I decided to write about my passion for gardening past, present and future.
I have been ill suffering with Lyme Disease since May 2003 but at last after long term antibiotic treatment getting my life back and can again enjoy my garden.
Tuesday, 13 July 2010
HAMPTON COURT RHS SHOW 2010
What a picturesque setting for this great if not the greatest garden show.
These are just a few of the small gardens.
After a while I realised that in fact what interested me with the gardens was the planting. Surprise surprise. The focal point in most of the gardens was usually some structure or folly mostly things I wanted to avoid taking photos of in preference for the plants.
See what I mean, although it would have been difficult to capture any of this lovely planting without including those ugly seats.
The other thing problematic at shows is the people, thousands and thousands like ants crawing everywhere. So to get any photos without people in was quite a feat in itself. I included the above plus people as it was something Rachel rather liked. I am not sure it would fit in her garden though.
Just the odd shot in the Marquees crowded as elsewhere. The day was so hot the hottest this year and really uncomfortable in or out of the Marquees.
I couldn't miss posting a photo of the roses.
or two.
And Rachel who accompanied me to the show, rather well covered due to the fact she is on Doxycycline which can have a very bad photosensitive reaction to sun. Yes some of you who follow my blogs have guessed, she had a tick bite recently and despite all my constant warnings she removed it incorrectly and as it had been attached probably about 24 hours we are not taking any chances. One member of the family with Lyme disease is more than enough.
I enjoyed all of your photos very much. It's so interesting to checkout all of the details in planting: the colours, the textures, the combinations, and the variety of possibilities. You are fortunate to have so many great gardens and garden shows accessible to you.
I enjoyed these photos more than the beebs coverage! I mean it, you shown so much of the gardens than I think they did. I wish I could of gone but this is peak season for me.
Hi Joanne, Those chairs really are hideous, LOL. I love the bedframe and the rusty flowers [different photo] My favorite photo is the one with the two-toned sweet pea obelisks. The thatched fencing is very cool and the green really complements the flowers.
It's a good thing Rachel has you to help her understand the seriousness of the situation. She has my get well wishes.
I'm so glad I didn't miss this post. I would love to see it in person one day. Thank you so much for the tour. Glad Rachel is on the antibiotic and I hope she'll be fine. I like her dress by the way, those "maxi dresses" are really popular here right now.
Hi Joanne, I agree ... I love the plantings... they are so lovely and natural. Wonderful post ... thanks for sharing this show. I have put a link to your site on my today's post. Still in my Lyme time. ;>)
I know I'm a week late but o'well still didn't want to miss it. What a great show to go to. I'd love to come there and see a few of them in person some day. You took super pictures.
Hi Joanne, I hope Rachel is OK. Thank you for sharing this garden show. I love the plantings too and how they are all so different and creative. Pity it was so crowded but at least it was crowded with garden lovers like us.
Hi Joanne. You've got an incomparable garden. I love to personally seeing them with my family. And one more thing, my day isn't complete without roses. Don't you bothered by bugs?
Yes I know it is August now but these were July photos and as with most things in my life I am running behind. Where does the time go? ...
LYME LIFE written 2009
I started suffering with arthritis in mainly my large joints especially my knees 6 years ago. The symptoms varied and I remember saying that every joint was affected except my elbows to one doctor. I was told it would be hormonal and to take the usual supplements cod liver oil or glucosamine ( I would certainly recommend buying shares in the companies producing these supplements) They had no noticeable affect.
All my symptoms deteriorated significantly over a few weeks, 4 years ago. Hips shoulders and knees being the worst and I started with muscle weakness in upper arms and upper legs. I had difficulty standing and walking across a room. I was unable to walk upstairs and my husband was making plans to convert to a downstairs bedroom. I had seen 5 doctors and 3 Rheumatologists and put on steroids for Poly Myalgia Rheumatica diagnosis. I had been diagnosed with Fibromyalgia and ME/CFS.
I have X rays and scans showing signs of osteoarthritis and Rheumatoid arthritis. I have been retired early from the Civil Service having lost my job not to mention my earning potential.
My illness seemed to progress through my body not affecting the same joints left to right at the same time. I had bursitis in left hip, right hip, left elbow. I had synovial thickening in both wrists. At that time I could not lift and hold a magazine so lifting a kettle I could only do if a third full and with two hands. Each joint in my hands fingers feet and toes were affected. I had swallowing difficulties and many other symptoms. None of this describes the endless and awful pain whenever I moved or the tiredness but inability to get quality sleep.
Two years ago my GP gave me Amoxicilin for a sinus/throat/chest infection. All my arthritis symptoms improved. The course ended the symptoms deteriorated I started a second course the symptoms improved. The improvement was more significant than when I had started taking steroids. This led my GP to suspect Lyme Disease. I laughed because we do not travel abroad but she said they had had other cases in the surgery in the early stages of tick bite and Erythma Migrans rash. She said, but you have not had a bite. I said oh yes I have I had two on my ankles with rashes, March 05 this was confirmed on her computer at the time I had seen a locum doctor. My worst symptoms were waking up feeling rigid and having to painfully flex every joint in my body before struggling to get up. The only other time I had experienced this was in May 2003 during a flu like illness like no other I had ever experienced. At that time I had a bite and similar rash on my right foot which lasted like the other rashes about four weeks. I had also consulted the surgery and it was dismissed as a virus. I walked our dog daily in the woods adjacent to our house where the deer roam, prime tick area.
