hi kath yes i think they are bringing them from other countrys thanks again for your prayers
joy
Search found 75 matches
- Sat Jan 10, 2009 5:42 pm
- Forum: Parents of OBPI Children
- Topic: please help we are desperate
- Replies: 11
- Views: 2874
- Tue Jan 06, 2009 6:30 pm
- Forum: Parents of OBPI Children
- Topic: please help we are desperate
- Replies: 11
- Views: 2874
Re: please help we are desperate
hi richard, great to hear from you hope you are well,thank you for all your info realy appriciate it, yes its a real rare condition he has all the doctors baffled, there is about 20 neuro surgeons coming from all over to have a look at him
,so fingers crossed.
joy
,so fingers crossed.
joy
- Tue Jan 06, 2009 6:15 pm
- Forum: Parents of OBPI Children
- Topic: please help we are desperate
- Replies: 11
- Views: 2874
Re: please help we are desperate
hi carolyn,
thank you so much for your prayers i will keep you up to date on whats happining,
joy
thank you so much for your prayers i will keep you up to date on whats happining,
joy
- Tue Jan 06, 2009 6:04 pm
- Forum: Parents of OBPI Children
- Topic: please help we are desperate
- Replies: 11
- Views: 2874
Re: please help we are desperate
<t>hi kath no we are not now going to america,<br/> we are seeing a fantastic surgeon who is hoping to do a muscle transfer if mark gets back the use of his hand first, america was only offering to do a nerve transfer which our surgeon says it is far to late now to have it done,so please god his han...
- Tue Jan 06, 2009 5:57 pm
- Forum: Parents of OBPI Children
- Topic: please help we are desperate
- Replies: 11
- Views: 2874
Re: please help we are desperate
hi there thank you so much for your kind words
joy
joy
- Tue Dec 30, 2008 5:52 pm
- Forum: Parents of OBPI Children
- Topic: please help we are desperate
- Replies: 11
- Views: 2874
please help we are desperate
<t>hi all its been a while since i have been on this site,<br/> mark was supposed to go to america to have a c7 transfer but as he is nearly 7 years into his diagnoses of bpn it is now to late he was then scheduled to have a muscle transfer in feb but 3 weeks ago mark lost the use of his hand he was...
- Wed Dec 03, 2008 6:36 pm
- Forum: Parents of OBPI Children
- Topic: mark losing power in hand
- Replies: 2
- Views: 1168
Re: mark losing power in hand
hi mark saw dr today he is not sure if he is being attacked by another virus and if so they will not go ahead with his muscle transfer we are devistated they also said it might be he damaged his arial nerve not realy sure what that is
joy
joy
- Tue Dec 02, 2008 7:21 pm
- Forum: Parents of OBPI Children
- Topic: met with dr kevin cronin
- Replies: 9
- Views: 2434
Re: met with dr kevin cronin
hithere you can find dr cronin in the mater hospital in dublin best of luck.
joy
joy
- Tue Dec 02, 2008 7:18 pm
- Forum: Parents of OBPI Children
- Topic: mark losing power in hand
- Replies: 2
- Views: 1168
mark losing power in hand
<t>hi all as you know my son mark was diagnosed with bpn over 6 years ago, he is due to have a muscle transfer in feb,now although he has no movement in his arm he had full function of his hand untill the other day he was unable to move it plus he was getting severe pain in the effected side of his ...
- Wed Nov 26, 2008 2:37 pm
- Forum: Newly Injured TBPI
- Topic: Muscle Transfer Info. needed!
- Replies: 11
- Views: 4671
Re: Muscle Transfer Info. needed!
hi there i think this message was meant for mike
joy
joy