Guest guest Posted November 30, 2009 Report Share Posted November 30, 2009 Dear Mea, Has he started the diet yet? My husband was dx'd with UC last month, has been on the diet 5 weeks, and says he has no more pain in his joints. He used to get up in the morning and hobble around until he "got loosened up" and now, he hope right out of bed! I know I've read that sugar and carbs (which turns to sugar in our bodies) contributes to inflammation which contributes to a whole host of other maladies. Blessings, MY HUBBY HAS UC FOR 7 YRS JUST DIAGNOSED WITH ANKYLOSING SPONDYLITIS Posted by: "mea" jesenia_daughtry@... jesenia_daughtry Sun Nov 29, 2009 8:52 pm (PST) WONDERED IF ANYONE ELSE HAS SAME DIAGNOSIS WITH UC. APPARENTLY IT GOES HAND IN HAND WITH UC. JUST NEED SOME UPBUILDING COMMENTS FOR ME AS WELL AS TO SHARE WITH MY HUSBAND. THE WORLD SEEMS TO BE COLLAPSING ON TOP OF US. HIS UC IS EXTREME AND NOW THIS OTHER CONDITION IS ALSO EXTREMELY PAINFUL AND DEBILITATING. ANYONE!!! THANKS Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 30, 2009 Report Share Posted November 30, 2009 I was diagnosed with AS this summer and given all the typical drugs. ie: mobic, hydrocodone etc. I did get relief but was not interested in being on narcotics long term. I got very good results from a chiropractor. The pain was gone within three or four visits and has been gone for months with maintenance visits. My AS is associated with crohn's and the pain was so bad I felt like I couldn't breathe. I had read some info claiming chiropractic was not safe with AS but my traditional doctor at the spine institute actually recommended it. It's worth a try.. > > WONDERED IF ANYONE ELSE HAS SAME DIAGNOSIS WITH UC. APPARENTLY IT GOES HAND IN HAND WITH UC. JUST NEED SOME UPBUILDING COMMENTS FOR ME AS WELL AS TO SHARE WITH MY HUSBAND. THE WORLD SEEMS TO BE COLLAPSING ON TOP OF US. HIS UC IS EXTREME AND NOW THIS OTHER CONDITION IS ALSO EXTREMELY PAINFUL AND DEBILITATING. ANYONE!!! THANKS. > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 30, 2009 Report Share Posted November 30, 2009 Hi- I have had UC for 3.5 years now. I am 36. Initially I used to have terrible pain in the back of my neck, which I thought was AS but the doc dismissed it and asked me take Tylenol. In any event, as I weaned off Pentasa and prednisone, it went away. So I don't know. I am new to SCD, but a lot of people here and elsewhere swear by it. You can help your husband try it, and it should work. What about yoga? Good luck and take heart. We're tons of us here to help each other out. -Andy. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 30, 2009 Report Share Posted November 30, 2009 At 10:51 PM 11/29/2009, you wrote: WONDERED IF ANYONE ELSE HAS SAME DIAGNOSIS WITH UC. APPARENTLY IT GOES HAND IN HAND WITH UC. JUST NEED SOME UPBUILDING COMMENTS FOR ME AS WELL AS TO SHARE WITH MY HUSBAND. THE WORLD SEEMS TO BE COLLAPSING ON TOP OF US. HIS UC IS EXTREME AND NOW THIS OTHER CONDITION IS ALSO EXTREMELY PAINFUL AND DEBILITATING. ANYONE!!! THANKS. Welcome to the group. I know a little about A.S., but I do know that SCD is just about the best thing you can do for gut issues. Just as a suggestion -- typing in all caps is considered shouting on this list -- and it's harder for most of us to read. You'll find plenty of support here. — Marilyn New Orleans, Louisiana, USA Undiagnosed IBS since 1976, SCD since 2001 Darn Good SCD Cook No Human Children Shadow & Sunny Longhair Dachshund Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 30, 2009 Report Share Posted November 30, 2009 Hi Mea I've had both UC and Ankylosing Spondylitis for about 12 years. (The arthritis is a