ReadyCrowd
Newbie
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Hello Andrew I am not T1 so can’t give you any practical advice but would just say it is very early days, it is a shock whatever type you are, the great thing is you want to do the right thing and learn how to manage it. This forum is an absolute godsend because it is the one place where you will get support and understanding in a friendly mannerHello there,
Hopefully I'm not breaking any rules by posting here. I was diagnosed on the 15th of October, so I'm not entirely confident I qualify as newly diagnosed even though I sure as heck feel that way. I'm going to be honest with you, the last couple of weeks have been a real struggle for me emotionally and physically; as it stands I'm deviating between the feeling that I'm finally coming to terms with my diagnosis and breaking down randomly during the day (usually when I wake up and before meal times). Aside from the stress and anxiety I'm feeling over all of this, the learning curve feels so steep right now due to the relentless torrent of information I've had to take in these past two weeks. I'm desperate for my life to return to some kind of normalcy but I feel as though I'm stuck in a loop.
I'm sorry in advance, I haven't even introduced myself and I'm here dropping a big old rant. My name is Andrew and I'm 35 years old. As it stands I'm currently waiting on the results of a GAD test; in the meantime I've been placed on insulin as the specialists here in Scotland strongly suspect I'm type 1 due to how quickly my symptoms appeared and escalated. I've come to understand that it's fairly rare to receive a type 1 diagnosis at my age and that I'm fortunate that it was detected before I had a major incident. My last (and first) a1c came back at 124 which I'm told is very high.
As it stands I'm trying my best to get familiar with counting carbs and dosing myself as best I can. I've been given a Libre 2 thingy and while it's been really useful I can't help but feel as though my life is turning into a graph as I focus on trying to flatten the spikes I'm seeing every time I stuff food into my face hole. While my healthcare team have been telling me I'm doing great for someone newly diagnosed, I feel as though they'd say that no matter what so it would be great if I could discuss the results I'm seeing and get some perspective. I've mostly been struggling with this alone because the people closest to me don't want to talk about it, which is rough because it's really what I need right now.
I'd really appreciate any questions, input, advice or even kind words you might have to offer.
Morning Andrew,Hello there,
Hopefully I'm not breaking any rules by posting here. I was diagnosed on the 15th of October, so I'm not entirely confident I qualify as newly diagnosed even though I sure as heck feel that way. I'm going to be honest with you, the last couple of weeks have been a real struggle for me emotionally and physically; as it stands I'm deviating between the feeling that I'm finally coming to terms with my diagnosis and breaking down randomly during the day (usually when I wake up and before meal times). Aside from the stress and anxiety I'm feeling over all of this, the learning curve feels so steep right now due to the relentless torrent of information I've had to take in these past two weeks. I'm desperate for my life to return to some kind of normalcy but I feel as though I'm stuck in a loop.
I'm sorry in advance, I haven't even introduced myself and I'm here dropping a big old rant. My name is Andrew and I'm 35 years old. As it stands I'm currently waiting on the results of a GAD test; in the meantime I've been placed on insulin as the specialists here in Scotland strongly suspect I'm type 1 due to how quickly my symptoms appeared and escalated. I've come to understand that it's fairly rare to receive a type 1 diagnosis at my age and that I'm fortunate that it was detected before I had a major incident. My last (and first) a1c came back at 124 which I'm told is very high.
As it stands I'm trying my best to get familiar with counting carbs and dosing myself as best I can. I've been given a Libre 2 thingy and while it's been really useful I can't help but feel as though my life is turning into a graph as I focus on trying to flatten the spikes I'm seeing every time I stuff food into my face hole. While my healthcare team have been telling me I'm doing great for someone newly diagnosed, I feel as though they'd say that no matter what so it would be great if I could discuss the results I'm seeing and get some perspective. I've mostly been struggling with this alone because the people closest to me don't want to talk about it, which is rough because it's really what I need right now.
I'd really appreciate any questions, input, advice or even kind words you might have to offer.
Hi @becca59, @PenguinMum, @Fazzy, @nicki92 and @Soplewis12 - thank you for dropping in and saying hello!
I'm doing the best I can to keep up with it all - I've recently been given my insulin-to-carb ratio of 1 unit per 18. Is that a high number? I've been given a target of 8 as of last week but I'm consistently finding that I'm dropping to numbers below that, so my healthcare team have offered to switch me to a half unit pen as they don't want me coming down so quickly from the 19 and 20 range I was at a couple of weeks ago. Is this something I should be concerned with? I've only just gotten used to taking the NovaRapid so for the meantime I've said I would think about it.
