So hello to all who either view & or sign my petition. Thank you

So i would like to share with all a part of my son’s ongoing “medical & medication” issues in the current abusive & neglectful unstable “one sided” placement with the current ab*sers of over 11 years & please be aware i will put up the link to the particular medication in question below.

On the 5th July 2021 my son was put on VYVANSE 30mg Capsules for “Alleged” ADHD but the medication can also be used for Binge Eating Disorder as well (which condition my son allegedly has) is anybody’s guess.

Please find below a list of date’s this medication was prescribed & supplied for Callum:

• 5th July 2021 - Vyvanse - 30mg (filled the same day) 
• 10th August 2021 - Vyvanse - 30mg (filled the same day) 
• 16th September 2021 - Vyvanse - 40mg (filled on 2nd October 2021)
• 17th September 2021 - Vyvanse - 30mg (filled the same day) 
• 29th October 2021 - Vyvanse - 40mg (filled the same day)
• 29th November 2021 - Vyvanse - 40mg (filled the same day)
• 29th December 2021 - Vyvanse - 40mg (filled the same day)

Now explain this to everybody neglectors & the “so called doctor & pediatrician Dr David Christie from Albury NSW” did you take into account any of the following medical issues or anything else wrong with callum before this putrid medication was prescribed for him & the issues that former pediatrician Dr John Douglas “flatly refuse to test for or address” at the first & second appointment” for Callum & he wasn’t to young to be tested for but anyway:

• are allergic to any other medicines, or any foods, dyes or preservatives
• take any medicines for any other condition
  have any other medical conditions or heart problems, including ischemic heart disease (such as angina or myocardial infarction), suspicion or presence of any cardiac or heart-related abnormalities, irregular heartbeats or rate, family history of sudden/cardiac death
• have epilepsy or other seizures or have had an abnormal brain wave test (EEG)

Now considering as follows a list of “alleged issues” that Callum “allegedly has” yet only the bs i have heard, such as:

• Callum has “alleged Apraxia”
• A alleged “learning disability”
• Some bs “gene problem” No evidence to back this up only helen’s bs in December 2013

Now this is notwithstanding that in September 2010 that Dr Douglas didn’t bother to request any testing for Food or Skin Allergies let alone test for Epilepsy (Alleged callum was to young to be tested for it) He was not.

Now since the 12th July 2010 - Present Date, everything that has happened to my little boy has been in the current “abusive placement” & is all down to the current neglectors & nobody else. Not me or his Maternal Grandmother D Vodden

If people like Jess Clark from Wodonga, Jill Allen & Jane Caldwell MCHN’s from Wodonga, along with Jasmin Wood, Sarah Bebbington (formerly Streeter) former CPS worker Diedre McDonald & a list of lies & others kept their nose out of how i raised my son regardless & stopped making up fake allegations (which couldn’t be found proven)

Then my son would be at home & safe from harm & abuse & he wouldn’t have been passed around or neglected

https://www.nps.org.au/assets/medicines/936ec4bc-7d4d-49df-8880-a53300ff8427-reduced.pdf