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Updated on 12/12/2024

The amount collected in our fundraiser is total amount from Siepomaga. It takes up to 3 business days to update the full amount. Thank you for every payment! 🚀

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This year has been a time of great change for me – both in my personal life and health. It seemed that I was getting back on track. My tests from March and June showed regression, but today's results show progress. It is often said that illness, or rather its progression, can be a symptom of recovery – I really want to believe that. After all the decisions I have made and the emotions that have accompanied them, I hope that things will only get better from here!

Unfortunately, my last MRI scan showed progression of changes in my liver and bones. Despite this, I am incredibly grateful that the rest of my body remains "clean". 😊

Standard treatment in Poland offers me chemotherapy – another one whose effectiveness is not certain. However, by pure chance I came across the story of a woman who was operated on in Germany, in Magdeburg, by Professor Maciej Pech – a specialist in liver diseases. The professor got to know my case and offered his help, of course in consultation with my doctors in Poland. I was offered one of two possible treatments: liver brachytherapy (2 or 3 treatments) or Liver radioembolization. The decision on the method will depend on the results of MRI using a special contrast. Subconsciously I feel that it will be brachytherapy.

But here comes the problem. Although everything is going well, Polish insurance is not valid in Germany. I can only have the procedure done privately, and the costs are enormous.

Medical costs

Radioembolization consists of two stays:

• First stay: evaluation for radioembolization - estimated cost is 9180 euro, to this must be added 535 euro flat fee for foreign patients, which gives a total of 9715 euro.
• Second stay: radioembolization - estimated cost is 27,375 euros, plus 535 euro flat fee, i.e. in total 27,910 euros.

Brachytherapy: the cost of one treatment is 6425 euro, to which should be added 535 euro flat fee, i.e. in total 6960 euroThe number of treatments needed depends on how many lesions can be removed during one visit.

When I thought I would no longer need to ask for help, life presented me with a new challenge. However, I have faith that everything will unfold as it should for my highest good.

Thank you for every form of support. ❤️

On May 22, I finished the 20th cycle of Paclitakel chemotherapy. After it, I am now receiving Endoxan, which is intended to maintain my 7-month treatment.

In the meantime, we checked my markers, which are very low, so it's really great. I also had a PET/CT scan performed, which showed that two lesions in the liver had disappeared, some in the bones had receded, but three were still present. My doctors' opinions are confirmed - they are satisfied with the results! I am too - of course I would like it to be nothing, but I am happy with these small and at the same time great successes!

Due to the fact that some changes remained in my body, I decided to perform a liquid blood biopsy, which is to show the number of circulating cancer cells and what receptors are floating in my blood, i.e. the so-called biochemistry of tumors, so as not to do a biopsy. I will know the results soon.

The day after my 37th birthday, I go to the gynecology ward to have my ovaries removed, so it will be an additional burden on the body, so I am not slowing down when it comes to supporting my body - both through infusions, diet and supplementation.

Recently I spent PLN 7,000 on the examination plus the infusions that I was recommended, so I still incur huge costs related to the treatment.

Fortunately, the culture results did not show anything dangerous. Only skin bacteria that were sensitive to all antibiotics were grown. So I underwent 10 days of antibiotic therapy. Due to all this, I couldn't have chemotherapy, so my treatment was extended until the end of May, up to 20 doses. In the meantime, I also received the results of the Maintrac test on circulating cells, as well as the effectiveness of the drug that was offered to me after chemotherapy. The circulating cell results are quite low, 250! This is a great result because I managed to get 1500! I have to wait another 2 weeks for the stem cell results. Unfortunately, the sensitivity results for the drug Capacetabine were only 30%, so there is no point in taking it because I would only be hurting myself, so we have to choose another drug, hoping that it will work. I can't check it anymore because the cost of such a test is another PLN 3,000. We will monitor the markers, which are now even lower than they were in March, so it's very good.

