ROSE BRENNAN
THE COURIER-MAIL
MAY 31, 2015
http://www.couriermail.com.au/news/queensland/stem-cell-tourism-continues-to-gain-popularity-despite-the-risks/story-fnn8dlfs-1227376236651
INCREASING numbers of desperate Australians are travelling overseas for a controversial medical treatment that is not approved locally.
Stem cell tourism continues to gain popularity among patients seeking a cure for conditions such as multiple *sclerosis, with clinics in countries from Singapore to Russia promising *solutions.
It comes despite warnings from *Australian health professionals that the effectiveness of autologous haematopoietic stem cell treatment (HSCT) is unproven, dangerous and comes with exorbitant costs.
Adult Stem Cell Foundation executive director Bruce Lahey said hundreds of Australians continued to seek out the service every year.
During HSCT a patient’s stem cells are extracted before they receive high doses of chemotherapy that wipe out their immune system. Weeks later the stem cells are transplanted back for the patient to develop a new immune system.
Young Regents Park police officer Ian Callaghan doesn’t have time to wait and will travel to Singapore for HSCT on June 1. The 33-year-old father of Noah, 16 months, was diagnosed with an extremely aggressive form of MS in 2013.
The disease has been making progress faster than expected and hasn’t been slowed by medication. If it continues, he will be wheelchair bound within a year and bedridden in five.
The senior constable suffers severe fatigue and numbness down the left-hand side of his body making it impossible to walk more than 200m.
His partner Amy, 27, is pregnant with twin girls who are due during his treatment.
He has made the selfless decision to delay returning to Singapore for the transplant, which will put his severely depleted immune system at risk, to see the birth of his daughters and spend time with them. When he returns to Australia after the transplant he will have to be isolated from his children to protect his new immune system.
For Mr Callaghan, the risks and the $125,000 to $150,000 price tag are worth it for the chance of becoming MS-free.
“I could die from the treatment and Australian doctors think that’s too risky. Or I could live the life of MS and try to live with it but it won’t be much of a life. You’re alive but you’re not living,” he said.
Mr Callaghan said he was angry and frustrated that the treatment isn’t available in Australia.
“The patients should be ultimately in charge of their own health and if they wish to seek certain treatments it should be available to them.
“The treatment isn’t voodoo magic. They’ve been doing it for cancer forever, and for MS for over 20 years overseas.
“They’re looking at about 80 per cent efficacy. It puts it into long-term remission.”
To help Ian go to: help-our-mate-fight-ms.net
THE COURIER-MAIL
MAY 31, 2015
http://www.couriermail.com.au/news/queensland/stem-cell-tourism-continues-to-gain-popularity-despite-the-risks/story-fnn8dlfs-1227376236651
INCREASING numbers of desperate Australians are travelling overseas for a controversial medical treatment that is not approved locally.
Stem cell tourism continues to gain popularity among patients seeking a cure for conditions such as multiple *sclerosis, with clinics in countries from Singapore to Russia promising *solutions.
It comes despite warnings from *Australian health professionals that the effectiveness of autologous haematopoietic stem cell treatment (HSCT) is unproven, dangerous and comes with exorbitant costs.
Adult Stem Cell Foundation executive director Bruce Lahey said hundreds of Australians continued to seek out the service every year.
During HSCT a patient’s stem cells are extracted before they receive high doses of chemotherapy that wipe out their immune system. Weeks later the stem cells are transplanted back for the patient to develop a new immune system.
Young Regents Park police officer Ian Callaghan doesn’t have time to wait and will travel to Singapore for HSCT on June 1. The 33-year-old father of Noah, 16 months, was diagnosed with an extremely aggressive form of MS in 2013.
The disease has been making progress faster than expected and hasn’t been slowed by medication. If it continues, he will be wheelchair bound within a year and bedridden in five.
The senior constable suffers severe fatigue and numbness down the left-hand side of his body making it impossible to walk more than 200m.
His partner Amy, 27, is pregnant with twin girls who are due during his treatment.
He has made the selfless decision to delay returning to Singapore for the transplant, which will put his severely depleted immune system at risk, to see the birth of his daughters and spend time with them. When he returns to Australia after the transplant he will have to be isolated from his children to protect his new immune system.
For Mr Callaghan, the risks and the $125,000 to $150,000 price tag are worth it for the chance of becoming MS-free.
“I could die from the treatment and Australian doctors think that’s too risky. Or I could live the life of MS and try to live with it but it won’t be much of a life. You’re alive but you’re not living,” he said.
Mr Callaghan said he was angry and frustrated that the treatment isn’t available in Australia.
“The patients should be ultimately in charge of their own health and if they wish to seek certain treatments it should be available to them.
“The treatment isn’t voodoo magic. They’ve been doing it for cancer forever, and for MS for over 20 years overseas.
“They’re looking at about 80 per cent efficacy. It puts it into long-term remission.”
To help Ian go to: help-our-mate-fight-ms.net