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Resuming roles in July, the new European Parliament and Commission will have a generational opportunity this year to overcome health inequities for people living with rare diseases, shaping policies that could address the urgent need for faster diagnosis and increased treatment options. Soraya Bekkali, MD, our SVP for EUCAN and International Business reflects on the opportunities and risks of this historic period in the region: http://spr.ly/604195Zil

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Jackie Damphier

Disabled Social Security Administration

1mo

What upsets me the most is the health care system here and the state of Tennessee does not take SLE lupus seriously and allowing people like myself to go without insurance I'll try to take my QMB away that I was entitled to through Medicare and you know what happens with lupus It attacks here kidneys, liver, respiratory, brain and your heart not to mention inflammation in your joints You know I'm suffering 24/7 in chronic pain and I can't get the help or assistance that I need and it's pretty darn sad that I have to suffer like this at 62 years old.

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