What's next? - On April 16, a new port was installed, and on April 17, another chemotherapy was administered (16). Further doses will be administered in the following weeks. Once completed, transition to supportive care. Further therapy to support my immunity, which amounts to approximately PLN 3,000 - 4,000 per month (there are more such treatments during the week when I am receiving chemotherapy).

Unfortunately, the funds in my fundraiser have decreased due to sensitivity tests, hence my huge request for donations. I trust that my oncological journey is coming to an end and I will soon be fully cancer-free!

The surgery was successful, Ola feels good and has no complications. She will probably have surgery to remove the lymph nodes in a week.

New news from me - I had an MRI at the beginning of March and the results are great, as are the results of all possible markers and bioresonance. The changes are rolling back, one has disappeared, and the most important thing is that the changes are no longer active! They do not have the so-called diffusion restriction. Holistic treatment works! We are going for total health :) but this road is bumpy...

I will be given chemotherapy drugs until the end of April. After completing chemotherapy, I will receive complementary treatment in the form of a drug called Capacetabine. It can also cause a number of side effects, but not as severe. I have to constantly perform my complementary treatments in the form of infusions, supplementation, hydrogenation - that's what I do, because you can see that it works :)

There's never a dull moment for me, and sometimes I really want to. After the last dose of chemotherapy No. 13, I developed angina and had to take an antibiotic, which I had not taken for 7 years. After finishing the treatment for angina, I started having problems with my infusion port - severe redness around it. The decision was made to remove the port and perform a culture test. I'll get the results soon, but regardless of the results, I'll have to install a new port on the other side. Fortunately, it is done under local anesthesia, but when it comes to stitching, it won't be very pleasant...

My doctor is still considering whether to continue chemotherapy or switch to complementary treatment. What is certain for today is that I will have a maintrack test, i.e. a liquid blood biopsy, which will examine my circulating and cancer stem cells - whether there are many or few of them, and will test my sensitivity to the drug that my doctor wants to give me.

Let's be honest, these drugs are a real pain. Unfortunately, the cost of maintrack research is another one PLN 6,000, so the funds from my collections will practically amount to 0..., so I am asking you for support again!

But! Recently I heard something so beautiful that captivated me: "I'm finishing chemotherapy at the end of April. And then it will be May...". The most beautiful month for me - full of sun, joy, the smell of lilacs, warm evenings. I end the entry with this good thought.

On November 13, I start the next series of chemotherapy - paclitaxel + carboplatin. These will be weekly infusions, as long as my health and bone marrow allow it. Luckily for me, this really is good news. The chemosensitivity results for these two substances are very high, even 75%, so just as I was heartbroken over 2 years ago because I didn't want it so much, today I approach it differently.

Of course, I do not neglect the side of strengthening the body. I've been through a lot over the last 2.5 years, my body makes me feel it, especially during the changing weather, and just as I never complained about pain and avoided painkillers, they are still in my life today. However, in order not to end it sadly, I am constantly and constantly striving for health, and as my friend Beatka says - I am walking towards life and the rising sun! :)

All treatments are available to me thanks to the help of my family, but most of all thanks to you, for which I thank you very, very much!!!

The last few months have been a continuous sine wave. Joy mixed with sadness and fear...

After the June description of the study, it would seem that everything is going well and there has been stabilization. I felt and feel really good, the blood test results are also OK. Of course, I didn't stop going for infusions and taking supplements, I also started ozone treatment. Unfortunately, the September CT scan showed changes in the liver. The changes in the bones are stable, but the changes in the liver are something new - and if they are something new, it means that the current academic and complementary treatments do not work. Outside the liver, a pathological axillary node appeared, from which a biopsy was performed. I am currently waiting for the receptor results to know which side to approach the overall treatment. I don't want to give up any of them, because even though something new has appeared, I know how complementary treatment supports me and drives my body so that pharmacological treatment does not weaken me.

