E 'should perhaps be clarified.
I have two blogs.
This was the first born with the idea of \u200b\u200bliving and sharing my experiences with Hodgkin's disease. Much practical experience as you have seen and see.
E 'Long time no write, and not by accident. Because I think in a blog "personal" can be written basically for two reasons (and there may be many other, for charity, but the most important are two).
The first is because I seem to have something interesting to tell. What I think, what they live. Others find it is pretty interesting, it may be useful in some situations, but the blog is "my". Actually I came to this kind of blog on the second try, and if anyone wants to read is www.klalla75.blogspot.com. From the little I know about blogs in general is very "current": a post photos, thoughts, quotes, videos, etc. ... that interest at that time.
The second reason, in my opinion, to write a blog, you have something to say that it may be useful to others because you have had similar experiences. There are many blogs and travel stories of this kind. In this case, the things written are not "fresh". When I started this blog was meant to be like this, and perhaps will continue to predominantly be. After months of chemotherapy and a job that I thought I had not seen and understood everything, but much of Hodgkin's disease and I wanted to tell.
|
| Christmas Tree "alternative" ... |
I wanted to write a blog on Hodgkin's lymphoma that was encouraging, telling about experiences from those who had already healed. For this there was a pause so long, in which I have not written.
I spoke with a psychologist and he confirmed that, at least among patients with Hodgkin's disease, self-help groups are difficult. Risks to find people "less sick" about you: what can they understand them? Or people who are not cured, and if it happens to me too? No no, not at all easy.
But last night I received this comment to a post:
"I have Hodgkin's disease and I did the cycle ABVD relapse after one month, I started another chemo BEACOOP the two months after relapse now I have to start radiation therapy, but I have already said that being aggressive can not exclude transplantation. I am desperateAt this point I can no longer remain silent. Also will take up this blog with the continuity that I can, the serenity that I can. Always convinced that together we can win. And that the lymphoma is only a part of life, and we live for the rest.
Giuliana "
0 comments:
Post a Comment