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Partners of HD Affe...
 
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Partners of HD Affected Individuals

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Topic starter
(@claudia)
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Joined: 3 years ago

Here you can share your thoughts, experiences, comments, and questions about being a partner of someone at risk or with an HD diagnosis – e.g., how your journey is together, what are the biggest challenges that you have to face, how do you provide support to your partner, etc.

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(@Anonymous)
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This is what Jose had to say about this topic in the Spanish version of this Forum:

Hi

I was a partner of a person affected by HD. Everyday life is complicated and, at the same time, educational. Why educational? Every day you must face new challenges, new ways of living. We are faced with the unknown and sometimes you handle it well and sometimes you don't know how to handle it. The main thing is to never give up and move forward with strength. Nothing and no one are going to solve our problems, so we must face them and go for it.

A hug for everyone 

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(@Anonymous)
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This is what Vlado had to say about this topic in the Slovakian version of this Forum:

Being the partner of a person with HD is a very painful thing. You see a loved one pass away in front of your eyes. But I'm still grateful for her smile and I enjoy her joy when she wins over me in board game. 🙂 

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