This is a difficult situation because both me and my family are approaching the issue for the third time. I am afraid, my husband is afraid, my mother, my aunt, my sister and probably my daughter are afraid, although the 7-year-old doesn't fully understand what is happening yet. My friends and the rest of the family are afraid. Nobody wants to hear words about the disease from the mouth of a 36-year-old...

While waiting for the biopsy results, I have already scheduled consultations with doctors who, together with my doctor, can come up with something best for me. Perhaps it will be possible to perform thermal ablation of my lesions. Apart from treating the physical body, of course, I do not slow down and I work emotionally through various types of therapies created by wonderful people, for whom I am extremely grateful.

As I asked before, today I am asking for your support, sharing and donations, because I have to start over again the whole process of developing a peri-oncological, integral approach to recovery. New consultations, additional paid tests, frequent and strong complementary therapies to block the path for cancer cells to reproduce in any way - this is currently my goal. Also (and probably above all) my goal is to heal the mitochondria so that the immune system recovers and can fight cancer cells on its own!!!

Thank you from the bottom of my heart, Ola and family.

I have good news - the CT scan from the beginning of June shows regression of the cancerous changes. I am glad that my various health-promoting activities are bringing results. I believe I'm on the right track. I constantly need systematic treatments to strengthen my body and support treatment and rehabilitation. This incurs huge costs every month, so the funds on my subaccount are "draining" at a dizzying pace. I am very grateful to you for every donation and I continue to ask for your support, without which I will not be able to cover all the costs related to the treatment.

Thank you!

The last few months have been intense - targeted therapy during which I took Abemaciclib, Faslodex, Reseligo and zolendronic acid. It was another challenge for my body.

The blood results weakened, so at the same time it was necessary to intensify the supportive treatment to strengthen the body. I will have a follow-up CT scan in the coming weeks.

Osteolysis caused by the metastasis resulted in a defect in the sternum. For this reason, I need specialized, manual rehabilitation to gently restore my body to its former condition.

The treatment costs are huge (approx. PLN 2,500 per month) and if it were not for your financial support, I would not be able to afford comprehensive activities.

I really want to continue to have the opportunity to use supportive treatment and private rehabilitation because I see its positive impact on my body.

Thank you very much for your support so far and I will be extremely grateful if you would like to continue supporting my treatment journey!

Unfortunately, once again I have to face an experience that is not the most pleasant. Recurrence in the sternum bone that has caused osteolysis of the sternum bone. Some changes were already visible in the imaging tests I had in September, but the radiologist simply didn't describe them...

If, if... - but there's no point in guessing. I have to get back on my feet and act, that's why the collection has been started again. I am collecting funds primarily for my strengthening activities and probably for rehabilitation, supplementation and numerous consultations.

I started taking Abemaciclib, so my body needs proper strengthening even more at the moment, which is why I am also undergoing supportive treatment to better endure the whole process. As a result, the costs of supplements taken have increased significantly.

Ola has had her last planned surgery and has her final prostheses. Imaging tests gave good results, there are no changes that could indicate recurrence. Ola also regularly tests the number of cancer cells. To maintain your current condition, it is important to continue treatment. Ola will undergo 3 more treatments of herceptin, then zolendric acid, and hormone therapy. Infusions supporting the body help maintain the results and rebuild the body's immunity, their cost is PLN 2,000 per month.

Yesterday Ola was on Herceptin 11, today she has 7 left. She had an ultrasound with elastography: ovaries, abdominal cavity and breasts. The results were very nice, everything was clean and unchanged!

On February 1, she will have blood drawn for a maintrac test, and on March 2, she will have surgery to replace the expanders with the final prostheses. Everything is heading in the right direction, keep it up!

Ola has already had her second surgery - lymph nodes removed, all are clear. That's excellent news! Ola is also starting chemotherapy and her first party is already behind her.

Ola is after surgery. We are waiting for histopathological results that will help determine further treatment.

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