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Struggling to find any trust in anything (kinda another vent post im sorry sorry)

Its weird bit before I was diagnosed I was mainly just getting the extra thirst and urinating systoms and have never felt like I was going to pass out or anything, so the diagnosis toon me by shock...but it's partly why I suspect I may not have good awareness
Diabetes is all about high blood glucose. It is an accidental overdose of medication for it which causes low BG ie hypos so you would not experience a hypo before you were diagnosed and it sounds like you have been actively preventing them since diagnosis which is a good thing in many respects but don't confuse never having a hypo with no hypo awareness.

I think most people fear hypos and it is totally understandable because they are potentially dangerous, but sometimes that fear is actually more debilitating than the reality and having the odd hypo and learning to manage them and developing confidence in both your body's response to hypos (ie hypo awareness and warning signs) and also your own ability to manage hypos is an important part of diabetes management and something that I think CGMs like Libre and Dexcom perhaps rob people of. It makes them feel vulnerable if they are without those devices.
Like everyone I feared hypos when I was first diagnosed and I didn't have CGM just finger pricks. The first few hypos were really scary, especially as I was alone when they happened and I rang someone close to me whilst I was having them and kept them on the line until I had recovered and let them know where I was in case I wasn't successful in treating it, but I have always been successful and that has given me the confidence in my own ability and the ability of my body but also confidence in my hypo treatment.... I use jelly babies and I call them my "Hypo Heroes". It is a delicate balancing act between trying to avoid hypos and learning how to manage them and if you have never had one then how can you be sure that your body will warn you and your hypo treatments will work.

Before I had had a nocturnal hypo, I used to wake up multiple times a night to assess if I might be hypo and sometimes I would actually get out of bed and go into the bathroom to finger prick to check, in the days when I didn't have Libre. Then about 8 months after diagnosis, I started exercising more and I had a whole week of nocturnal hypos even though I reduced my basal insulin and ate carbs before bed. That week taught me that my body will wake me up and my hypo treatment will work and surprisingly it stopped me from being so frightened of them because it gave me confidence that I can manage them. I still get nocturnal hypos (and indeed daytime hypos) despite my best efforts but I am so much calmer and more relaxed about them now because I have that confidence and I will just pop a jelly baby or two into my mouth and chew them really well and go straight back to sleep. The fear for me was far more debilitating than the reality and once I conquered the fear and gained confidence, the hypos were far more easy to deal with. I now sleep like a log every night unless my Libre alarm wakes me up and sometimes I even sleep through that! My body will usually wake me up in the low 3s at night but I get hypo sensations between 4.2 and 3.6 during the day depending upon how fast or slow my levels are dropping and what I am doing.
I take a break from CGM every now and then for a few days. What surprises me is that even though I have confidence in my own body's ability to warn me of going hypo and confidence in my own ability to manage hypos and I spent my first year of diagnosis without CGM, I still feel vulnerable the first night I go to bed without it, so I dread to think how scary the idea of going without CGM feels to people who have never managed their diabetes without it and never had a hypo and never developed confidence in their own body and their ability to deal with a hypo and I do wonder if the technology is doing people a disservice in allowing them to prevent themselves from gaining that experience and confidence.
 
