Ok , have had my "Woe Is Me" time and I am back .
Marmite you go girl , up and posting already ! Just go easy on yourself .
Ned definitely go speak to Macmillan . They specific people that work for them that just deal with the money side of things . And if you are in a union , speak to your rep . Not only will they be able to advise you , but some unions (nursing ones over here) give you grants when you are sick .
Also if you have any insurance policies on your mortgage , check them for critical illness cover or income protection cover .
And if all this fails , there are all sorts of benefits out there you could be entitled to , again Macmillan are the best people to do all that for you .
Camel I had all my lymph nodes cleared when I had my mx . The worst thing about it to be honest was getting the drain removed after ! The armpit area felt like I had a rolled up newspaper under there .
Who was it asking about FEC chemo ?
I had 6 rounds of them . My worst side effect was the sickness . They gave me a syringe driver which pumped anti sickness meds into me 24 hours a day for 5 days after each chemo . It was a wonderful thing .
Make sure they give you one of those if you get nausea .
My Onc said that if I felt ill whilst on chemo then she wasn't doing her job properly !
My chest and neck are glowing red now , and pretty sore . (neck looks like I have been induldging in some serious bouts of passion
)
Only have 4 more sessions to go , for which I am eternally grateful !
Next set of appointments are with the Surgeon to discuss reconstruction options . I really don't know what to ask her , but she's bloody good at her job so I will just allow myself to be guided by her .
Then in February it's my dreaded 3 monthly CT scan time - eek !
Made beef and broccoli stir fry for dinner tonight , with homemade egg fried rice . Just waiting for DH and the DC to get back from Mass then it's chow down time !
Hope you are all having a great weekend .
Amber - sofa , now !