I was diagnosed with B12 deficiency in 2012 and the realisation that clinicians are taught very little about this very common condition dawned swiftly. I wanted to make a difference to people like me who were searching for correct information and help. Please see my mission statement.
Since my own diagnosis I have driven my family and friends round the twist – badgering those with symptoms to get tested. If someone breaks a finger nail, they’ll cheekily ask me if I thinks it’s B12 deficiency. The following line in Sally Pacholok’s book confirmed that my behaviour was normal!- ‘your families will tease you about your over zealousness in educating them about the dangers of B12 deficiency’ – I am pleased to report that those who did get tested and were found to be deficient are now driving their family and friends round the twist too.
One particular friend, Laura inspired me to create this website http://www.b12deficiency.info, I think she wanted me to shut up! I wanted to raise awareness about B12 deficiency and everything I was doing was falling on deaf ears.
I am a lay person and each time I would be asked – ‘are you a medic’? Nobody really was interested.
This website now provides the vehicle to help us all access great support and information. In the beginning my main source of information was the book- ‘Could it be B12? An epidemic of Misdiagnoses, Sally M. Pacholok R.N.& Dr Jeffrey Stuart, – and then later I found Pat Kornic at her excellent support group: https://www.facebook.com/groups/174928999276739/ – These people are my particular ‘Life Savers‘ but everyone who features on the page deserves championing.
I want to thank Laura for inspiring me, Ryan for his excellent typing skills, and my fantastic husband Damian for building the original website and for allowing me to bore him about B12 everyday!
www.b12deficiency.info and if you share the information, please credit the site.
Please sign and share my petition –