I have carefully reread this entire post and I don't think there is another way to interpret the "sugarcoating" and now the reference to minimizing major brain surgery to be directed to anyone's post other than mine. This thread is about a Mom whose son is going through a very tough decision making process that we all have faced or are still facing. I tried to give emotional support so that she could step away from that burden 24/7. You don't need to clarify again or state that it is difficult to communicate intent in this type setting. You obviously feel my support was misdirected and potentially harmful. Your emphasis on the fact that bad things can happen is why I avoided this forum prior to my major brain surgery a month ago. I knew bad, potentially devastating, life changing things could happen. I'm pretty sure everyone that has done any research after their diagnosis is aware that this can be serious. You may feel my brand of support isn't helpful. I'm not sure that telling people over and over that bad things can happen is helpful. For those of you in watch and wait, choosing radiosurgery or microsurgery or in limbo wondering if the treatment chosen will be the end of the journey or the beginning of a longer journey....good things can happen too. I wish everyone the very best on their respective journeys. It appears I'm not a good fit for this forum and I appreciate you pointing that out so many times in this one thread.
Thank you Kathleen. You have been very helpful. Sometimes the kindest thing you can do for someone is tell them the truth and not sugar coat things. Thank you so very much! I'm sorry your tumor had regrown 7 years after they removed it all with microsurgery. Thank you for sharing your two cents. I agree with you that major brain surgery should never be minimized.
The only contribution I've made to this thread since we last spoke was to Kathleen, where I praised Kathleen for her comments (see quote above).
My comments were friendly, positive, and in the spirit of the ANA forum.
With all due respect, I never quoted your post, and your name was never mentioned since we last spoke.
I'm sorry if you disagree with my point of view or misinterpreted my remarks; however, with all due respect this thread is not about you. Opposing points of view are more than welcome and even encouraged on the forum so long as they are respectful.
If you disagree with my point of view regarding sugarcoating, then we can "agree to disagree" as the saying goes. Everyone has passionate views, and at the end of the day we are all on the same team.
Not that I should have to defend my self; however, as many on the forum know I was initially diagnosed at Michigan Ear Institute last summer. The reference about "brain surgery should never be minimized" comes directly from their website! The Michigan Ear Institute's website under the section "SIZE OF TUMOR." Please take a look for yourself.
I was simply passing along Michigan Ear Institute's words of wisdom, which is a good thing in my opinion. I stand by my comments.
Michigan Ear Institute says "surgery should never be minimized, and the risks of surgery include death." As far as I know, death is not a side effect of radiation.
Our fellow forum member, and senior contributor PaulW, had a friend die on the operating table from the surgery. So yes, the risk should never be "sugarcoated" or minimized in my opinion. I hope anyone considering treatment factors that into their decision making process. As the proverb goes...a true friend tells both sides of the story.
I feel like I'm walking on egg shells around here before I post.
Best wishes.
http://www.michiganear.com/ear-services-acoustic-neuroma.html