Emerging Anew: Budding and Reblooming (The cycle never seems to end.)

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The blog has been largely quiet for the last few months as I’ve been reentering and reshaping my life. What’s nice to know, at least for my own sake, is that this blog is not going to go away anytime soon. As hokey as it sounds—like me, or even you—it’s just going to continue to grow and change.

Rhododendron hybrid at the Espy House in Oysterville, WA.

I want to grow and change. I want to be like my formerly feral cat who’s grown to trust me more and more. For this love she’s shown me, I fixed her fence again about a month ago. I’m not going to say that she does the dishes now, but she’s quite happy with the respect I’ve shown her.

Currently I’m seeing so many things again as if for the first time and part of what’s kept me away from my typically long and meandering posts has been a reticence to describe my new life because it is taking time for me to watch it as it unfurls.

Vine Maple (Acer circinatum).

I’m emerging too and with the amount of restorative exercise I’ve been doing I’m looking like myself again. One cannot describe how much illness changes you inside as you suffer through the pain. In my case, I struggled for years on my own.

Though I’m better now, and so much stronger physically, for the last few months I’ve had to continue battling Hereditary Angiodema while at the same time accepting the fact that two falls down staircases have caused some serious damage to my back and neck. It is difficult to accept that I didn’t seek the help I needed at the time I needed it. Daily I’m reminded of this, and daily I’m learning to think about it differently while acknowledging I did the best that I could at that time. I needed help though in my daily life, and I needed a lot of support. Accepting that I still do, and that I need to ask for it from now on, is something I see now as an immediate need as I better define what living with dignity means to me.

With allergies and food intolerances it’s been difficult for years to eat but I’ve taken charge of that too. Having spent a lot of time with a Scandinavian friend with similar issues helped me a lot last year. Sometimes we cooked for one another too. It really helped me to rebuild my confidence and as my health has improved I’ve had more endurance in that arena too. Cooking is a big part of who I am.

A shrimp and basil casserole I made with a recipe from the island of Elba. It has tomatoes and potatoes too and that’s just about it.
Handmade cannoli I made for my boyfriend’s birthday. Yes, I even made my own shells too.

My online seed shop has recently been remodeled and cleaned up a bit too. I’ve been working on many other responsibilities as well. Highlights of my days include moments when I can sneak outside to discover new blooms on my old garden friends.

Slowly, I’m weeding the garden back into shape. Last year I didn’t work outside much at all. It was simply too painful. This year, I am trying really hard to take my garden back.

Iris fiorentina. 

There are the new-to-me flowers too. Even if I’ve seen them a million times in print or online, seeing them up close and in person makes such a difference. I’ve been visiting friends’ gardens more and more and I love it when I’m surprised by what I can only call “new material”.

Sparaxis tricolor.

The classics have been comforting me this spring. After years of living with great stress and uncertainty I’m finally calm enough to really soak up and appreciate their beauty.

Tulip hybrid in the company of a peony.

The return of my green rose has brought me great comfort and gardener pride. With the high temperatures we’ve been having it’s blooming early this year.

Their black pepper scent was much missed.

Rosa viridiflora.

With a return to the kitchen, I’ve become interested again in cooking with herbs and other plants. I’ve been wanting to raid my neighbor’s calendula for years and this is finally the year for me to do it. Have you cooked with Calendula before? Just curious.

Calendula officinalis.

Lastly, I’ve been returning to my roots and have been enjoying the natural beauty of the region I live in once more. There is so much meaning in everything I see and do now after so many years of struggling personally, professionally, and in my private life. Sometimes I wish that this process could speed up and end but in order to grow, I see clearly now that this takes time and care. I must tend to myself first and then to my garden. In the end, we’ll all be much stronger and more disease and pest resistant.

Oh, and I’m getting really excited now about being part of a presentation—along with some other garden blogging friends—on June 8th out at Joy Creek Nursery. Should be fun to really think about the topic of garden blogging over the next few weeks.

