Just a thought....
Don't compare your life to others'. You have no idea what their journey is all about.

Sunday, 28 September 2014

Traitorous actions

I feel like a traitor…. to myself and all I believe in. While I’m not comfortable with my latest actions, I’ve made my peace with them - for now. On Friday, two days after my visit to a very persuasive surgeon, I caved and took my first Tamoxifen. I was not struck by lightning. Neither did I break out in hives.

tamoxifen

I do, however, feel as though I’ve crossed to ‘the dark side’.

Mr C, my surgeon, spent a lot of impassioned time telling me that I was taking grave risks with my health. He said that if I were to agree, he’d have me on the cutting table by the next morning. He wanted to know if I was seeing some other practitioner. I knew what he meant by ‘practitioner’ and that he was imagining voodoo just by the way he said it. I came very close to telling him I was seeing a witch doctor just to see his reaction. Two things here… first, I’m not in the care of a witch doctor (I just know someone’s going to assume that not knowing my warped sense of humour) and second, I’ve learnt that surgeons don’t have a funny bone, so I quietly snickered to myself and kept my peace. The only way he was going to let me walk out of that hospital with my records was if I agreed to take Tamoxifen.

Tamoxifen is a drug that blocks oestrogen. Oestrogen is the hormone that feeds my cancer. You can read more about it here. I’m not a fan, not even slightly. It is, however, the least ghastly of my ‘conventional’ choices. If Tamoxifen works the way the surgeon wants it to, the cancer will, at the very least, stop growing - something I believe it’s done anyway. The side effects scare me, not the menopause one, but the others. There’s the risk of a blood clot and the risk of the cancer going ‘yippee’ and making the Tamoxifen create the very oestrogen problem it’s trying to resolve, which will mean an even more aggressive cancer. Then there’s the risk of a very aggressive cancer of the uterus in 5 years, which is directly caused by Tamoxifen. This information, by the way, doesn’t come from an ‘alternative’ website, but from the Tamoxifen itself.

So while I’m not happy taking Tamoxifen, I’m only giving it a tiny corner of my life. The rest is dedicated to health-building, nourishing and healing foods, drinks and supplements. I have more supplements now than I care to count, but we’re hitting this thing with All we’ve got. Perhaps, with my will to be healthy, Tamoxifen will only do good and maybe, just maybe, it will do what it’s meant to do and fix at least one part of the complexity that is this cancer.

Technorati Tags: ,,

Tuesday, 23 September 2014

What’s wrong with you?

great love

I saw an article on Twitter on loving your cancer: http://omtimes.com/2014/08/loving-cancer-good-health/ My knee-jerk reaction was, “Are you crazy??” Love… I mean… Love something that has the potential to kill me or at the very least cause me a whole lot of misery? Love? Ok, so I read the article and it was good. More thoughts on that later.

My nightly research, wandering, link-hopping led me on a further path that had this love theme coming up regularly. My dear friend, Michelle, gave me the link to some music, which took me to Youtube and, being the compulsive link-clicker I am, I was soon going on to other related music. One link led to another and I found myself revisiting Ho’oponopono. Ho’oponopono is a Hawaiian practice of forgiveness and love. There is a lot to it, but, in short, it is a prayer you recite with healing intention:

I’m sorry
I love you
Please forgive me
Thank you

This prayer can be directed at any one or any thing. At no time does it mean you condone the ‘wrong’ that’s been done. This is also no pat, meaningless apology, just heartfelt love and a letting go of all negative emotions relating to the person, event, thing - or yourself. Yes, you could say it to yourself or parts of yourself.

I’ve used this prayer before, though very rarely. To be honest, I usually forget it exists. Once, I had a confrontation with a colleague at work. The next day, I dreaded going to work fully expecting a continuation of the confrontation - I don’t do confrontation very well - as the situation hadn’t been resolved the day before. In my flurry of tension over the situation, I decided to do some Ho’oponopono. I, rather dramatically, held my hand over my heart, focussed on the colleague and recited the prayer a few times. Arriving at work, the colleague couldn’t have been nicer. She apologised! She also explained why she’d acted the way she had. Now I don’t know if what happened was a result of the Ho’oponopono or just co-incidence. I’m going to choose to believe my little forgiveness ritual had its desired effect. I’ve used it since on other situations and had good effect. It may well just be because of my own mental state being altered. That’s also good.

