Wishing the best for you bud.Ripping huge farts!
A week ago Monday, I had my first round of chemotherapy, two days worth. They gave me medication to take which turned to be even worse poison than the chemo. On Wednesday I was able to hold it down after chasing it with pho broth. Thursday was a different matter, no pho broth, my brain sent my stomach the signal "get that garbage outta there". I'll spare the gory details of what happened next, it lasted from Thursday afternoon until 5:00 AM Friday morning.
This week was somewhat better, I felt like Curly Howard. He said he tried to think but nothing happened, I had waves of nausea but nothing happened. I was told by the nurse who administered the chemo that I could eat what I wanted but I had to avoid alcohol and spicy food. I tested what she told by having Thai Green Curry for lunch. Not long after, I had the most horrendous after taste in my mouth. It was like I had eaten Ceiling Cat's pussy with Homelander eyes. Then it got spectacular, the spirit of Andre the Giant possessed me. I started ripping some of the longest, loudest farts in my life...it was extraordinary. Needless to say that new Korean Restaurant that opened up in my neighbourhood will have to wait. My oncologist will have to explain why she though I could handle two poisons at once.
Jake explains how Andre got the Fezzik role in The Princess Bride.
I'd like to know, how did they diagnose your cancer? For me my spleen became enlarged, without taking that into account my GP assessed I'd given myself sunstroke by overexerting on my hike during a very hot and humid day.He called me back after the cardiologist requested a blood test. I had a stent put in in the winter of 2021.Worthers were my salvationWhen I lost my tastebuds....oddly enough They were the only things I could taste...no other foods.
Von, you can do this! Get well and beat this fucking cancer.Thanks for all the well wishes, I'm hoping that I'll be well enough to eat Christmas gnocchi. Funny thing, fresh fruit makes me nauseous but canned fruit doesn't. I don't want to become dependent on the nausea medication, so I eat peaches in syrup when I sense it coming on. I bought individually wrapped mallowpufs for the Halloween collective basket. I won't be taking part.
1st time..woke up in morning stretched my neck side to side..and noticed tightness on right side...felt around and notice small lump..size on my pinky nail...since S/O is a nurse ..she che ked and said get to the DR....and rest is history
I also did a barium swallow and it showed a large mass under my breastbone plate..didn't know it was there..A-symptomatic..if I didn't find the little lump the larger mass would kept growing until it was too late
2nd time..lump just above clavical did biopsy and yup back again..
3rd time ..was having coughing fits to point of choking..Did CT SCAN..and several tumors surrounding my esophagus..had to use experiment chemo drug cus on my A-Fib and closeness to heart..so couldn't do just radiation..
As far as foods
Hard liquor out
Beer is beverage of choice now
Spicey foods out
Semi bland in
Thats interesting about Healh Canada but not surprising to me - I've dealt with them on the diagnostics side for 30 years and it's so sad that they so often have their heads up their ass. Glad you were able to afford what I'm sure was a hefty price tag to get treatment. I think a lot of people may not even be aware that alternative places for treatment exist.At PMH they could not come up with DX. The problems in Canada they do not perform mutation study after Bone Marrow biopy. What I have is very rare forum of blood cancer. I decided to attend MD Anderson, after BM and genetic mutation. Proper DX was made. In Canada there is not one single hematologist who is familiar with the condition at the time of my DX.
What Is Waldenstrom Macroglobulinemia?
Waldenstrom macroglobulinemia (WM) is a type of non-Hodgkin lymphoma (NHL) that produces large amounts of an abnormal protein (called a macroglobulin). Learn more here.www.cancer.org
PMH now has hired top doctors from Dana Fabre on contract basis to teach their faculty. Health Canada still does not allow mutation studies. Unreal. I have been in Clinical remission for almost 7 years.
It's all in the mind brother..and support of family...I wanted to say fuck it and curl up and wait for the inevitable...but I still had so much I wanted to do..so I just decided FUCK YOU!!!Mingia! I though I was tough but you thumper19474 have me beat by a country mile. The oncologist put me on steroids to reduce the swelling in my neck. I wasn't expecting shitstorm which happened due to me over indulging during Thanksgiving. Even though I had priority I still spent 9 hours in Emergency.
Here's a food recommendation for you, not only will the brain tolerate, it welcomes it. I have whenever I have a noticeable energy crisis and cant get out of bed.
For 2 years PMH made my life hell. They could not make DX and kept pushing drugs on me.Thats interesting about Healh Canada but not surprising to me - I've dealt with them on the diagnostics side for 30 years and it's so sad that they so often have their heads up their ass. Glad you were able to afford what I'm sure was a hefty price tag to get treatment. I think a lot of people may not even be aware that alternative places for treatment exist.
I know we don't know eachother but I'll be thinking of you pal. You got this. Keep hanging in there. Kick cancers ass.Ripping huge farts!