Just wanted to say that this makes me angry on your behalf. You may want to look at changing hospitals or making a complaint. One face to face appointment after diagnosis and then being told not to call them for support is not right. Anxiety after diagnosis is common and needs to be treated seriously. Ignoring someone or making them feel like a nuisance is not helpful and will just result in poor mental health. I know they are stretched but this doesn't seem right to me. We have the same telephone message system as you but I have never been made to feel like a nuisance and I do talk to them about my mental health struggles because it is relevant to my diabetes (I am AuDHD - autistic and ADHD, I have anxiety and PTSD and can get really panicky, obsessive and scared of my diabetes at times) and they have been supportive.
My local hospital is the largest in the county, only one of two that have a emergency department so we often take in patients from the surrounding towns aswell. and its the only one that's remotely close. So sadly not feesable to change. And I'm a milienal who hates "complaining to the mamager" type attitude..but I probly should stand up for myself more. I will looking what I can doing that regard
One of the frist things they did when I started to get overly fixated on the sensor is threaten to take it off me and revoke my prescription to force me to use only my fingers if I didn't bring down my sensor usage (aka don't look at it as much) which while might have been a bluff..it left me with a bad taste. There exact words where "we've done it before when people over-stress about it and we can do it again" which..yeah felt like a threat
Also once during a bad patch, the person who rang be back ended the conversation with "by the way you've been ringing us every other day recently, please unless it's an serious problem don't ring us untill next week" so since them I've been ringing them less because I just don't feel listened to
 
My local hospital is the largest in the county, only one of two that have a emergency department so we often take in patients from the surrounding towns aswell. and its the only one that's remotely close. So sadly not feesable to change. And I'm a milienal who hates "complaining to the mamager" type attitude..but I probly should stand up for myself more. I will looking what I can doing that regard
One of the frist things they did when I started to get overly fixated on the sensor is threaten to take it off me and revoke my prescription to force me to use only my fingers if I didn't bring down my sensor usage (aka don't look at it as much) which while might have been a bluff..it left me with a bad taste. There exact words where "we've done it before when people over-stress about it and we can do it again" which..yeah felt like a threat
Also once during a bad patch, the person who rang be back ended the conversation with "by the way you've been ringing us every other day recently, please unless it's an serious problem don't ring us untill next week" so since them I've been ringing them less because I just don't feel listened to
I understand, I hate confrontation too but that attitude is shocking and should be addressed. Look up PALS (Patient Advice and Liaison Service) at your hospital. Go and speak to them or write them a letter detailing how you have been treated (like in your posts here). PALS is a good place to start and they will be able to support you and advise you going forward.
 
Hi Sara,
I'm really glad you came back to post again. Everything you're saying makes total sense, and honestly, none of it sounds like overthinking - it sounds like someone trying really hard to stay safe and do things right in a system that hasn’t made that easy for you. You've been managing so much with very little meaningful support, and the fact that your levels have stayed stable is a huge credit to your care and effort, even if it doesn’t always feel like it.
It looks like you're doing all the right things: you're comparing finger pricks, you're noticing patterns with your sensors, and you're actively looking for solutions. That’s a lot to juggle, especially when anxiety is in the mix too. And the truth is, no tech is perfect - both sensors and meters can be temperamental, and variation in fingerprick readings (even from the same spot) is frustratingly common. You're not imagining it or doing anything wrong.
The way your team has handled things - especially that comment about taking the sensor away and discouraging contact - is not OK. It’s not you being “too much”, but it does sound like they are being too limited. You deserve support that takes your mental health seriously and recognises that managing diabetes isn’t just about numbers - it’s about anxiety, fear, isolation, and daily decision-making, too. You’re not a nuisance for needing help and support with all of that.
I totally get not wanting to be that person who “complains to the manager”, but self-advocacy doesn’t have to look like confrontation. Sometimes it just looks like keeping a record of what’s happened, or sending an email that says, “I’ve been left feeling really unsupported and I want to understand my options.” If writing feels more doable than calling, that can be a powerful way to start. Even something like putting together a short bullet list of what hasn’t felt OK - or forwarding part of what you’ve shared here - could help make your voice heard without needing to go full formal.
If changing hospitals isn’t realistic (and that’s fair), maybe there’s a patient liaison, or even a GP you trust more, who could help advocate with you. You shouldn't have to fight for support alone.
Also, I'm not sure if you’ve tried calling or emailing our helpline, but they can be a supportive bridge while you’re waiting. They’re used to talking through exactly the kind of emotional and practical overwhelm you're feeling right now, and can help you put things into perspective or help in making all the things you'd like addressed in your next appointment. They're honestly great when you need that extra point of view.
Also - thank you for explaining so clearly where your fear of hypos comes from. That “unknown” is scary for a lot of people, especially if you live alone and haven’t had one yet. It’s not irrational, it’s protective. What you’re doing - managing gently, preventing lows while learning as you go - is completely valid. Building confidence takes time, and there’s no one right way to get there.
Please keep talking here as much as you want to. You're not alone, and your voice matters - not just because of what you're dealing with, but because you're handling it with so much honesty and care. As you can tell, people here are always happy to help, support and share their experiences too, which I think helps a lot when things get overwhelming, so don't be afraid to reach out whenever you need to.
Take care and keep being kind to yourself - you’re doing a lot better than you think. <3
 
