Does any one take a colon/UC Chrons anti iflammatory like asacol/apriso?

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therearemiracles
Veteran Member


Date Joined Dec 2006
Total Posts : 3457
   Posted 4/1/2010 12:58 PM (GMT -6)   
Hi I was just wonder in anyone take an anti inflammatory for the colon or gut, if so are you feeling relief with this drug along with your antibiotics? I may have to start the anti inflammatory for my gut.
Thanks
Very mild left sided (could have fooled me with the "mild")  UC.Just found out 4 years into it I might have Lyme's Disease, going to a LLMD in December. Confirmed Lymes on 12/8/09 before my new antibiotic protocal from my LLMD, I  Started and stopped LDN ON 1/25/09 to mid May no improvements. Tried Asacol, Pentesa, Colozol, Sulfasulsadine and Lialda, they made me worse. A range of antibiotics (for 10 days here and there), not much better. Supplements: No UC meds at this time. Started Doxy and Cedfinir too rough on stomach, stopped those.Started Bicillin injection 1/12/10, once a week of injections.On Zithromax and Flagyl as well, about 2 year protocol to rid myself of bacteria Babesia, Chylmadia Phenomia and Borresliosis. Taking Oxy Aloe Flush and liquid vitamins, curcumin and CO Q10


Razzle
Veteran Member


Date Joined Aug 2007
Total Posts : 4396
   Posted 4/1/2010 10:45 PM (GMT -6)   
What anti-inflammatories would you try for your gut? In your signature, you mention all the usual ones used for UC made you feel worse. I have the same problem from the 5-ASA class of meds (given to me for "Crohn's," which I & my LLND both think is actually gastrointestinal lyme and not Crohn's) - I get rashes or systemic allergic reactions from all of the 5-ASA meds that I've tried.

If I were in your situation, I'd take enteric coated omega-3 essential fatty acid supplements (shown in clinical studies to be as effective for UC as the 5-ASA meds), probiotics (also proven to help UC in clinical studies), and possibly steroid enemas (work best on left-sided UC from what I understand)... Systemic steroids would not be a good idea unless you have no other option. I would also stay away from 6MP/Imuran/Azathioprine, Methotrexate, Remicade, Humira, etc. - these meds significantly reduce the immune system's ability to fight Lyme and other infections.

Another thing that may or may not make a difference for you is reducing consumption of preservatives (specifically sulfite preservatives)...there was a study done in the UK that showed reduced symptoms & flareups of UC in the group that reduced the consumption of red meat and packaged foods containing sulfite preservatives. I don't have the link to the study anymore, but it was very interesting. I know another person with UC who experiences a UC flare when they eat sulfite preservatives.

Take care,
-Razzle
Chronic Lyme Disease, Chronic Bartonella (clinical dx only), Gluten & Sulfite Sensitivity, Many Food/Inhalant/Medication/Chemical Allergies & Intolerances, Asthma, Gut issues (dysmotility, non-specific inflammation), UCTD ("Secondary Lupus-Like Syndrome"), Osteoporosis, chronic Lymphopenia, etc.; G-Tube; Currently weaning off TPN.
Meds:  Pulmicort, IV Doxycycline, Heparin (to flush PICC line), Claritin, Singulair, Domperidone, Colloidal Silver (topically & nasally), probiotics, Liver support herbs, Ailanthus, digestive enzymes, homeopathy.

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