Aleksandra Pomorska

COLLECTION FOR:

rehabilitation, supportive care, doctor visits, medications and other supplements

UPDATES:

Aktualizacja z dnia 15.04.2024 r. 

Wyniki posiewu na szczęście nie wykazały niczego groźnego. Wyhodowały się jedynie bakterie skórne, które były wrażliwe na wszystkie antybiotyki. Przeszłam więc 10 dniową antybiotykoterapię. Przez to wszystko nie mogłam mieć podawanej chemii, dlatego moje leczenie zostało przedłużone do końca maja, do 20 podań. W międzyczasie otrzymałam także wyniki badania Maintrac na komórki krążące, a także na skuteczność leku, który był mi proponowany po zakończonej chemioterapii. Wyniki komórek krążących są dość niskie, bo 250! Jest to świetny wyniki, ponieważ potrafiłam mieć 1500! Na wyniki komórek macierzystych muszę poczekać jeszcze 2 tygodnie. Niestety wyniki wrażliwości na lek Capacetabina wyniosła tylko 30%, więc nie ma sensu, aby ją brać, ponieważ jedynie robiłabym sobie krzywdę, dlatego musimy wybrać inny lek licząc na to, że będzie działał. Nie mogę już jej sprawdzić, ponieważ koszt takiego badania to kolejne 3000 zł… Będziemy monitorować markery, które obecnie są jeszcze niższe niż były jeszcze w marcu, więc jest bardzo dobrze.

Co dalej? – 16.04 założenie nowego portu, a 17.04 podanie kolejnej chemii (16). W kolejnych tygodniach podanie kolejnych dawek. Po zakończeniu przejście na leczenie podtrzymujące. Dalsza terapia wspomagająca moją odporność, która miesięcznie wynosi ok 3000 – 4000 zł (w tygodniu gdy mam podawany chemioterapeutyk, takich zabiegów jest więcej).

Niestety środki na mojej zbiórce stopniały ze względu również na wykonane badania wrażliwości, stąd moja ogromna prośba o wpłaty. Ufam, że moja onkologiczna droga dobiega już końca i niebawem odetchnę pełną piersią wolna od raka!

Updated on March 21, 2024.

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 The changes are rolling back, one has disappeared, and the most important thing is that the changes are no longer active!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 perform my complementary treatments all the time 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 like 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'm 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.

Updated on November 7, 2023. 

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 organization. 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!!!

Updated on October 5, 2023. 

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 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 my current 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.

Update of 26/07/2023 

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 "melting" 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!

Updated on May 27, 2023.

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!

Updated on March 3, 2023

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 it...

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.

Updated on April 22, 2022

Updated on 13/01/2022

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!

Updated on October 21, 2021

Updated on May 27, 2021

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

Updated on April 13, 2021

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

Updated on March 26, 2021 

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

DREAM: