NeuroTalk Support Groups

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NeuroTalk Support Groups (https://www.neurotalk.org/)

- Reflex Sympathetic Dystrophy (RSD and CRPS) (https://www.neurotalk.org/reflex-sympathetic-dystrophy-rsd-and-crps-/)

- - Nerve block (https://www.neurotalk.org/reflex-sympathetic-dystrophy-rsd-and-crps-/97314-nerve-block.html)

baseballfan

08-11-2009 11:46 PM

Nerve block

Hi All,

Will you please keep me in your thoughts and prayers tomorrow, I am having my 2nd sympathetic nerve block. :grouphug::grouphug::grouphug::grouphug::grouphug:

Thanks and hugs to all,

Kate

hope4thebest

08-12-2009 01:46 AM

Hi Kate,
I've had six without sedation..
Try and go in in a relaxed state...they played some music for me during my blocks..that was helpful!! Maybe you can bring some of your own soothing music that you like if they will allow that!!
My lumbar blocks took about 20 minutes to half an hour..before you know it, it's done!
Let us know how it goes!!

Take good care!
I'll be thinkin' 'bout ya!!
Hope4thebest (((((( hugs))))))

daniella

08-12-2009 10:58 AM

Sending thoughts. I hope you get relief.

hopeful

08-12-2009 10:02 PM

I will keep you in my prayers. I think the nerve block is my next step. Hope all goes well for you!

Dubious

08-12-2009 11:32 PM

Quote:

Originally Posted by hopeful (Post 551158)

I will keep you in my prayers. I think the nerve block is my next step. Hope all goes well for you!

Hi Kate,

I have had 7 blocks since my CRPS DX last June 08. They always help me, for 2 or 3 months anyway! Hopefully your issues are ones of SMP that will respond to the blocks favorably. I do have a complication from the last one that is unrelated to CRPS. Prayers and best of luck to you!

Dew58

08-13-2009 03:13 AM

Hope you are doing well since your block:hug:

baseballfan

08-14-2009 01:42 AM

Thanks

Hi All,

Thanks for all the prayers and good thoughts:). You are all greatly appreciated. This is a great group of people who are very supportive and helpful.

Anyway since having RSD I have had one sympathetic nerve block on the left and one on the right. In total I have had 8 or 9 ESI/nerve blocks from 2003, the sad part is I had never had a ESI/nerve block hep me. I always hope and tell my usband to hope maybe this is the one that will do the trick.

After talking to my husband I don't think or really want another ESI/Nerve block again. But you never know, I will never give up on having hope that something someday will work.

I know I need to tell my story from 2003 until now in the introduction area to make it easier for all of you since your missing over 6 years if pain history.

:grouphug::grouphug::grouphug::grouphug::grouphug: :grouphug::grouphug::grouphug:

Thanks,:)

Kate

Dew58

08-14-2009 01:59 AM

http://i44.tinypic.com/6qxshe.jpg

Thinking of you, Kate.

CRPSbe

08-14-2009 05:37 AM

Kate,

This one didn't help either? Maybe it's too soon to tell... or... I hate giving up hope on things too, but maybe there are other things out there for you that you haven't tried yet. I'm wondering why they keep doing the blocks if they don't work...

Hang in there!

bassman

08-14-2009 07:21 AM

Quote:

Originally Posted by baseballfan (Post 551612)

Hi All,
I had never had a ESI/nerve block hep me. I always hope and tell my usband to hope maybe this is the one that will do the trick.

Kate

Kate,

Yes, that sometimes happens. Treatments that the doctors say "always help" do not a thing for us RSDers. I have had a few cortisone injections given by orthopedic physicians that do absolutely nothing. Only the topical anesthetic feels good.

After eight or nine blocks, I would personally agree that it is time to move on to trying something else. Either the doctors are missing the nerves altogether, or it just does not work for you. Why take the time and effort for an end result of nothing?

Hoping for better futures for you,

Mike :hug:

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