I know that when I start dropping below 6 my vision goes blurry and I begin to feel irritable, tired and lightheaded but I'm not sure whether that's related to the diabetes. After a bit of Googling online, it looks as though blood glucose readings above 4 should be too high for me to be feeling the effects of low blood sugar - so I'm starting to wonder whether it's all in my head.
I appreciate your concern - I've let my DN know about my situation and I'm hoping she'll point me in the direction of some support groups in the near future. Unfortunately (like many people I'm sure) I've lost contact with most of my friends over the COVID period and done a pretty good job of alienating myself. I do live with my brother, but apart from him the rest of my family lives in the United States so talking with them isn't easy. I think the timezone differences, distances between us and their lack of knowledge of type 1 has made the whole thing a bit more complicated than it normally would be. The general attitude towards my diagnosis has been disbelief (I'll be the first type 1 in the family) due to my age and how healthy I am in general - something I think is made more difficult by the fact I'm still waiting on the results of my GAD test.
If I'm being honest, even if I could speak to them I'm sick of the platitudes. They don't want to believe the specialists are right so any conversation on the subject is shut down with a "don't worry, when you get the test results back you'll see you're type 2" and it's driving me crazy. While I appreciate the sentiment behind the words, it's what I want to hear and it's preventing me from accepting the true reality of my situation. Apart from that, I don't know how much it matters - diabetes is diabetes at the end of the day and we're all on the same boat regardless of the type. I would much rather believe the specialists who diagnoised me and move forward under the assumption that I'm type 1 if only to avoid being dissapointed down the road.
@Soplewis12 I'm with NHS Tayside. So far my healthcare team have been brilliant! How have they been where you are?[/QUOTE
Hi Andrew,
I think 1 unit of insulin to 18 carbs is a decent ratio for someone new to insulin (I'm just going to assume that you are type 1 for rest of information) most type 1's lgo through a honeymoon period & their insulin requirements can be quite low. You don't mention a basal insulin so can only assume that you are just on fast acting at the moment. Most type 1's bolus insulin ratios are 1:10, mine are breakfast 1:10, lunch 1:8 & dinner 1:10. It can affect your eyes by BG coming down too soon after a long time being high, You're body is currently used to working with high BG so won't like it when you go in to normal range but slowly but surely it will get better.
I was also the first type 1 in my family but I was lucky enough that a sister was a nurse who understood the changes needed to help me initially. I made a big mistake of just getting on with it, didn't talk to anyone about how distressed I was, how hard it was so everyone assumed I was doing great.
If you feel you have no-one who understands the complexity of living & coping with type 1 check to see if your health board have someone you can talk to. It can be quite a lonely condition to try & cope with.
On a lighter note my mum & kids still don't understand hypo & hyper!
NHS GG&C have been great.
Best of luck
Hi & Welcome @ReadyCrowd to the club nobody wants to be part of ... they are a really friendly, knowledgeable, approachable bunch around here so any questions just ask away ... we have all been were you are at the momentHello there,
Hopefully I'm not breaking any rules by posting here. I was diagnosed on the 15th of October, so I'm not entirely confident I qualify as newly diagnosed even though I sure as heck feel that way. I'm going to be honest with you, the last couple of weeks have been a real struggle for me emotionally and physically; as it stands I'm deviating between the feeling that I'm finally coming to terms with my diagnosis and breaking down randomly during the day (usually when I wake up and before meal times). Aside from the stress and anxiety I'm feeling over all of this, the learning curve feels so steep right now due to the relentless torrent of information I've had to take in these past two weeks. I'm desperate for my life to return to some kind of normalcy but I feel as though I'm stuck in a loop.
I'm sorry in advance, I haven't even introduced myself and I'm here dropping a big old rant. My name is Andrew and I'm 35 years old. As it stands I'm currently waiting on the results of a GAD test; in the meantime I've been placed on insulin as the specialists here in Scotland strongly suspect I'm type 1 due to how quickly my symptoms appeared and escalated. I've come to understand that it's fairly rare to receive a type 1 diagnosis at my age and that I'm fortunate that it was detected before I had a major incident. My last (and first) a1c came back at 124 which I'm told is very high.
As it stands I'm trying my best to get familiar with counting carbs and dosing myself as best I can. I've been given a Libre 2 thingy and while it's been really useful I can't help but feel as though my life is turning into a graph as I focus on trying to flatten the spikes I'm seeing every time I stuff food into my face hole. While my healthcare team have been telling me I'm doing great for someone newly diagnosed, I feel as though they'd say that no matter what so it would be great if I could discuss the results I'm seeing and get some perspective. I've mostly been struggling with this alone because the people closest to me don't want to talk about it, which is rough because it's really what I need right now.
