My daughter takes around 40 tablets a day WHEN SHE IS WELL and more when unwell. It’s time to #reviewthelist for prescription charges Cystic Fibrosis Trust
As a member of the Prescription Charges Coalition, we’re joining the The PDA National Pharmacy Association RCGP in calling for an urgent review of the exemption list for prescription charges in England. Find out more: prescriptionchargescoalition.co.uk #ReviewTheList
Cystic Fibrosis Trust #ReviewTheList my box of medication that has to sit under the stairs as no room left in the cupboard!
It will now cost almost £10 for a single item on a prescription in England - for many people living with Turner Syndrome this is unaffordable. That’s why we’re supporting the Prescription Charges Coalition in calling for an urgent review of the exemption list. #ReviewTheList
From age 16 my son will have to pay for prescriptions- this is just one daily snack …if in Wales or Scotland he wouldn’t, if he had most other long term health conditions he wouldn’t - #reviewthelist cf patients in England are penalised
A stroke already costs so much, but today it only got more expensive. A single item on prescription in England will now cost £10. 💊
With the Prescription Charges Coalition, we want to #ReviewTheList of exemptions and spare stroke survivors these charges: bit.ly/3weJLs0
As members of the Prescription Charges Coalition, we’re joining the The PDA, National Pharmacy Association, RCGP, Royal Pharmaceutical Society in calling for an urgent review of the exemption list for prescription charges in England.
➡️ Find out more: prescriptionchargescoalition.co.uk #ReviewTheList
My daugter was born with CF. She didn't choose her condition.
Her medication isn't optional. It keeps her alive. She shouldn't have to pay for these life saving drugs - CF prescriptions need to be made exempt! #reviewthelist Jeremy Hunt Health and Social Care Committee
Following on from the great community effort led by Nick Smith, today we hear from James, Jade and Lucy about why #freeprescriptions should be available for everyone with #cysticfibrosis . #ReviewTheList (1/2)
Last month, as part of the Prescription Charges Coalition, we wrote to the Health Select Committee Jeremy Hunt asking for his support in our mission to #ReviewTheList so that people in England with long-term conditions can access their vital medications for free.
We strongly oppose the rise in the prescription charge today as it’s simply unaffordable for people in England living with immunodeficiency. We’re joining the Prescription Charges Coalition in calling for a review of the exemption list. prescriptionchargescoalition.co.uk #ReviewTheList
Prescription charges are rising again. Patients with #lupus have to pay for these. These are my daily medications. I would not be alive with out them. Calling on Jeremy Hunt Health and Social Care Committee to urgently #ReviewTheList #immunocompromised #Evusheld - can I ask my followers to #RT
Cystic Fibrosis Trust Health and Social Care Committee Just a sort out of one of our medicine cupboards #reviewthelist ..with the cost of living up, the post code uk lottery must end for life threatening conditions
Prescription charges rise in England by 20p today and have risen 📈15 times faster than the price of milk 🥛since 1979. Children's Liver Disease Foundation support the call for Lord Bethell to #ReviewTheList urgently
It will now cost almost £10 for a single item on a prescription in England - for many working age ppl living with Genetic Conditions. This is unaffordable. buff.ly/3wkli4w #ReviewTheList
