Samantha Walsh has lived with type 1 diabetes for over five years since 2017. After her T1D diagnosis, she was eager to give back to the diabetes community. She is the Community and Partner Manager for T1D Exchange and helps to manage the Online Community and recruit for the T1D Exchange Registry. Prior to T1D Exchange, Samantha fundraised at Joslin Diabetes Center. She graduated from the University of Massachusetts with a Bachelors degree in sociology and early childhood education.
I selected “Other”. I use GlucaGen Hypo Kits, but I don’t live in the United States. (I’m from the UK (United Kingdom of Great Britain and Northern Ireland.))
I have 3 of those little red boxes. A friend gave me one several years ago, the doc at the VA sent 2 over the last few months. While I see the logic of having it, until the Attack Pit or Saber Tooth cat grows thumbs they’re useless (live alone).
@Steven Gill. I ‘hear’ you, sir. They’re only ever used by those around me as by the time I get a warning sign that hypoglycaemia is ‘on the way’ it’s too late as I’d already be unconscious. The first I know about it is when I’ve already been given the injection and I’m on my way recovering. I can usually feel where I’ve been injected and realise [realize] that my clothing has been removed. (I sweat profusely when I’m experiencing a hypo.) 😉
I had a gvoke hypopen prescription but my insurance this year does not cover it. The glucagon prescription that they do cover is GlucaGen® HypoKit® and according to their website ‘Novo Nordisk is permanently discontinuing the manufacture and distribution of GlucaGen® HypoKit® in the U.S. on July 1, 2024.’ I’m hoping that when this happens, my insurance will cover either GVoke or Baqsimi.
Early on in my diabetic life, I know I was given one of those kits. Never was used and was then thrown out. The endo office I go to now is always wanting me to get one of the Rxs listed. But after not needing anything like that for a very long time (probably 25-30 years), why would I spend that kind of money on something that I would end up throwing away? After 57 years of dealing with diabetes, I’m kind of stubborn about some things. 😬
As a T1D for 50 years, I have never had a prescription for or used any form of glucagon. Have you ever had a need to use it? Is juice/candy not good enough?
THe hold Novo kit – but it’s long expired
I selected “Other”. I use GlucaGen Hypo Kits, but I don’t live in the United States. (I’m from the UK (United Kingdom of Great Britain and Northern Ireland.))
I have 3 of those little red boxes. A friend gave me one several years ago, the doc at the VA sent 2 over the last few months. While I see the logic of having it, until the Attack Pit or Saber Tooth cat grows thumbs they’re useless (live alone).
@Steven Gill. I ‘hear’ you, sir. They’re only ever used by those around me as by the time I get a warning sign that hypoglycaemia is ‘on the way’ it’s too late as I’d already be unconscious. The first I know about it is when I’ve already been given the injection and I’m on my way recovering. I can usually feel where I’ve been injected and realise [realize] that my clothing has been removed. (I sweat profusely when I’m experiencing a hypo.) 😉
@Steven Gill. I forgot to add, sir, that those red boxes are orange on this side of the ocean. 😉
Amphastar Pharmaceuticals, Inc. Glucagon Emergency Kit
I had a gvoke hypopen prescription but my insurance this year does not cover it. The glucagon prescription that they do cover is GlucaGen® HypoKit® and according to their website ‘Novo Nordisk is permanently discontinuing the manufacture and distribution of GlucaGen® HypoKit® in the U.S. on July 1, 2024.’ I’m hoping that when this happens, my insurance will cover either GVoke or Baqsimi.
I have an Rx for Baqsimi and GVoke Hypopen. I prefer using Baqsimi.
Early on in my diabetic life, I know I was given one of those kits. Never was used and was then thrown out. The endo office I go to now is always wanting me to get one of the Rxs listed. But after not needing anything like that for a very long time (probably 25-30 years), why would I spend that kind of money on something that I would end up throwing away? After 57 years of dealing with diabetes, I’m kind of stubborn about some things. 😬
I do not understand why Medicare does not cover any of these products. I had to pay over $500 for two Gvoke pens that have a one year expiration date.
I have never had to use it so far. But having them is like having insurance. You never know when you’ll need them.
Medicare should at least pay for one at a minimum.
As a T1D for 50 years, I have never had a prescription for or used any form of glucagon. Have you ever had a need to use it? Is juice/candy not good enough?
Gvoke syringe to allow for smaller glucagon dose.
I don’t know. I have one but don’t know the brand. I recently got a new one that is delivered via the nose.