My local hospital is the largest in the county, only one of two that have a emergency department so we often take in patients from the surrounding towns aswell. and its the only one that's remotely close. So sadly not feesable to change. And I'm a milienal who hates "complaining to the mamager" type attitude..but I probly should stand up for myself more. I will looking what I can doing that regard
One of the frist things they did when I started to get overly fixated on the sensor is threaten to take it off me and revoke my prescription to force me to use only my fingers if I didn't bring down my sensor usage (aka don't look at it as much) which while might have been a bluff..it left me with a bad taste. There exact words where "we've done it before when people over-stress about it and we can do it again" which..yeah felt like a threat
Also once during a bad patch, the person who rang be back ended the conversation with "by the way you've been ringing us every other day recently, please unless it's an serious problem don't ring us untill next week" so since them I've been ringing them less because I just don't feel listened to
Don't take this the wrong way, but I think they're right. As you said yourself, you've become "overly fixated". Neither the sensor nor the finger prick are going to give accurate results. The only thing we can hope for is that they're accurate to themselves. This way we can use them to detect trends. But constant fixation on these numbers is the way of madness. And when you consider that implications that stress has for blood-sugat (Many other things, also) it can become a self-fulfilling negative cycle.

If it is becoming an overbearing worry, you might be better off without it.
 
Diabetes is all about high blood glucose. It is an accidental overdose of medication for it which causes low BG ie hypos so you would not experience a hypo before you were diagnosed and it sounds like you have been actively preventing them since diagnosis which is a good thing in many respects but don't confuse never having a hypo with no hypo awareness.

I think most people fear hypos and it is totally understandable because they are potentially dangerous, but sometimes that fear is actually more debilitating than the reality and having the odd hypo and learning to manage them and developing confidence in both your body's response to hypos (ie hypo awareness and warning signs) and also your own ability to manage hypos is an important part of diabetes management and something that I think CGMs like Libre and Dexcom perhaps rob people of. It makes them feel vulnerable if they are without those devices.
Like everyone I feared hypos when I was first diagnosed and I didn't have CGM just finger pricks. The first few hypos were really scary, especially as I was alone when they happened and I rang someone close to me whilst I was having them and kept them on the line until I had recovered and let them know where I was in case I wasn't successful in treating it, but I have always been successful and that has given me the confidence in my own ability and the ability of my body but also confidence in my hypo treatment.... I use jelly babies and I call them my "Hypo Heroes". It is a delicate balancing act between trying to avoid hypos and learning how to manage them and if you have never had one then how can you be sure that your body will warn you and your hypo treatments will work.

