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General Parenting
B’s obsession
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<blockquote data-quote="B’smom" data-source="post: 740129" data-attributes="member: 23359"><p>Is that what your son is diagnosed with? How did they diagnosed him so many years after the fact? </p><p></p><p></p><p>He is not currently. We did go for a MRI last year and they said that everything was normal (I requested it because I have a condition where my cerebellum hangs to low and caused nerve damage). </p><p></p><p>If it was encephalitis, would it still be visible almost 8 years later on a screen?</p><p>My fear is that we’ll never know the answer. I do feel that’s it’s a piece to the puzzle that is B and it would help give us answers. And maybe a better direction on how help him better.</p><p>His first psychiatrist spoke about sending him to a developmental peadiatrician but then he was admitted to the treatment centre.</p><p></p><p>We definitely have to jump through hoops in Canada to get to certain doctors. I’m not sure how I would be able to convince the doctors to refer him to a neurologist.</p><p>The government won’t even approve genetic testing for him because “he’s not severe enough” Sounds like I need to do a better job advocating. I have the day off, I guess I have more phone calls and appointments to make today <img src="data:image/gif;base64,R0lGODlhAQABAIAAAAAAAP///yH5BAEAAAAALAAAAAABAAEAAAIBRAA7" class="smilie smilie--sprite smilie--sprite1" alt=":)" title="Smile :)" loading="lazy" data-shortname=":)" /></p><p>Thank you!</p><p></p><p></p><p></p><p></p><p>SWOT- that’s heartbreaking! I can’t imagine being passed around like that with no care.</p></blockquote><p></p>
[QUOTE="B’smom, post: 740129, member: 23359"] Is that what your son is diagnosed with? How did they diagnosed him so many years after the fact? He is not currently. We did go for a MRI last year and they said that everything was normal (I requested it because I have a condition where my cerebellum hangs to low and caused nerve damage). If it was encephalitis, would it still be visible almost 8 years later on a screen? My fear is that we’ll never know the answer. I do feel that’s it’s a piece to the puzzle that is B and it would help give us answers. And maybe a better direction on how help him better. His first psychiatrist spoke about sending him to a developmental peadiatrician but then he was admitted to the treatment centre. We definitely have to jump through hoops in Canada to get to certain doctors. I’m not sure how I would be able to convince the doctors to refer him to a neurologist. The government won’t even approve genetic testing for him because “he’s not severe enough” Sounds like I need to do a better job advocating. I have the day off, I guess I have more phone calls and appointments to make today :) Thank you! SWOT- that’s heartbreaking! I can’t imagine being passed around like that with no care. [/QUOTE]
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