I've never written about Karinna, because I've been home and she's recovered physically and mentally very well. The first check-up was supposed to be in early October, but I noticed a ganglion increase again, so the doctors here decided to come early for investigations. Analyses, pet ct, MRI. Indeed my observation has come true, the ganglion has grown, and besides the visible one there are others around it, plus the lungs and cervix.
Since I'm not quiet like that and her doctor, she didn't like those ganglia even if it's not a relapse of the disease, and I hope it isn't. Well, along with other doctors, they're looking for the best solution for Karinna. Today I went to the surgeon to see if she needed surgery, the surgeon said yes, but here we have a problem. The ganglion that is visible can easily remove it but does not know how to proceed with the ganglia that descend to the lungs, and he in turn must work with other doctors to make a decision . Okay it's not
I get a lot of messages, and I apologize for not being able to answer every one of you. As soon as I have news I'll let you know.
It seems that our happiness lasted only 1 month but with the help of the Good Lord, v9m overcome and this obstacle, as we have overcome them all with brio, and my Karinnuta will be victorious again, I know that the Good Lord will be by her side as it always has been.
We kiss you and wish you a beautiful day

Hello our dear 💗
I don't know how or with what to start. With the news, with the gratitude I have for all the people who have been with us? I begin with the news, I'm sure you've been waiting with your breath, just like us. Following the final investigations and analyses, the news is that, KARINNA , GARGARITA NOASTRA INVINS THIS NEMILOASA BOAL . yes, that's right, the torment, her suffering is over. The good Lord was by her side, and he never let her. She will still undergo home treatment, which is extended for 1 year, all chemotherapy. Following investigations, the MRI found that she has a cyst on her left kidney, so she will be closely followed by a pediatric nephrologist. The usual tests, will have to be harvested weekly, as usual. Tonight we will set off for Romania, we will come by ambulance. After so many months, of torment, of suffering, of helplessness I'm still confused and even in shock, I still can't believe it's all over. We'll be back in control in a month and a half. I still can't believe that in a little while I'm going to hug my big girl, see them together, see my parents again.
I bow to you 🙇 ♀️, without you, my child would not have been today, so good. First of all, thank God, thank God, thank you for not turning your face away from my child, for holding with your teeth for her to be piternica and to rise from the bed of the disease, thank you on my behalf, every time you gave me strength, to get over the helplessness of the mother. Thank you beautiful people, for being with us, God give you everything. Thank you from the bottom of my heart "Association Save a Heart" especially Lord Vlad Pie for all your support, you are a wonderful man with an enormous soul. Thanks Narci Nargıs, a being so dear to me 🥰 thanks for everything, you were always with us, even when you couldn't physically, thank you that no matter the time, desperate being in the hospital you spent hours talking to me on the phone, you're wonderful, thank you. Thanks Gina Keloğlu, thanks for being with us, all the time, you were always available, when it was the hardest, you didn't move off our section 🙏 you're wonderful. Last but not least, thank you to the Turvia Medical Framework, I am forever grateful that you have healed my child, and given him the chance to have a normal childhood and life.
Thank you from the bottom of my heart to all of you who have been with us. Even if we leave, I'll keep you updated on Karinne's condition, I know you love her, because you've proven it. Thanks for your financial support, for your beautiful words, for your prayers.
All I want is for all the little children trying to heal and get up from the bed of the disease.
We embrace you with love. 🤗🤗🤗💗💗💗

Karinna yesterday started treatment with iodine, today being the first day of imaging in MIBG. She was very good, I managed to put her to sleep for the 25 minutes she was in the machine 🙏 so she was not given anesthesia. After finishing, the doctor wanted another five-minute video, because he thought something suspicious in the neck area. (she also has a ganglion at the tumor removal operation). I'm very anxious about that. Tomorrow we have the second imaging in MIBG, and the last by the way, but it will be anesthesia, because the time in the device will be longer, and the machine will move to be able to catch it from all angles. Then we'll wait for the final results, check with our oncologist to see what else he tells us. I pray to the good Lord that everything will be well and she may have escaped this disease, that she may have been defeated and never come back

Good evening our dear son 🤗 know that I have not written for a long time, but we have been in a continuous waiting . Today we started the investigation. Today we had the MRI 🙏 following that tomorrow to go again to the hospital because, Karinna must repeat the covid test, to make sure that everything is okay for next week's imaging, next week Monday we will start iodine treatment, (Monday to Friday). Tuesday and Wednesday we have imaging in MIBG.
We hope with all our heart that next week at the end we will have all the answers, and if everything is ok, the doctor said he would allow us to come home until the first check-up, of course with treatment at home.
Karinna feels very good, being energetic, playful and eating
Much was, little is left 🙏 this little seems to me an eternity.

