Hypopara patients deserve better quality of life - make it easier for Hypopara patients to access Forteo

Yes its far too expensive for the average me especially since I am 77 years old and on a service pension

This medication is way too expensive. Also after being on it 6 months I am now diabetic

Can you get this in NZ???

Please make this drug available on the pbs for these rare sufferers. All illness should be treated equitably and fairly for all human being, all Australians. Have compassion for those that suffer life changing illness everyday, for the rest if their lives. Consider their quality of life, the time they may not have remaining. Consider yourself lucky that you do not have it. Help .

Good idea

For my daughter

I have hypopara and i was shocked that i was not even aware there was another drug available for my condition number one but my goodness who could afford it. it could give so many people a better quality of life and be able to deal.with syptoms so much better.

The medication cost is too expensive. We need more support from the government to subsidise the medication and invest more in research for rare disease like hypoparathyroidism.

Glad to help

Everyone needing this just to try and have a normal life should have help accessing it. Imagine if it was one of your lived ones.

Pease put om PBS - help to save lives

Please add it to the PBS, makes a change to someones life

Just give them the medication cheaper they need it to live a better quality life!

Mother in law needs this. Please put on pbs

Helping a friend see better days

A signature for me and my son. both living with hypopara!

As a Hypoparathyroidism patient I would pray you make this accessible for all.

I worked with a clinical nurse, who has had to give up her profession because of this condition, please listen to the pleas and assist with the funding and help these suffering this condition to have some quality

Please help people with this terrible disease live a better life

My husband, and 2 sons both have hypoparathyroidism due to a genetic fault. We pay hundreds a month for their scripts, and then add 'over the counter' meds which don't count to the Pbs safety net. I have never even heard of this medication, presumably because it's so expensive! Just because not many people suffer from this shouldn't mean they miss out on opportunities for better health.