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	<title>Comments on: What can reasonably be done for Primary Progressive Multiple Sclerosis?</title>
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		<title>By: Hannah</title>
		<link>http://managing-multiple-sclerosis.com/ms-symptoms/what-can-reasonably-be-done-for-primary-progressive-multiple-sclerosis#comment-1087</link>
		<dc:creator>Hannah</dc:creator>
		<pubDate>Tue, 30 Jun 2009 06:03:19 +0000</pubDate>
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		<description>My mother has ppMS and has experienced the same treatment as you. Unfortunately treating your symptoms is all that can be done, especially as you have had this for 9 years. There is a lot of research into new drugs for MS but not for the progressive types only the relapsing remitting types. My mother had a few steroid courses which showed an improvement for a short term period, but I would be very cautious about steroid treatment as they come with serious side effects such as  hypertnesion and osteoporosis .
I am very pleased that you are doing better than expected, and I hope you continue to do so. I&#039;m sorry I can&#039;t offer any more help or ideas about it - I&#039;m sure your neurologist is doing the best he can.</description>
		<content:encoded><![CDATA[<p>My mother has ppMS and has experienced the same treatment as you. Unfortunately treating your symptoms is all that can be done, especially as you have had this for 9 years. There is a lot of research into new drugs for MS but not for the progressive types only the relapsing remitting types. My mother had a few steroid courses which showed an improvement for a short term period, but I would be very cautious about steroid treatment as they come with serious side effects such as  hypertnesion and osteoporosis .<br />
I am very pleased that you are doing better than expected, and I hope you continue to do so. I&#39;m sorry I can&#39;t offer any more help or ideas about it &#8211; I&#39;m sure your neurologist is doing the best he can.</p>
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