He discharged us today 💃. I was hoping we wouldn't go back to the hospital unless we had checked in. The doctor decided that we go to the hotel, in his urine he found a microorganism, that's why we have home treatment. On Friday we are going to go for checks and tests, and we will probably also determine when we will start the investigations 🙏🙏🙏. Last night they gave her a erythrocytes transfusion, because her tests are dropping after treatment. With God's help her condition will improve even more after the period of aplasia 🙏🙏🙏.
Thank you from the bottom of our hearts for continuing to be with us, and you will still think of us, and you give us messages every day, which is a huge 🙏🙏🙏.
Many kisses from us 💋💋💋💋

Hello, our dears. We're hospitalized. Yesterday Karinna had surgery, her condition after the operation was a grandmother's. He's been put back on, so we can continue treatment. Today we are going to start the last chemo cure, which will be reduced by 25%, due to problems encountered on the course. We hope, with the reduction of the dose, that we will not have any more aggressive side effects as before. After this cure we will begin the investigations, and in the wake of them we will see what we have to do, if she needs further treatment, or this is where we finish everything. I hope with all my heart, to end this, and this will be our last internment. Then we'll see what the neurologist will say if we're going to have physiotherapy sessions because of the legs. Our journey is not over yet, but I hope it will be over as soon as possible.

Hello, our dears, 💖💖 I haven't written 🤗🤗 in a long time. Elena's condition has improved, everything is under control now, the infection has fallen considerably. We're still in the hospital, she's undergoing treatment for fungus and antibiotics. We see what the infection doctor will say about the treatment for the fungus, if there are enough 10 days of treatment, tomorrow he will discharge us, if the doctor says we have to follow 14 days of treatment, we remain hospitalized 🙏🙏.
As you know, we would still have a cure and we should finish, but it is not clear what will happen, because the last two cures have been so strong that we have always faced infections. We don't know yet how she's going to be given the treatment, she's not wearing any more, through her veins she can't, that they're going to give in, and so there's no more veins in Karinna, the last ones with the ports, makes the gentlemen, to have signs of doubt, so you'll have to make a commission first, in which a decision will be made regarding Elena. , how to administer the treatment, and how it will be the last cure. Our doctor, she told us that we are struggling with a very severe diagnosis, she has to follow all her chemo belts

Elena's condition improves by the day the infection has decreased, she recovers slightly. She's not sitting in her butt yet and she's not very receptive, but every day we take one step. The infection decreases, she no longer needs oxygen, manages to catch one thing vu hands, and can move alone. Today they told us the results of the fungus, she really has Candida Albicans but with God's help we get rid of it if it progresses every day a little bit, it's a sign, that it responds to treatment for the fungus. I went to Eco at the heart today, everything is in normal parameters, we still have to do to the liver, we hope that the fungus did not get to walk at all in the body.
She's very scared, her brangives us headaches, she gives in every day, she gets tested every day, as is normal, and she has to be stung many times, because she has no veins.
All evil for good with God's help overcome this obstacle, easily with small steps.
You're wonderful people, thinking of us in such large numbers. We kiss and hug you with love!

You're all wondering about Elena's condition, I'm sure of that, which is why I want to keep you all informed. She was a little better today 🙏 she didn't get a fever that often, but the danger didn't go by. Despite all the efforts made by the doctors here, the fever has still persisted, and she has not recovered with anything. I can't even bend a leg, it's just standing right, and sitting in the butt no longer specific. Today she also had her second dose of immunoglobulin, as I told you, that she is also undergoing immunoglobin treatment with the hope of being well. ( $4000 is the cost of immunoglobin). Today, there's a lump on his body, the doctor told us it's because of the very high fever and he's never leaving again. Because all her tests are coming out good, and they can't figure out how to figure out where this infection starts, now the doctor has told us that, along with the other doctors, they decided that tomorrow to go back into surgery, to remove the port, that would be the only start of the infection, considering that in the past we faced problems because of the other port in the country. Following, that the following treatments are done through a catheter, attached to the neck, head or wrist of the foot but that's what we'll talk about next. Tomorrow's surgery will be performed depending on her condition tonight, if the condition is for the better, there will be no more surgery, but if the condition is still that way, they will put her in. I'll keep you updated.
We talked a little bit about chemotherapy, we only had one cure left, and we were going to finish the treatment, it's not known exactly, if the next cure will go to the treatment doses or change the treatment protocol, first to get rid of this infection that, grows by the day with all the efforts made by the medical professional.
We kiss and hug you with love!

