Help & Save Sarah

Help & Save Sarah Sarah is 7 year old lovely girl fighting with DMG that is a very aggressive cancerous brain tumour.

21/11/2023

21/11/2023
I want to thank everyone who pray for Sarah's health. She came back miraculously, at home and doing better Alhumdulillah.
There is also a bad news that this episode happened because there is progression and bleeding in her tumour that is why she have swelling in her brain. She came back this time, still she has become so weak. There is a strong possibility that she may decline faster now.
We don't know how much time we have left with her but we want to make everyday memorable.
It makes my heart swell with pleasure that Sarah has been loved and so many people who prays for her and thinking about our family. I appreciate it a lot and want to thank everyone. Please keep praying and supporting . https://gofund.me/4d9b0822

Sarah was alright when she woke up in the morning. She was changing clothes when she started feeling weird. Then she did...
18/11/2023

Sarah was alright when she woke up in the morning. She was changing clothes when she started feeling weird. Then she did few vomitings, I brought her to the hospital. She started losing alertness and became less responsive.
Right now, We are waiting for scan results, i hope we get some better news. She never had seizures but today she went through extreme seizures. She is not answering when I call her name. Just randomly moving her hands. Ya Allah !!! Please let my Sarah awake ameen.

13/11/2023I m posting after a long time. Sarah has been doing really well, we were hopeful that she may be able to defea...
13/11/2023

13/11/2023
I m posting after a long time. Sarah has been doing really well, we were hopeful that she may be able to defeat this monster.
But today, we got the bad news that her tumour is grown into the spine too and is progressing. I don't have words to explain what I am feeling now, all I see is her eyes that has hope that she would be better one day.
She will start school tomorrow, I don't know how long she would be able to continue going to school. The only thing that is important is she stays happier.
It is really hard time for us. We knew this is coming but wasn't expecting it this much earlier. Please remember her in your prayers. We need a miracle. May Allah give us strength ameen.

24/09/2023 Sarah is doing alright Alhumdulillah. We are relying on self healing not any specific medication. She has bee...
24/09/2023

24/09/2023
Sarah is doing alright Alhumdulillah. We are relying on self healing not any specific medication. She has been denied for CAR-T cell therapy at UCLH. Now we have started searching for other ways. Herbal and homeopathy are the options too.
Also waiting for green signal to start school as soon as possible. Sarah is very excited to go back to school.
Also planning to take her for another holiday before her scan in November.
Remember her in your prayers. Keep donating and supporting her with your love.

Sarah's Instagram and pages https://www.facebook.com/profile.php?id=100090666475532 https:โ€ฆ Uroos Atif needs your support for Help & Save Sarah

As Help & Save Sarah  has been doing better, we took it as an opportunity to chill and relax. No hospital, no needles, n...
13/09/2023

As Help & Save Sarah has been doing better, we took it as an opportunity to chill and relax. No hospital, no needles, no stress of what may happen, we switched on our rest modes and went to Antalya. We spent the best family time and Sarah Atif enjoyed every moment of it.
I wish Sarah becomes completely healthy and we would be able to go back again.
Remember her in your prayers.
https://gofund.me/4d9b0822

23/08/2023Sarah had a wonderful hydrotherapy session today and she enjoyed every moment of it.  ๐Ÿค—๐Ÿ˜—๐Ÿ˜˜ I have never seen he...
23/08/2023

23/08/2023
Sarah had a wonderful hydrotherapy session today and she enjoyed every moment of it. ๐Ÿค—๐Ÿ˜—๐Ÿ˜˜ I have never seen her this much happier lately. O Allah !!! Please keep my daughter happy and give her complete health. Please show us a miracle.
https://gofund.me/69f537ed

Thank you so much Sky News for inviting us for the interview. I hope Government would take effective measures to spend t...
18/08/2023

Thank you so much Sky News for inviting us for the interview. I hope Government would take effective measures to spend the funding allocated for Brain tumour research. Sarah got a chance to meet the wonderful people like Anna, Laura, Hugh Adams and others. Everyone was amazed with her energy and lightening shoes. ๐Ÿ‘Ÿ๐Ÿ‘Ÿ ๐Ÿ’™๐Ÿ’œ๐Ÿ’šโค
Please keep donating as we will have to find more treatments for Sarah.
https://gofund.me/1f1db4b8

