Hello - I was wondering, as usual, about the bantering about of the word "expert" ???
Quite a few of my shareposts discuss this .. and my question is always the same , when it came to doctors who claim to be "experts" in the field of MS or Fibro ...
Now I see we have experts popping up all over the place here ? Expert bloggers, expert moderators, expert in what ???
What I am trying to say is , there is no such thing as an expert .. especially when it comes to the medical field .. no such animal .. the real experts are the patients who have to live with this crap everyday .. and their opinions or feelings describe the expertise with which they live ..
Sometimes I have accused some open "forum" writers of "hijacking" posts .. this can be said for some of the writing I see here .. seems when people write in their journals and shareposts , boom, an "expert" comes along and writes something so contrived as if they alone thought of these "feelings" ..
This is why I only subscribe to a few shareposts .. Dr. Gross and Kristen ... a mother of two who shared her experiences as a newly diagnosed patient , and find their writings to be the most "honest" should I dare say ...
I don't need another "expert" telling me what I feel or think ... so what is the deal ? Why should I feel like a pat on the back is needed , when some of these "experts" should know that MS is different for all of us .. and what makes their "opines" better ?
We don't get paid to do this, we aren't given any credible proof that they are "experts" , and you are probably wonderig why I am on this particular subject ...
A friend pointed out that while it is always good to share our thoughts and feelings and to have respect for others , it is a two way street ... so why is one persons "blogging" considered "expert" , over another ?
And who really is to say what is true and not true .. and why do people insist on giving accolades to those who get paid to be an "expert" ... I am confused ?
I believed this place to be a place where all can express freely, and that the "hiring" of "experts" to tell us what we think or feel is too wierd for me .. just my opinion ...
Letting go of these emotions are my choice, letting go of these is my job .. and i often turn here to just write about "my experiences" and they are real .. when I hear or see the words "expert" or "paid" , I get nervous ... let the experts go to congress and get us all the help we deserve , but I won't allow myself to "taken" by "experts" ever again ... I don't trust them ....
People should write the truth about themselves, their experiences and not come here and try to "sell" us all on "sharing" .. it should be voluntary, and honest and real ... again, just my opinion, but life isn't all roses , even for the "normal" people ... it stinks, it is polluted, it is sad, it is hurtful and shameful ...


Hi AGSerra1,
Thanks for your post, albeit a frustrated one. I just wanted to address some of the points you brought up because I think we are in total agreement on some of them. For example, I agree that the term "expert" might be fairly arbitrary and that the real "experts" are the ones who live with it every day. I would argue, however, that Mandy, Jake, and Gina all deserve the word because they are dealing with MS every day. I do not think their objective is to be preachy, but instead to share their experiences with the day to day struggles in hopes of both connecting with others who are similar and engaging in a therapeutic exercise. Another major goal of this site is to create open and respectful conversation, which could not be possible without differing opinions. In that light, I thank you for your thoughts and hope you keep them coming.
Best,
Sofia
Dear Sofia and all else,
I deal with MS each and every day too and I would not give myself a title of an EXPERT.
Albeit I know a great deal about MS and much more than most Physicians in General and maybe even more than many general neurologists.. However still, I have no medical degree and therefore can never carry the label of being an expert.
I have been sharing MS related Info for several years. Have my e-newsletter "Stu's Views and MS Related News", have my MS website. library of over 1200 ms articles and my MS Blog.
And yet, each carry my disclaimer that I am not an expert in the field of MS nor a medical practitioner.
To do anything less, would imply the wrong message.
Regards,
Stuart