Hi there..I just saw the PM Dr and...
 

I advised him that the nerve blocks did not work. Now he gave me a dvd on SCS..I am not familiar with any of these stuff and it sounds scary. He said I would need a psych eval?? Is this true..Anyone that had this done or know anything could you explain? I truly appreciate it and thanks in advance

Hi Mom.

There is a new "sticky" at the top of the page for SCS. It's new this week, so not much on there yet. My Ortho thinks I would be a good candidate too. Check it out!

I have SCS and posted on the new forum,but to answer your question YES a psyc. evaluation is required by the DR. and insurance Co. prior to implant._Carol

oh okay..i was thinking they were doing it because they thought i was crazy lol. I will check the forum out thanks..

I've had 2 scs implanted and 2 removed. I now have a painpump which I LOVE> I've posted on the other stick so you can read my story.

Hugs
Mary

Seems to be protocol... first goes the blocks..then sugestion of SCS.. at the same time trying meds... do lots of homework..read our posts..I have the SCS..didn't work for me..some it does...the pump seems to have more success... but lots of Dr. are not offering that up..the phych eval.. is required by the insurance co. prior to implantation... ..So sorry your blocks were not successful... Hang in there the best you can...

Soft hugz, kathy

Scs
 

If you go to seach this forum and type in SCS you should be able to read a lot about them.

Thanks everyone for your help. I will certainly take a look at the posts. Just makes me frustrated when I try something and find out it really is not working. Now im back to square one :(

Ya..Mom... we can relate! I am so sorry......:hug:

I will use your screen name and keep smiling:) I have been in awful pain nonstop everyday and i just hate that fact that all i can do is try and bare it. I don't want to be a nag or a pain to anyone. I find this site helpful. I did check out the scs forum and decided that i will not go with that procedure. I am nervous about having a foriegn objectg in my body and having to do deal with something like that permanently I don't think i can do that. There has got to be something else. I will keep searching until I find something. Thanks again everyone and i pray and hope you are feeling pain free

Mom...
 

Thank you..that warms me that you should use my screen name..i hope it brings you comfort as it is my heart felt wish... Funny just as you just said...I repeated that a minute ago too... to a dear friend of mine..."not to be a nag or a pain" but keep searching... my disability lady is impossible.... just this morning she is like a wart on my hip (and my Dr.'s)... making life impossible..I know they seem like just words but we must all keep a positive feeling and not give up hope.. know at times it almost feels like it would be the obvious most smart route..we can not go there.. not even together.. My rules..I called it..

Hugz for strength...Mom..:hug:

As you already know...Keep Smilin!!

Thanks hun I appreciate it:)

My ..
 

pleasure, Mom..that is the least I could do to help you.. it's my pleasure!!!!

KS:hug: