maryodriscoll
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Hi everyone, well ladies in particular.
I have to share this with you as I am so angry and I don’t want anyone else to have to go through this. 4 years ago I visited the doc to discuss contraception to change from the pill. I had various options discussed and most were deemed not good apart from a coil or an implant. I was told that out of all the options the implant was the best option for diabetes as the coil had infection risks and the others hormone complications but as the implant was only progesterone it would not affect my control.
One year later I was having some problems physically and hormonally. My control had become irratic and there seemed to be no logical pattern. I was concerned that it was the implant so I went back to the doctors. I was told that it was highly unlikely that the control issues were due to the implant but in case there was risk that it was not working they would replace it with another implant.
For the next 3 years I had increasing control issues. I developed retinopathy and experienced a lot of pains in my hands, elbows, knees and other places which I saw various doctors for and a rheumatologist only to be told there was nothing they could find and it was probably fibromyalgia. I developed a frozen shoulder which I ended up paying £500+ to a osteopath to help with. I kept questioning if it could be the implant and repeatedly told (with a grin) it was highly unlikely. my HbA1c was in the region of 7.5 to 8 and only managed to keep it that low by testing 10 times a day and injecting/correcting 8 to 10 times a day. The swings daily were anywhere between 1.8 and 30 with the daily, monthly and weekly measurements from my meter averaged 10. I now have big lumps in my injection sites too. I had a lot of imotional problems during this period due to the immense pressure to keep things as controlled as I could and still failing. I developed numbness and pins and needles in my hands a feet. I was exhaused emotionally and physically and my sleep patterns were awful, waking 5+ times a night. I was put on amtryptaline for the pains and to help with the sleep problems.
3 months ago, despite reticence by the doctors, I had the implant taken out. The doctor who did it kept trying to persuade me it was a mistake not to replace it and that it would not be the cause of my issues or my control and in fact it was more irresponsible of me to risk getting pregnant.
I have just had my HbA1c taken. It is 6.9. My average meter readings are below 8. I am hoping that the retinopathy and neuropathy will improve with time and the pains will go away - who knows.
Without a doubt - it was the implant. Why do the doctors not know this!?!?!?!
I have to share this with you as I am so angry and I don’t want anyone else to have to go through this. 4 years ago I visited the doc to discuss contraception to change from the pill. I had various options discussed and most were deemed not good apart from a coil or an implant. I was told that out of all the options the implant was the best option for diabetes as the coil had infection risks and the others hormone complications but as the implant was only progesterone it would not affect my control.
One year later I was having some problems physically and hormonally. My control had become irratic and there seemed to be no logical pattern. I was concerned that it was the implant so I went back to the doctors. I was told that it was highly unlikely that the control issues were due to the implant but in case there was risk that it was not working they would replace it with another implant.
For the next 3 years I had increasing control issues. I developed retinopathy and experienced a lot of pains in my hands, elbows, knees and other places which I saw various doctors for and a rheumatologist only to be told there was nothing they could find and it was probably fibromyalgia. I developed a frozen shoulder which I ended up paying £500+ to a osteopath to help with. I kept questioning if it could be the implant and repeatedly told (with a grin) it was highly unlikely. my HbA1c was in the region of 7.5 to 8 and only managed to keep it that low by testing 10 times a day and injecting/correcting 8 to 10 times a day. The swings daily were anywhere between 1.8 and 30 with the daily, monthly and weekly measurements from my meter averaged 10. I now have big lumps in my injection sites too. I had a lot of imotional problems during this period due to the immense pressure to keep things as controlled as I could and still failing. I developed numbness and pins and needles in my hands a feet. I was exhaused emotionally and physically and my sleep patterns were awful, waking 5+ times a night. I was put on amtryptaline for the pains and to help with the sleep problems.
3 months ago, despite reticence by the doctors, I had the implant taken out. The doctor who did it kept trying to persuade me it was a mistake not to replace it and that it would not be the cause of my issues or my control and in fact it was more irresponsible of me to risk getting pregnant.
I have just had my HbA1c taken. It is 6.9. My average meter readings are below 8. I am hoping that the retinopathy and neuropathy will improve with time and the pains will go away - who knows.
Without a doubt - it was the implant. Why do the doctors not know this!?!?!?!