There is more than in the underline of the personal information to the story that one must dig deeper. Use a spade shovel, right now you are using a flat head. So deep that the community has been miss led, folks have made as a poster, which you are on the right track and openly see the BS. Points. Had the disease reportedly trailears. Years means, that one has suffered from CRPS/RSD at least 10 years or more. This case is only coming up on 3. This is taking in account of all recorded sites and crossed referenced; including medical professionals feeding off her postings since this the paper trail began.
Which has leading followers being down a bad path. With your posting of education on the individual made me want to dig deeper into finding the truth, which you point out should be bold in shared. Especially, with the short comings and miracles of losing 40 lbs to brag of being in a size 4. While I guess saying that the rest of the CRPS / RSD community we are fat if we do not fit in the criteria or critical enough to have access to dogs who are trained for people in worsen case scenarios. So now that specially trained dog is now being accessed as a pet, the money and time alone invested in the adaptive dog is now unable to help a real person who needs this help.
Is the special trained dog able to be returned and allowed to readapt to a severe individual since she has a new body and can walk, bend, care for and attend to her personal needs.
Guess that care hasn't taken off, as you pointed out.
Now the well noted by her is not able to raise a family. A 5 year old child. She was in Portland Oregon paper. Standing erect and appearing to able to move about, smiling and becoming pain free. I noticed for person improving miraculously physically and mentally, made me wonder. Where is this family she is struggling to raise? Most people who a recovering would want this experience sharing of a survivor not just of a person who a disease, but the coping and supportive family who are also coping.
Since it is clear residents of Oregon and all the old medical blogging over time. Especially, noted in her own private and personal blogs. Since court record library and open cases of legal action kind of intrigued me. Single dad actually appears to be raising said child on his own. Makes one wonder. What else of the untold story is?
This just makes me uneasy in having the disease myself over 10 years and was looking upto this individual as being hope and inspiration. More uneasy and feel partially betrayed. I am a l studying law and chose my own disease as a debate in a legal situation. Especially fighting for disability and pain. Amanda has had some variable good information to support. She is writing a book. Since my opinion is seeing her now as a poor character given one sided story and the overall evidence.
Just say, keep up with your opinions and character questioning of credibility because someone needs to see the other side of the coin. I ran into a reference of her writing a book. I won't be buying it because now I don't even trust if the posts are worthy and could be more harmful than good.