Going through my mailbox a little later, a sentence jumped out at me, “What’s wrong with you?” It’s what we’re asked when something’s out of place. Or simply a “What’s wrong?” There’s so much negativity and fear in those words. It’s something that’s been brought home to me over and over with this cancer deal. Fear. Negativity. The doctor’s tone dropped to indicate severity. It was all over his voice and body language long before he got the words out, which were also negative, “I’m afraid I have to give you the news…” Why afraid? Why all the fear around cancer? Oh I can understand the fear! I can understand the anger, nay, the rage. I can understand the upset. But that’s the whole problem with sickness in our society. It’s wrapped up in fear because we aren’t in control of our bodies. We’ve handed that control over to the medical institutions and the supermarkets.

Today, I choose to take back control. I choose to love this thing that’s teaching me so much - ok, I’ll at least try. I choose to forgive my body for betraying me and this tumour for turning my life upside down. I choose to love my body and give it what it needs, treating it well. I choose to make mindful choices with what I put into my body. It’s my home, after all, and the vessel I will live in for many years to come. In moving into a home, I like to paint it a bright colour and make it beautiful, choosing my furnishings carefully. Why not with my body?

So, to this cancer I say…

I’m sorry
I love you
Please forgive me
Thank you

Monday, 22 September 2014

A moment of weakness

struggleI really need to take some photos instead of using random bits from the web.

I’m tired. Truly tired. I’ve just realised why I love working so much. It takes me out of myself and gives me a break from the incessant thoughts that are running havoc through my mind. I’m so tired of looking at it and trying to decide if it looks better or worse than yesterday. I’m tired of the constant research, looking for the next ‘magic pill’ or having to decide whether x is good for me or bad for me or only good under certain circumstances or measured quantities.

Heading to the kitchen for another lunch of sweet potato and broccoli - thank goodness I love eating those - I broke down. It’s moments like these when I almost want to go to the doctors and just let them do their thing. At least all the decision-making and responsibility will be taken out of my hands. I know that is why people do it. It’s just so much easier to let someone take over. Oh to have someone who can do that… a bit like the motherly neighbour who bustles in with a “Never mind love, let me do it.”  The trouble with that is that I’d then feel guilty and, you know, guilt is another sick-creator. Positive is healing. Negative is a downward spiral that ends in hospital wards.

Not to worry. I’ll be over this soon, the mood, that is. The rest? I don’t know.

“The more you ask how far you have to go, the longer your journey seems”

which reminds me of a blog I wrote a time ago and a lesson learnt on a hot walk in Mossel Bay. I can’t find the blog now and more’s the pity. I could do with that lesson. In a nutshell, I was carrying a number of bags on a long walk and the woman with me (who was carrying far more) said that the faster we walk, the quicker we’d get there and be able to rest. It was far more profound and memorable than the way I’ve managed to put it here, but you get the idea.

I did, however, while hunting for the blog I was after, find this…

"We're a quarter of the way through the year. I'm pretty much half-way through my life. In terms of my dreams and goals, the clock is ticking - very loudly. My life so far has been one of revving engines, tyres spinning in mud, occasionally moving a few inches ahead, even more occasionally moving ahead by a couple of feet - very often just sinking further into the mire.

My tendency to find humour in life has been a survival tactic. If I don't, the misery and, yes, bitterness may just swallow me up. Like many take a pill against what ails them, I take smiles, laughter and positive snippets daily, sometimes hourly. It's my 'silver bullet' against melancholy."

It seems, though my life has changed beyond recognition… there are some things that never change :)

I’m no optimist

A dear friend, in fact, a few friends, called me an optimist. The lady overseeing my case at the hospital also ‘admired’ my optimism. Here’s the crunch though… I’m not an optimist. Jurgis will tell you that. I’m often the one that sees where the problem in something may be. I’m definitely not a pessimist though. I consider myself to be a realist. I’ll see where the problems are and choose to look at the solutions. That, I think, is the important part, the choices I make and where they lead me. Yes, they do lead me to come across as an optimist because my “On the bright side…” outlook is a Choice.

After my diagnosis, I set about working on complete mind/body healing. You’ve by now seen my previous blog on the nutritional changes I made. This part isn’t so much a case of ‘changes’, as it’s mostly stuff I’ve been doing all along, as a case of intensifying that work.

