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	<title>Scleroderma Warriors | Lulu Mckenzie | Activity</title>
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				<title>Lulu Mckenzie replied to the topic  in the forum Scleroderma Warriors General Discussion</title>
				<link>https://sclerodermawarriors.org/reply/580/#post-707</link>
				<pubDate>Sat, 15 May 2021 21:21:03 -0500</pubDate>

									<content:encoded><![CDATA[<p>Is anyone here on methotrexate or have been at some point? If so is it OK to have a glass of wine? My rheumatologist said that I shouldn’t drink at all but I’m wondering if I can have an occasional glass of wine. Thoughts?</p>
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				<title>Lulu Mckenzie replied to the topic  in the forum Members</title>
				<link>https://sclerodermawarriors.org/reply/579/#post-705</link>
				<pubDate>Fri, 14 May 2021 14:21:05 -0500</pubDate>

									<content:encoded><![CDATA[<p>Do they have a scleroderma specialist near where you live? My first indication was a rash on my neck, then the swollen fingers, your onset sounds much like my own. I’m on Cellcept now and it’s amazing the difference it’s made, I am now able to walk just fine without any aid and my skin has softened. Everyone reacts differently to medication but i&hellip;<span class="activity-read-more" id="activity-read-more-121"><a href="https://sclerodermawarriors.org/reply/579/#post-705" rel="nofollow ugc">Read more</a></span></p>
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				<title>Lulu Mckenzie became a registered member</title>
				<link>https://sclerodermawarriors.org/activity/p/61/</link>
				<pubDate>Thu, 13 May 2021 20:03:34 -0500</pubDate>

				
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