Plants Make Me Ill (Revisiting Chronic Illness in the Garden)

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With all of the recent changes it has been difficult for me to sit and think about being chronically ill. Mostly that’s because it’s what I thought about for so many years; the diagnosis robbed me of many things and it hurt deeply. Gardening kept me busy, but mostly I read about it. Actually being outside all of the time was another thing altogether and that became more and more difficult as I became more ill. But who out there amongst us isn’t an armchair gardener at one point or another?
Now I am feeling better, so I don’t have as much time to sit and think, but the avoidance is mostly due to my not wanting to accept or even acknowledge what I’ve seen as a roadblock and an obstacle for so long. So much of my current divorce has to do with the illness, but it is certainly not everything and I know that too.
Peony bloom I snapped from the sidewalk.

Currently, when I don’t have plans with friends on Friday nights, I take leisurely 6-mile walks to Powell’s Books on Hawthorne and then I walk back home through Mt Tabor Park. These are productive walks where I not only get the much needed exercise I’ve missed for the last decade or so, but I also get to feel the joy I used to feel at just looking at things—mostly plants.

Rockery overflowing with Basket of Gold, Aurinia saxatilis.
During these walks I am in awe of how thrilling it is to be able to breathe and to walk. And although plants do still make me a bit ill—at least their pollen that is—I am learning how to better manage my asthma and to feel the symptoms in my body. For so long I was unable to do so because I’d become so numb from all of the swelling but I can feel a lot now.

Walking past Portland Nursery still makes me giggle a little since it’s no longer an escapist refuge for me as it once was when I could barely get anything done all day.

Seeing the cherry blossom petals scattered on the sidewalk while standing amongst them has made me smile with pleasure this year. They won’t be here for long and this year I won’t have to see them solely from the car as I fly past them. I savored them the other night because they’ll be gone next week.

No one knows this yet but I have lived at the base of Mt Tabor Park for almost 8 years and it was only within the last few months that I’ve been able to visit all of its reservoirs.

False Solomon’s Seal, Maianthemum racemosum.

Finding native plants in the park has been a great boon too.

Vine Maple, Acer circinatum.
Lastly, while up at the park, walking and thinking about chronic illness, I thought a lot about the native Vine Maple. It is so tiny among giants, stretching for the sunshine, doing its best as an understory resident. Thinking about how much I’ve always liked this tree, and how calm I’ve felt beneath them spring, summer, or fall, seeing them during my walk home in the woods of Mt. Tabor felt like coming across another old friend.
Somehow this comforting end to my walk on Friday helped me to find the courage to do some research into what to call the current stage of my chronic illness experience. From inside, I have felt so much certainty about so many things but I haven’t understood at all why. I have felt very isolated, but I just knew that if I looked hard enough I would find something—and I did!
Just as my disease is new and unknown, so too are the studies of people living as I do. We become chronically ill as adults, suffering for many years with uncertainty and change, there comes a moment when we face death, we get through it, and then with extra medical attention, we improve suddenly after something is changed or adjusted. We are the lucky ones. Many living with chronic illness will never get this opportunity and I think knowing this is part of the catalyst for what happens internally to some of us. I, like many others, have been rewarded with just the outcome we’d spent so much time trying to let go of so as not to create false hope within ourselves. We had to learn to live in that moment between enduring and suffering, committing to ourselves not to dream about being able to live in the reality I have just reentered—one with so much more freedom.
One study said that there may only be 5-10% who experience what they called self-reformation, but I think that further study will show a higher number of people who enter into this process. Medical science seems to improve daily and there will be more people like me. There must be others out there already too who, like me, simply don’t know what to call what they’re going through.
Here are the phases that have so far been identified, but I am putting them in my own order, as they occurred within myself: need for reciprocity (to help others who are suffering), value suffering, appreciate one’s abilities, a disregard for material things, maximizing today, reordering priorities and exiting from unsatisfying relationships.
This last one is the tricky one. It shows my part in the divorce, and I agree with what I read about other people in my situation. When I read the experience of one woman, I was shocked to see myself in her words. This list also points forward for me, and what I read also made me think so much about plants and gardening—funny how that always seems to happen. I am sure that many of you out there already understand this too in your own lives.
Plants might still make me a teeny tiny bit ill with allergy or an immune response but there is no way I am ever leaving the garden again. All roads seem to lead right back to plants in my life and that’s just the way it’s going to be…