As an introduction, if you have 20 minutes to spare, do watch this video. Dr Lissa Rankin puts it much better than I ever can…. the mind/body connection and our innate ability to heal ourselves. It was that intuition I listened to when I told them I would prefer not to have surgery or chemo.

Here are some of the modalities I’ve used in the past and am now using to heal my mind and my body…

Affirmations: Every night, as I go to sleep - in fact, this is what I did while undergoing the bone and CT scans - I recite affirmations. Back in Brazil, I recorded one and I play this to myself on my phone whenever I need to stop and take a ‘breath’. “All is well. Everything is working out for my highest good. Out of this situation only good will come. I am well. I am healed and healthy. I am happy.” There is more. This is just a snippet. I go from that into a number of gratitude affirmations.

EFT: Emotional Freedom Technique - you can read more about it here: I practice EFT on my way to work every day. EFT helped me with the sheer emotional overwhelm that came with the cancer diagnosis and helped me work on the emotional issues that led up to my getting cancer when there is no apparent family history of cancer. I don’t need to tell you that our emotions and our health are linked very closely. Each day, whenever I thought of it, I’d tap on my weak immune system and the safe and painless flushing of toxins from my body. I’d also tap on any other issues I had as they came up.

One night, shortly after my diagnosis, I revisited an old therapy I’d used before, TAT. Click here to learn more. TAT seems very simplistic, but it’s very powerful (just like EFT). The idea behind TAT, as with EFT, is to clear the past (even historical) events and/or traumas relating to a condition. Either way, I used TAT on the cancer. Like many, I had a huge number of fears around the word and a few traumatic experiences where I’d been exposed to close friends who’ve died of the disease. After doing TAT, I went to sleep as normal, but had a dream. On waking up from that dream, I knew, with absolute certainty, that I’d be clear of cancer in 3 months. It wasn’t a belief, but a knowledge.

After the TAT and my initial rounds of EFT, I found that all the emotional charge related to the word ‘cancer’ was completely gone. When hearing or saying the word, I may as well have been talking about an annoying pimple. It’s still like that. When people react to my diagnosis with alarm, I find myself wondering… what is this drama you speak of and wanting to comfort them, as they seem so upset by it.

Every night, if I shower (no, no…. get that thought out of your head… of course I bathe daily!), I listen to grounding music. I have a few meditations that ‘ground’ me to the healing powers our our Earth. It makes visualising the healing energy that is around me doing its work. If I bath, I have meditations that allow me to heal as I’m lying there in my bicarbonate of soda (‘baking soda’ to my American friends) and breathing exercises that help oxygenate my body and cells.

Another practice that I don’t do nearly often enough, is Qigong. It’s best described as “the art and science of using breathing techniques, gentle movement, and meditation to cleanse, strengthen, and circulate the life energy (qi)”.

Back in Brazil, Jurgis developed a large mole on the side of his head. This mole grew very rapidly and got very much darker. It went from a tiny spot to a large area almost an inch in length. I was worried enough to photograph it to see how it was changing. If it changed any further, we’d agreed that he needed to see doctor to get it cut out. When I next checked his mole, it was gone… not even a trace. I now have before and after photos. Jurgis just decided that it wasn’t welcome and he told the mole just that. Then, he put it out of his mind and went about his life. The mole vanished.

Such is the power of the mind. Such is the power that I am using on this cancer.

Not so simple

20140914_183916_PerfectlyClear

I’d love to say “I did this and was healed”, but, for a start, I’m still at the start of a very long healing process and, secondly, what I’m doing towards that healing is multi-faceted and not as simple as the explanation I gave at the hospital. I’ll try to sum it up in one blog, then explain more in further blogs. My apologies for taking so long to get this out, but I’ve been plagued by a nasty headache, which has rendered me unwilling to do more than is absolutely necessary.

First and foremost has been a healing of the mind. One of the biggest factors in causing cancer is stress. For me, this has meant working really hard on my mindset, not just believing, but knowing the cancer is beaten. I’ll blog more on this separately, as there was a lot involved. Some have labelled me as optimistic. I want to take this moment to say that I am most definitely not a ‘glass half full’ type of person, but a realist who will see the glass is half full and make conscious plans to fill it!

