A Pain Survivor Community
Silvia replied to Nicole Hemmenway's discussion It’s been a year!
Silvia replied to pmdd's discussion For those new to RSD...it is possible to have a life, a happy one...maybe not now, but it is possible to get the pain under control. How many have the pain under control?
Silvia left a comment for Stacie Cavallaro
Stacie Cavallaro left a comment for Silvia
Silvia commented on Relentless Agony, aka "Joe"'s group Wisconsin & Surrounding States
Silvia joined Relentless Agony, aka "Joe"'s group
Silvia left a comment for Stacie Cavallaro
Silvia replied to Nicole Hemmenway's discussion I believe.
Stacie Cavallaro left a comment for Silvia
Stacie Cavallaro said… Hi Silvia,
I feel very badly for you and your son. I certainly hope he does not need another surgery as that may actually make the CRPS even worse. You are so right - this is an awful disease and there is no cure for it. We will have this forever in our systems. For me, my husband and I enjoy going to clubs to listen to bands play but the vibration of the music hurts too badly. I can only stay for a short while and then I have to leave. Being so young, does your son have support from his friends? Some people just cannot handle being with someone with a disability. I know because I have lost many friends due to this. It is a shame as we are still the same person - just with a problem, that is all. But someone who cannot handle this is really not a friend anyway. You sound like a very good mother - but do not forget that you need to talk also - as his caregiver. My husband is caring and supportive, but I feel so bad that I have ruined his life. He has given up so much for me. He gets very angry when I talk like that, though.
Well, I wish the best for you and your son. And please keep me posted on his progress. I really do care.
Stacie
Stacie Cavallaro said… Hi Sylvia,
I notice that you joined HoH about a month ago and I just want to welcome you to this wonderful site. I think you will find that every member is so caring and compassionate.
I am sorry to hear that your son may have RSD (aka CRPS). I was diagnosed with this disease in 2006 and it has been a battle ever since. This is a very nasty disease, and it has consumed almost my entire body. The pain is horrendous at times and I truely feel so badly for your son, and for you as well. I hope that your son is receiving the proper treatments and that the doctors are able to stop the disease from spreading. And I hope that you as his caregiver are developing your own support system, as it is very important for you to be able to express your feelings, as well.
I wish you and your fmily the very best.
Stacie
Hi Silvia! I am so sorry it took me a day to connect, but I wanted to thank you for joining HoH. We are so glad you are here and I cannot wait to get to know you better.
We are all here to support, inspire and encourage each other through the ups and downs of pain. I know through my own journey how important it was for me to connect with others who were also enduring many of the same challenges and experiences. I hope you feel empowered through reading others responses and sharing your own. We all have something to offer each other. Sending love and healing wishes your way...keep holding onto hope!
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