Product review of medical foods for PKU - Low Protein Diet

update

"Massive thanks to Simon Harris TD for his support & work to help PKU patients in Ireland get access to more prescription foods. PKU is a small community in Ireland but with his help & lobbying from parents and friends (6,000 representations were made) from June 2017, for the first time in 6 years, we will have access to new synthetic prescription foods for our kids. Simon Harris promised he would help and he did. Thanks to everyone else who helped us by signing a petition, liking a post or emailing a TD. It is a small but important step for PKU patients in Ireland PKU Association of Ireland" and also from Adults with PKU, Homocystinuria, Galactosemia and Allied disorders who require a low protein diet for life in order to maintain basic overall health.

Last 36 hours of petition before sending

Please reshare this petition to give it a last push accross social media and email family friends and work mates your childs friends parents and anyone else you have contact with to do the sane.Many thanks to the 1172 to thoose of you who have signed thus far.

Best wishes,

Gwen Kennedy

Adult with HCU an allied isorder of PKU

Share this petition

Help this petition to reach more signatures.

How to promote a petition?

• Share the petition on your Facebook wall and in groups related to the topic of your petition.
• Contact your friends
  1. Write a message where you explain why you have signed this petition, since people are more likely to sign it if they understand how important the topic is.
  2. Copy and paste the web address of the petition into your message.
  3. Send the message using email, SMS, Facebook, WhatsApp, Twitter, Skype, Instagram and LinkedIn.