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Another new finding !
Key Player in Parkinson's Disease Neuron Loss Pinpointed ScienceDaily (Oct. 19, 2012) — By reprogramming skin cells from Parkinson's disease patients with a known genetic mutation, researchers at the Salk Institute for Biological jjStudies have identified damage to neural stem cells as a powerful player
Key Player in Parkinson's Disease Neuron Loss Pinpointed ScienceDaily (Oct. 19, 2012) — By reprogramming skin cells from Parkinson's disease patients with a known genetic mutation, researchers at the Salk Institute for Biological jjStudies have identified damage to neural stem cells as a powerful player
Hidden
in
Cure Parkinson's
12 years ago
I am Living (it up) with Parkinson's and Other Things
Diagnosed with PD in 1998, probably inflicted with it for a couple years before that, I decided to make the most of the poker hand I had been dealt. Put on Mirapex early on, I soon became a compulsive gambler and after that became, divorced, fired, lost all my property but literally the clothes I was
Diagnosed with PD in 1998, probably inflicted with it for a couple years before that, I decided to make the most of the poker hand I had been dealt. Put on Mirapex early on, I soon became a compulsive gambler and after that became, divorced, fired, lost all my property but literally the clothes I was
wordworks2001
in
Cure Parkinson's
12 years ago
Mylofibrosis
Hi everyone. Three weeks ago my husband diagnosed with mylofibrosis after PRV for six years. However his marrow sample was sent to another hospital for checking and we were told yesterday that the other hospital have said it is accellerated PRV so that is his diagnosis. We were told that he is in the
Hi everyone. Three weeks ago my husband diagnosed with mylofibrosis after PRV for six years. However his marrow sample was sent to another hospital for checking and we were told yesterday that the other hospital have said it is accellerated PRV so that is his diagnosis. We were told that he is in the
tissi
in
MPN Voice
12 years ago
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Welcome to my life...... HS... I hate it!!!! :)
I contracted HS when I was 18. (32 years ago - Yeah! I'm old). I was told straight off from a works nurse that it was only dirty people who get puss lumps under their arms. I had a massive lump under my right armpit. Because of this, I kept it and didn't consult my GP. However, it quickly spread to the
I contracted HS when I was 18. (32 years ago - Yeah! I'm old). I was told straight off from a works nurse that it was only dirty people who get puss lumps under their arms. I had a massive lump under my right armpit. Because of this, I kept it and didn't consult my GP. However, it quickly spread to the
Bio-thingey
in
MY SKIN
12 years ago
has anybody had an ankle fusion opp that has not worked?
my opp was in november 2011,i have now had my ct scan back and the fusion has not taken at all,it has even made my
bone
graft
i had 15 years ago dissapear.i am now being told i'm on the waiting list again for another opp..i want and need a second opinion but don't know how to get 1.please help any1 :
my opp was in november 2011,i have now had my ct scan back and the fusion has not taken at all,it has even made my
bone
graft
i had 15 years ago dissapear.i am now being told i'm on the waiting list again for another opp..i want and need a second opinion but don't know how to get 1.please help any1 :
dannyb
in
NRAS
12 years ago
MF BMT (SCT) Transplant Survivor
Hi, I was diagnosed with MF in 2010 and had a Stem Cell Transplant in March 2011, I live just outside London. I do buddying for MPDVoice and have just taken one buddy through transplant and have two more heading that way. Thanks to the internet I have MF-BMT friends around the globe at varying stages
Hi, I was diagnosed with MF in 2010 and had a Stem Cell Transplant in March 2011, I live just outside London. I do buddying for MPDVoice and have just taken one buddy through transplant and have two more heading that way. Thanks to the internet I have MF-BMT friends around the globe at varying stages
MFBMT2011
in
MPN Voice
12 years ago
epelipsy and Lupus
Hi every one Would like to say think this is a great sight nice to know am not alone, was diagnosed with rhymatoid arthrits at 5 always suffered with my joints,tiredness ect, wasnt till my kidneys started packing up they then told me I had SLE have had ups and doewns over the years with sweling, rashes
Hi every one Would like to say think this is a great sight nice to know am not alone, was diagnosed with rhymatoid arthrits at 5 always suffered with my joints,tiredness ect, wasnt till my kidneys started packing up they then told me I had SLE have had ups and doewns over the years with sweling, rashes
Andrewc
in
LUPUS UK
12 years ago
AMN/Mystery disease
I am computer challenged! I am like a cave woman in training in this computer/technological world! FYI, I have, never, ever done a blog, before! I am suffering from AMN, big time, and would love some help!!! I KNOW THAT I COULD BE OF HELP AND YOU COULD BE OF HELP TO ME! I have an amazing story
I am computer challenged! I am like a cave woman in training in this computer/technological world! FYI, I have, never, ever done a blog, before! I am suffering from AMN, big time, and would love some help!!! I KNOW THAT I COULD BE OF HELP AND YOU COULD BE OF HELP TO ME! I have an amazing story
relay
in
AMN EASIER
12 years ago
no symptoms, sporty, 80% LAD blockage to CABG or not?