Before I had had a nocturnal hypo, I used to wake up multiple times a night to assess if I might be hypo and sometimes I would actually get out of bed and go into the bathroom to finger prick to check, in the days when I didn't have Libre. Then about 8 months after diagnosis, I started exercising more and I had a whole week of nocturnal hypos even though I reduced my basal insulin and ate carbs before bed. That week taught me that my body will wake me up and my hypo treatment will work and surprisingly it stopped me from being so frightened of them because it gave me confidence that I can manage them. I still get nocturnal hypos (and indeed daytime hypos) despite my best efforts but I am so much calmer and more relaxed about them now because I have that confidence and I will just pop a jelly baby or two into my mouth and chew them really well and go straight back to sleep. The fear for me was far more debilitating than the reality and once I conquered the fear and gained confidence, the hypos were far more easy to deal with. I now sleep like a log every night unless my Libre alarm wakes me up and sometimes I even sleep through that! My body will usually wake me up in the low 3s at night but I get hypo sensations between 4.2 and 3.6 during the day depending upon how fast or slow my levels are dropping and what I am doing.
I take a break from CGM every now and then for a few days. What surprises me is that even though I have confidence in my own body's ability to warn me of going hypo and confidence in my own ability to manage hypos and I spent my first year of diagnosis without CGM, I still feel vulnerable the first night I go to bed without it, so I dread to think how scary the idea of going without CGM feels to people who have never managed their diabetes without it and never had a hypo and never developed confidence in their own body and their ability to deal with a hypo and I do wonder if the technology is doing people a disservice in allowing them to prevent themselves from gaining that experience and confidence.
Honestly I admire people who have the confidence to take break from cgms...but i don't see my anxiety being able to work. Tough it

I think alot of it acty comes from one weird moment I had.. I was still very new to it but it realy scared me for some reason
On the run up to Christmas I was starting to feel a bit better, was only checking my libre a few times an hour and genuinely started to feel like I was getting on top of things
I cooked my meal (it was salmon brochlie(spelling?) Baby corn and a small bit of carbs (potato). This is a meal I have had lots of times before with no bad effects. But this time I don't know what hapens. I wasn't near a hypo (according to my libre) or anything before I Injected my novarapid, I ate my tea as normal and then about 5 mins after I has finished and clean my plate away and just sat down to relax I got the alarm on my sensor saying I was at 4.5. And it was so bizarre to me, I waited the 15 minutes before eating but nothing longer than that, but the graph just shown a sharp decline despite me having just eaten, this dosent normaly happen to this extreme it normaly just goes down a bit then starts to level out as a eat. So I got up a but to see I'd maybe it was a a compression low but instead it kept going down to 4.2...I didn't test it which was stupid bit at the time I had forgotten that advice and just ended up eating a half of a chocolate digestive and it brought me back up to ok levels (if slighlty higher than if I had eaten my pretty healthy meal) Later when I looked back on the graph it was like it has besrly happend, so when I told my diabeties team about it the next day they (kinda correctly I guess) told me I didn't have a hypo because I didn't reach a number below 4, which ok fair.. but I was still weirded out that it happend right after I had eaten, normaly when I dip lower than normal it's in the gap between meals not right after it, then then it's not that dramatic

It definitely made me be more hyper aware right after meals before..and kinda brought back the hyper fixation I had started to go away from setting me back from square one
 
I understand, I hate confrontation too but that attitude is shocking and should be addressed. Look up PALS (Patient Advice and Liaison Service) at your hospital. Go and speak to them or write them a letter detailing how you have been treated (like in your posts here). PALS is a good place to start and they will be able to support you and advise you going forward.
It's funny the difference of attitudes between here and reddit, on there when I spoke about my diabeties team and the problems I feel with them I baiscly got told
"Sounds like your a difficult patient and the problem is you"
But here has been much more supportive
Which honestly put me off making an account here for ages..glad I did. Thanks everyone
 