Thus started my very lengthy search about Lyme Disease leading me through http://www.lymediseaseaction.org.uk/ to a doctor who specialises in this illness. He confirmed my GP's suspicions. I never had a positive blood test but then they are antigen tests and there is much research that shows they are unreliable. In my case the year of steroids and many weeks antibiotics could have affected the results. So with a clinical diagnosis and following ILADS International Lyme and Associated Disease Society guidelines I continued on antibiotics for two years. Both my doctors continued to treat me despite the Health Protection Agency advising against long term antibiotics. I am now nearly 100% recovered I have no pain or muscle weakness. I can walk upstairs something I could not do for three and a half years. I can garden do house work and live a normal life. I still need to pace myself and with only a few months to 60 will not be looking to return to work.
Life is such a joy.
Sadly there is much controversy about Lyme Disease and doctors in UK are taught that it is so rare. Well where I live in Guildford I have been in contact with a dozen other people with it so perhaps not so rare as HPA would like us to believe. I am in touch with nearly 2000 other patients through a chat line Eurolyme most had been misdiagnosed with several other illnesses.
Look at UK charity http://www.lymediseaseaction.org.uk/ if you want to read more about this illness. There are many MP's taking an interest in the problems surrounding diagnosis and treatment see above charity links into a recent meeting at the House of Commons.
Thank goodness there are some thinking doctors around who have courageously treated me against opposition and I have made such a miraculous recovery albeit rather a lengthy one.
One day there will be many more people who are helped with their chronic illnesses when IDSA starts taking note of what our courageous LLMD’s are doing following ILADS Guidelines.
ME/CFS, Fibromyalgia, Poly Myalgia Rheumatica, Arthritis, Bell’s Palsy, MS,MN, ALS, Parkinson’s, Alzheimer’s, Heart Block, Stroke, Psychiatric, gastric problems the list is endless. Not all suffering from Lyme Borrelia but how many are even properly assessed for it.
What a great show. I love the roses too.
ReplyDeleteI hope Rachel will be fine after her tick bite.
FlowerLady
I do hope Rachel will do OK on Doxy!!
ReplyDeleteEven though there were crowds of people you managed to get photos that did not have many people in them
That takes real talent
I enjoyed all of your photos very much. It's so interesting to checkout all of the details in planting: the colours, the textures, the combinations, and the variety of possibilities. You are fortunate to have so many great gardens and garden shows accessible to you.
ReplyDeleteYour posts are always so super gorgeous..just wonderful! Beauty everywhere! Wonderful post!
ReplyDeleteKiki~
Oh no poor Rachel I hope she is okay - she looks fab!
ReplyDeleteI LOVE the rust (the flowers and the iron double bed) and the tumble down shed, oh I like the look of that show. Thank you for sharing xx
Hi Joanne
ReplyDeleteI enjoyed these photos more than the beebs coverage! I mean it, you shown so much of the gardens than I think they did. I wish I could of gone but this is peak season for me.
I hope Rachel is ok.
It looks like great fun. Maybe someday. Yes, take no chances. We check ourselves over everyday in summer.~~Dee
ReplyDeleteHi Joanne, Those chairs really are hideous, LOL. I love the bedframe and the rusty flowers [different photo] My favorite photo is the one with the two-toned sweet pea obelisks. The thatched fencing is very cool and the green really complements the flowers.
ReplyDeleteIt's a good thing Rachel has you to help her understand the seriousness of the situation. She has my get well wishes.
I'm so glad I didn't miss this post. I would love to see it in person one day. Thank you so much for the tour.
ReplyDeleteGlad Rachel is on the antibiotic and I hope she'll be fine. I like her dress by the way, those "maxi dresses" are really popular here right now.
Beautiful gardens and lovely roses... oh, and I love love Rachel's dress! ;)
ReplyDeleteCielo
Glad you had a really great day despite the heat and the crowds.
ReplyDeleteHi Joanne, I agree ... I love the plantings... they are so lovely and natural. Wonderful post ... thanks for sharing this show. I have put a link to your site on my today's post. Still in my Lyme time. ;>)
ReplyDeleteI know I'm a week late but o'well still didn't want to miss it. What a great show to go to. I'd love to come there and see a few of them in person some day. You took super pictures.
ReplyDeleteHi Joanne, I hope Rachel is OK. Thank you for sharing this garden show. I love the plantings too and how they are all so different and creative. Pity it was so crowded but at least it was crowded with garden lovers like us.
ReplyDeleteHi Joanne. You've got an incomparable garden. I love to personally seeing them with my family. And one more thing, my day isn't complete without roses. Don't you bothered by bugs?
ReplyDelete