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MajaParticipant
Thank you!! ๐ Yes, I am kind of far away.. but… 15 years ago we would have had to write letters and put a stamp on them and waaaait ;o) lol. Hugs back at you! ๐
MajaParticipantOkay, I found it and sent it to you. Love and hugs, Maja
MajaParticipantDear Dr. Diana, sorry it took me so long to answer. I live in Germany, I am not in the states. I will have a look at the symtoms checklist and try to fill it out – if I find it lol ;). Yes, that would be interesting to find out if I might respond to that medicine. – And, yes, I know, it might not be fibrosis – it is all kind of confusing. ๐ Sending you big hugs!
MajaParticipantDear Dr. Diana. Thank you for your answer!! ๐ I understand that.. –Where else did you develop fibrosis? I am quite sure that “my” kind of gastroparesis that I have will most likely be due to fibrosis of my stomach and also most likely of other muscles in my stomach. Same with my uterus and the polyp I got there. And the muscles in my mouth`s cheeks being fibrotic and causing scars and wounds and swellings inside my mouth etc. Fibrosis causes a lack of blood supply/tightended muscles, nerval over-activity I think in my body in these tissue areas that are most affected. My tissue tells me exactly by feeling really cold in the areas.. Also tend to get swellings from that inside on the linings and mucosas.. What do you think where does fibrosis most likely occur in EDS, in what kind of tissue? Muscles, even fat?, connective tissue itself?, fascia, tendon-like tissue…I would love and to know more about it. (And MRI prob won`t show these kind of fibrosis I guess..) Hugs to you – hope you will manage to get rid of the fibrosis in your shoulder!
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