Oh God please let this work😢 it's so painful and it hasn't been mentioned no marathons, no momey raised on tv nothing. I wasnt supposed to live long im 48 my neice died at 5 with this.
Research and development costs are extremely expensive and considering fewer than .05% of the world’s population has Sickle Cell, there are only so many people that this medication will even be a consideration for. Capital investors need to get a ROI too or else they will stop investing in these sort of groundbreaking discoveries.
The american health care industrial complex milks us for all we're worth. Medical bills #1 reason for bankruptcy in u.s.a. GQP wanted to block negotiating on medicare prescription prices.
@@nickgardner1408aren't hospital ward bills exorbitant though? There's constant horror stories of 5 grand bills for hospital visit for broken fingernail for example. Why can't they have cheap wards with minimal cheap equipment, and ease off on legal sanitary requirements that cause prices to inflate so much? When this treatment is developed in more common sense countries, it'll be 10x cheaper to fly to Mexico for it, expect to see the rest of the world leapfrogging the West on health matters, while the West gets bogged down in extremely over-the-top health measures that end up doing the opposite of benefiting public health.
@@motherofallemails CRSPR has massive costs that first need to be distributed amongst all recipients. CRSPR had to hire the best and smartest scientists to work around the clock for 13 years racking up billions of dollars of dept. Those scientists don’t come cheap so someone had to pay those scientists and for their equipment to discover a cure that no one was even 100% sure was possible of working, meaning they could lose their entire investment. Now that they were successful, those who paid for it to be discovered need to be paid back and then some for taking that risk. If they are not, no one will ever invest in companies like this because there is zero incentive to and if that happens, those diseases will just go uncured and people will just continue to suffer and die. Over time the cost will come down as technology gets better but not everyone has decades to wait. It’s a sad truth but a truth none the less.
Many people with doctoral degrees are paid for years and years to do come up with a treatment. Now that the treatment is available, it requires months of care and monitoring by health professionals, who also have salaries. As it becomes more common, the price will go down. Plus, this would likely be covered by health insurance onlce it's no longer experimental. The media has a policy of making people feel angry.
I need more information about this treatment and if there is a possibility of a cure in the United States, things happen easier, the forms of treatment. I'm from Brazil looking for more news about sickle cell anemia.
The cost of this therapy is $2.2 million per person. For a cure that is predominantly plaguing the black/hispanic community (1/365 black AA) to promote a cure for a disease that most AA with the disease won't ever be able afford is not helpful in my opinion. There's no way an insurance company would dare cover this treatment. It just an advertisement of showcasing medical advances that is clouded in false hope.
While it's experimental, it is covered by the research grant. When it is no longer experimental, the price will come down and government programs and many insurances will likely cover it, if the positive outcomes are high.
There's much easier and cheaper ways to rejuvenate any type of cell within the body.Once you have seen how STC30 plantbasted stemcells works it will blow your mind.
In fact, there is now a group of scientists working with this technique for create a therapy against hiv, but it is still in the experimental phase, so there's still a time left to see something result
They have the best treatment for various skin disease and they make use of Africa magic herbs. Give a try, you did thank me in the future. They ship discreetly worldwide
I so much admire your kind gesture Dr Igudia, indeed you are a life saver. Coming across your channel on my worst HSV2 stage was a blessing, your remedies were top notch. I’m grateful to God I made you my physician
I am from India, Assam resident of Mankhowa Tea Estate 15 no line, my younger sister is suffering from sickle cell anemia, is this technology available in India,She is 23 years old and been a sickle cell anemia patient from childhood,,we don't have such much money for her treatment
I am happy for this break through. My cousin would love to have this treatment to be free of this pain for 41 years. Lower the price. We are not rich.
Maybe the price will go down. 2.2 mil is unreachable for almost everyone.
2.2 million dollars how dare you price something that high you should be ashamed of yourself
Wow 😮!! That’s Amazing!! Absolutely speechless… this is groundbreaking news
No, someone with sickle cell can have pain any where not just in the joints. She is just young at this point.
