LaneyMcg

Hi janner,
Having read your post and all the replies I think everything has been said because you are truly amazing, not just in the vast knowledge you have on mel but for me the fact you have stuck around all these years to help people whilst NED yourself makes you a fantastic unselfish lady who is a beacon of light at a scary time. You helped me in 2006 when I was diagnosed 2a breslow 2.7mm. You translated my pathology/histology report ( I never know what it’s called). And helped e make sense out of what I was convinced was my death sentence.
please continue being the wonderful guiding force for so many, and I hope one day soon all on here will be NED because melanoma would be no more.
My thoughts and prayers are with all the warriors still fighting.
Love across the pond
Laney xx

Hi janner,
Having read your post and all the replies I think everything has been said because you are truly amazing, not just in the vast knowledge you have on mel but for me the fact you have stuck around all these years to help people whilst NED yourself makes you a fantastic unselfish lady who is a beacon of light at a scary time. You helped me in 2006 when I was diagnosed 2a breslow 2.7mm. You translated my pathology/histology report ( I never know what it’s called). And helped e make sense out of what I was convinced was my death sentence.
please continue being the wonderful guiding force for so many, and I hope one day soon all on here will be NED because melanoma would be no more.
My thoughts and prayers are with all the warriors still fighting.
Love across the pond
Laney xx

Hi janner,
Having read your post and all the replies I think everything has been said because you are truly amazing, not just in the vast knowledge you have on mel but for me the fact you have stuck around all these years to help people whilst NED yourself makes you a fantastic unselfish lady who is a beacon of light at a scary time. You helped me in 2006 when I was diagnosed 2a breslow 2.7mm. You translated my pathology/histology report ( I never know what it’s called). And helped e make sense out of what I was convinced was my death sentence.
please continue being the wonderful guiding force for so many, and I hope one day soon all on here will be NED because melanoma would be no more.
My thoughts and prayers are with all the warriors still fighting.
Love across the pond
Laney xx

Hi I too am in the UK I am under the christie hospital in Manchester. Original diagnosis in 2006, with 2.7mm on upper back snlb clear. Sending thoughts and prayers to your girlfriend but it’s fabulous that your educating yourself to help her.
Hope all goes well.
Laney x

Hi I too am in the UK I am under the christie hospital in Manchester. Original diagnosis in 2006, with 2.7mm on upper back snlb clear. Sending thoughts and prayers to your girlfriend but it’s fabulous that your educating yourself to help her.
Hope all goes well.
Laney x

Hi I too am in the UK I am under the christie hospital in Manchester. Original diagnosis in 2006, with 2.7mm on upper back snlb clear. Sending thoughts and prayers to your girlfriend but it’s fabulous that your educating yourself to help her.
Hope all goes well.
Laney x

I am so sorry for your terrible loss. My thoughts and prayers are with you x x x

I am so sorry for your terrible loss. My thoughts and prayers are with you x x x

I am so sorry for your terrible loss. My thoughts and prayers are with you x x x

Hi I think that you may be in the uk, I am too and unfortunately our drs seem to be a little behind on treatment options compared o our friends in the US. I was diagnosed in 2006 with 2.7mm mel clarks level 3. I had WLE that had clear margins and SNB that showed no node involvement. So there is def hope after diagnosis. Make sure your dr is. Melanoma specialist, and ask lots and lots of questions. Never feel like a nuisance. You have come to the right place for advice as everyone here knows what it is to feel out of their depth and scared. We are all with you hoping for positive outcome. If your in the UK I go to the Christies hospital in Manchester.
Laney
X x x

Hi I think that you may be in the uk, I am too and unfortunately our drs seem to be a little behind on treatment options compared o our friends in the US. I was diagnosed in 2006 with 2.7mm mel clarks level 3. I had WLE that had clear margins and SNB that showed no node involvement. So there is def hope after diagnosis. Make sure your dr is. Melanoma specialist, and ask lots and lots of questions. Never feel like a nuisance. You have come to the right place for advice as everyone here knows what it is to feel out of their depth and scared. We are all with you hoping for positive outcome. If your in the UK I go to the Christies hospital in Manchester.
Laney
X x x

Hi I think that you may be in the uk, I am too and unfortunately our drs seem to be a little behind on treatment options compared o our friends in the US. I was diagnosed in 2006 with 2.7mm mel clarks level 3. I had WLE that had clear margins and SNB that showed no node involvement. So there is def hope after diagnosis. Make sure your dr is. Melanoma specialist, and ask lots and lots of questions. Never feel like a nuisance. You have come to the right place for advice as everyone here knows what it is to feel out of their depth and scared. We are all with you hoping for positive outcome. If your in the UK I go to the Christies hospital in Manchester.
Laney
X x x

Thinking of you and looking forward to hearing your surgery went well.
Love and hugs
Laney x
Love across the pond x

Thinking of you and looking forward to hearing your surgery went well.
Love and hugs
Laney x
Love across the pond x

Thinking of you and looking forward to hearing your surgery went well.
Love and hugs
Laney x
Love across the pond x