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Myasthenia Gravis For support and discussions on Myasthenia Gravis, Congenital Myasthenic Syndromes and LEMS. |
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12-23-2009, 08:15 PM | #21 | |||
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Tom
sorry you have to have more chemo. You are still in my thoughts as you go through all you have to. take care Kate
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12-24-2009, 08:18 AM | #22 | ||
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Sorry I haven't posted until now.
I hope you enjoyed your visit to my country, even if you did pay a visit to the NHS! I am so sorry that you need to have more chemo, be brave and strong. Sending lots of positive energy your way. Love Rach |
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12-24-2009, 08:35 AM | #23 | |||
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losing one battle doesn't mean that you have lost the war.
hope you will be able to celebrate next christmas in London, without having to meet the NHS, celebrating your remission. best, alice |
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12-24-2009, 08:55 AM | #24 | ||
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Tom,
I was very sorry to learn you will have to undertake more chemo. Pls let us know how you are progressing and know that you are in my thoughts. Sue |
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12-25-2009, 10:08 AM | #25 | ||
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We had a neuro-oncologist look at my MRI yesterday and it was clear to her that these effects are due to more lymphoma.
We're starting high-dose systemic methotrexate and intrathecal cytarabine today. Yes, chemotherapy on Christmas. I appreciate everyone's advice. I might update here occassionally a few more times to share news, but since this isn't actually MG-related I'll keep it to a minimum. |
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12-25-2009, 10:35 AM | #26 | ||
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Tom,
Again I am so sorry. You beat it once and you can beat it again. Would love hearing from you with some updates. I will continue to keep you in my thoughts & Prayers. Everyone here is pulling for you. Take care. Hugs, Pat |
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