A five-year-old girl that her parents described as “little firecrackers,” fights in ultra row brain tumordefuse chances after receiving 12-monthly forecasts.
Rosie Hassall, from CheshireHe started experiencing heavy headaches and unusual eye movements in November 2024.
In the beginning, the doctors suspected the migraines, the condition that runs in the family. However, Rosie’s Symptoms aggravated.
The pain in his head became so intense to struggle to cry, laugh or even sneeze. Analyzed eye test revealed suspicious nerve damage, which led to the scan of the MRI.
Only three days before Christmas arrived a devastating diagnosis: Kiwi size brain tumor. The biopsy confirmed the tumor was cancerous, unequal and incredibly aggressive, probably developing within a few days or weeks.
Rosie’s parents, Charlotte and Stefan Hassall, both 36, told us the forecast of his daughter nine to 12 months.
The rarity of her condition makes the forecast uncertain, prompted the family to share his story to lift consciousness And potentially help others to face similar battles.
They advocate hope that Rosie will break the chances and “prove doctors wrong.” Family temptations began with apparently innocent symptoms, emphasizing the importance of permanent medical assistance when faced with inexplicable health problems.
“Rosie is a fighter, we can see how much she struggled since she had this and I hope she proves the wrong and can find them out,” Charlotte said from real life.
“She will be the one who passes through it, but you never know if not, we can help another family down the line through what we pass. “
Rosie began to experience pain in his head and strange eye issues in November 2024. Years.
“We didn’t think of anything from that, but in the next few days, the pain worsens,” Charlotte said.
“We had a tea night and said she learned to cover her, but the left eye actually cheered in the other way.
“Then we realized that something happened.”
Charlotte took Rosie to appoint a doctor where she thought he could experience migraines – a condition he works on both sides of the family.
She also visited opticians, the form Express, but the reason for Rosie’s symptoms could not be found as her eye and vision work as normal.
Rosie then started to become “really good,” she took her to Leighton Hospital in Cheshire, where she was prescribed by antibiotics after the doctors found white spots on her throat – but Charlotte said “never picked up from there.”
“She had 27 episodes of this pain in her head and doctors were a little stunned about what could be,” she said, adding that they were also able to give Rosie Calpol to help in pain.
“She was so bad, rolling in the pain on the floor, was really uncomfortable and really praised.
“She tried to cry, but it was so painful, she couldn’t laugh or sneeze because it hurts.”
After looking for another eye test of SpecsaversWhere did Charlotte say that the symptoms of her daughter became “much worse,” I thought that Rosie suspected the nerve damage in her left eye and she headed for an ophthalmologist.
Rosie turned the “thorough” tests before being sent for the MRI scan at the 19th Leighton Hospital. December.
The family is 22. December received search results, which revealed a six-cent-center tumor in his brain.
“Everything just stops, everything goes quiet,” Charlotte said.
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On the same day, Rosie was subjected to contrast – where the color is injected to make certain tissues and blood vessels appear clearer – before the family headed in Alde Hey Children Hospital in Liverpool and the presence of tumors confirmed.
The family could go home for a Christmas day, but they should have returned to the hospital Boxing day In order for Rosie to undergo biopsy on 27. December.
26. January The family received Rosie’s official diagnosis, which was a “new entity” of pediatric bithalamic glioma.
Bithalam gliomas are incredibly rare tumors that make up less than 1 percent of brain tumor diagnosis, in line with brain tumor research.
“We were told from the beginning, it was unreleased about where the tumor was sitting, we were told that it was a very aggressive tumor,” Stefan said.
Charlotte added: “They said it was a literary question for days or weeks that could happen and grow pretty quickly because the symptoms have just come.
“Although he has pediatric gashalem glioma, it’s a new entity, it’s a very rare form of cancer that has – when Google, you can’t find a lot.”
Rosie will still have chemotherapy treatment, after previously passing radiotherapy, and it will be scanned every three months to monitor the growth of the tumor.
The family is informed at the average forecast for batalamike gliomas between nine and 12 months, but they remain positive because they know that Rosie is a fighter.
“Rosie is amazing and just tried to continue as much as he could, she was such a hard car,” Charlotte said.
They hope to share a rocky trip, others will benefit from further research and information in the future.
“If someone knows more about your cancer, we can learn from it and help other families,” Charlotte said.
The family launched the GofundMe Support page such as Charlotte and Stefan took free time to take care of Rosie and help her enjoy the days that have a hospital, ease of £ 33,000.
To learn more, visit Family For Family Here: GofundMe.com/f/support-rosie-and-hor-family-through-brain-cancer