We all ask you about Elena's condition, I get a lot of messages, but I don't have time to answer each of you, I apologize. Her condition didn't improve. The fever still persists, and it seems that nothing can handle it to stop it. Today our doctor decided to do an X-ray on his lungs, we are waiting for the results, because he has symptoms, he has been taken and the sample for Coronavirus we will wait for the results with his breath. He's been tested, the CRP is still, grown, taken from the port, considering that we've had problems in the past, but at the moment there's nothing about the port, what tests have come out. It's also attached to oxygen. We've been on the brink of intensive care, we haven't crossed the hump yet, but we're still here on the oncology ward, I hope the good Lord will help us stay here, and not take her to therapy, here, hospital policy, don't let mom sit next to the baby. From today we started immunoglobin treatment, it is not in our proforma treatment, so the costs are extra, I do not know exactly how much it will cost, but as soon as I find out, I will let you know, must do 5 days treatment with immunoglobin. In parallel with the antibiotic, he'll also get a treatment for the fungus. Because of the fever, and her pulse, sometimes it's high. Everyone's trying to keep her in position as long as possible.

I pray to the good Lord to keep her in position and she will be fine. I can't answer all of you, I'm sorry.

Hello, our dear son 🤗 I haven't written anything to you, but time hasn't allowed me. We were discharged yesterday, being all right, but today, we are back in the hospital, hospitalized, because Karinne's condition did not allow us to stay "home", so we came back because she was getting high fever😪, infection 😪. We're staying in the hospital until she recovers, and our doctor will decide we can be discharged safely. Unfortunately, this is the disease 😪 I no longer trust anything, when it comes to treatments, infections of anything, the condition can change from one second to the next. We kiss you and wish you a wonderful day 🤗

Elena's SMS fundraising campaign is over. As a result of the campaign, 27,409 SMS messages were collected 🤗🤗. Thank you so much for getting so involved, thank you to everyone who sent sms.uri, everyone who told a friend to donate. 🙏.
I especially thank Mr. #CodinMaticiuc,for the involvement 🙏 and the Save a Heart Association for giving us the option to donate via SMS.
The fundraising campaign will remain open until the oncologist, following the investigations, tells us that everything is fine, and there will be no need for any other treatments 🙏.
We embrace you with love, and we kiss you, you are wonderful people

Following the fundraising campaign by SMS between 15.05.2020-14.06.2020, 27409 text messages were sent for little Floria Elena.

Thank you for your support and trust!

We are on the fourth day of treatment, Elena has carried out the treatment well so far, only on the first night she vomited, but we fixed this problem and it was not repeated. Today, however, the tests started to drop, so he got a blood transfusion, hemoglobin was small, so it required. 🙏🙏. We continue with the treatment, on Sunday, we should finish it 🙏🙏 with God's help we will carry out this cure. If on the 17th, there will be good tests and they won't be falling drastically, next week months, they should discharge us. This is where the virus was again given a state of emergency, and the doctors prefer to be as close to them as possible, for any unforeseen occurrence 🙏🙏. Everything's going to be fine 💖💖.
Thank you for still being here, next to our 🐞, and fighting side by side with us. Please continue to do so, please distribute, any distribution can mean a donation, donation that can save Elena's life🙏🙏.
➡️Elena kisses you and asks you to stay by her side 🙏🙏

🔴🔴 Today we also have the SMS option, it will be limited, it will be active for Elena 30 days, so please take advantage of this, give as many messages as possible, collect some of the necessary money.⬇️⬇️

From 15.03.2020 until 14.05.2020 little Karina Elena Floria will have allocated for fundraising the short number of SMS 8832

A simple SMS will change his life!

