nausea feeling

[pulisa]

I'm glad that your blood test results show that you are healthy and that you believe the evidence that you don't have a sinister illness.

[unsure_about_this]

I'm glad that your blood test results show that you are healthy and that you believe the evidence that you don't have a sinister illness.

Thanks

My skin feels less itchy and the marks are slowly fading .

[unsure_about_this]

I been in to the doctors about my skin problem, he thinks it a fungal problems, which is causing the itchiness , i still thinking this either lymphoma, non hodkins etc. the marks seems to be fading slowly.

I need to pick up prescription tomorrow as it was too late to pick it up today

Also worried that the itchy is cause by liver disease, because i have googled it.

today 28/4/22 i picked up my antifungal cream

[unsure_about_this]

I was also given some shampoo for my hair.

The marks on my skin are slowly fading and on my legs. itchiness has gone down a lot, but still worried that every itch is too do with cancer, like skin, lymphoma, nhl, leukemia, liver cancer, liver disease , kidney disease, skin cancer, pancreatic cancer etc

I have been given some more tablets to try for my anxiety, i been told to take them once per day, and told to try to take them for longer,

[unsure_about_this]

I been taking these tablets for a bit now, but it still making my anxious about my poo, with consistency, how often I go (I go a more regularly now, because I am eating more fruit and vegetables) which helps me soften my poop up, instead of straining. also worried about bowel incontinence, I can control my bowel movements, just need to get better toilet paper to wipe more easier

I am worried still about if I got bowel cancer, because my poo consistency ,

my niece is a lot better now.

[pulisa]

Latest with my health worries.

I managed to get a GP appointment Wednesday just gone, she was a fantastic doctor, who listened, she checked my blood pressure, my weight, felt my stomach area, listened to my heart and lungs (as she asked me to breath in and out) because of my NF I am getting a blood test done , I am getting to get more phone calls from the GP now. I am going to be referred to get more help, maybe mindfulness with local buddhism centre, I don't know.

She talked to my worries about the big C , very unlikely I am at risk. as I don't smoke, drink and my weight is okay (could be a few more kgs heavy) but if she saw my parents both my parents are not over weight.

When I talked to her about my bowels movements, she was not too concerned about colour, as I would be showing signs if there were a problem.

As for cancer, she said if I had anything serious wrong with me I would know about it.

Do I believe my GP yes, as she took the time.

Important to remember what the GP told you, Phil. Has there been any news about your referral for more help with your HA?

[unsure_about_this]

Important to remember what the GP told you, Phil. Has there been any news about your referral for more help with your HA?

Not yet, since the GP who I saw in March left the practice, I told the new GP about i had no news. but will keep trying

[worryguts999]

A big thank you for this positive and informative post. Just about how I feel most of the time, especially appointments+social situations, pounding chest, pins+needles and the dreaded nausea. Always feel better when out of the situation and back in "safe place" mode. Never actually sick, but, as pointed out, it's the fear of the symptom. A brilliant and clear explanation-has helped me a lot-I will read often and maybe things will improve. Thanks again.

[unsure_about_this]

Hoping my anxiety goes away soon, as fingers cross me and my parents are off to Hungary later this year in September, already booked, it was either that or Poland, maybe in 2023 Poland.

I am getting more and more gurgling noises from my stomach and bottom lately , must be all the fruit etc I been eating, In the past I been told I have IBS

[unsure_about_this]

I had my latest appointment at the hospital with my frozen shoulder I am moving to the next stages of it, and will get more movement back in around 6-12 months. I also having physio now, we are not rushing this. slow and steady. the specialist I been seeing he is 3 months ahead of me as is 95% there.

I am about 10 o clock on a clock getting my arms up, I was around 7pm a few months ago. struggling , could not sleep properly