Recent Posts
Height 5'6" HW 263 SW 239 LW 142 From size 20/22 to size 5/6
At 4 years out I crept back up to 180 now working my way back down. CW 173 size 10
Kelli - I do very much appreciate your honest answer. My Rheum said he would not be OK if I were in any type of flair but my blood tests are so whacky he keeps saying to me ... are you sure you feel OK? LOL
I'm waiting for the final approval and I'll see my Rheum on Feb 12 - one more time before surgery to see how the tests are going this month!
My gut is saying go for it as I should only get stronger once I'm at a normal weight.
Thanks for writing.. I did have surgery while on Prednisone on 8/26/2009. My Dr. wasn't concerned about it so I went through with the surgery..
It is very important you notify the anesthesia Dr. of your use of Prednisone. They have to give you an extra dose before you go to sleep.. That is the most important part. I made sure when the Dr. came in to talk to me he was aware of my prednisone use even if the nurses wrote it in my chart. My Dr had me take Vit. E prior to surgery to help straighten my tissue which is broke down and thin when using Prednisone.
After surgery, I seemed to be doing great. I even got out of the hospital 1 day early only staying for 24 hours. Unfortunately, I had complications a couple days later that I am still dealing with today. I have had 3 more surgeries since then and I am still experiencing pain and discomfort. My RNY Dr. says it is lupus related while my lupus Dr. says it is not.. I am not sure at this point what has caused my complications so I am going to a specialist out of state.. I have been to the ER and hospital multiple times since surgery. I have lost lots of weight 70lbs however, if I had to do it again, I am not sure I would have had the surgery because of the complications.... Some people get upset when I say that but I am just being honest about the situation.
Lupus is a disease that is very hard to treat and diagnose and so often when Dr.'s don't know what is wrong they blame "Lupus".
I hope this helps.. Every situation is different and all I can say is follow your gutt... Every situation is different and you may do great..
If I can assist you anymore, please don't hesitate to write...
Sincerely,
Kelli
Thanks!
Gracie
All my docs are very pleased with my progress. Of course, since surgery, I have a low white blood cell count. They ruled out all the likely suspects (short of doing a bone marrow biopsy) and everyone decided it was my autoimmune disease going "wonky" as a result of t he WLS. So, my wonderful team of docs is just keeping a close eye on me as I shrink down to nothingness.
Good luck Robin!
Elli
Glad you all lurk cause here I am ... a SLE pt for 15 years now almost to VSG. I take 6 mg of Prednisone a day and 400 mg of Plaquinil. My lupus doc does not see any problem at all with having WLS and at my first visit with surgeon he made no indication there would be a problem at all. I hope that is the case.
I'm going to review all the other posts to see if there is any other info from all of you prior to this week on personal experience.
Thanks - Robin
Hi Kelli - I'm new on the boards here and just coming across your post. what was the outcome? I've taken 6 months of classes and asked about prednisone on a number of occasions and no one seems to have an issue with it. I've never been able to get off of it (for 10 years now) but only on 6 mg a day.
For anyone else *****plied to this thread previously, I'd love to hear your responses. I'm looking at the VSG mostly due to my lupus and the thought I may need to take meds that the RNY won't allow.
Thanks all ... Robin
Right now all my joints are swollen, my skin is a mess with psoriasis lesions and I can't get rid of the same damn sore throat ..even through three courses of antibiotics. Oh well just another day in the life of those with autoimmune challenges