It may be that you were more sensitive to the insulin that day because you had done some extra activity earlier or perhaps left it a bit too long between injecting and eating or you absorbed the insulin a bit quicker than usual or your levels were just a bit lower than usual when you injected which can make the insulin act quicker.
The important thing in that situation, where levels are dropping and you take some faster acting carbs to bring you up particularly if you already have food in your stomach is to chew your hypo treatment thoroughly because if you just have a couple of chews and then swallow, they will sit on top of the other food in your stomach waiting to be digested and sort of get diluted and slowed down by that food. Also the cells inside your mouth can absorb glucose directly into your blood stream, so releasing the glucose in your mouth will give you a quicker response than your stomach plus your mouth is closer to your brain which is where you want the glucose to get to if you are actually hypo.
Next thing to be aware of is that Libre is least accurate when levels are falling or rising fast and then change direction because you have eaten glucose or injected insulin. The nature of the algorithm in the system is that it will take usually at least half an hour to stop showing your levels dropping in that situation even when they started going back up 10-15 mins after eating your fast acting carbs, so DO NOT rely on Libre in those situations because it will make you panic and think that your fast acting carbs have not stopped the drop, when most likely they are actually bringing you back up. Libre and probably other CGM are not reliable in these situations and you should finger prick if you are concerned. My Libre can show me as 4.3 with a vertical downward arrow and 2 well shewed jelly babies will turn it around and bring me back up but Libre will continue to show me dropping, sometimes down to low 3s, but when I look at the graph later I didn't actually go below 4 and it was just the algorithm over exaggerating the drop. I have experienced this enough times now to know without finger pricking that it is just Libre being slow to catch on that levels have changed direction and I just ignore it when it says I am still dropping. If I have any concerns I will finger prick 15 mins after taking the glucose but mostly I just wait and it catches on about 30-40mins later that levels have in fact come back up and things were not nearly as bad as it was showing. It is just an irritating quirk in the system that, at the time you need it to be most reliable, it is actually least reliable, but that is why we are advised to finger prick 15 mins after glucose treatment and not rely on it.
 
Don't take this the wrong way, but I think they're right. As you said yourself, you've become "overly fixated". Neither the sensor nor the finger prick are going to give accurate results. The only thing we can hope for is that they're accurate to themselves. This way we can use them to detect trends. But constant fixation on these numbers is the way of madness. And when you consider that implications that stress has for blood-sugat (Many other things, also) it can become a self-fulfilling negative cycle.

If it is becoming an overbearing worry, you might be better off without it.
Don't take this the wrong way, but I think they're right. As you said yourself, you've become "overly fixated". Neither the sensor nor the finger prick are going to give accurate results. The only thing we can hope for is that they're accurate to themselves. This way we can use them to detect trends. But constant fixation on these numbers is the way of madness. And when you consider that implications that stress has for blood-sugat (Many other things, also) it can become a self-fulfilling negative cycle.

If it is becoming an overbearing worry, you might be better off without it.
Oh on that point they are right but i realy dont think straight up threats are the way to help any situation. I'm self aware enough to know that I fixate and my mental health is very reliant on my sensor, but I mentioned how much it deteriorated when I had to go without one right? I was a mess and was finger testing almost compulsively every like five minutes, and was scared to death about going to sleep, I even started having some more darker thoughts which is when I the. Reached out to get referred for therapy.

I mean I keep waiting for that moment where I feel a hypo or one suddenly happens so I can show myself it's not that scary but It hasn't really happened yet...maybe if it dose I'll get more confidence and then I can think about taking some breaks...but right now without the sensor I would struggle to cope I think
 
Unfortunately hypos are scary and the first few particularly so, so I am not sure that one hypo will create that confidence. It took many hypos for me to develop it including 6 nocturnal hypos in one week. I would not wish that on anyone and I was alone at the time, but it did solve the problem for me as I realised that I could deal with them and that was without CGM but Libre didn't have high and low alarms then anyway.
 
Oh on that point they are right but i realy dont think straight up threats are the way to help any situation. I'm self aware enough to know that I fixate and my mental health is very reliant on my sensor, but I mentioned how much it deteriorated when I had to go without one right? I was a mess and was finger testing almost compulsively every like five minutes, and was scared to death about going to sleep
Try not to put yourself down, you are not 'fixated', you are anxious and trying to do the best you can (and you are doing well) with very little support which is leaving you feeling overwhelmed (which is completely understandable).

