“Dr. Kritthai Page Sudiwa: Latest Follow-up Results 6 Months After Lung Cancer Diagnosis”

Dr. Kritthai Page Sudiwa Sick of lung cancer spreading to the brain Revealing the follow-up results 6 months after illness, the latest good signal has arrived.

(16 Apr. ’23) Doctor Kritthai Thanasombatkul 28 years old who opened the page fight diwa Telling about the experience of being sick with “lung cancer”, posting pictures while traveling to Japan. with a message through the page Review your own story since cancer diagnosis. And most recently, a follow-up examination after 6 months of treatment indicated that

Hello, today I’m going to review my story a bit.

Median time to progression 6 months

This 6 month number is very important to me, it means that 6 months after diagnosis, 50% of people will develop this type of lung cancer. with increased cancer invasion and resistant to the main treatment being provided

October 2022

the beginning of the story I was diagnosed with lung cancer that had spread to the brain. I had surgery Get a full body exam receive chemotherapy, radiation

November 2022

After all the side effects, hair loss was gone.
I started to set a new foothold on myself.
decided to open the page fight diwa came up to intend to pass on some small things and it can really deliver

December 2022

The first treatment was followed up at 3 months. The computed tomography showed that the nodules in my lungs were smaller. and the cancer has not spread to other organs The overall disease remains calm.
but a lump in the brain not like that
Because the drug that I got it through the brain very little. Cancer in my brain so I’m happy.
I learned that Our life is extremely uncertain. In the end we will die and we don’t know what day it will be.

January 2023

My condition has improved a lot. I was able to go back to exercising almost as usual, playing basketball, cycling, going to the gym, getting fit back to how I was before the illness.
I have returned to teaching students. got back to work Start making plans to return to normal life.
I have shared with you all my views on the work that we want to do until the last day.

February 2023

Follow up in the brain 3 months after complete radiation.
Even if the lump that was radiated would collapse
But there are 3 new cubes added.
I decided to take a look first. Let me go talk to Nong Suan Kularb first. and talk about it after that If you remember, in that post, I wrote:

“I probably can’t say that anymore and I probably don’t even remember ever coming here,” which I mean exactly.

because after going to the rose garden I came back for another brain exam. the lump that was encountered last time twice as big Together with the addition of new cubes. Now I have 13 stones in my head and I also have seizures.

I needed a full head irradiation treatment. to eliminate cancer that is likely to have spread throughout the brain Which means that my normal brain tissue will also be exposed to radiation. Resulting in deterioration of my brain for sure. just more or less only fast or slow To study another doctorate degree would be very difficult. Even if I don’t want to But it really is the best choice.

March 2023

I started getting light all over my head. how bad luck My brain is swollen I had increased intracranial pressure. I vomited out of my nose with the same force as my mouth.
I slept in the hospital to observe the symptoms. and receiving steroids to suppress inflammation in the brain The medicine works great. But at the cost of its side effects.

After half a month in the hospital I went home and wrote a post saying “Why can’t we die yet?” Because during that hospital bed I really miss giving up.

I have to say here that I am most impressed with this post since the page was opened. Because this post is more than just people saying hello to encourage me. But the people on the page are encouraging each other. Thank you very much everyone. so cute

Two days later I had another severe headache. Brain computed tomography results say The clot in my brain is bleeding and the blood increases the pressure in my brain. I may need surgery to drain the blood.

Fortunately, in the end, the blood supply was not enough to require open brain surgery. Headaches are more likely to be a side effect of radiation. But have to wait for X-rays with electromagnetic waves to see each other again. In the meantime, continue taking anti-inflammatory drugs to reduce brain swelling. which when taking this drug in a row for a long time Causing to take medicine to prevent fungal infection in the lungs along with All blood values ​​were destroyed. Both exercising and dieting well, taking the drug consistently at the maximum dosage. But the bad cholesterol in the blood is much higher than the normal value. It’s a fat value that if I had constricted arteries, it wouldn’t be surprising at all. They also had to take anticonvulsants and anti-dementia drugs every morning and evening. I have pain in my ribs that I don’t know if the cancer has spread to my bones.

Previously, I had booked a ticket to Japan. but from the symptoms described Makes the hope that I will be able to travel and watch it is very funny. Two days before the day of flying to Japan I’m still admitted.

But I tried my best to prepare, prepare medicine, write my history. in case if something happens over there Japanese doctors will surely shed tears for the history that I have prepared. (But the best thing is not to meet him)

very unbelievable
that I went for a walk with Peem in a garden full of cherry blossoms I took Pim to see Mount Fuji. to breathe clean air go to eat delicious food, go to an amusement park wearing a pair of kimonos and I ate Kobe Beef

Yes, I’m still taking massive pills, sleeping 2-3 hours a day, still constipated and constantly monitoring myself seriously.

But I still went with the hope that everything would be okay.

Every morning I wake up Everything that I can still see Every meal that I have eaten everywhere i have gone Every activity that I have done is extraordinary.
Every day that I received I deliberately used it like it was the last time. (because it might really be my last)
I don’t know Am I waking up to see this?
I don’t know Will I have a chance to visit again?
I don’t know I’ll be the first half. or the second half

April 2023

okay

It is now 6 months after I was diagnosed with terminal lung cancer.

“What if it doesn’t respond to treatment?”
“If the disease relapses Or the disease is not peaceful?

It’s a worry that I can’t try to do anything to change its outcome.

I can only take care of my body and mind the best I can. Be patient with everything that comes your way in life.
And hope that everything will be okay.
I can only really hope.

I encountered a lot of disappointments as well. It takes a lot of willpower to come back and fight. But I held on to that hope. ‘Cause it seems the only thing I have

I don’t know what happened first.
Because there is life, there is hope.
or because there is hope there is life

I told Phim on the day I was going for the 6 month follow-up that

“No matter what the outcome He will not die as soon as he knows the result. This evening, we will continue to eat delicious food as usual.”

I had CT scans of my chest and abdomen. Including brain electromagnetic waves

and the 6-month follow-up result was that the right lung nodule had collapsed in half from its original size. The small lump in the left lung is almost completely gone. All of the lumps in the brain are still there, but they are calm and no new lumps have formed in other organs. There was no spread to the bones, liver, kidneys, lungs, or lymph nodes. Only the enlarged pleural lump presses on the ribs causing pain. which can be irradiated at the point of the cube

I have become the “second half” now.

A group of people whose statistics from research cannot tell how long they will live. And the next interesting number is The proportion of those who survived at 5 years was about 20%.

I wish it was me

If I were to summarize the lessons from Nong Cancer during the 6 months that we have been together, it would be that

“Life is uncertain. Eventually we will all die. live in the present Live each day like it’s your last. If there is anything that can be done for others share some good fortune with him and no matter how bad life is Don’t lose hope in life at all.”

day offSongkran like this Many of you may be using the range.day offReward yourself with a trip. Many of you probably have the opportunity to return home to be with family or loved ones. May everyone use the time in front of you to the fullest. Let it be like it’s the last day Because we really don’t know. How will Songkran next year be? Can we still meet?

I’d like to go home and have dinner first.

helloSongkran Dayyes
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I think we have traveled together for a long time as well.
It would be good if there was a “Su Diwa, a collection of books”
Let’s follow.