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Reply
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 Pam
  Welcome to the RSD family. My name is Janine I am the founder of this group.  I am sorry it has taken me so long to respond but I have been in the process  of a move and I have been away from a computer for awhile. My replies will  be sporadic for awhile as I will continue to be away from my computer during  my transition.
  I am so sorry to hear of another victim of the monster. I would like to  suggest to you that you seek counseling now though as it will help you to  adjust to what the future holds. This is something I suggest to everyone, it  sure helped me. RSD is so unpredictable, it is as individual as every person  is so there are no concrete answers as to what is next for any of us. What  is tue for one is not true for some one else. While it limits itself to one  area of the body for one person another may end up with full body symptoms,  while it may spread slowly in one person it spreads quickly in another. For  these and many other reasons it is best that we take care of ourselves in  every way, not just our bodies but our minds and spirits also.
  Always listen to your doctor but never think of your doctor as God. Question  everything and learn as much as you can. When you think you have all the  answers there is always another question to ask about this disease. You can  never research enough! Everyone of us who has had this monster for any  lenghth of time has done our share of research and we continue to do so.  Never be afraid to ask us about any procedure the doctors want to do on you,  and never have a procedure done without asking questions of those of us who  have had the procedure done! We are here to help that is why I set this  group up. We don't want anyone to feel alone in this.
  When you have those days where you feel like crying call on us. We have very  caring ears. Many of us are on line and are willing to chat at all hours of  the day and night. Right now I am unavailable but I know annie and mirage  are online quite a bit and are very good listeners. They are very willing to  help.
  Take care of yourself and know that you are not alone.
  Luv and hugs
  Janine
 
  "Winners Never Quit and Quitters Never Win"
 
 
 
 
  >From: "mallo" <[email protected]> >Reply-To: "RSD Helpline Support Group"  ><[email protected]> >To: "RSD Helpline Support Group" <[email protected]> >Subject: new with RSD >Date: Wed, 3 Sep 2003 15:14:05 -0700 > >----------------------------------------------------------- > >New Message on RSD Helpline Support Group > >----------------------------------------------------------- >From: mallo >Message 1 in Discussion > >Yesterday I went to the doctor and they told me that I had RSD.I`m 51 and  >not sure what to think.I`ve cry on and off today thinking why me. I had  >Ulner Nerve surgery last year( left arm)and they think thats how I came  >down with this.This all new to me not sure what will come next.My next stop  >is going to be Pain MGT Anesthesia and I hope this will help. I`ve been out  >of work for 3 months and plan to go back in 2 weeks I hope I can handle it.  >Thanks for listening to me  Pam   P.S Any good books that I can read up on  >about RSD > >----------------------------------------------------------- > >To stop getting this e-mail, or change how often it arrives, go to your  >E-mail Settings. >http://groups.msn.com/rsdhelplinesupportgroup/_emailsettings.msnw > >Need help? If you've forgotten your password, please go to Passport Member  >Services. >http://groups.msn.com/_passportredir.msnw?ppmprop=help > >For other questions or feedback, go to our Contact Us page. >http://groups.msn.com/contact > >If you do not want to receive future e-mail from this MSN group, or if you  >received this message by mistake, please click the "Remove" link below. On  >the pre-addressed e-mail message that opens, simply click "Send". Your  >e-mail address will be deleted from this group's mailing list. >mailto:[email protected] Pam
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