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I think that it would be terrific if Congress could pass the Andrea Sloan CURE Act to start improving the compassionate use process.

If my Democratic colleagues and other Republican colleagues that have not cosponsored it are not willing to cosponsor it, please do not object so we can pass this bill and so we can give these patients and their families the right to hope.

I think that they have done an excellent job of doing everything, within their regulatory power, to approve things.

Thank you again. Matt, gosh, about 15 years ago, my brother-in-law was diagnosed with ALS, and so, we lived what you are going through.

If 'Right-to-Try' legislation gets passed at the Federal level, just as it has at State levels, we are not going to see the dramatic shift tomorrow that we hope to see.

How do 'Right-to-Try' laws ensure that patients can afford their treatments?

What help, Mr. Garr, should be offered to patients and to pharmaceutical companies to ensure that patients can afford these drugs?

I appreciate your willingness to continue a conversation about what we all know is an important issue that is critical for Americans seeking access to potentially lifesaving treatment.

I am proud of the FDA's 'Gold Standard.' I am proud of what the FDA does.

We are asking for a very specific carve-out for a very small exception that does not necessarily--well, it does not cost us any money.

We need to move toward personalized medicine, in these cases.

Treatment should not be up to somebody who has no involvement in my medical treatment.

It will also force companies to have one point of contact at the company for somebody like Matthew to call.