16/08/2023 " The only reason a warrior is alive to fight". Our fearless Sarah is an example of it. Things didn't go her ...
17/08/2023

16/08/2023
" The only reason a warrior is alive to fight". Our fearless Sarah is an example of it. Things didn't go her way but she fought back, willing to undertake a new course of treatment. Her charm enlightens everyone around especially me as a mum. Her optimism gives me confidence to believe in miracles. May Allah make things easier for her, Ameen. Remember her in your prayers.
https://gofund.me/69f537ed Help & Save Sarah

After the whole week of treatment and staying at hospital, Sarah has improved a lot Alhumdulillah. Hopefully they will d...
07/08/2023

After the whole week of treatment and staying at hospital, Sarah has improved a lot Alhumdulillah. Hopefully they will discharge her soon. She has become too weak and gets tired after little activity.
We are not going back to the trial for ONC201 again. New hunt has begun to find the other ways of treatment. Keep donating.
Sarah and other children with and needs a lot of support. This journey is very hard.
Being a parent breaking every day and getting back ourselves up is not easy but its our test by Allah.
I hope Governments would start to put more money in for the research of Brain tumours.
A lot of families are in need for it throughout the world.
https://gofund.me/4d9b0822

Our brave Sarah is in ICU and fighting with this horrible drug reaction. We have finally decided not going back to the t...
01/08/2023

Our brave Sarah is in ICU and fighting with this horrible drug reaction. We have finally decided not going back to the trial. We were sure it was Paxalisib last time but she is unable to tolerate ONC201 too. Please remember her in your prayers. We want her to get better soon, we want her to be happy, is it that difficult !!! may Allah give her complete health. Ameen
https://gofund.me/4d9b0822

The day started with the start of 2nd round of PNOC022 trial at Prinses Mรกxima Centrum voor kinderoncologie, Utrecht and...
01/08/2023

The day started with the start of 2nd round of PNOC022 trial at Prinses Mรกxima Centrum voor kinderoncologie, Utrecht and ended at Northwick Park Hospital, London.
Sarah has suddenly become unwell when we got home. Doctors are trying their best to find out why did she get high fever with such elevated BP and Heart rate. She is still in Resus. Please pray for Sarah.

30/07/2023Leaving for Netherlands, let's see if Sarah would be able to start 2nd round of PNOC022 trial. Need prayers al...
30/07/2023

30/07/2023
Leaving for Netherlands, let's see if Sarah would be able to start 2nd round of PNOC022 trial. Need prayers always. Our brave ans pretty Sarah is excited but scared too, due to the side effects of the medicine last time.
https://gofund.me/4d9b0822

29/07/2023

19/07/2023
Posting it late, We celebrated Sarah's birthday in London with friends and family (though her actual birthday is 17th June). She got her favourite LOL cake from Mnash Delights. We had memorable moments, we have never seen Sarah so happy โค๐Ÿ’™๐Ÿ’œ. Keeping praying and supporting our lovely and brave daughter.
https://gofund.me/4d9b0822

25/07/2023Sarah is still recovering with the drug reaction. Her skin is extremely dry and itchy all the time. She is irr...
26/07/2023

25/07/2023
Sarah is still recovering with the drug reaction. Her skin is extremely dry and itchy all the time. She is irritable most of the time these days. She doesn't want to be like this. We don't know whether we will go back to 2nd round of trial or not. I can't put my daughter in more pain.
Today we spent the day at Great Ormond Street Hospital and Children's Charity for skin review and bloods. Brain tumours are cruel.
https://gofund.me/4d9b0822

10/07/2023Trial has been on halt for 2 weeks. Sarah's liver enzymes are really high. She will have ultrasound and more b...
10/07/2023

10/07/2023
Trial has been on halt for 2 weeks. Sarah's liver enzymes are really high. She will have ultrasound and more bloods tomorrow at Prinses Maxima.
We will be going back to London on 12th July. We are hopeful that after her liver becomes healthy she would be able to resume the trial again.
Worst part is the skin that has very bad rashes with extreme itching. She also had a biopsy for her skin today.
It very hard as a parent to see your child in pain and unable to fix it. This helplessness kills. We are praying and trying to comfort her as much as we can.
Remember Sarah in your prayers.
https://gofund.me/036781c6

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