commen side effect of UC) For more than 1/2 that time I've been able to manage on Asacol + some sort of NSAID (currently it's Mobic) Most of my flares have been managed my Prednisone. For the most part I've found that when I keep the UC in check, the Arthritis was in check too (but I needed the meds) Last November I took an antibiotic and wound up in the hospital with a severe flare that's not totally under control yet. I found SCD in early July (I'm now 5 months in). While my D isn't totally under control yet, I do see improvements. I see even more improvement in the arthritis. I now take the Mobic ~2 times a week - instead of every day. When I wake up my joints don't feel stiff and locked and my back and neck have a full range of motion. You don't mention how long your husband has been on SCD, but I truly think that the diet will help both conditions. Hope that insight helps and that your husband feels better soon! --Merissa > > WONDERED IF ANYONE ELSE HAS SAME DIAGNOSIS WITH UC. APPARENTLY IT GOES HAND IN HAND WITH UC. JUST NEED SOME UPBUILDING COMMENTS FOR ME AS WELL AS TO SHARE WITH MY HUSBAND. THE WORLD SEEMS TO BE COLLAPSING ON TOP OF US. HIS UC IS EXTREME AND NOW THIS OTHER CONDITION IS ALSO EXTREMELY PAINFUL AND DEBILITATING. ANYONE!!! THANKS. > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 30, 2009 Report Share Posted November 30, 2009 HI, THANKS SO MUCH FOR WRITING BACK. HE IS NOT THE ONLY ONE WITH THIS PROBLEM. LIKE HE THINKS. HE WAS ON THE DIET FOR ABOUT 3 WEEKS AND FELT REAL WEAK AND "WORSE OFF" . HUNGRY ACCORDING TO HIM. HE GAVE UP ON THE DIET. HE HATED THE HOME MADE YOGHURT AND FOUND IT TO HARD TO CONTINUE. NOW HE IS GOING TO GO ON REMICADE WHICH THE ARTHRITIS DOCTOR RECOMMENDED AND ALSO THE GI DOCTOR. I REALLY WISH HE WOULD JUST GO ON THIS DIET BUT HE HAS JUST CONVINCED HIMSELF TO GOING ON REMICADE. IT BREAKS MY HEART BUT WHAT ELSE CAN I DO I DON'T KNOW. Subject: Re: MY HUBBY HAS UC FOR 7 YRS JUST DIAGNOSED WITH ANKYLOSING SPONDYLITISTo: BTVC-SCD Date: Monday, November 30, 2009, 9:45 AM Hi MeaI've had both UC and Ankylosing Spondylitis for about 12 years. (The arthritis is a commen side effect of UC)For more than 1/2 that time I've been able to manage on Asacol + some sort of NSAID (currently it's Mobic)Most of my flares have been managed my Prednisone.For the most part I've found that when I keep the UC in check, the Arthritis was in check too (but I needed the meds)Last November I took an antibiotic and wound up in the hospital with a severe flare that's not totally under control yet.I found SCD in early July (I'm now 5 months in). While my D isn't totally under control yet, I do see improvements.I see even more improvement in the arthritis. I now take the Mobic ~2 times a week - instead of every day. When I wake up my joints don't feel stiff and locked and my back and neck have a full range of motion.You don't mention how long your husband has been on SCD, but I truly think that the diet will help both conditions.Hope that insight helps and that your husband feels better soon!--Merissa>> WONDERED IF ANYONE ELSE HAS SAME DIAGNOSIS WITH UC. APPARENTLY IT GOES HAND IN HAND WITH UC. JUST NEED SOME UPBUILDING COMMENTS FOR ME AS WELL AS TO SHARE WITH MY HUSBAND. THE WORLD SEEMS TO BE COLLAPSING ON TOP OF US. HIS UC IS EXTREME AND NOW THIS OTHER CONDITION IS ALSO EXTREMELY PAINFUL AND DEBILITATING. ANYONE!!! THANKS.> Quote Link to comment Share on other sites More sharing options...
Recommended Posts
Join the conversation
You are posting as a guest. If you have an account, sign in now to post with your account.
Note: Your post will require moderator approval before it will be visible.