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Kate Learoyd
@PKUFamily
That’s my momma! My inspiration. twitter.com/nspku/status/1…
Retweet of status by @BerryS730
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Kate Learoyd
@PKUFamily
75 more signatures needed to reach target! Give this a helping hand with a signature and Retweet please Petition ·… twitter.com/i/web/status/1…
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Kate Learoyd
@PKUFamily
@jaowsty76 All the best Jason
Kate Learoyd
@PKUFamily
Happy Christmas folks. NHSE is not funding #Kuvan for #Pku “this time”. The mood in @NSPKU is chin up and fight. … twitter.com/i/web/status/1…
Kate Learoyd
@PKUFamily
England @NICEcomms has a lovely process for evaluating rare disease, called HST. Like unicorns and rainbows i… twitter.com/i/web/status/1…
Kate Learoyd
@PKUFamily
I tell Amelie last night that we’ll be seeing Anita @MetabolicsBCH @macdonj on Friday. She tells me ‘Neeta is my best friend’
Retweet of status by @gemmaltreanor
Kate Learoyd
@PKUFamily
Lovely Damien raising Money for #NSPKU on Salomon Trail Marathon Wales 16 June 2018 uk.virginmoneygiving.com/fundraiser-dis…
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Kate Learoyd
@PKUFamily
It’s a fab day but some families out there will spend hours battling a child over #pku supplements. No family sh… twitter.com/i/web/status/9…
Kate Learoyd
@PKUFamily
Healthy choices mean different things to different people:
Aspartame is neurotoxic to people with the rare disease… twitter.com/i/web/status/9…
Aspartame is neurotoxic to people with the rare disease… twitter.com/i/web/status/9…
Retweet of status by @phedupcampaign
Kate Learoyd
@PKUFamily
PKU children do though #pku @NSPKU twitter.com/drayzze/status…
Kate Learoyd
@PKUFamily
@IanAustinMP Is that a bet @IanAustinMP ? Perhaps we can ask MPs to eat the same tiny protein allowance as their c… twitter.com/i/web/status/9…
...but wait! There's more!
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fakhright
@fakhright
astaghfirullah peng.krim guaaaaaaaa..............a *salto sambil solat*
