NorthWest Biotherapeutics Inc (NWBO)

[Lykiri]

Thanks abeta for sharing Hannah's story!
Keeping everything crossed that they can raise the money for her treatment!
https://www.justgiving.com/crowdfunding/gail-iredale?utm_term=zxmewna3z&fbclid=IwAR1so6BL1BGU4a5K9LJuaALIOodkp0qAqQ259eCNibkIxE_1H7yIbScNJRI

$NWBO people. Hannah has GBM4 & is now post resection with her tumour stored correctly by Ashkan but the crux of the matter is they need to raise £150k to begin getting the DCVax made. They are at £30k so far...

Dig deep people, her life is on the line!https://t.co/b2EvJbKSdk

— Tommy Bax 🇬🇧 🇹🇼 (@TommyBaxendale) July 7, 2023

"But I discovered Professor Keyoumers Ashkan in Harley Street and the fact that he is working with dendritic cell vaccine (DC Vax) - not available on the NHS - which means that a vaccine can be created from her blood and the tumour she had removed originally to kickstart the body into realising there is a cancer present which her immune system needs to fight. The number of jabs she would need would depend on the response by Hannah's immune system.
"The treatment has previously been shown to extend people's lives and so there is a 30% chance of living five years, when more cures might be known, from 1%. As a mother, I have to take it and make sure we raise enough money to make it possible."

https://www.derbytelegraph.co.uk/news/local-news/if-dont-raise-enough-money-8560910?fbclid=IwAR2Y11XGpOLmekarY0rG4AmNOU2ps5hqCwcCZZtHkjy9dqeG8lmLWEf15bo
Hannah's mum:

Help for Hannah
June 14, 2023
Please share Hannah’s story… we need to raise awareness xxx
Once upon a time, life was wonderful, easy, relaxed and I truly felt content and happy with 2 healthy children, a home, food in the fridge and a roof over my head.. when life was turned upside down in July of last year, when we were told she had a massive brain tumour. We were by her side every day and night and watched as she couldn’t swallow for weeks, suffered excruciating head aches and sickness, weight loss and eventually had a GN tube fitted and was eventually transferred to QMC for evaluation. Her tumour was evicted on the 4th of august and we felt so blessed the surgery went well despite leaving her with seizures.. for 7 weeks we waited for the removed tumour to have a whole genetic profiling and then… The arse literally fell out of our world. While Hannah was seizing we were told Hannah’s tumour was cancer, a rare horrible terminal cancer with no cure. Can you imagine for just 1 second the gravity and reality of being told that? Well that’s where my strength came from. That moment, that look in my girls eyes as we told her, watching your child’s face crumple at the news no one expects to hear at only 19…
That’s where I found my strength to fight for her, that’s what I close my eyes and see when I feel beyond exhausted and ready to give up, that’s what I remember when I literally beg for donations, because pride comes way lower on the scale for me than the love I have for my girl….That really was the beginning of her journey through this cancer before the endless daily trips to Nottingham for radiotherapy and chemotherapy and night after night in hospital.. She has never complained...
We will carry on until we reach the dc-vax cost of 250k and keep going after that to raise funds for research so no parent has to sit there helpless and no one has to sit there to be told there is no cure for this beast of a cancer. I love you Hannah … I love all of you that are tirelessly supporting her.. she’s a human with a life ahead of her.. thanks to all of you… now buy some raffle tickets .. love you all!

Listen to this amazing girl and her mum. (DCVax-L around min.7)
INTERESTING QUOTE REGARDING NHS (National Health Service)

The trial still has patients, a lot of patients alive at the 7 year mark since the trial happened…

https://www.facebook.com/louise.k.ford/videos/217490237426936