Before the official diagnosis came through, I started planning my regime. The first step I took was to cut out ALL sugar and sugar-related products. For someone who loves chocolate, this was rather traumatic, but necessary, as sugar feeds cancer. See more here: https://www.youtube.com/watch?v=WJsqpg4JpeY - I selected this video because it’s short and sweet, but there’s plenty to be found online about the sugar/cancer fiasco. This led directly to my next step, to alkalise my body. Sugar, for one, is highly acidic and yes, I had far too much of it in my system. Cutting out acidic food was part of the deal, but to actively alkalise my body, I started drinking lemon water (one lemon squeezed into a litre of water) with the aim of drinking two bottles a day. For those who will ask, lemon converts to alkaline in your body, so yes, it is acid, but doesn’t stay that way. Sometimes I make it. Sometimes I don’t. Switching to high alkaline foods came with that particular package deal.

I switched back to goat’s milk, as goat’s milk isn’t acidic like cow’s milk. It helps that I think that goat’s milk is awesome on so many levels. Cow’s milk (throw all beef products into that category) is loaded with hormones too and hormones are a huge no-no (my cancer is oestrogen positive), not just for me right now, but for everyone! There’s a huge belief in Croatia about the cancer-healing properties of goat’s milk as well. I can live with that. My only cheese is a slice of goat’s milk cheese too. Regular cheese now has me rolling in agonies of acid reflux within seconds. Who would have thought it? I’ve been a huge cheese fan for so long!

VEG! Good thing I love my veggies. I’ve pretty much eliminated meat products, only occasionally treating myself to a bit of chicken, salmon or… as we’re having tonight, venison. The whole hormone thing comes into play here. I’m being very selective and this is my treat. My usual meal, if I have one at all after juicing and smoothies, is pictured at the start of the blog. What you see there is a salad with rocket (yum!!), tomato and goat’s cheese, with a dressing of yoghurt (more on that in a minute), flaxseed oil, hemp oil and a little rock salt… then some veggies. The brassica family are particularly good.

Breakfast is probably my favourite meal though. I’m on the Budwig protocol: http://www.budwigcenter.com/the-budwig-diet.php. I don’t use quark, but organic yoghurt with live cultures. Breakfast is (aside from juicing) a bowl of meusli with yoghurt, flaxseed oil, hemp oil, ground flaxseed, a little honey and a handful of blueberries.

Strictly speaking, I’m meant to be juicing all day, but, practically speaking, that isn’t possible with work. At work, for lunch, I eat cold (avoid microwave like the plague!) sweet potato. It’s alkalising and gives me energy in my high-activity job. I nibble on brazil nuts too. Brazil nuts are high in selenium, which is a mineral that stops cancer growth in its tracks.

On the subject of minerals and such, the next part is supplements. At the beginning, I was on garlic, hawthorn and olive leave extract - garlic and olive leaf have anti-cancer properties. Hawthorn strengthens the cardiovascular system, which means all that precious oxygen will get around better. Cancer hates oxygen. Oxygenating my body has become a life-mission. Another supplement is turmeric, or more specifically, curcumin. I have some pineapple first, as the bromelian in pineapple weakens the cell walls, so all the micro-nutrients I’m consuming can get in. Before taking my turmeric, I also take black pepper, so the piperine can increase the bio-availability of the curcumin - ie. increase absorption by the body.

More recently, I’ve added chaga mushroom extract to my regimen. This could be a blog on its own. Basically, in Siberia where the mushroom is harvested, there is no cancer! This is because the locals there drink chaga mushroom tea in place of coffee. There’s a heap of information on the subject online, so I won’t go on about it here. I also take grapeseed extract, my own precious supply of Japanese knotweed tincture and periodically also feverfew tincture. Each of these are valuable in the fight against cancer. Japanese knotweed and feverfew can’t be taken continuously though, so I give myself a few doses on a weekly basis.

I want to do a whole blog on the mind/emotion treatment, which is, to me, the most vital part of my ‘fight’ against cancer, so keep an eye out for the next blog. There’s enough in here to chew on in the meantime, don’t you think? I’m open to any and all questions, though I hope to be doing follow up blogs explaining various parts of this regimen. For the most part, there’s a ton of information online. All I can add is knowledge gleaned from my database and the books I have on hand.

