After time travel, I can only beat up the national football team

Chapter 244: Report safety, current situation and the time for resuming updates!
Recently, my mother and I are both doing clinical work, I am in Tianjin and she is in Jinan.

I am doing genetic clinical research on hemophilia A. After one month of medication, the coagulation factor content has increased from 0.5 to more than 90.

This has returned to normal levels, because the normal coagulation factor content is between 50-150.

However, this gene therapy has many hidden dangers, the main one being liver damage, which increases the risk of liver cancer, and these are only stage I mice.

Now, I have to take hormones every day to maintain and enhance factors, and I have to take them for three months before I can stop.

But if the factor content decreases once you stop taking the hormone, you have to continue taking it.

I feel that hormones are not a good medicine. Not only will they cause hormone face and a big belly, but they will also affect many body indicators.

My face and stomach are obviously abnormal now, and there are many red spots on my body. I feel nauseous after taking hormones at night, and I also get excited and insomnia. However, my appetite does increase, which needs to be controlled, otherwise my face and stomach will get bigger.

These are actually minor matters. I was supposed to be discharged from the hospital this Wednesday. But the speechless thing is that when I did a color ultrasound before discharge, I found a 1.1cm*0.7cm mass on my liver.

So, I had another MRI that afternoon, but to my surprise, it was still unclear.

Today, I had an enhanced MRI done again. The outrageous thing is that the enhanced MRI still could not completely confirm the diagnosis. I really didn't expect this.

The doctor said that my case is really atypical and only a biopsy can provide a true diagnosis. However, considering that my genetic medicine acts on the liver, a biopsy is not suitable for the time being. In the end, the only diagnosis is that I have a high probability of hemangioma and inflammatory granuloma. The probability of cancer is very small. It is recommended that I have a follow-up examination within two months.

I am a little panicked now. There is hope for hemophilia temporarily, but then I get liver cancer. I might as well not do this clinical work.

However, the hospital had informed me of the risks in advance, and I decided to accept it after considering it. So even if I was so unlucky in the end, I would have to accept it.

I actually know that phase I gene therapy is very risky, but I have no choice but to take the risk of doing this clinical trial.

My mother's condition was not optimistic. After two chemotherapy sessions, chemotherapy was no longer effective. She had already had bone metastasis and began to have difficulty walking.

So, if I have trouble taking care of myself and start struggling after walking a thousand meters, then it would be really difficult.

At that time, my mother's hospital probably didn't have any good options, so the doctor recommended that my mother participate in a clinical trial, which was also a phase I clinical trial.

We had no other choice at the time because we couldn't afford the medicine out of our own pocket and the medicine that could be reimbursed was not very effective, so we could only be guinea pigs.

Now my mother has participated in the clinical treatment for one and a half months. The bone metastasis has been well suppressed and it is not so painful for her to walk anymore.

However, after a comprehensive CT scan this Wednesday, it was found that the lesions on the organs had not changed much and had not shrunk significantly, but they had not worsened.

I don’t know whether this is a good or average effect. Anyway, there seems to be no other way to treat cancer in the late stage except having money.

Coincidentally, my mother and I attended our respective clinics at almost the same time, and then had follow-up examinations every Wednesday.

We are both safe for now. I hope we can stay safe forever and I also hope my liver can work longer.

(End of this chapter)