is going in on Tuesday at 11 AM at UCDMC. And I will start dialysis Wednesday, the 21st at 6 AM.
Saturday, January 10, 2009
Perfect Match

My sister Silvia's crossmatch results came back as a 100% match. Hector had only been a 50% match. The crossmatch took a long time because the transplant clinic is so slow, it took them 2 weeks to get the kit to her. She is coming up to visit on the 16th, for her all day evaluation and testing. I had a blood test Mon., saw my primary physician on Wed., and I called the dialysis clinic on Thursday to tell them I want to start dialysis. My ankles have become swollen, my ammonia breath is back, I can't sleep, my blood pressure is out of control (even with extra medication, usually 160/110), my potassium still gets too high sometimes, my phosphorous is very high (even with medication) and for 2 days, my fast heart beat would wake me and I would see red flashes when I opened my eyes. My doctor doesn't know what the flashes mean. The dialysis lady said she'd call me back in 1 1/2 weeks to schedule me. I thought she was joking. They've been begging me to do dialysis for months and now that I finally decided I need to do it, they are going to make me wait. I'll probably change my mind by the time they call me back. I called my doctor to tell her and she says she will try to find another place for me to do dialysis.
Labels:
antigens,
Denise Acosta,
dialysis,
high potassium,
kidney donation,
Silvia Encinas
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