Augh… there’s so much here! I think I’ll leave it at this for now. I can’t say which part is doing the healing work - my bet is on the mind/emotional part that I still have to write about - but it’s working and I’m healing! EDIT: I neglected to go into the juicing. I juice at least 5lb of carrots daily, often with celery, cucumber and spinach added. That's a LOT of juice!

Thursday, 11 September 2014

Half the battle won!

healing

Today was the most exciting day I’ve had in a long time. Since my diagnosis, my days have been filled with work and tests and exhaustion. Cancer is exhausting, not just the disease itself, but the amount of effort going into research and lifestyle to ‘fix’ it.

Yep, I’m a fixer. From the day I was diagnosed… even before that… I’ve been researching and working on my personal healing. A total cure is what I’m aiming for. No less.

I was called into the hospital for an appointment today to discuss my test results and my prospective surgery, scheduled for Monday, the 15th. I was nervous, naturally. I arrived at the hospital only to be told that the surgeon, ironically, had ‘taken ill’ and I was to see my Breast Cancer Advisor, the lady who has been overseeing my case. She’s a nice lady, so I didn’t mind at all. She sat me down and started with the scan results. Bone scan clear. CT scan has ‘tiny nodules of activity in the lungs’, but inconclusive, as they’re too small and there’s no way of telling what ‘activity’ they are. A follow up scan for those will be done in 6 months, but they’re not considered an issue at all right now. To clarify, anything can turn up as ‘activity’. If I had unprocessed food in my stomach or digestive tract, it would have shown up as ‘activity’ there. A fractured bone would show as ‘activity’, as would a stomach ulcer. I’m not in the least worried about that aspect, especially not in the light of what came next.

Mary (not her real name) said that the next phase of treatment was up to me, whether I wanted chemo first or surgery first. She knows my views on the subject, so she wasn’t really surprised when I said I wanted neither. I’ve asked for 3 drug- and surgery-free months in which to heal myself, then a re-evaluation to see if it’s necessary at all. I explained that I know, without a shadow of a doubt, that my cancer has been halted and that my body is healing. She wanted to know why I was so sure. I’ve been taking regular photos of my lump (yes, it’s very visible), so I was able to describe the changes to her.

Sensitive readers may want to avoid this part…

The lump itself was ugly. It was raised and a dark, bright, purple, surrounded by angry red. Over the top was a thick crusty scab, not caused by an injury. It was part of the cancer growth. The scabbing occurred very suddenly, about a week before my first hospital visit. Recently, after 3 days of intense itching, the scab fell off leaving a very healthy pink skin underneath. The purple has diminished and is now just a small area. The red is gone completely. The skin around the lump, that was previously a mix of greyish-red is normal flesh colour. The lump itself no longer feels as though it has a life of its own and there’s no more pain! I had constant stabbing pain in that lump!

The best news for today was the lymph glands though. Before, the swollen lymph glad was visible to the naked eye when I raised my arm. I could feel it. Every doctor who examined me could feel it. It was noticeable on the ultrasound and big enough to take a sizeable biopsy from. That biopsy came back as cancerous. Today, Mary found no lumpy lymph gland. She asked if she could call in a second opinion and yet another surgeon came in. He hunted (boy did he hunt!). He examined both armpits thoroughly and said there were NO compromised lymph glands! No swelling at all! He suggested that the previous swelling was just because it was fighting the primary cancer. Mary then told him of the biopsy and he accepted that it had gone down, assuming that I’d been on chemo.

My point was made! My body is healing itself! It’s so exciting! My metastasis has disappeared… completely regressed! With this in mind, she agreed that my 3 month request was not that far fetched and was curious as to what I was doing to achieve this. I told her some… the full truth may have been hard for her to take. I’ll still blog that.

So… that’s my ‘shout it from the rooftops’ big news. I’m certainly one very excited and motivated bundle of happy right now. It makes saying “No” to the chocolate at work so worth it : )

Thursday, 28 August 2014

Voldemort!