SENT SMS 8832 ELENA MESSAGE

Floria is fine, she's all recovered, there are still small problems but she'll soon recover completely
Finally, our final proforma has arrived. $55,000 (51,000 euros) cost my little girl's life.
It's hard for me to write, it's hard for me to think but to say to a whole world, but...

He still feels very well, except when the veins in the bran and he needs to be stung, or he has to have blood taken daily for tests.
Fortunately the infection started to drop considerably, she recovered very well after last week's surgery. We come with good news, tomorrow he goes back into surgery, to get his port installed, around 12 o'clock 🙏 sure and this surgery will be a success, doctors know what they're doing 🙏🙏. I hope this time we don't have any more problems with the infection at the port.
Genetic tests arrived yesterday. It's good news, and it's bad news. One part came out negative, and the other positive, what the doctors feared the most, came out negative. She's in the middle grade. It's not the best grade, but thank God it's not the last stage. He'll recover, but we need you to recover our 🐞🐞.
The doctor today said the time has come for the next course of chemotherapy, but we'll see after tomorrow what decision will be made. If we stay hospitalized to do his treatment, he'll give us a few days to breathe, and we'll come back to do the treatment.
The treatment plan has been established. We have three more chemotherapy cures in the protocol, one cure from A8 and 2 from A9, and then the RMNs will start, then they will put it in a special device for neuroblastoma, MIBG, 2 days in a row for imaging and if everything is as planned, our suffering is over 🙏🙏. Only she has the power to carry all this, and with any luck we'll only return to Turkey for checks.
To do all this, we need you, so we can cover the cost of treatment, we still don't have a final proforma, I just know they're going to exceed $60,000, when I get the proforma I'm going to attach it here.

Dearly beloved, today we have finished the treatment! Karinnuta is fine 💖💖 her tests are fine, and the infection has started to drop, from a medical point of view everything is ok.
We'll be hospitalized for a few more days until the port is all right. It looks like this easter we'll do it in the hospital, but at least she's fine 💖💖 we'll continue with treatment for the infection. With God's help, next Easter year we will make it at home with our loved ones 💖💖 with the eldest girl.
🔴🔴 Please stay with us until the end, until our 🐞🐞 is well, and regains his right to childhood.

Elena Floria didn't feel very well last night or in the morning, the temperature persisted, so the doctor decided that today we should take a break from treatment, and keep her under surveillance 🙏 if she feels good today and no longer makes temperature, we will continue tomorrow, now we are on antibiotic 🙏🙏🙏. She still can't rest 😥, today she ate a little banana 💖💖💖💖

Elena sends you kisses 😘😘

Our 🐞🐞 will fight 💖💖💖

Please continue to join us, distribute as many as possible, any distribution may even mean a donation, a donation that can save Elena's life 🙏🙏

Dearly beloved, we today checked in for the first course of chemotherapy 🙏🙏, the tests were good, so the doctor decided to stay hospitalized, so that tomorrow we can start treatment 🤗.
We thank you from the bottom of our hearts to all who have remained with us, to those who have made this possible internment of ours 🙏🙏 please remain with us 🙏🙏. God give you everything tenfold 🙏🙏.
Karinnuta is feeling well, I was hoping to feel just as well during treatment and that there would be no problems. Also today, our fighter is doing 10 months of life, I would not have wanted to celebrate them in a hospital bed, in a foreign country, but surely in the future we will have countless days to celebrate, with your help, my little girl will know her childhood

God protect us all.
They come with news, not very good. The operation performed in the country, which the doctor removed from there, was actually a metastasis of the disease, we do not yet know where the "mother cell" is in the body. Things, at least for me, have taken a turn back. All her CDS, and paraffin blocks will be sent to another hospital, to determine the risk of the disease! 😥 Time is precious for Karinna, and we can't wait too long, so we can't wait for the results from the other clinic so Monday has to be admitted, at the moment we're going to get a proforma payment for a single course of chemotherapy, and we have to pay it urgently by Monday, the chemotherapy cure will last somewhere at 6 days , plus the period of aplasia, and in the meantime, we hope to have the other results, to determine everything that is to be established in her disease, and only then will we receive a proforma payment for the entire treatment, and if necessary for transplantation. 🙏🙏
We ask you from the bottom of our hearts to stay with us, without you, we fail, without you Karinna my little girl will never know 😥 childhood. At the moment, her life costs money 🙏🙏 that's why I beg you to stay close to us, so I can see her grow up and play 🙏🙏.