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Posted on 11/3/21 at 8:01 pm to Horsemeat
Best of luck. I have no advice to give you, but I have a niece getting ready to go through a similar procedure at Duke the first of the year, removing her bone marrow, cleaning it, and replacing it. She will be there for 3 montsh.
Good luck and prayers your way.
Good luck and prayers your way.
Posted on 11/3/21 at 8:02 pm to Horsemeat
I wish you the best and have faith that you will get through this. My wife underwent a sudden life threatening medical condition (brain aneurism) and we know for a fact that the power of modern medicine is awesome. She was granted a new life and we are ever grateful. You are in our thoughts and prayers.
Posted on 11/3/21 at 8:17 pm to Horsemeat
Praying for you! You can do it!
Posted on 11/3/21 at 8:20 pm to Horsemeat
I have done it and it isn’t fun but is also not pure misery.
I had stage IV Diffuse Large B Cell Lymphoma twice. The relapse required about 4 months of Hyper cvad chemo and radiation treatments. Treatments were given inpatient at Emory Winship.
At about 4 months, I had my own stem cells harvested and stored for the transplant that took place a month later.
The prep for the transplant include a few days of high dose chemo and total body irradiation. The TBI and high dose chemo was to kill all of the bone marrow in my body before the new was re-introduced. Of course, without the re intro, you would die.
After the transplant, which was done in my hospital room with 2 attending doctors, I stayed inpatient for 2 weeks. Once they considered me to be stable, I went to stay at the ACS Hope Lodge about 2 miles away for 2 more weeks before going home.
The worst part was the nausea that came immediately after the high dose chemo and TBI sessions. Sometimes the nausea meds couldn’t alleviate it but it was just dry heave vomiting off an on for 15 or so minutes.
It’s not fun for sure but it isn’t pure misery either. You’ll be fine with a positive disposition.
I had stage IV Diffuse Large B Cell Lymphoma twice. The relapse required about 4 months of Hyper cvad chemo and radiation treatments. Treatments were given inpatient at Emory Winship.
At about 4 months, I had my own stem cells harvested and stored for the transplant that took place a month later.
The prep for the transplant include a few days of high dose chemo and total body irradiation. The TBI and high dose chemo was to kill all of the bone marrow in my body before the new was re-introduced. Of course, without the re intro, you would die.
After the transplant, which was done in my hospital room with 2 attending doctors, I stayed inpatient for 2 weeks. Once they considered me to be stable, I went to stay at the ACS Hope Lodge about 2 miles away for 2 more weeks before going home.
The worst part was the nausea that came immediately after the high dose chemo and TBI sessions. Sometimes the nausea meds couldn’t alleviate it but it was just dry heave vomiting off an on for 15 or so minutes.
It’s not fun for sure but it isn’t pure misery either. You’ll be fine with a positive disposition.
Posted on 11/3/21 at 8:33 pm to bmela12
quote:
Don’t play around with the prevention stuff like breathing exercises and mouth washes
Forgot about this. When your appetite already sucks, you don’t need thrush/esophagitis making things worse. Use nystatin/magic mouthwash regularly. And make sure to swish and swallow (that’s what she said) to prevent esophagitis, and not swish and spit.
Don’t forget to get immunizations when recommended by your oncologist. Not trying to start a covid pissing match, talking about tetanus/mmr/etc. And make sure family doesn’t take the intranasal flu vaccine just before transplant. Injection is fine.
Posted on 11/3/21 at 8:43 pm to Horsemeat
My Cousin recently did this to treat bone cancer. He came through it very well. He’s doing fine and is in remission,
I wish you all the best and I will say a prayer for you.
I wish you all the best and I will say a prayer for you.
Posted on 11/3/21 at 8:47 pm to Horsemeat
My brother donated not once but twice to save a woman’s life. Last he heard she is still alive. Unfortunately, he never got to meet her.
Posted on 11/3/21 at 8:50 pm to Horsemeat
Wish I could answer your questions and offer more than thoughts and prayers. They seem an inadequate platitude, but I offer them sincerely.
This post was edited on 11/3/21 at 8:51 pm
Posted on 11/3/21 at 8:55 pm to lynxcat
I donated 10 years ago, almost to the day, based off a swab taken in 2001 while on campus in Fort Collins. Donation was not bad at all, hope the recipient is doing well but I have no idea how it worked out. If you have the chance, get yourself in the registry.
My only regret was not getting the ‘Bone Donor’ t-shirt I asked for. Seriously though, get in the registry. Prayers for your recovery.
My only regret was not getting the ‘Bone Donor’ t-shirt I asked for. Seriously though, get in the registry. Prayers for your recovery.
Posted on 11/3/21 at 9:17 pm to Horsemeat
Sister went through this, she is still cancer free six years. All the best, you got this.
Posted on 11/3/21 at 9:21 pm to Horsemeat
My 78 year old grandmother went through exactly this going on two years now.
It isn’t fun, but you can do it. Being tired all. Of. The. Time. Was her biggest gripe. Biggest thing she preached was the ability to stay away from the world for almost a year while your immune system is essentially reconstructed.
