MS Contin vs bupernorphine: Dr changed me from... - CLL Support

CLL Support

22,512 members38,670 posts

MS Contin vs bupernorphine

dooner6 profile image
6 Replies

Dr changed me from MS Contin to bupernorphine - anyone else done this ?

Written by
dooner6 profile image
dooner6
To view profiles and participate in discussions please or .
Read more about...
6 Replies
cllady01 profile image
cllady01Former Volunteer

dooner6, what is your current situation for having this medicine? It will help us to know how to answer you, if we know more about your situation.

I believe you replied to a post one time a couple years ago and stated you have Waldenstrom macroglobulinemia.

Are you being treated and it would help to know what your treatment is.

Hoping you feel well enough to answer my inquisitiveness.

dooner6 profile image
dooner6

Still have tthe Waldens and a failed lumbar fusion from 2004 - pain 7-8.

dooner6 profile image
dooner6 in reply to dooner6

Failoed lumbar laminectomy - NOT fusion. Sorry.

cllady01 profile image
cllady01Former Volunteer in reply to dooner6

I can't vouch for any given pain medicine, and especially for what you must be feeling. I certainly hope you get some relief from the new medicine.

It appears you are in the process of getting off the stronger med. and the new one is said to be a way to moderate severe chronic pain that is acceptable, but not as addictive and will better allow you to breathe as it is said to "have a much lower likelihood of respiratory depression.

Just keep your Dr. apprised of any changes you find to be concerning.

Best wishes for a good result.

dooner6 profile image
dooner6 in reply to cllady01

Thanks very much - needed to hear ...

haposwald profile image
haposwald

From oral to a patch? For me MS Contin got to be a true Pau with its addicting qualities I was truly glad when that was gone from my system! The buro patch seems to be taking care of all the chronic and most acute pain that I have from 3 cervical herniations and type 1 diabetes perifical neuropathy , but the patch has its side effects as well . Doesn’t do good in sweaty or wet conditions and the adhesive is pretty tough on the skin m. It’s a once a week on/ off and has been a miracle for me. Goid luck

You may also like...

Bebtelovimab vs Paxlovid

Wondering if anyone has experience with Bebtelovimab? Son has been isolating in his room with covid

Ibrutnib vs Acalabrutinib

Venetoclax - Morning vs Night

Has anyone's doctor advised the best time to take Venetoclax as far as it working...

Acalabrutinib: tablets vs capsules

VO2 max Vs Lymphocytes