I'd really appreciate any questions, input, advice or even kind words you might have to offer.
I know that when I start dropping below 6 my vision goes blurry and I begin to feel irritable, tired and lightheaded but I'm not sure whether that's related to the diabetes. After a bit of Googling online, it looks as though blood glucose readings above 4 should be too high for me to be feeling the effects of low blood sugar - so I'm starting to wonder whether it's all in my head.
Hi I have been type 1 for nearly 2 years and I am 52. So it came as a shock to me, plus I don't know anyone else who has it either.Hello there,
Hopefully I'm not breaking any rules by posting here. I was diagnosed on the 15th of October, so I'm not entirely confident I qualify as newly diagnosed even though I sure as heck feel that way. I'm going to be honest with you, the last couple of weeks have been a real struggle for me emotionally and physically; as it stands I'm deviating between the feeling that I'm finally coming to terms with my diagnosis and breaking down randomly during the day (usually when I wake up and before meal times). Aside from the stress and anxiety I'm feeling over all of this, the learning curve feels so steep right now due to the relentless torrent of information I've had to take in these past two weeks. I'm desperate for my life to return to some kind of normalcy but I feel as though I'm stuck in a loop.
I'm sorry in advance, I haven't even introduced myself and I'm here dropping a big old rant. My name is Andrew and I'm 35 years old. As it stands I'm currently waiting on the results of a GAD test; in the meantime I've been placed on insulin as the specialists here in Scotland strongly suspect I'm type 1 due to how quickly my symptoms appeared and escalated. I've come to understand that it's fairly rare to receive a type 1 diagnosis at my age and that I'm fortunate that it was detected before I had a major incident. My last (and first) a1c came back at 124 which I'm told is very high.
As it stands I'm trying my best to get familiar with counting carbs and dosing myself as best I can. I've been given a Libre 2 thingy and while it's been really useful I can't help but feel as though my life is turning into a graph as I focus on trying to flatten the spikes I'm seeing every time I stuff food into my face hole. While my healthcare team have been telling me I'm doing great for someone newly diagnosed, I feel as though they'd say that no matter what so it would be great if I could discuss the results I'm seeing and get some perspective. I've mostly been struggling with this alone because the people closest to me don't want to talk about it, which is rough because it's really what I need right now.
I'd really appreciate any questions, input, advice or even kind words you might have to offer.
Hi @becca59, @PenguinMum, @Fazzy, @nicki92 and @Soplewis12 - thank you for dropping in and saying hello!
I'm doing the best I can to keep up with it all - I've recently been given my insulin-to-carb ratio of 1 unit per 18. Is that a high number? I've been given a target of 8 as of last week but I'm consistently finding that I'm dropping to numbers below that, so my healthcare team have offered to switch me to a half unit pen as they don't want me coming down so quickly from the 19 and 20 range I was at a couple of weeks ago. Is this something I should be concerned with? I've only just gotten used to taking the NovaRapid so for the meantime I've said I would think about it.
I know that when I start dropping below 6 my vision goes blurry and I begin to feel irritable, tired and lightheaded but I'm not sure whether that's related to the diabetes. After a bit of Googling online, it looks as though blood glucose readings above 4 should be too high for me to be feeling the effects of low blood sugar - so I'm starting to wonder whether it's all in my head.
I appreciate your concern - I've let my DN know about my situation and I'm hoping she'll point me in the direction of some support groups in the near future. Unfortunately (like many people I'm sure) I've lost contact with most of my friends over the COVID period and done a pretty good job of alienating myself. I do live with my brother, but apart from him the rest of my family lives in the United States so talking with them isn't easy. I think the timezone differences, distances between us and their lack of knowledge of type 1 has made the whole thing a bit more complicated than it normally would be. The general attitude towards my diagnosis has been disbelief (I'll be the first type 1 in the family) due to my age and how healthy I am in general - something I think is made more difficult by the fact I'm still waiting on the results of my GAD test.
If I'm being honest, even if I could speak to them I'm sick of the platitudes. They don't want to believe the specialists are right so any conversation on the subject is shut down with a "don't worry, when you get the test results back you'll see you're type 2" and it's driving me crazy. While I appreciate the sentiment behind the words, it's what I want to hear and it's preventing me from accepting the true reality of my situation. Apart from that, I don't know how much it matters - diabetes is diabetes at the end of the day and we're all on the same boat regardless of the type. I would much rather believe the specialists who diagnoised me and move forward under the assumption that I'm type 1 if only to avoid being dissapointed down the road.
@Soplewis12 I'm with NHS Tayside. So far my healthcare team have been brilliant! How have they been where you are?
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