Leva DUK's post is excellent advice. Try the helpline if you can, it might give you some support in the interim.

While you are waiting for the mental health referral, do you have any numbers you can call for support such as the crisis team, Samaritans, mental health matters (MHM, Shout (a text message service) etc? Especially if you are having 'dark thoughts' as you put it. They are there to help, I have used them (Samaritans, Shout and MHM) and they are helpful.
 
It may be that you were more sensitive to the insulin that day because you had done some extra activity earlier or perhaps left it a bit too long between injecting and eating or you absorbed the insulin a bit quicker than usual or your levels were just a bit lower than usual when you injected which can make the insulin act quicker.
The important thing in that situation, where levels are dropping and you take some faster acting carbs to bring you up particularly if you already have food in your stomach is to chew your hypo treatment thoroughly because if you just have a couple of chews and then swallow, they will sit on top of the other food in your stomach waiting to be digested and sort of get diluted and slowed down by that food. Also the cells inside your mouth can absorb glucose directly into your blood stream, so releasing the glucose in your mouth will give you a quicker response than your stomach plus your mouth is closer to your brain which is where you want the glucose to get to if you are actually hypo.
Next thing to be aware of is that Libre is least accurate when levels are falling or rising fast and then change direction because you have eaten glucose or injected insulin. The nature of the algorithm in the system is that it will take usually at least half an hour to stop showing your levels dropping in that situation even when they started going back up 10-15 mins after eating your fast acting carbs, so DO NOT rely on Libre in those situations because it will make you panic and think that your fast acting carbs have not stopped the drop, when most likely they are actually bringing you back up. Libre and probably other CGM are not reliable in these situations and you should finger prick if you are concerned. My Libre can show me as 4.3 with a vertical downward arrow and 2 well shewed jelly babies will turn it around and bring me back up but Libre will continue to show me dropping, sometimes down to low 3s, but when I look at the graph later I didn't actually go below 4 and it was just the algorithm over exaggerating the drop. I have experienced this enough times now to know without finger pricking that it is just Libre being slow to catch on that levels have changed direction and I just ignore it when it says I am still dropping. If I have any concerns I will finger prick 15 mins after taking the glucose but mostly I just wait and it catches on about 30-40mins later that levels have in fact come back up and things were not nearly as bad as it was showing. It is just an irritating quirk in the system that, at the time you need it to be most reliable, it is actually least reliable, but that is why we are advised to finger prick 15 mins after glucose treatment and not rely on it.
I think that the thing about the incident that kinda shook me, the fact that things weren't as safe and predictable as they seamed until then. I have since learnt that that's unfortunately part if the deal with type 1..things can just happen, it was a but if a hard pill to swallow when I asked the my diabetes team what could have caused it and they told me they couldn't give me an answer. But I didn't hold that against them unlike the other times they where more dismissive.

I knew that anything below 4 was a hypo, I was told I should have tested which I will admit I was panicked so I kinda wasn't thinking rational, but since was told again that you should treat hypos of finger readings only, then wait 15 after you treat the hypo (I have jelly babies and dextrose drinks) before checking again. Makes sense considering the lag the sensor has
 
Oh on that point they are right but i realy dont think straight up threats are the way to help any situation. I'm self aware enough to know that I fixate and my mental health is very reliant on my sensor, but I mentioned how much it deteriorated when I had to go without one right? I was a mess and was finger testing almost compulsively every like five minutes, and was scared to death about going to sleep, I even started having some more darker thoughts which is when I the. Reached out to get referred for therapy.

I mean I keep waiting for that moment where I feel a hypo or one suddenly happens so I can show myself it's not that scary but It hasn't really happened yet...maybe if it dose I'll get more confidence and then I can think about taking some breaks...but right now without the sensor I would struggle to cope I think
From an outside perspective, I'd say that what looks to you like a threat is actually something that would be done for your own benefit...and a good thing.

