Sorry been very quiet lately but I'm - to be blunt - knackered π Still up and down the M6 to see MIL and I'm so tired that I can't think straight. I can just about manage to shove some slap on - usually whilst B is driving - so I can play the ' I'm fine' game.
I've been keeping up with your posts - so much has been happening! Good and bad...Twitchy feeling so poorly, so unlike her. She's amazing and has wonderful advice, I'll just send her my love and hope that she's soon on the mend π Wendy! What a fabulous outcome. You're my inspiration chick. I've read your letter and I could cry tears of joy - which does sound rather odd considering you've just been diagnosed with SLE! But you know what I mean π onwards and upwards my friend, so proud of you π
Well...as I out in the posts title, I have my second opinion next week - next Thursday at 3:30 at the London Lupus Centre - not sure if I'm allowed to say with whom the appt is. I am now pooping myself as this really is last chance saloon! I know I'm being daft but after 10 years of misdiagnosis or being told it's all in your head, it's kind of scary.
I love this forum - it has been a God send to me. I'm still fighting not only for me but for the countless others who will be told to bu***r off, there's nothing wrong with you. Still scared thoughπ
With love and thanks,
Charlie xx
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Charliebear68
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Let us know how you get on. Best of luck with your appointment. I haven't been there myself but I've only heard good things about the London Lupus Centre.πΈπ»
I know just how you feel. Even though I finally got my diagnosis in march I won't believe it until I see it in writing. I'm scared that they will change their minds and the searching will start again. People just don't understand the need for an actual diagnosis a name to all the symptoms and a reason why we feel so ill. I really hope you get the answers you need π€
ππΌ Am with sam13...even after 6 years of diagnosis, PTSD due to 40 years in the diagnostic wilderness means I'm ever-ready to be given that b***** o** line...to my face, in writing, whatever π
Hang on in there charliebear...this consultant could be a Big Happy Surprise...this could well be your True Detective π€·ββοΈ: it happens!
You are such a thoughtful person π Still thinking of others..I have been keeping up with posts and I'm afraid I did giggle when I saw your bright pink tablets...I hope you have to chew or suck them! They're ruddy huge!
I'm hanging in chick - by my fingernails! Before they break off anyway π π
B says we need 'House' to rule things out and be a detective! Great minds eh??
Keep fighting my friend and I'll be in touch soon πππ
ππππ that's why I included the photo of the psychedelic pink tabs: hoped everyone would at least chuckle! how you swallow these tabs depends on whether you're treating symptoms of constipation or diarrhoea...you always chomp gently on the tabs (which turn into pink glue once chomped) to break them up a bit...then fast as poss you wash them down with water (lots of water if you're managing slow transit dysmotility, less if it's fast transit π)
Hello Charliebear68! Thank you for your very kind words!!!! Waiting to see my GP and get a response from the Health Board, wondering nervously how they will react. I really, really hope that your appointment goes well. I know how you are feeling. I was so nervous about my appt in London! I didn't sleep much the night before. In a hotel room in London, very noisey and so many thoughts running through my head. I was feeling sick with nerves the next morning. Like you. Thinking what if after all this fuss, he agreed with my diagnosis? What if he wants to reduce my meds? What if he says I can't help you any further, this is as good as it gets for you. These appts are hugely important for us aren't they, bound to be nervous. Is your other half going with you? Can't believe you are still making that journey! How is the MIL doing? Best wishes, Wendy x
Exactly! I can't seem to think of anything else! My mind just wanders off...no change there though π
I think the health board will need to eat humble pie! Seriously, you have done something amazing! You challenged them and won - I know how difficult it has been for you and dealing with red tape at any time is daunting but on top of being g poorly?! You're awesome babe πππ
My darling B is definitely coming with me - I wouldn't remember anything afterwards...plus he'll stop me being a jabbering wreck! When I'm stressed, I either clam up or have verbal diarrhoea with a few Spoonerisms thrown in for good measure...
MIL is still in step down - hopefully she can go home soon - I cannot even begin to tell you how upsetting this has been, all I will say is that it is a disease to be old in the UK, heartbreaking.
Thank you for your lovely message and I'll have you in my thoughts and hope your meetings go well - do let us know. I'll be thinking positive thoughts next week and will be on the forum for courage π
Thank you ππ This forum is such a lifeline. The support from my friends that I have found on here is overwhelming! I'm so touched by the lovely messages but that is where I draw my strength. Together we are strong.
Thanks Charlie, I absolutely couldn't agree more, this is the place to beπ, I think I'd still be feeling very lost in limboland without you all. Big Hugs π€ π¦ππβοΈπXx
Good luck Charlie for next week. Hope it goes well for you, no reason why it doesn't. I too have heard good things about the hospital!. As a dear friend says to me Courage Charlie. X
Just found this post - been so sorry for myself all week that I missed it. Firstly thanks for the amazingly nice things you said about me! I went pink and it wasn't the viagra for once!
So much good luck to you for the appointment. Mind to maintain eye contact, have your A1 sheet of worst symptoms in bucket points and breathe deep each time you feel panic. So hope this works out and agree totally about ageing, nhs and disease re your MiL - it's rubbish. Xx
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