"Call him Voldemort, Harry. Always use the proper name for things. Fear of a name increases fear of the thing itself."
~Dumbledore

I have my own personal Voldemort - not quite in the sense of the character, but in the sense of having a monster I’ve been afraid to name for too long. This past couple of weeks, I’ve finally given it a name. Before the test results came through, it was ‘The Big C’ - talk about a name to inspire fear! I now just call it cancer. See? It even loses its capitalisation!

fear wolfVoldemort... or wolf... or whatever form the worst fear takes.
(The artist is unknown to me, so if anyone knows who to credit,
feel free to let me know)

Back in Brazil, I discovered a lump in my breast. I duly went to the doctor and was told it was just a fatty deposit. Switch to ‘ignore’. I’m good at that… ignoring something I don’t want to deal with. We then left on an adventure across the oceans with England being the destination, so we could be closer to Tat. A couple of months ago, the ‘fatty deposit’ changed and very soon became something that was most definitely not just a fatty deposit, so back to the doctor I went.

To give the doctor some credit, I’d hate to ever play poker against her. She gave nothing away, but booked me for further testing ‘just to be sure’. I went for the obligatory mamo. Then ultra scans. Then the biopsy. The mamo is awful. The ultra scan, messy. The biopsy… combine raw fear of the disease with fear of the ‘gun’ that punctures the hole with discomfort and the pain when they take a sample beyond the lump to check for spread. There were two of those… one for the lump itself and another for my lymph glands.

A few days later, I had my appointment to review the results, Invasive Ductal Carcinoma (IDC). People suddenly start talking quieter in serious tones. I lost it with the surgeon who broke the news when I told him I’m pro-active and asked him what I could do/eat/drink to promote healing before the surgery. “Oh, just eat healthy and do a bit of exercise,” was his response. No foods or chemicals to avoid - and we all know there are many carcinogenic foods and chemicals out there. He had absolutely no advice at all, not a shred of wisdom to share. Let’s just cut it off and pump you full of harmful chemicals and radioactivity and be done with it. At that point, my anger kicked in. I’ll nail this damn thing, yes, I will!

So, from the point of view of the specialists, the programme is as follows: Next Thursday, I go for a bone scan and a CAT scan to see if there’s cancer anywhere else in my body. On the 15th of September, I’m booked in for a mastectomy. It’s still up for debate as to whether or not they want me to do chemo before or after the surgery. A lot depends on the results of next week’s tests.

I am, however, not the average patient ;) I came home and, after the first tears, rants and blind hysteria, I sprang into action. I’m not without resources. I will do everything in my power to avoid ‘modern medicine’s solutions the cancer. I am pro-active and have started an intense treatment programme of my own. Perhaps I’ll write about that in another blog. Perhaps not. I know that there are those that will try to shoot me down in flames for what I’m doing, but I’m Not going to take this lying down and I will Not have treatments forced on me that will, I believe, do more harm than good. I do, however, intend to be around for many more years, so, trust me, I won’t be stupid about this. I am, in the end, a realist, and will do whatever it takes to heal.

So there’s my Voldemort…. a pitiful beast in the end and one I can fight. I know there will be scary moments and downright frightening encounters, but I have around me so much love and support that there’s no way I can lose!

Sunday, 18 May 2014

Nature's Mandalas

image

None precisely symmetrical our perfect, but all incredibly
beautiful and unique!

image

image

image

image

The daisies come with special thoughts of Kippy in Nevada

image

image

image

image

image

Sunday, 20 April 2014

Posies and ringlets

I love my job! I get to meet the most fascinating people all day every day. Yesterday, it was a little old lady with a halo of perfectly (and I mean perfectly) coiffed ringlets. She must have spent hours on her hair. Picture young Shirley Temple as an eighty-plus lady…. same hair.

ringlets

Sharp as a button, she was, in her woven green coat. She looked like she had stepped straight out of a 50’s magazine. But this pint-sized dame showed me a thing or two! She’d been sewing all her life and wanted to know if she could buy the fabric instead of having the curtains made up for her. She knew what she wanted and brought samples of her sofa cover in to match the fabric.

Needless to say, she spouted feet and inches to me. My metric ‘everything-in-multiples-of-10’ brain objected in a scramble of numbers that spun dizzily. Not a problem to the genius I was talking to. She was never taught metric, but converted the measurements for me without skipping a beat! That was when she told me she’d retired 15 years ago from My Job! Yes… the very job I was doing! Back when Montgomery had concessions in the Co-op. I’d like to bet she could still do it and sweep me under the rug too. She turned down the offer to replace me, though, as she had a ‘little boy’, aged 90, back home she needed to care for.

I can only hope that I have a fraction of this lady’s spunk and wits when I’m her age. Grow old gracefully? That’s for dull folk!