Again, don't take this the wrong way, but your justification for keeping using a sensor i.e that your health anxiety is even worse with finger-pricks seems to perhaps point to a more general health anxiety that might respond to a more general set of anxiety treatments etc.
 
Try not to put yourself down, you are not 'fixated', you are anxious and trying to do the best you can (and you are doing well) with very little support which is leaving you feeling overwhelmed (which is completely understandable).

Leva DUK's post is excellent advice. Try the helpline if you can, it might give you some support in the interim.

While you are waiting for the mental health referral, do you have any numbers you can call for support such as the crisis team, Samaritans, mental health matters (MHM, Shout (a text message service) etc? Especially if you are having 'dark thoughts' as you put it. They are there to help, I have used them (Samaritans, Shout and MHM) and they are helpful.
Thanks, alot of this i think I needed to hear, although I realy feel like "fixated" is the best way to describe is especially back in feb when i had multiple sensora fail and had to wait through we weekend till the replacement comes on monday, I couldn't go through 5-10 minutes without feeling the need to test my finger, I could stop myself like 70% of the time but the conclusion was there and strong, incouldnt relax or think of anything else

I did try the crisis team frist and foremost, they saw me once a day for 3 days. they then pushed be to self refer with my GP for a more long term solution. And now I'm here waiting.
One sort of nasty wrinkle if I have to have any more interactions with the crisis team then my referral will be null and void because you can't seek help from another place while using this service, but Samaritans are OK if I just need to talk, MHM has been okay and have helped be develop breathing exercises to calm myself. But often say my diabeties team is the best place for much concerns.

Diabeties uk helpline is what actuly reminded me about this forum, as in terms of emotional support they seam limited, they also suggested looking for local diabeties support group. And I did find one which i think is run by DUK, but things haven't gone well..

The group meets every 2 months, which honestly I wish it was sooner but ide take what I could get. The frist time I think the problem was i forgotton to be added to the email list when i asked, so I never got the info about joining the zoom meeting i even checked my spam and nothing. The next one earlier this month I did get the joining info (I was worried because he said he normaly sends out the info a week beforehand and I again saw nothing..until I checked my spam..which I hadn't checked cos last time I found nothing) but as I sat in zoom waiting for the meeting to start it had to be cancled becuase he couldn't log into his zoom account due to some issue of it needed a OTP... so so far it's not realy been helpful
 
From an outside perspective, I'd say that what looks to you like a threat is actually something that would be done for your own benefit...and a good thing.

Again, don't take this the wrong way, but your justification for keeping using a sensor i.e that your health anxiety is even worse with finger-pricks seems to perhaps point to a more general health anxiety that might respond to a more general set of anxiety treatments etc.
Yeah I have health based anxiety, and am on the waiting list to get help for it. I am currently on trazodome for anxiety and am open to trying other things, I just want to try them with therapy instead of before, because my triggers are around my sensor and my diabeties I need extra help in managing when things go wrong.

Unfortunately it's just left me here struggling until get to the front of the waiting list
 
Honestly I admire people who have the confidence to take break from cgms...but i don't see my anxiety being able to work. Tough it

I think alot of it acty comes from one weird moment I had.. I was still very new to it but it realy scared me for some reason
On the run up to Christmas I was starting to feel a bit better, was only checking my libre a few times an hour and genuinely started to feel like I was getting on top of things
I cooked my meal (it was salmon brochlie(spelling?) Baby corn and a small bit of carbs (potato). This is a meal I have had lots of times before with no bad effects. But this time I don't know what hapens. I wasn't near a hypo (according to my libre) or anything before I Injected my novarapid, I ate my tea as normal and then about 5 mins after I has finished and clean my plate away and just sat down to relax I got the alarm on my sensor saying I was at 4.5. And it was so bizarre to me, I waited the 15 minutes before eating but nothing longer than that, but the graph just shown a sharp decline despite me having just eaten, this dosent normaly happen to this extreme it normaly just goes down a bit then starts to level out as a eat. So I got up a but to see I'd maybe it was a a compression low but instead it kept going down to 4.2...I didn't test it which was stupid bit at the time I had forgotten that advice and just ended up eating a half of a chocolate digestive and it brought me back up to ok levels (if slighlty higher than if I had eaten my pretty healthy meal) Later when I looked back on the graph it was like it has besrly happend, so when I told my diabeties team about it the next day they (kinda correctly I guess) told me I didn't have a hypo because I didn't reach a number below 4, which ok fair.. but I was still weirded out that it happend right after I had eaten, normaly when I dip lower than normal it's in the gap between meals not right after it, then then it's not that dramatic

