Sorry to hear your lovely son Linas has neuroblastoma. Have you heard of the charity Families Against Neuroblastoma? If not, they may be able to help you. It is run by caring neuroblastoma families. They organise days out for neuroblastoma families,a support network, information about treatment, and helping to fundraise for treatment abroad when the UK has not been able to help. The website is http://www.familiesagainstneuroblastoma.org/ Please get in touch with them. I hope your son is doing OK and wishing him all the best. Thanks Caroline
Hi My son Ashley faught neuroblastoma for 2 1/2 years he was also treated in oxford. sadly he passed away in september 2010. We are a local family in milton keynes and i would like to help you if i can, put you in touch with a charity that can offer support and help you launch an offical appeal for whatever linas needs, we went down the route of alternative therapies and seeking treatment in other countries. i would strongly recomend you look into the types of treatment avaible in germany and america for nb. I can also put you in touch of some organisation that may be able to help you finacilly. Sending much love and strength to you and linas. clair hyde angelfeathers81@hotmail.com x
Sorry to hear your lovely son Linas has neuroblastoma. Have you heard of the charity Families Against Neuroblastoma? If not, they may be able to help you. It is run by caring neuroblastoma families. They organise days out for neuroblastoma families,a support network, information about treatment, and helping to fundraise for treatment abroad when the UK has not been able to help. The website is http://www.familiesagainstneuroblastoma.org/ Please get in touch with them. I hope your son is doing OK and wishing him all the best. Thanks Caroline
ReplyDeleteHi My son Ashley faught neuroblastoma for 2 1/2 years he was also treated in oxford. sadly he passed away in september 2010. We are a local family in milton keynes and i would like to help you if i can, put you in touch with a charity that can offer support and help you launch an offical appeal for whatever linas needs, we went down the route of alternative therapies and seeking treatment in other countries. i would strongly recomend you look into the types of treatment avaible in germany and america for nb. I can also put you in touch of some organisation that may be able to help you finacilly. Sending much love and strength to you and linas. clair hyde angelfeathers81@hotmail.com x
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