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afterthought on recent MHRA/patient involvement post in UK

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I was invited to participate in a patient conference at MHRA HQ, in relation

to the issues we are now discussing, a little while ago, Sept?, and as I was

unable to get to London I sent in written feedback on SSRIs.

This came my way as a member of the LMCA, Long-Term Medical Conditions

Alliance, in my role as HepAction. My afterthought is that perhaps there might

be

some mileage, yet again, from SSRI patients/activists joining this

organisation also as another way to get representation and information?

I can also give info on a good likely source of funding for anyone needing

help with expenses in doing any of this work. I had no funding, I do now, when

I applied to join th LMCA and they waived their fee.

Mo

Practise random kindness and acts of senseless beauty

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I was invited to participate in a patient conference at MHRA HQ, in relation

to the issues we are now discussing, a little while ago, Sept?, and as I was

unable to get to London I sent in written feedback on SSRIs.

This came my way as a member of the LMCA, Long-Term Medical Conditions

Alliance, in my role as HepAction. My afterthought is that perhaps there might

be

some mileage, yet again, from SSRI patients/activists joining this

organisation also as another way to get representation and information?

I can also give info on a good likely source of funding for anyone needing

help with expenses in doing any of this work. I had no funding, I do now, when

I applied to join th LMCA and they waived their fee.

Mo

Practise random kindness and acts of senseless beauty

Link to comment
Share on other sites

I was invited to participate in a patient conference at MHRA HQ, in relation

to the issues we are now discussing, a little while ago, Sept?, and as I was

unable to get to London I sent in written feedback on SSRIs.

This came my way as a member of the LMCA, Long-Term Medical Conditions

Alliance, in my role as HepAction. My afterthought is that perhaps there might

be

some mileage, yet again, from SSRI patients/activists joining this

organisation also as another way to get representation and information?

I can also give info on a good likely source of funding for anyone needing

help with expenses in doing any of this work. I had no funding, I do now, when

I applied to join th LMCA and they waived their fee.

Mo

Practise random kindness and acts of senseless beauty

Link to comment
Share on other sites

I was invited to participate in a patient conference at MHRA HQ, in relation

to the issues we are now discussing, a little while ago, Sept?, and as I was

unable to get to London I sent in written feedback on SSRIs.

This came my way as a member of the LMCA, Long-Term Medical Conditions

Alliance, in my role as HepAction. My afterthought is that perhaps there might

be

some mileage, yet again, from SSRI patients/activists joining this

organisation also as another way to get representation and information?

I can also give info on a good likely source of funding for anyone needing

help with expenses in doing any of this work. I had no funding, I do now, when

I applied to join th LMCA and they waived their fee.

Mo

Practise random kindness and acts of senseless beauty

Link to comment
Share on other sites

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