It isn’t fun, but you can do it. Being tired all. Of. The. Time. Was her biggest gripe. Biggest thing she preached was the ability to stay away from the world for almost a year while your immune system is essentially reconstructed.
Posted on 11/3/21 at 9:26 pm to Horsemeat
Multiple Myeloma?
I am sure others have a similar procedure, but what my mone ended up doing was having her own stem cells harvested they they NUKED her with Chemo then gave her back her cleaned up stem cells. She was never healthy enough to do the bone marrow transplant which was suppose to be a much longer term solution.
I am sure others have a similar procedure, but what my mone ended up doing was having her own stem cells harvested they they NUKED her with Chemo then gave her back her cleaned up stem cells. She was never healthy enough to do the bone marrow transplant which was suppose to be a much longer term solution.
Posted on 11/3/21 at 9:28 pm to Horsemeat
I don’t, but I have bone problems and have had two major surgeries dealing with my issue, and from what I hear bone marrow surgery is the most painful surgery there is and by far. Say no to the opioids and get dosed up to the eyeballs in THC instead. It’s going to suck, but it is definitely the step you need to take. Godspeed my friend.
This post was edited on 11/3/21 at 9:29 pm
Posted on 11/3/21 at 10:19 pm to Horsemeat
I completed an Autologous stem cell transplant in August of last year at MD Anderson. bmela12 is pretty much spot on with what you will experience. I was there during the Texas lockdown for covid. We had to rent an apartment in the medical center area. First week was base line blood work, tests and inserting of my port. Second week was stem cell harvest. Third and fourth week was hospital stay. Fifth and sixth week was spent laying low in apartment, visiting the hospital every day for baseline bloodwork until counts came up.
I'm pretty hard headed and went in with the attitude of making this treatment my b$%^h. I pledged to myself that I would walk the halls and eat something every day no matter how bad I felt and I stuck to it. I was told by the nurses that exercise and nutrition go a long way in shortening the recovery. I don't know what kind of chemo they will give you, but I was advised to eat plenty of ice during the first couple days to minimize throat symptoms. I've had 3 PET's and everything is headed in the right direction. I am currently redoing all of my childhood immunizations as they are erased just as your immune system will be. You are bigger than the treatment and disease. Most importantly, don’t let the procedure overwhelm you mentally. Yes, it’s a ton of crap, but find a project or something to focus on while in the hospital. Hang in there brother. You and your family are in my prayers.
I'm pretty hard headed and went in with the attitude of making this treatment my b$%^h. I pledged to myself that I would walk the halls and eat something every day no matter how bad I felt and I stuck to it. I was told by the nurses that exercise and nutrition go a long way in shortening the recovery. I don't know what kind of chemo they will give you, but I was advised to eat plenty of ice during the first couple days to minimize throat symptoms. I've had 3 PET's and everything is headed in the right direction. I am currently redoing all of my childhood immunizations as they are erased just as your immune system will be. You are bigger than the treatment and disease. Most importantly, don’t let the procedure overwhelm you mentally. Yes, it’s a ton of crap, but find a project or something to focus on while in the hospital. Hang in there brother. You and your family are in my prayers.
Posted on 11/3/21 at 11:29 pm to Ric Flair
quote:
Did the stem cells smell like spaghetti o’s?
Ha! I remember it tasting like tomato sauce. Weird stuff. Oh and the “re-entry” of cells was the most anticlimactic event. I don’t know what I was expecting, but 30 minutes maybe and you were back to your soap opera?
I just did CAR-T and the cell infusion tasted like canned corn. Spot on.
Posted on 11/4/21 at 12:00 am to bmela12
I have nothing to add as far as experience with this, but I do want to say that reading this thread from the beginning has been very inspirational to me. The experiences that some of you have had (and lived to tell about) are truly remarkable. And your willingness to share is also a blessing.
Next time I "think" I'm having a bad day, I will think about this thread and realize that I really have no clue what a "bad day" is compared to what some of you have experienced.
Best of luck to you Mr. Horsemeat.
Next time I "think" I'm having a bad day, I will think about this thread and realize that I really have no clue what a "bad day" is compared to what some of you have experienced.
Best of luck to you Mr. Horsemeat.
Posted on 11/4/21 at 12:13 am to Horsemeat
Keep the rubber side down and the bugs off the glass
Posted on 11/4/21 at 12:59 am to Horsemeat
Wish you the best. I was lucky enough to save a person through transplant. Sign up for Be the Match guys.
Posted on 11/4/21 at 1:16 am to Horsemeat
My only experience was as a potential donor. I was a match for someone when I was stationed in Korea. They were about to plan for me to fly to DC then the recipient decided not to go through with it. Of course, they couldn't tell my who it was or why they decided to decline. It was sad actually or perhaps that person made peace.
Overall, cancer sucks. I have had family members go through with it. I have one cousin battling colon cancer at the moment. I hope and pray for the best, Horsemeat.
Overall, cancer sucks. I have had family members go through with it. I have one cousin battling colon cancer at the moment. I hope and pray for the best, Horsemeat.
This post was edited on 11/4/21 at 1:18 am
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