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Carol

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Hello Carol and welcome to the group. I don't take

cytoxan but I do have breathing difficulties from the

rp (although it is much better than it used to be).

This is something to be cautious about and I would

suggest a phone call to your doctor to check it out.

Whatever meds you are on for rp you generally have to

stay on them quite a long time, then change to

something else!! Usually equally horrible!! The trick

is finding the balance that is right for you.

I am much better since I have been diagnosed and on

meds. I take methotrexate, plaquenil and prednisone

at the moment.

I hope you feel better, and feel free to jump in, ask

questions or relate your experiences!! Take Care,

Love Liz

__________________________________________________

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Hello Carol and welcome to the group. I don't take

cytoxan but I do have breathing difficulties from the

rp (although it is much better than it used to be).

This is something to be cautious about and I would

suggest a phone call to your doctor to check it out.

Whatever meds you are on for rp you generally have to

stay on them quite a long time, then change to

something else!! Usually equally horrible!! The trick

is finding the balance that is right for you.

I am much better since I have been diagnosed and on

meds. I take methotrexate, plaquenil and prednisone

at the moment.

I hope you feel better, and feel free to jump in, ask

questions or relate your experiences!! Take Care,

Love Liz

__________________________________________________

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