Oh God please let this work😢 it's so painful and it hasn't been mentioned no marathons, no momey raised on tv nothing. I wasnt supposed to live long im 48 my neice died at 5 with this.
Very expensive
Yes, it costs 3.1 million.
My cousin is 45 years old with sickle cell and he has being going through for years. Help!
*SCOPEHILLARY*
His T.e.l.e.g.r.a.m handle
They make use of African magic herbs for treatment of various types of diseases and they ship discreetly worldwide
They cured my niece of diabetes
With the cost of this, most people will not be able to afford it.
Exactly so wats the point n den u pay all dat money n boom u die by some accident or some other thing.....money can't buy life
True
No one pays for health bills. This would have to be paid through government medical programs or insurance
@@deedebdoo who say no one pays for health bills I wish not in my country
Ground breaking ❤
How do they come up with these prices?
Research and development costs are extremely expensive and considering fewer than .05% of the world’s population has Sickle Cell, there are only so many people that this medication will even be a consideration for.
Capital investors need to get a ROI too or else they will stop investing in these sort of groundbreaking discoveries.
The american health care industrial complex milks us for all we're worth. Medical bills #1 reason for bankruptcy in u.s.a. GQP wanted to block negotiating on medicare prescription prices.
@@nickgardner1408aren't hospital ward bills exorbitant though? There's constant horror stories of 5 grand bills for hospital visit for broken fingernail for example. Why can't they have cheap wards with minimal cheap equipment, and ease off on legal sanitary requirements that cause prices to inflate so much?
When this treatment is developed in more common sense countries, it'll be 10x cheaper to fly to Mexico for it, expect to see the rest of the world leapfrogging the West on health matters, while the West gets bogged down in extremely over-the-top health measures that end up doing the opposite of benefiting public health.
@@motherofallemails CRSPR has massive costs that first need to be distributed amongst all recipients. CRSPR had to hire the best and smartest scientists to work around the clock for 13 years racking up billions of dollars of dept. Those scientists don’t come cheap so someone had to pay those scientists and for their equipment to discover a cure that no one was even 100% sure was possible of working, meaning they could lose their entire investment.
Now that they were successful, those who paid for it to be discovered need to be paid back and then some for taking that risk. If they are not, no one will ever invest in companies like this because there is zero incentive to and if that happens, those diseases will just go uncured and people will just continue to suffer and die.
Over time the cost will come down as technology gets better but not everyone has decades to wait.
It’s a sad truth but a truth none the less.
Many people with doctoral degrees are paid for years and years to do come up with a treatment. Now that the treatment is available, it requires months of care and monitoring by health professionals, who also have salaries. As it becomes more common, the price will go down. Plus, this would likely be covered by health insurance onlce it's no longer experimental. The media has a policy of making people feel angry.
I need more information about this treatment and if there is a possibility of a cure in the United States, things happen easier, the forms of treatment. I'm from Brazil looking for more news about sickle cell anemia.
There is a cure
There is a cure
This specialist treat various skin diseases with African magic herbs. If you care for recommendation
How can one get such treatment in Nigeria
Thats disgusting to charge these egregious prices for live saving medicine
There is no way any insurance company will cover 2.2 million dollars! NO WAY ! those pharmaceutical companies should be ashamed !
I don't believe a true cure would hurt. 6 months of argeous pain. That's 😮😮.
The cost of this therapy is $2.2 million per person. For a cure that is predominantly plaguing the black/hispanic community (1/365 black AA) to promote a cure for a disease that most AA with the disease won't ever be able afford is not helpful in my opinion. There's no way an insurance company would dare cover this treatment. It just an advertisement of showcasing medical advances that is clouded in false hope.
exactly! hopefully it becomes more affordable with due time
2.2m Is crazy.I just don't want to be suffering from crisis especially in winters 😞😞
While it's experimental, it is covered by the research grant. When it is no longer experimental, the price will come down and government programs and many insurances will likely cover it, if the positive outcomes are high.
