Just joined

[paulasmith75]

hi all! I have been told I have Morphea by my Hemotolagist reading my results out. I know I have Raynaurd symptoms but not been tested. I have a phone videk appointment on Saturday so I will know were im at. I have a few different health issues but I dont want to boar you all. Thank

[MissusTee]

Hi there,

I have had limited scleroderma for 34 years, and I have 3 other autoimmune conditions. Make sure that you have a list of questions to ask, as it may be a while until you get seen again with the coronavirus pandemic. If you have any questions just ask.

[newbe]

Please do not feel you are boring us, this website is exactly where you can vent your spleen (so to speak) and get some encouraging advice. We are all a mixed bag.

[PeacockPrincess]

I'm also not diagnosed yet but have suspected reynard's. Although the doctors didn't want (couldn't be bothered) to look into it yet unless/until it gets worse. :/

[Magsterly]

Don’t overthink or worry. I started 20 yrs ago with white finger and pain holding cold items. I would have to drop them! True - the pain is worse but I’m not debilitated yet! I live healthy and exercise exercise exercise. I’m hoping none of the more severe stuff happens. I’m trying to believe at 48 that maybe it will level off 😉