Just a quick note to let everyone know that I have spoken to the writer, the editor, the people at Beta Seron, the President and the board chair of the local MS chapter.
The editer has been in several meetings since this article was printed. He has also spoken with the writer and the gentlemen from the local MS chapter.
The writer has been to my house to run a human interest story about someone living with MS.
The editor has asked me to write a 650 word article to go along with the story. I started that piece and then forwarded it on to the President of the local chapter so that he could make sure it said what he wanted it to.
The folkes at the Beta Seron office have decided to watch the article to see if any other papers run it.
The local MS chapter is trying to coordinate with the editor what gets published.
My husband had his letter to the editor published in the paper on Tuesday.
I am hoping with the MS Walk on April 26 that the article and sidebar will show up next Sunday, April 20.
I am doing everything I can think of to correct this gross misrepresentation of MS.
If anyone has any idea or thoughts please let me know.
Thanks