Hi I'm looking to speak to new friends on Facebook as you lot of ladies are truly amazing and your knowledge is better than the nurses if any one is on Facebook please add me jreinke@live.co.uk
Friends: Hi I'm looking to speak to new... - My Breast Cancer ...
Friends
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HI Jenny1410
Hope you're doing OK? I think this forum is probably the best place to find likeminded ladies to talk to. Facebook is a bit Public for the kind of questions we like to ask/answer.
I'm personally on FB but don't discuss my health or wellbeing.
There is the option to message anyone on here directly so if you find you have things in common or have the same type of cancer & you both want to chat it's easy to do.
If you read through the various posts you might find someone in a similar situation to yourself. Or you can raise a topic/question & someone usually has some input!
I'm on self enforced R&R at the moment, so l have time on my hands! l have an auto immune disease that's playing up & l don't want to have to increase my steroids!
Remember there's always someone around to chat & we even have at least one lady from Australia so day or night you could get a reply.
Best Wishes 💐
Mrs Nails 💅🏼
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Yep that's what Iv been doing on this page things I talk about that family can't see it's just that Iv been down for so long that I need to get back on track so deleted most of my people on Facebook because they didnt understand or was not going throu it I just want to see what other survivers get up to and to move forward thanks for your reply
I see Jenny, just more 'normality' l have to be honest I've stopped seeing a lot of people's posts, kept them as Friends but not all the rubbish they post! 😂
Where are you up to now in your treatment? I finished my Chemo November 2015, still wearing a wig as my hair has not grown back as well as I'd have thought it would.
We're celebrating our 40th Wedding Anniversary this year so an exciting year ahead. Off to the Far East on the Queen Mary2 to kick the Celebrations off! I have a long standing auto immune disease that many of my family & friends don't understand & that frustrate's me so much as the only thing my friends ask about is "How is my hair" 🙆🏻aagghh!
Keep in touch
Mrs Nails 💅🏼
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Finished radiotherapy end September didn't have chemo but now my other arm pit is hurting they all say it's too soon it's in my head and its unusual to have two mammograms in one year so I have to wait till march and keep pushing for it my recovery has been long and hard and I haven't seen any change in the scaring since day one I also have noduals in my throat daily headaches now thought to be due to high blood pressure ,it's been a long year otherwise all good
Great seeing news about your cruise lovely to have something to look forward too. Is this your first? We are 30 yrs married in May where does time go eh? Have a fantastic cruise - im jealous ha ha x
Hi Hidden
Yes, really looking forward to Our Cruise 🚢 I can't believe where 40 years went! We've been very lucky & taken many Cruises preferring them to other types of holiday now.
I had to cancel the Cruise for My Big 60 as l was mid Chemo so this is why we're pushing the boat out now, sorry for the pun!
I see from your later post you now have ME/CFS l'm so very sorry to hear this, it must be awful for you. I have PMR (Polymyalgia Rhematica) which also causes fatigue, l'm resting at the moment to try n keep the steroids as low as possible along with another drug which is basically a low dose Chemo!
The main thing is I'm here, l have a wonderful husband, my boys are both happily married & we are looking forward to Celebrating Big Style this year 🥂
Keep in touch
Angela aka Mrs Nails 💅🏼
Good for u pushing the boat out and doing it in style. We were on the last trip the QE2 had before being sold my my what service. Like u we got the bug and we had a trip of a life time flew to australia then cruised home 80 or so days my what an experience. Sadly two months later bang good old breast cancer but won the battle. Know ive just had a mastectomy following 2nd diagnosis but my wonderful memories of these trips keep me going. All trips in uk now as we have furbaby. Am lucky enough to have a motorhome so it fits all our holiday needs for now. Loved hearing all your news enjoy x
Sorry darlin
I can't put this on fb there are family and friends that don't know about this fact as they can't / won't cope with it ....
I found here is amazing the ladies with different stages and knowledge are so helpful and supportive xxxx good luck xxx
Hi I am on Facebook, happy to link up, I had mastectomy may 2015 no chemo or radiotherapy as I had the mastectomy, could have opted for lumpectomy but didn't want radiotherapy, now on letrozole, send me you full name and I will look for you, I am Deb Warman.
Jennifer reinke picture of baby pink headband yer I had mastectomy but a small lump got left behind so had to have radiotherapy I think that's what upset me the most thanks for adding me
Would love to keep in touch but not on fb my email address is valeriewhyte@hotmail.co.uk send me a message anytime. Ive been through the mill but on the up on how to turn my life around. My treatment left me witj ME/cfs so life for me is very restricted. Hope u get some folks to chat too and send some get well wishes too x
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Jennifer reinke if you want to add me thanks
So glad you have joined us... this page is amazing let's you ask questions that you can't ask anybody else,also if there is a problem you always get an answer.... so welcome aboard x
I'm already friends with you on Facebook. Although I don't post every day, I do go on several times a day to check posts, so if you fancy a chat just leave a message xxx
I had chemo mastectomy radiotherapy and all the thing removed under don't call sorry can spell it not on tablets fist 2 lot gave made sick but have tamoxiffen now I had cancer in left bust still not got one bust