Cancer and Addisons

Hi all I've been on forum for quite a few years now.

Haven't noticed anyone with both.unless I've missed it .

But thought I'd let people know what's going on with me lately ,

Beginning of the year my PSA (cancer count) rose up quite fast and quite high ,so oncologist put me on New meds, nearly three months ago since then My blood pressure is going mad mainly low so oncologist and Addisons specialist told me to increase my fludrcortizone, for my heart,from 1 1/2 to 2tablets a day, about two weeks later,no improvement so doctor and oncologist tell me to increase to 3 tablets day a week later phone call from Dr stop extra tablet my sodium levels have dropped dangerous levels so i carry on with low BP , spoke to Addisons specialist this morning explained everything everything he told me I should never have increased dose to 3and those tablets would not decrease my sodium levels,its more than likely that My new cancer meds are making My Addisons meds metabolize to fast in my body so they don't last long enough to do there job properly,at last something is making sense.

Now hes arranging a all day blood test at hospital so I have to Go early have tablets with blood test either side by about an hour, morning, lunch and evening,to see if meds are going out of My body to quickly.

Then at least I should know one way or the other than hopefully someone will figure out what to do..

Sorry if I'm ranting a lot but three months of being told one thing then another im getting rather fed up,fed up is rather mild to what I actually think, but thought id keep it clean,.

Hope everyone is keeping safe,keeping positive and keeping fighting.

Billy

  • Hi Brian ,if i remember right (cotton wool brain not helping) adrenaline rush is controlled by certain glands so that could be why no rush .

    Hope specialist told you your immune system is shot down as well , hydrocortisone does improve it but if you get ill you need increase your hydrocortisone intake to help body fight infection even common cold, although I think your glands are working so much or you would be on fludrocortisone as well,. Cannot remember if you had a 24 hour water sample and 12 hour blood tests to check hydrocortisone is staying in body properly and make sure dose is right .

    Trying to get fit is a problem but can be done just takes alot longer than normal  .

    Hope things go smoothly for you now you've a stable carcinoma getting sorted Addison's wise over Christmas . keeping positive is a good help ,and we called how you feel as the new normal,we All feel different once cancer is around us .

    Take care keep positive and safe .

    Billy

  • Hi Billy 

    never had a 24hour water test  but my cortisol levels are good being controlled by the hydrocortisone ,although it is like a self medicating prescription if there is any infection which has happened ,the general rule is double the dose for 6 days  or till the infection is under control ,but I find a quick call to the hotline or your local hospice can sort you out ,they tend to be on top by calling me every 2 weeks ,

    I don't know how bad your energy levels but mine go as far as getting up and a quick wash then 30 mins to recover or up and down the stairs a few times then it's a struggle to go up a third time ,but no one has told me why this is happening as my heart and lungs are fine even though my  O2 drops and heart rate goes over 110bpm ,so it is a mystery to me till I see the specialist whoever he might be ,so we go on cos we are still here 

    Brian 

  • Hi Brian.    Before I was diagnosed i was struggling at work with lack of energy, metal fabrication and welding,we had a trolley with 18in numatic tyres and pulling it ten feet and id had it completely out of breath and sweating like mad even outside in winter,I found out later the glands, slowly shut down the body hence struggling and you lose strength ,it takes alot longer to get strength and energy back,then to lose it ,Took me years and still not as good as before illness . but 70 years old doesn't help

    Take care keep positive and safe.

    Billy

  • Hi all my cancer frends.

    Just another update BP is up to 105/60 most days now energy improving but still bad days now and again cancer count 0.14 has been lower so keeping eyes on it.

    Brenda is still improving getting back to normal (Very bossy, but after 50 +years together im usto it.

    Head still useless trying jigsaws to get it going.

    Hope you are all keeping positive and safe especially traveling.

    Billy .

     

  • Hi all my dear cancer frends .

    Chaos lately started feeling better and BP rose over yippee, then started lacking energy again, BP ok just over 100 ,.mostly.   my darling Brenda had uti and problem getting antibiotics and she went really high throwing things about moving things around continues talk about anything and everything, carer called police said i was at risk, they called ambulance,in hospital till hit a nurse so assessed and put in psychiatric hospital. Bella could have cancer having op Friday to remove lump and test it  .so as i say chaos . Hope others are having better luck .

    Brenda complained her mobility scooter wasn't very red, her favourite colour, I've managed to paint it nearly all red .took a few days. 

    Take care all keep positive and sure. 

    Billy

  • Hi Billy 

    Hope the chaos is in retreat and that Brenda's uti is responding to treatment. Also fingers crossed for Bella.

    Take care

  • Sorry for not keeping up to date bit chaotic lately .

    im lacking energy again,do abit and stop when I find myself puffing.

    PSA is rising slowly again . oncologist is thinking of stopping my Enzalutamide (cancer meds) for a couple of months to see if I get energy back or if something else is causing energy level being low .

    Brenda is in psychiatric ward and been sectioned always has a nurse with her just incase . She's always so happy, says all the men want to marry her and she's plenty of boyfriends, she likes to dance teaching others as well, (she usto do ballroom dancing before she met her first husband but he was jealous so she stopped .

    Brenda still cannot remember any of our married life together , but can still remember her first husband.

    I'll get up to date hopefully when tablets stop and see what im like . 

    Thinking of my forum friends .

    Love Billy xxxx

  • Billy,

    Sorry you're having such a tough time. Hope change in meds helps. Low BP and low energy makes life very tough.

    Sorry to read Brenda got sectioned. At least she's happy. 

    Also sorry to read about Bella. Hope she's still able to enjoy some tasty meals. 

    His nibs a lot worse. Thought NHS wrote him off, but maybe not quite yet. I'll post an update in a few months. 

    Take care, Billy! 

  • Hi dear Jess,im always very cautious when they mention changing meds for my cancer,as couple of times they have reacted with my Addison meds and put me in a coma and it can kill me after coma.  I've got both oncologist and endocrinologist,(glandular specialist (Addisons)), trying things which could work but got to try then she what happens with me,(bit of a guinea pig.).

    i always take Brenda her favourite sweets and drink, she loves lemon sherbet, and grape juice .

    Hope weather is nice where you are, cloud and cold here . been out to shop on scooter well covered up.

    Take care keep safe and positive .

    Love Billy xxxx

  • Hi there my ol buddy ....

    So sorry to here your lass is in unit ... life is really not fare to you ... and yet you still reach out to others ... how amazing is our new lass Jess.... if every one was like her, the world would be a kinder place ... I'm so glad to see everyone holding her hand ... 

    Well don't get on here much now ... looking after grandkids takes so much energy, but I adore them, any ways wanted you to know I'm thinking of you ... hope bellas lump turns out not too bad... big vertual hug as always Chrissie xx