New Member Parent of Son with type 1 diabetes

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Jzeb

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Hi
I am feeling overwhelmed at the moment as my Son has been diagnosed with charcot foot. Drs didn't pick up on it for a number of Months.
He has had diabetes sine he was 3 years old. He is 30 now.
He has a cast on his left foot and has just told me he has same symptoms in his other foot. I am so afraid and upset for him. Very worried. He doesn't live near either.
Has anyone any advice or anything that might help or be useful to know. thank you
 
Hi
I am feeling overwhelmed at the moment as my Son has been diagnosed with charcot foot. Drs didn't pick up on it for a number of Months.
He has had diabetes sine he was 3 years old. He is 30 now.
He has a cast on his left foot and has just told me he has same symptoms in his other foot. I am so afraid and upset for him. Very worried. He doesn't live near either.
Has anyone any advice or anything that might help or be useful to know. thank you
Welcome to the forum, you must feel rather helpless being far away. I believe @Flower lives with Charcot foot but if you use the search at the top right you should find some posts related to the topic.
 
Hello and welcome @Jzeb

I’m so sorry to hear about your son and how overwhelmed and worried you are for him.

Unfortunately Charcot seems to be misdiagnosed too often or diagnosed late once damage has occurred. It does mimic other conditions such as cellulitis, sprain, infection & that can make diagnosis challenging. It is a long term complication that can really stop you in your tracks. Being in a cast long term on crutches is a struggle and waiting for Charcot to settle down takes patience. It can be managed successfully and have a good outcome with time ,please don’t despair.

It can happen in both feet so your Son needs to seek help about that asap. My right foot and ankle are very damaged and badly misshapen and still in a cast today after many years. My other foot has fractured multiple times & is held together with metal but thankfully hasn’t changed shape & is my ‘good’ foot.

I hope your son has access to a good multi disciplinary team & clinic looking after him - orthopaedics, podiatry etc as well as care from his diabetes team. It really helps to get blood glucose in good stable range as well as blood pressure, cholesterol & all the normal diabetes stuff we juggle. Charcot can settle down given time and good monitoring but damaged feet remain very high risk and vulnerable to ulcers & skin breakdown due to altered weight distribution through the feet.

Surgery can be done if necessary once the initial flare up & bone destruction has settled and there are good results from surgery. Other options are air boots/braces & custom shoes & insoles. There is some current research on using artificial bone to stabilise joints.

There was an article on Charcot foot recently in Balance magazine with new research etc. I’ll find it & post tomorrow hopefully.

I hope you and your Son are doing ok. Charcot foot is a real shock & challenge but there is hope for a positive outlook. Wishing you both well .
 
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Welcome to the forum @Jzeb

Sorry to hear about your son’s diagnosis with Charcot Foot :(

I hope he is getting good information from his clinic, and the cast on his foot helps to stabilise things.

There’s an overview of Charcot foot here
 
Hello and welcome @Jzeb

I’m so sorry to hear about your son and how overwhelmed and worried you are for him.

Unfortunately Charcot seems to be misdiagnosed too often or diagnosed late once damage has occurred. It does mimic other conditions such as cellulitis, sprain, infection & that can make diagnosis challenging. It is a long term complication that can really stop you in your tracks. Being in a cast long term on crutches is a struggle and waiting for Charcot to settle down takes patience. It can be managed successfully and have a good outcome with time ,please don’t despair.

It can happen in both feet so your Son needs to seek help about that asap. My right foot and ankle are very damaged and badly misshapen and still in a cast today after many years. My other foot has fractured multiple times & is held together with metal but thankfully hasn’t changed shape & is my ‘good’ foot.

I hope your son has access to a good multi disciplinary team & clinic looking after him - orthopaedics, podiatry etc as well as care from his diabetes team. It really helps to get blood glucose in good stable range as well as blood pressure, cholesterol & all the normal diabetes stuff we juggle. Charcot can settle down given time and good monitoring but damaged feet remain very high risk and vulnerable to ulcers & skin breakdown due to altered weight distribution through the feet.

Surgery can be done if necessary once the initial flare up & bone destruction has settled and there are good results from surgery. Other options are air boots/braces & custom shoes & insoles. There is some current research on using artificial bone to stabilise joints.

There was an article on Charcot foot recently in Balance magazine with new research etc. I’ll find it & post tomorrow hopefully.

I hope you and your Son are doing ok. Charcot foot is a real shock & challenge but there is hope for a positive outlook. Wishing you both well .
Thank you so much for taking the time to write about your experience s. That's so awful for you. It sounds like it's a long journey with ups and downs.
Yes it did seem difficult to diagnose.
It is definitely going to be a challenge.
I wish you well too.
 
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