Hello everyone! It's been a while. I've been busy training for the MS 150 here in Dallas. We got one day in, the other was rained out.
Anyway, my apologies if this has been discussed here but it's new to me. While fundraising for the MS 150 a coworker of my husbands discovered that she did not have MS she has Hughes Syndrome. The way she came about it was a bit strange, our insurance wouldn't pay for Tysabri so she went to this Neuro that, honestly, we thought was a quack. He put her on a strange diet and no medication. Her disability was progressing pretty quickly and we were a bit worried. I don't know her - just stories that my husband told me. SO, apparently he did two simple blood tests and voila, she has sticky blood. She is now on blood thinners, and physical therapy and doing really, really well. Amazing, and I'm so happy for her.
Is this something that is well known? I've never heard of it and my neuro (of course) seems dubious.
Here's the info:
http://www.hughes-syndrome.org/symptoms.htm
Thoughts?
Thanks. Have a wonderful day.
Jenn
Anyway, my apologies if this has been discussed here but it's new to me. While fundraising for the MS 150 a coworker of my husbands discovered that she did not have MS she has Hughes Syndrome. The way she came about it was a bit strange, our insurance wouldn't pay for Tysabri so she went to this Neuro that, honestly, we thought was a quack. He put her on a strange diet and no medication. Her disability was progressing pretty quickly and we were a bit worried. I don't know her - just stories that my husband told me. SO, apparently he did two simple blood tests and voila, she has sticky blood. She is now on blood thinners, and physical therapy and doing really, really well. Amazing, and I'm so happy for her.
Is this something that is well known? I've never heard of it and my neuro (of course) seems dubious.
Here's the info:
http://www.hughes-syndrome.org/symptoms.htm
Thoughts?
Thanks. Have a wonderful day.
Jenn
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