My husband is a 50 year old, very fit (mountain bikes 4 * 1.5 hours per week, 1* 3 hours and plays squash 2 times) - he is a pilot so regulary does stress ecg's which all showed no problems and superfit. His family has CAD history so he took a preventative CT scan which showed calcium score of 144 and
My husband is a 50 year old, very fit (mountain bikes 4 * 1.5 hours per week, 1* 3 hours and plays squash 2 times) - he is a pilot so regulary does stress ecg's which all showed no problems and superfit. His family has CAD history so he took a preventative CT scan which showed calcium score of 144 and
zimbali
in
Cholesterol Support
12 years ago
Do you have problems healing?
I had a skin graft in January due to a malignant melanoma (possibly linked to MMF) and the donor site is refusing to heal. I am 8 weeks post op and the nurses in the plastics clinic have tried everything they can think of. Does anyone have any suggestions please? I am fed up with having a dressing
I had a skin graft in January due to a malignant melanoma (possibly linked to MMF) and the donor site is refusing to heal. I am 8 weeks post op and the nurses in the plastics clinic have tried everything they can think of. Does anyone have any suggestions please? I am fed up with having a dressing
Hidden
in
LUPUS UK
12 years ago
Has anyone had a stem cell transplant for their scleroderma?
onthemend
in
Scleroderma & Raynaud's UK (SRUK)
12 years ago
home neb machine
Hi, I have a friend with a 9 year old with asthma due to XLP damage to his chest and they need to buy a home neb machine for him for when his chest is really bad. Recently he had to go into hospital overnight for saline neb which helped but his parents have never been offered advice re buying a machine
Hi, I have a friend with a 9 year old with asthma due to XLP damage to his chest and they need to buy a home neb machine for him for when his chest is really bad. Recently he had to go into hospital overnight for saline neb which helped but his parents have never been offered advice re buying a machine
Hidden
in
Asthma Community Forum
16 years ago
Bone Marrow Transplants
I know this is off topic, but I think it is something that is really important. Adrian Sudbury started a petition to make it compulsory for kids to learn about bone marrow and plateleys donation. He's trying to get to 10,000 signitures by the 23rd of this month! Give him a hand people! http://petitions.pm.gov.uk
I know this is off topic, but I think it is something that is really important. Adrian Sudbury started a petition to make it compulsory for kids to learn about bone marrow and plateleys donation. He's trying to get to 10,000 signitures by the 23rd of this month! Give him a hand people! http://petitions.pm.gov.uk
Hidden
in
Asthma Community Forum
16 years ago
Leg Ulcers - Can anyone suggest anything that might help?
I HAVE HAD ULCERS ON MY ANKLES AND FEET FOR THE LAST 10 YEARS. I HAVE HAD SKIN GRAFTS IN HOSPITAL AND TRIED ALL SORTS OF DRESSINGS BUT CANNOT GET THEM TO HEAL. CAN ANYONE ONE SUGGEST ANYTHING THAT MIGHT HELP?
I HAVE HAD ULCERS ON MY ANKLES AND FEET FOR THE LAST 10 YEARS. I HAVE HAD SKIN GRAFTS IN HOSPITAL AND TRIED ALL SORTS OF DRESSINGS BUT CANNOT GET THEM TO HEAL. CAN ANYONE ONE SUGGEST ANYTHING THAT MIGHT HELP?
jabba
in
Scleroderma & Raynaud's UK (SRUK)
13 years ago
RA and Surgery..
After that surgery was once again needed on feet again, repair of some metal work along with fusion of more joints and a
bone
graft
operation. The
bone
was taken from each my shins and then placed in my feet along with more pins and screws.
After that surgery was once again needed on feet again, repair of some metal work along with fusion of more joints and a
bone
graft
operation. The
bone
was taken from each my shins and then placed in my feet along with more pins and screws.
Hidden
in
NRAS
13 years ago
Is it life changing?........
Cancer has touched a number of family members throughout my life - not that long at 44, but it really affected me most when my Mother was diagnosed at 50 and died at 51. I must admit, it had a pretty profound affect on me and my family and although it was over 15 years ago it still remains with
Cancer has touched a number of family members throughout my life - not that long at 44, but it really affected me most when my Mother was diagnosed at 50 and died at 51. I must admit, it had a pretty profound affect on me and my family and although it was over 15 years ago it still remains with
PeterThomas
in
Tenovus
13 years ago
Hi.I have had WG for just over 4 years now. I have been on Rhituximab for just
over a year and I have been told that I will probably need to have a bone marrow transplant. Has anyone else needed this procedure for WG. Any information would be greatly appreciated. Thanks.
over a year and I have been told that I will probably need to have a bone marrow transplant. Has anyone else needed this procedure for WG. Any information would be greatly appreciated. Thanks.
jimny
in
Vasculitis UK
13 years ago
Intro and history.....any advice welcome
Hi Everyone, I'm new here but hope to learn so much from you all. Hope this isn't too long, and would welcome any comments. I was diagnosed as having serious CAD at the end of Nov 2010. the resultant emergency angiogram at Sheffield NG showed i needed either a CABG or a total of 5 Stents over
Hi Everyone, I'm new here but hope to learn so much from you all. Hope this isn't too long, and would welcome any comments. I was diagnosed as having serious CAD at the end of Nov 2010. the resultant emergency angiogram at Sheffield NG showed i needed either a CABG or a total of 5 Stents over
smithy
in
Cholesterol Support
12 years ago
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