A week ago Monday, I had my first round of chemotherapy, two days worth. They gave me medication to take which turned to be even worse poison than the chemo. On Wednesday I was able to hold it down after chasing it with pho broth. Thursday was a different matter, no pho broth, my brain sent my stomach the signal "get that garbage outta there". I'll spare the gory details of what happened next, it lasted from Thursday afternoon until 5:00 AM Friday morning.
This week was somewhat better, I felt like Curly Howard. He said he tried to think but nothing happened, I had waves of nausea but nothing happened. I was told by the nurse who administered the chemo that I could eat what I wanted but I had to avoid alcohol and spicy food. I tested what she told by having Thai Green Curry for lunch. Not long after, I had the most horrendous after taste in my mouth. It was like I had eaten Ceiling Cat's pussy with Homelander eyes. Then it got spectacular, the spirit of Andre the Giant possessed me. I started ripping some of the longest, loudest farts in my life...it was extraordinary. Needless to say that new Korean Restaurant that opened up in my neighbourhood will have to wait. My oncologist will have to explain why she though I could handle two poisons at once.
Jake explains how Andre got the Fezzik role in The Princess Bride.
Wow .This seems to be more about hospital and provincial protocol rather than the welfare and health of the patient. This pisses me off but I've dealt with Cancer doctors being idiots.For 2 years PMH made my life hell. They could not make DX and kept pushing drugs on me.
Everyone can get 2nd opinion from Md Anderson for about 1.2K. They will request the slides from the hospitals but not all the hospitals are willing to give it. My aunt who attended Sunnybrook ended up in Hopkings. They requested slides 7 times but to no avail. They started from scratch and she is doing well. Her daughter is US citizen and she hardly pay for any medication.
My biggest worry at the moment is preventing my blood from going hypoglycemic, that could kill me. I drank two cans of ginger ale last night, just checked my blood sugar and got a reading of 5.2 just above the low end. Once I get to another round of chemo, I have to take the steroids again, that will spike my blood sugar to almost double digits. The oncologist put me on steroids for a week after my throat stated to swell.It's all in the mind brother..and support of family...I wanted to say fuck it and curl up and wait for the inevitable...but I still had so much I wanted to do..so I just decided FUCK YOU!!!
BRING IT!
I was on prednisone..for 5 days after each treatment..had me wired..couldn't sleep antsie...full of energy...called the S/O...while she was on nights..told her...and she said if I was so wired..then clean the oven!!...LOLMy biggest worry at the moment is preventing my blood from going hypoglycemic, that could kill me. I drank two cans of ginger ale last night, just checked my blood sugar and got a reading of 5.2 just above the low end. Once I get to another round of chemo, I have to take the steroids again, that will spike my blood sugar to almost double digits. The oncologist put me on steroids for a week after my throat stated to swell.
I won't give up either, Arnold would say I was a pussy.
I have 4 tablets of Dexamethasone to take before and after the chemo. The oncologist would not have sanctioned chemo if the swelling of my neck didn't go down. That would have been annoying, having to go through a real life M.A.S.H scenario with a straw in my planger gap so I could breathe. The roids worked.I was on prednisone..for 5 days after each treatment..had me wired..couldn't sleep antsie...full of energy...called the S/O...while she was on nights..told her...and she said if I was so wired..then clean the oven!!...LOL Gotta have a sense of humor during those times
I wish you all the best with your recovery. You got this!I'm assuming Oakvilleguy's father didn't have access to zofran, anti-nausea medication the oncologist put me on. I should have asked what type of chemo I was on. I'll know as I'm scheduled for another round after Remembrance Day. You're right about the loss of tastebuds, which is why I went for the Thai Green Curry. Not expecting the horrid mouth feel I had aftermath...like I'd just eaten Sexy Hucka's rancid pussy. I couldn't get away with one cheek sneaks after I went Andre, everybody would have known.
thumper what were you diagnosed with, I have Non Hogkins Lymphoma. Being such a hard luck guy, the Mario Lemeiux version was not in the cards.
In other news Bill Maher should invite Francesca Fiorentini on Real Time.
Gators which MD Anderson Clinic did you go to, the one in Ohio or in Dallas? I've never been to Texas always wanted to go there. I had trouble understanding some of what you wrote and didn't want to look like a Friends moron.At PMH they could not come up with DX. The problems in Canada they do not perform mutation study after Bone Marrow biopy. What I have is very rare forum of blood cancer. I decided to attend MD Anderson, after BM and genetic mutation. Proper DX was made. In Canada there is not one single hematologist who is familiar with the condition at the time of my DX. PMH now has hired top doctors from Dana Fabre on contract basis to teach their faculty. Health Canada still does not allow mutation studies. Unreal. I have been in Clinical remission for almost 7 years.