Multimillion-dollar companies don’t need to reach out to patients
and caregivers, so I was happy to receive an invitation from Novo Nordisk to
attend an advocate summit with the less than happy title, “The Future of Diabetes.”
I’m not exactly sure why the title seemed uncomfortable to
me.
My guess is I don’t want Diabetes to have a future.
They spoke with me beforehand via conference call and asked
what I hoped to glean from our meeting, as well as what I hoped for my
children’s future. They didn’t have to
ask these questions, but I was impressed that they did.
This would be the first time Novo Nordisk has ever invited
patients and their caregivers to a forum. There was only a small group of us,
as I believe they were testing the waters to see how it would all play out.
They were very respectful and kind, and seemed extremely interested in
everything we had to say. I knew we weren’t going to solve the world’s problems,
but I was thankful that we had their audience, even just for one day.
There were a couple small presentations, and a small
overview of new medications that had come onto the market. Most notably:
Tresiba.
I was not familiar with it, probably because it isn’t
indicated for children yet, but my guess is that will change in the next year
or two.
Tresiba is a long acting medication that I’m told is flatter
than any other basal insulin on the market. It lasts for at least 42 hours, although
you still would give an injection every 24 hours. The exciting thing is missing
a dose isn’t a problem, you can just take it when you remember as long as there
are at least 8 hours between injections. As an example, if you normally give
your child their long acting insulin at bedtime, and then forget one night, you
can give it to your child in the morning, and STILL give them their regular
dose that night before bed again. As I understand it, it stores in the body differently
and won’t cause lows. Also, the missed hours won’t cause highs. That wasn’t the
only exciting thing: It has a 56-day shelf life. That’s almost three months it
can be out of the fridge and still remain viable. Nice! There was a young woman
that attended the forum who uses Tresiba and is super impressed by it. She says
it has completely knocked out her dawn phenomenon and she doesn’t have wonky
blood sugars during her menstrual cycle anymore. She used it for months,
keeping her pump on only for bolusing. Eventually she moved to MDI completely. I’m
not saying this will be your experience, and I’m not trying to sell it to you,
I promise. I just thought you’d want to hear what I heard. Information is power. Something to look forward to, for sure.
Obviously, the cost of insulin was brought to the table. And
obviously, it isn’t their fault. I’m only being slightly sarcastic here; Technically,
it really isn’t there fault, and they do have concern about the cost…it is the current payer system in the United States makes
them play the game like this. Even so, considering their profits, I’m pretty
sure it’s not upsetting them as much as it’s upsetting us. There was a plea
from another advocate to see Novo’s profits as a good thing. They can use this
money to make new medications for us, and build new research facilities and
production plants as they are doing now. I can't really argue with that. But for me, someone who has seen
families suffer because of the cost, I’m not sure I’m sold on the tradeoff. Ideally,
I’d like it if patients could work together with big companies, like Novo
Nordisk, and go to Capital Hill to excite change in the way our payer system
works in the United States.
I asked them why they didn’t have a program to help those
who can’t afford the cost of insulin, and it turns out they do! What?! I’ve
never heard of it. I didn’t know anyone who has heard of it, or shared that
information, and I’m active in the Diabetes Online Community. They even have a
website. (cornerstones4care.com) They have a copay program that for 2 years
will ensure you don’t spend more than $25 a month on their insulin…as long as
your insurance isn’t with a government program. (It will pay up to $100 of your
copay per 30-day refill.) The copay program information can be found HERE.
There is also a financial assistance program that you must
meet specific criteria for. You can find the information HERE.
Both of these links are hard to find on the website. There
was significant discussion about that, and I’m confident our voices were heard.
Happily, I signed up for the copay card, and in less than 5 minutes I had one
making its way into my hands via my printer.
The last discussion was led by Novo’s invited guest, Dr.
Gary Scheiner. He asked us to talk about what we think Novo should focus on
short term and long term. He asked about innovation, and what we’ve found to be
the most significant change in our lives. Even more than a pump, I felt like
Novolog and Humalog were the most significant changes in my boys’ lives. Living
with insulin that had to be injected a couple hours before eating was rough. It
was life changing to be able to give him insulin when they ate, letting them
dictate when they would like to eat instead of the insulin itself. Pumps were
also the best innovation…but it’s been almost 15 years since both of those have
entered our life…I’m ready for something new.
Long term, all I asked for was something to ease the worry.
A faster, smarter insulin would be ideal. Something that would deliver what my
boys needed, when they needed it. This coming from a woman that chooses the
boys current insulin pumps just because there are a few less buttons to push.
In my book, a little less worry goes a long way. As we circled around the table
other people echoed my sentiments, including those that work at Novo Nordisk.
I’m very thankful that Novo Nordisk initiated dialog with
the patient and caregiver community. This is the first stone thrown into the
pond, and as a result, I hope the ripples will bring around change in the
future. As a side note, it felt good to have Todd Hobbs in the room. He is the
Vice President and Chief Medical Officer for North America at Novo Nordisk. He
is Type 1 himself and has a son that was diagnosed at age 5.
They started their presentation with information about the
company, and said they hope to go out of business someday.
That’s a ballsy thing to say.
I’m glad they said it.
PS: Charlie Kimball
Another PS: All the information in this article relies mostly on my memory. Please talk to your doctor, and research reputable websites with any questions you may have.