It definitely made me be more hyper aware right after meals before..and kinda brought back the hyper fixation I had started to go away from setting me back from square one

That happens to me sometimes @Sara Grice I’m eating or have just eaten and my glucose has gone down a bit not up. Although your team are technically correct that 4.5 isn’t a hypo, I don’t think there’s anything wrong in what you did, having a few carbs to push you up a little.

If you feel your team aren’t supportive with the emotional burden of Type 1, could you try a counsellor? Sometimes having someone listen helps get your thoughts straight. I’ve used a counsellor before and was pleasantly surprised at how helpful it was. They can help you reframe things and the fact they just listen is really good.
 
That happens to me sometimes @Sara Grice I’m eating or have just eaten and my glucose has gone down a bit not up. Although your team are technically correct that 4.5 isn’t a hypo, I don’t think there’s anything wrong in what you did, having a few carbs to push you up a little.

If you feel your team aren’t supportive with the emotional burden of Type 1, could you try a counsellor? Sometimes having someone listen helps get your thoughts straight. I’ve used a counsellor before and was pleasantly surprised at how helpful it was. They can help you reframe things and the fact they just listen is really good.
When you counsellor is that different to a license therapist? Because I am currently waiting for that. If it's something different I'll have to make sure it won't effect my current referral with the NHS therapy service I'm waiting for
 
When you counsellor is that different to a license therapist? Because I am currently waiting for that. If it's something different I'll have to make sure it won't effect my current referral with the NHS therapy service I'm waiting for

I’m not sure @Sara Grice Mine was definitely a counsellor rather than a therapist. I can’t see how it would affect your referral for a therapist because it sounds like they’re different things. Not only that, the NHS wouldn’t know what you’re talking to a private counsellor about. As an example, if somebody was waiting for an NHS XYZ Therapist (I made that title up) and in the meantime they got divorced and wanted to speak to a counsellor to improve their self-esteem or help them re-focus on their life priorities, that would be quite different.

However, if you’re worried it might cause you problems, you could check first.
 
When I had a referral there was quite a waiting list. I found a counsellor and worked with them. When I got the NHS support I took a break from the counsellor but in the end felt they complemented each other so worked with them both for the time that the NHS support was available. I continued with the counsellor for quite a few years. Very helpful in putting my diabetes in its place d enabling me to get on with life.
 
I’m not sure @Sara Grice Mine was definitely a counsellor rather than a therapist. I can’t see how it would affect your referral for a therapist because it sounds like they’re different things. Not only that, the NHS wouldn’t know what you’re talking to a private counsellor about. As an example, if somebody was waiting for an NHS XYZ Therapist (I made that title up) and in the meantime they got divorced and wanted to speak to a counsellor to improve their self-esteem or help them re-focus on their life priorities, that would be quite different.

However, if you’re worried it might cause you problems, you could check first.
Oh private therapy is definitely something I could look Into, I dunno how much it will cost me, if I can add it into my budget.
I will check with the palce I am waiting for frist but I think it's just actuly only about the crisis team, since the crisis team deals with people who need alot more Intense support than the NHS therapist could provide, so if they hear you have used them while being referred they null your referral I think.

So it should be ok
 
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