Bone Marrow Stem Cell Transplant Live from Top US Hospital
Bone Marrow Stem Cell Transplant Live from Top US Hospital
Last Updated on Wednesday, 30 March 2011 10:29 Written by Administrator Wednesday, 30 March 2011 10:29
here’s a long overdue update as to how the chemotherapy and stem cell transplant are going. I’ve been in the hospital for just over a week now and I’ve been too weak really to be posting anything, but today I got off my ass and made it happen. I’m even getting medicinal marijuana for my nausea
Video Rating: 5 / 5
just found out today that im getting a stem cell transplant, I know what you are going through with not keeping down any food. the marijuana pills do not work either
just found out today that im getting a stem cell transplant, I know what you are going through with not keeping down any food.
I have had Parkinson’s for 6 years & doing reasonably well!Do you do any Stem Cell procedures with/for Parkinson’s?What I think I need is stem cells directly into the area of the brain that is causing my Parkinson’s symptoms. Blessings, Richard Robert Amerine 5705 Locust St.,Kansas City MO ,USA 64110 Phone # (816) 444-4668 ra5705@gmail.com
my mom is going thru 2nd transplant starting april 2nd…the 1st time( 10 years ago) was? from her own cells saved… but this round will be by means of umbilical cord blood cell infusion and cell from her brother who was a match…GOD BLESS ..fyi we are doing a video journal as
My sister had her stem cell transplant in January of 2010. Has similiar symptoms as you do. Can’t hold anything down and constantly throwing up. Her doctor prescribed “marinol”, it’s kind of like marujuana. Hey whatever works. It not only increased her apetite but has taken the nausa and vomiting away. She was taken compazine and zofran, but at least the marinol is doing the job of 4 cause she is able to also sleep.
I have my stem cell transplant coming up – April 2010. Thank you for the info. PS you look great without hair
Stem cell transplant is probably the most difficult and stressful experience anyone can go through, from a patient perspective, as well as the one who is the caregiver.
We often tell the caregiver of our transplant patients that they have the hardest job of all. And they do. Kudos to all of them.
These people, both patient and designated caregiver, need loads of support.
good luck praying from tx
im 14 and about to have a stem cell transplant for slow responding 3b hodgkins lymphoma disease
Your transplant was right after mine. I got out the middle of Feb. I had a Tandem Autologous Stem Cell Transplant for Hodgkin’s Lymphoma. SUCKED. I’ll try to find some other videos of yours to see how things turned out. My hair is about 2 inches long!!! woohoo!!!
Hey sulo4life, everyone’s different and it depends a lot on the chemo you have. I had high dose melphalan and wasn’t sick once and didn’t miss a meal. Some people aren’t so lucky. I also had all the premeds (anti-emetics) and took ativan and compazine every day.
Hey, I’m going through the same thing. Where is this hospital at?
Hey…Thank you so much. That’s extra special to me coming from someone who’s been through it. I’m home now and getting stronger by the day. I would love to hear more of your story…
Hey. I had my BMT a year and a half ago. I wish you well going through this phase. I found being kept in the hospital very hard. I’m an artist and I painted a little bit.
They tried to give me the nabilone (marijuana derivative) but I threw it up! I wish you the best.
Hello Jason, I found your site through “hellsbells36″ – anyways I’m so sorry for all this your going through! I really really wish you the best! I can only imagine what your mother is going through as well – this has got to be so hard for you guys! please hang in there (keep fighting) – big big kiss to you from france! jody
Hey man,
Hang in there buddy. I have had friends in this predicament and they made it just fine. I’ll be glad to add your name to my friends list that made it. Take care, Tim
you still look cute by the way even without the hair! hope the nausea goes away with the medicine they give you also, thanks so much for the update jason. luv Hells x
Hey Jason so glad to finally see a new video you are always in my thoughts dear Jason, you are so brave and i just want you to know i am thinking of you. xxxx Helena from the UK xxx