What autoimmune disorder has celiacs, gastroparesis, cystitus, vulvadynia and sub clinical hypothyroidism?
Autoimmunes as you list are all related to each other as they are HLA type conditions. If you have one, you are more likely to have others. There does not need to be one primary autoimmune disorder. Are you being strict with your gluten free diet (i.e. being wheat free as well) and have they started you on thyroxine yet? Both those things will improve your gastroparesis and vulvadynia. Improving the vulvadynia will improve the cystitis.
Does anyone have or know of a person with gastroparesis?
I have been living with gastroparesis for about a year now. Mine is pretty severe, to the point that I cannot tolerate any solid food without vomiting and have lost about 1/3 of my bodyweight.
Changing your diet is going to be necessary, at least in the short term. Soft food, low in fat, low in fibre. Things like soups, yoghurts, pasta and similar foods are best . Have you tried any of the medications that increase the motility of your stomach? These were no good for me because of side effects, but a lot of people use them with great success - the two main ones are domperidone and metaclopramide. Another possible option is botox injections into the pyloric sphincter (where food leaves your stomach). This has very mixed results, but I am actually going to be trying it next week.
It's probably easier for you to ask any questions you might have than for me to ramble on here, so if there is anything in particular that you want to know please feel free to email me :-)
Autoimmunes as you list are all related to each other as they are HLA type conditions. If you have one, you are more likely to have others. There does not need to be one primary autoimmune disorder. Are you being strict with your gluten free diet (i.e. being wheat free as well) and have they started you on thyroxine yet? Both those things will improve your gastroparesis and vulvadynia. Improving the vulvadynia will improve the cystitis.
Does anyone have or know of a person with gastroparesis?
I have been living with gastroparesis for about a year now. Mine is pretty severe, to the point that I cannot tolerate any solid food without vomiting and have lost about 1/3 of my bodyweight.
Changing your diet is going to be necessary, at least in the short term. Soft food, low in fat, low in fibre. Things like soups, yoghurts, pasta and similar foods are best . Have you tried any of the medications that increase the motility of your stomach? These were no good for me because of side effects, but a lot of people use them with great success - the two main ones are domperidone and metaclopramide. Another possible option is botox injections into the pyloric sphincter (where food leaves your stomach). This has very mixed results, but I am actually going to be trying it next week.
It's probably easier for you to ask any questions you might have than for me to ramble on here, so if there is anything in particular that you want to know please feel free to email me :-)
1:06 AM
Ken Mark









