Rheumatoid Arthritis Support Group
Rheumatoid arthritis is a chronic, inflammatory, multisystem, autoimmune disorder. It is a disabling and painful condition which can lead to substantial loss of mobility due to pain and joint destruction. The disease is also systemic in that it often also affects many extra-articular tissues throughout the body including the skin, blood vessels, heart, lungs, and...
I think because health care is a provincial jurisdiction, each province has their own plan. My sister has MS in Ontario and she cannot be covered, because she was not on the plan prior to her diagnosis. Shades of American health care.
Unless I am mistaken, BC is also the only province less that charges a monthly premium for BCHCP. Even in Alberta it is now free.
Hope the Enbrel helps straight away & makes things better.
It is always interesting to read on DS the different experiences that we share about our access to Drs, Specialists & the drugs that we so desperately need. I still find it hard to understand why the process accessing drugs is pathed with stress, heartache & difficulty when I believe all sick people should be able to access drugs easily.
I was on Enbrel in 2009 after failing about 4 other drugs and my Rheumy completed the paperwork & sent it away to Australian Health Department for approval. I received in the mail a prescription for Enbrel & filled it that day. 4 Enbrel injections cost me $32.00, that is $8 each. On the Enbrel box it showed that the real cost was $1,500 and that was the cost to the government. There was no stress for me & if I was a pensioner or on disability, I would've got 4 Enbrel injections for $5.
Australia has a PBS scheme (Pharmaceutical Benefits Scheme) that is subsidised by our government (i.e. taxpayers). The PBS Board decides which drugs to subsidise according to the benefit for the patients & negotiates prices with the drug companies. I have never experienced any stress about not being able to afford the med's that I need & cannot understand why other western countries don't support their chronically ill. It often leaves me feeling so sad to hear the cries of people on this site who cannot access the med's that they need.
Unfortunately, Enbrel wasn't the right drug for me but I can afford what I need. I realise that I am lucky to access the medical care here that I need, but I don't think that should be a privilege in a western country, but a basic right.
Cheers, Anna
H
Our basic health coverage is somewhat mandatory... you can't even see a GP unless you want to pay out-of-pocket for it. I've been on the BC plan I switched from my parents plan at 18. The basic plan has absoutely no drug coverage.
If you don't sign up for the fair pharmacare or make too much money you get no help with drug costs. I was able to sign-up after I was diagnosed though.... I find that a bit shocking (Ontraio won't cover her). How can a pre-existing condition be turned down by government health care? My Rhuemy had to fill out paperwork for a "Special Authority" before I could get coverage - but that was no problem - my rhuemy fibbed a bit on the form - he said I was sero-positive - I'm not. He was convinced I had RA and wasn't gonna let them slide out of paying. They have changed the criteria now - it doesn't matter anymore.
In BC pharamacre is run by the government and provided you meet thier criteria for the disease, age, income - you are covered.
She must not meet one of the disease criterias they have established for MS... in otherwords her doctors can't get her special authority approved. MS is one of those conditions there's no blood tests for ETC. Makes it hard to define.
Anna - don't get me wrong I do have coverage... its just complicated and ill managed. Dealing with the government can be frustrating - the gov't machine doesn't seem to have much common sense. It sounds like your experience was much more pleasent than mine.
Thank you for both of your comments.