My Fibroscan result has just come in at 7kpa!!!
3 1/2 years after a diagnosis of cirrhosis with ascites..
Keep believing……..
My Fibroscan result has just come in at 7kpa!!!
3 1/2 years after a diagnosis of cirrhosis with ascites..
Keep believing……..
Brilliant 👏🏻
Congratulations! Awesome news !
I hope to be right behind you. 🥳🥳🥳❤️
That's great but I'm just wondering does that mean you still have cirrhosis or it's gone
It was inflammation rather than scarring. So no I don’t have cirrhosis
So the doctors were wrong I'm beginning to wonder my fibroscan was 63 bow 14 two years later bloods all normal no symptoms
They couldn’t tell early on because of the inflammation, so the working diagnosis was cirrhosis. But I I got well quite quickly and I tracked all my bloods and US reports, pushed for Fibroscans etc because I knew I didn’t have cirrhosis. You have to advocate for your own health, I would have been left on the cirrhosis pile if I hadn’t of pursued what I thought was right. Good luck 👍
I am so inspired by this...my bloods all went normal in 6 weeks and I had an elastology of 11.8 then in Nov 9kpa - they are saying cirrhosis but I feel great. My ultrasounds say fairly homogenous with minimal contour irregularity and normal echogenicity and trace ascites...did you have any of that? I am praying that I can get out of the cirrhosis umbrella...I am doing everything I can to try. Still waiting for a hepatologist (since July)..I took things into my own hands and drove 14 hours to pay for a fibroscan which was a bad idea...it was at a clinic (I am in Canada) that focuses on weight lost and stuff..I guess in hind sight more of a salon really for women...they do have a fibroscan there though and so I drove and paid...they gave me a result of 32.1 kpa and 162 CAP...I took it to my GP who said it was not worth the paper it was written on..lmy 14 hour drive home was hell thinking that I had progressed that quickly and here I thought I was stopped and showing signs of reversing...note to anyone out there - DO NOT DO THAT lol.
How were your ultrasounds reading deanw41? Just love to have a comparison...when you presented what things looked like for you...such a positive post!
Hey, well my ultrasounds alway say different things, they are not that accurate and are very subjective. The last one said slightly fatty and they have varied over the last nearly 4 years. My latest bloods show my platelets are nearly in the normal range which again is promising. 146k. I’ve been doing intermittent fasting for the last year, it’s working for me. It’s the process of Autophagy- have a look it’s very interesting! Keep believing you are better , never underestimate the power of the MIND. Do all the obvious right things in terms of self - care.
That Fibroscan you had seems a bit random?! If your Dr discounts it then, put it down to experience.
Do NOT be deterred, keep going!!! To healing……and beyond!!!! 💥💥
Hey Dean! Do you have the same type of ultrasounds done each time? Are they done at the same place? Do you know if they compare them to the previous ones?
Mine show that they are compared to the previous ones, since they are done in the same hospital system.
Mine have been pretty logical overall. 😌
How’s the fasting going ? I’m hungry just thinking about it. 😂
Hey Mary, well mine get done at different places in different machines by different people! That equals different opinions! Subjective reality!! Do you get the actual reports written by the US tech? I do and that’s how I know they say different things, the Dr letter just says no significant change!
Haha, still fasting!! Autophagy all the way baby 🤣
I don’t get reports by the techs- they take the scans. The radiologists (doctors) reads them. I can see the report by the doctor - the actual measurements and interpretations. It is different doctors but they compare it to the previous report.
I keep track of the measurements and descriptions and can make an overall comparison of changing parameters.
The last one did say “mild morphological changes of cirrhosis.”
Some trends I have noted: spleen size decreasing (even though I didn’t have “splenomalgy”). Measurements improved. Descriptive words seem much more favorable. Went from nodular to smooth, and increased echogenicty to normal, but I am hoping that is not a mistake ! 🤣😁
I still need to check out that autophagy I’ve read there are some good results from it for various health issues.
Sounds like you might have had a lot of inflammation at the start and that’s why your score is comping down. Keep well and have yearly Fibroscans!
No, docs wasn't wrong, this can happen with alcoholic hept.
What can happen?
A person can be diagnosed with cirrhosis with alcoholic hept., you can even have ascites, bleeding varices, when they stop drinking the liver can regenerate, some ppl just get lucky when they completely stop drinking, sadly , many go back to drinking or say they will cut down ,which really makes people with autoimmune liver disease angry. You should be fine if you keep up the good work, congrats!
When I was in hospital with ascities and had a drain the diagnosis was decompensated cirrhosis. Interesting they said inflammation with the same issue. So glad you are doing well. It gives hope. Take care.
Hi, I had the same My report came F3 12.8 kpa
6 months later I went for a scan
With a clean up.
The report came as 5.66 kpa .
deanw41 oh my goodness....I sooooo hope you reply to me on this one...so you presented with ascites...I did as well but I am a 9.0 kPa now and my liver is still a little enlarged 15.8 cm...my belief is that the ascites was caused to being VERY inflamed (17.4 cm in July) - I have no other signs of it and feel completely fine.
You had ascites correct? The Dr said now that it was due to inflammation? Oh please tell me yes, that would make so much more sense for me. My liver is fairly homogenous with normal echogenicity and a mildly irregular contour at the subs capsular...nodular contour was showing but in the two ultrasounds late Oct the nodular contour was not listed.
Congrats to you - I LOVE these stories!!
Hello! Yes, mine was inflammation! I only had one episode of ascites and it never came back. You have to keep pushing these consultants otherwise you end up on the cirrhosis pile, no significant change is what I’m STILL getting from my consultant. Outrageous!!!!
Wow, congrats Dean! So happy for you (cough, jealous). 🤣You still have to be active on this forum though.
You give me hope as I approach my 6 month check up where I’m telling my specialist the only thing keeping me from moving to another state is the clinic.
Thank you and I’ll stick around I’m sure! Best of luck for you upcoming check up.
How are things with you?
Hi…that’s amazing. Sounds like you’re doing really well. Don’t leave the forum though…it’s always great to hear from you.
There are only two ways you get ascites. Either from alcoholic hepatitis or Cirrhosis. That how it was explained to me from my hepatogolist. Ask your doctor about it.
brilliant news!! Can I ask did ur platelets go back in range?
Excellent news
Hi dean did you ever have a ultrasound if so what did it say please was it normal
What's fibroscan mate? I'm sorting a date to go in for TIPs procedure if you no what that is? Still worrying about it but being drained every fortnight with about 25pint ov fluid on Ave being taken. Hope you doing well 👍
Was that your first fibroscan or had you had one before...awesome job!! Congrats!