← Return to CRPS - anyone suffering with complex regional pain syndrome

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@bobberoo

Foot issues and CRPS symptoms:

I’ve had CRPS symptoms for over a year and it’s time I go somewhere to get treated and I’m not talking about just nerve blocks small device is inserted in the spine, I need to figure out where to go to get my nervous system re-balanced the Academy injections or lidocaine injections. Help please 🙂

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Replies to "Foot issues and CRPS symptoms: I’ve had CRPS symptoms for over a year and it’s time..."

Hello, I am sorry to hear you have been suffering and not finding relief.
Can you tell me a little more about what you have tried so far? Do you know the cause of the foot pain, or did something happen to get you into this cycle?
It will be easier for others to respond with a little more information about your history.
Sue

Makes sense. Now I just need to figure out how I’m gonna do that with the mayo clinic so I guess I’ll be getting on the phone soon 🙂 thanks!

Hello @bobberoo. Thank you for sharing more of your background with @sueinmn so that she and other members can provide you with support you are seeking!

Because there is an existing discussion on CRPS, you will notice that I have moved your post here: https://connect.mayoclinic.org/discussion/crps-anyone-suffering-with-chronic-repetative-pain-syndrome/

I've done this so that you may also connect with other members going through similar situations. Members such as @nursejudith @suecutuli and @grannyzoo may be able to join you as recent contributors to this discussion to share some additional support.

Do you have an appointment scheduled somewhere at this time or are you looking for care recommendations?