Yes and it costs 2.2 million dollars per patient.!! It also involves chemotherapy. And it takes 6-7 months.
Who will pay the 2.2 million dollars???
All my money in the bank is $1000
99% patient can't afford this treatment, who will help them 😢
Good news for my family
Its too expensive 😭
Why does it only happen in this nationally
There's much easier and cheaper ways to rejuvenate any type of cell within the body.Once you have seen how STC30 plantbasted stemcells works it will blow your mind.
Could you please provide more details or additional information?
Anyone know if this would work for other diseases like immune diseases?
They are editing T cells like they edited these heme cells. Those edited T cells are in developement for lupus right now, 3-5 years before approval
All praise to Jah Jesus Christ 🙌🙌🙌🙌🙏🙏🙏🙏👏👏❤️❤️❤️ Amen! And Amen!
Can't ya utilize CRISPR to edit, or modify, DNA of bacteria or viruses???? Hmmm.......
In fact, there is now a group of scientists
working with this technique
for create a therapy against hiv,
but it is still in the experimental phase,
so there's still a time left to see something
result
Great tips! I recently started using the ANEMIA CARE PACK from Planet Ayurveda, and I’m feeling amazing. Thank you for the wonderful content!"
My baby girl 11yrs she is sickl cell, 🇰🇪🇰🇪🇰🇪, can we get this treatmeant soon??
If you care for recommendation, you can get the best African magic herbs treatment from this specialist
*SCOPEHILLARY*
His T.e.l.e.g.r.a.m handle
They treat various types of disease with Africa magic herbs and the best at that and they ship discreetly worldwide
Y la cura del VIH???? Cuando tendremos
*SCOPEHILLARY*
Dude's on T.e.l.e.g.r.a.m
They have the best treatment for various skin disease and they make use of Africa magic herbs.
Give a try, you did thank me in the future.
They ship discreetly worldwide
@@LauraFernandez-jx7dj???????????????
@@LauraFernandez-jx7dj?????
My childhood friend died in 2020 at the age of 32 😢
I so much admire your kind gesture Dr Igudia, indeed you are a life saver. Coming across your channel on my worst HSV2 stage was a blessing, your remedies were top notch. I’m grateful to God I made you my physician
I am from India, Assam resident of Mankhowa Tea Estate 15 no line, my younger sister is suffering from sickle cell anemia, is this technology available in India,She is 23 years old and been a sickle cell anemia patient from childhood,,we don't have such much money for her treatment
*SCOPEHILLARY*
His T.e.l.e.g.r.a.m handle
This specialist specialize on African magic herbs for treating various types of disease and the ship discreetly to any location
They cured my cousin with diabetes and they are the best
Did you find any more information my indian brother?
Hopefully, the costs will come down. Since it's not really a cure if it can not be given yo the people thst need it.
Sickle cell protectives them/us from malaria😊
Wow, fantastic because their life span is short with the average age in early 50s. I bet medicine is very expensive and insurance may not cover it .
Good news 😂😂😂😂😂😂😂😂😂😂❤❤❤❤❤❤❤❤❤ thank you
The cost is so expensive it’s not worth it! Y’all will never understand sickle cell disease 🤦🏾♂️
$2.2 million dollars for a shot???? pssshhh😮💨
Umm.. it's literally gene editing what u expect it to cost $1 ??
It's 7 months in the hospital.
What a game changer
Only for maybe 1% of ppl. Majority of people don’t see $70k a year where will they get $2.2M
$2 million!!! This is so political! 😮
Scientists and doctors who have been working on this for years, haven't been working for free.
2.2 welp guess I'm going to die with this disease
I'm praying you healed without the burden of price!!
Amen
Why do people in the media talk the way they do? It’s absolutely annoying and so fake. For the life of me I don’t understand it.
AMP TRYING TYMES GOOD NEWS FINALLY. ❤
All peoples hairs problems is
2.2 million !
Good news 😂😂😂😂
Bring it back