MSN Home  |  My MSN  |  Hotmail
Sign in to Windows Live ID Web Search:   
go to MSNGroups 
Free Forum Hosting
 
Important Announcement Important Announcement
The MSN Groups service will close in February 2009. You can move your group to Multiply, MSN’s partner for online groups. Learn More
RSD Helpline Support Group[email protected] 
  
What's New
  
  Welcome  
  Message Boards  
  General  
  Group Rules  
  Welcome Newbies  
  Our Toolbar  
  Monthly Check In  
  NEW CHAT ROOM  
  Kid's Introduction Page  
  RSD Intro's  
  Coping With RSD  
  FAMILY INTRODUCTIONS  
  RSD Questions  
  ADVOCACY PROJECTS  
  RSD News  
  A Laugh A Day  
    
  Pictures  
  Poems n Such  
  Healthy Recipies  
  Workman's Comp  
  RSD an Pregnancy  
  Help Wanted  
  Prayer Request  
  Caregivers  
  
  
  Tools  
 
General : ulcers
Choose another message board
 
     
Reply
 Message 1 of 5 in Discussion 
From: eels  (Original Message)Sent: 3/12/2008 7:55 AM
hi everyone
Hope you r all feeling the best possible 2day. My husband Dave, got a scs implant about 4 weeks ago now. It seems to be working well.The problem we have now is he keeps getting new ulcers / lesions every day. He used to get them b4, but no where near as bad as now. We actually watched one forming yesterday. His skin reddened and then melted away [like a lighter put to plastic]. The fluid and blood surfaces. and then the sore ulcerates. They are on his feet and legs up 2 his knees. I dress them everyday with Silvazine cream, but the Doctor and his specialist have never seen anything like it and dont know what 2 do. I read that the scs can aggravate the rsd and cause these, but does anyone know if there is anything he can take or do to stop or slow them down. Also, does anyone know of a rsd doc in Queensland Australia. We have a great pain doc but I think we could do with someone that specialises in RSD. If anyone can help, please let me know. Thanks. from Eels xx


First  Previous  2-5 of 5  Next  Last 
Reply
 Message 2 of 5 in Discussion 
From: MSN NicknameTami62Sent: 3/12/2008 11:34 AM
Hi eels,
 
So happy to see you are still with us in the group. My husband is getting ready for the spinal stimulater and I was wondering what information you might have to share. Where did you find the info on the stimulater causing ulcers. One of our other members also has issues with ulcers and lesions and she found a cream that works pretty well for her. I'll see if I can find the information on it and send it to you if you send me your email. She said it works better than anything the docs have given her but I don't know what they have tried on her. If you like I can see if she would send you an email so she can give more details. I am relieved to hear that the implant seems to be helping him. By the way, you are only the third caregiver I have met and I feel we need as much support as those who suffer. If you have any suggestions for our site to help improve the support for family I would welcome it. I'd really like to see the family and friends get more involved and active in the group. I think it would help everyone. Please save my email and contact me any time. I'm so glad to know you are there.
 
Talk to you soon.
Tami
 
 

Reply
 Message 3 of 5 in Discussion 
From: MSN NicknamefranknberrieSent: 3/14/2008 7:10 PM
I can tell you if it were me I would get that electronic device out of my body, I was offered an SCS but I read so many negative articals and actually took my brother to an emergency room to get his removed because of other problems the temporary version caused, I think they are as backwards as a frontal labotamy.

Reply
 Message 4 of 5 in Discussion 
From: MSN NicknameTami62Sent: 3/22/2008 6:13 AM
Hi Frank,
I would like to here what information you have on the SCS. Scoti's doc is going to ask for it for Scoti. Please share any citations you have.
 
Thanks
Tami
 

Reply
 Message 5 of 5 in Discussion 
From: eelsSent: 3/27/2008 4:34 AM
hi, Daves ulcer are still really bad and he also got one on his hand. The RSD has now spread and is in both hands and both legs. He is still not sorry he got the scs though, as the pain is more bearable with it. We get a lot of info from Dr Hooshmands RSD Puzzles. Its easy to google it. Also, Dave has been really dizzy and faint. We went to the Docs and is Blood pressure reduced 25 points from sitting to standing position and his pulse was racing. Has anyone had this. I am scared that is immune system is stuffing up. The Rsd puzzle list says that it can attack the immune system. Also for the ulcers we got this new dressing called Mepilex. You only change it each week, and because no air gets to it, the ulcer heals quicker and doesnt get the germs in. Also Dave doesnt have to go through the agony of me having to clean and dress the wounds daily. I would post some photos, but are not sure how to. Hope everyone is having a good day. Love Eelsxxxxxxxxxxxx

First  Previous  2-5 of 5  Next  Last 
Return to General