Joanne's Cottage Garden: CLEMATIS SEASON BEGINS IN MY GARDEN

Monday 4 May 2009

CLEMATIS SEASON BEGINS IN MY GARDEN

NELLY MOSER

Thanks to Frances of Fairegarden for her advice which prompted me to look at zoom.

I know I posted on Clematis in an earlier post but one can't have too much of Clematis.

GILLIAN BLADES

THE PRESIDENT

JOSEPHINE

MONTANA ELIZABETH

ELSA SPATH

21 comments:

Frances4 May 2009 at 20:00
Hi Joanne, thanks for the link love! You are so right, there cannot be too much clemmies. That is what we call them since there seems to be dispute about the proper way to say the name. We have several of the same ones, Josephine, Nelly, Elsa. The President has a fabulous center! So happy you are happy with the photography. So much to learn, so little time to read that owner's manual! :-)
Frances
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Joanne4 May 2009 at 20:40
Frances Thanks for your comment. At least in a post it doesn't matter if you say clematis or clematis.

The only problem with some clematis photographs especially the blues and mauves is thet the red comes our more true whereas the eye does not see the red the same so to our eye they are less red than in a photograph. I read this I think in Ray Evison's The Gardener's guide to growing Clematis.

I expect on some sophisticated equipment this could be adjusted out.
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Anonymous4 May 2009 at 21:05
NEVER to many clematis/clematis. LOL You say tomato but clemmies is cute - ya I like that. Keep showing them Joanne since you have so many!
Hey even on some easy equipment you can adjust the color. Someone recomended IrfanView to me years ago - not just to adjust color but to reduce and everything. You don't have to go into a program and all that - just click on your picture and it comes up. Oh forgot - and it's FREE!!!
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Snowbabies4 May 2009 at 21:20
Beautiful colours, we've just planted 2 new varieties of these today.
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Joanne4 May 2009 at 21:20
Hi Raingardener Thanks for the tip. I'll have a try.
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Joanne4 May 2009 at 21:23
Hi Snowbabies Make a note of their names or you will kick yourself when the labels disintegrate in years to come. I have a paper plan for my Clematis and roses as I forget their names occasionaly it has helped at times when I chat with another enthusiast usually my Dad.
I don't bother with other plants though although i like to know their names.
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Carolyn4 May 2009 at 22:17
Oh! I love your clematis.I have most of the same varieties but not in bloom here for awhile.
carolyn
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Catherine@AGardenerinProgress4 May 2009 at 22:45
I agree, never too much clematis. I'm on the hunt for 'Josephine'. Your pictures are so pretty. Mine are growing so fast right now and have lots of buds.
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Hermes5 May 2009 at 06:10
"but one can't have too much of Clematis"
how true that is. President is the first I ever grew and glad to see it in all its glory.
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Roses at Wedgwood House and Gardens5 May 2009 at 06:58
Raingardener/Joanne, I use Irfanview, and I was just thinking of what Joanne was saying about the red tones. My camera often makes things too warm and when I edit and size my pics, I often reduce the red a notch and it makes all the difference. I love Irfanview and have been using it for about three years now. My computer techie put me onto it when I was getting frustrated with Photoshop. I love it and it is so easy. So, I recommend it too.

Anyway, just love your clemmies (good one Frances). I am not really that succesful with them, but keep trying. I have a habit of severing them at their base, mistaking them for an old foxglove stem or whatever on my first weed and clean in the Spring grrrr! I do it almost every year, crazy! They come back, but not with avengance! Montana Elizabeth, looks similar to the Rubens, one which I would love to have. What is the difference between the two, do you know?

Anyway, I think I am caught up with your posts, thoroughly enjoyed taking the time, at last.

Thanks again for sharing and have a great week in Lancashire!
Pauline! :)
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Joanne5 May 2009 at 08:11
Carolyn something for you to look forward to then.
Catherine Josephine is lovely and that's why I had to post it although it has been munched I suspect by earwigs. Have a look at Belle of Woking, blue and Arctic Queen white both as lovely as Josephine.
Hermes It does seem to do so well and repear flowers during the summer. At present there are lots of lovely big buds.

Pauline Thanks for the tip I will have a try when I return from Lancashire.
You could be right about Rubens I will have to check it out. Trying to get Bindweed out of Clematis has damaged many a shoot but so far they have recovered. Mike will not be coming with me so he will take care of the watering while I am away.
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lady jicky5 May 2009 at 09:31
I try and try with clematis but its so hard to get the roots in the shade and then there is our drought which does not help!
I adore your plants and I am going very green with envy! LOL
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Joanne5 May 2009 at 12:04
Lady jicky Hi I would persevere once they get established they can manage better during the dry weather. try growing them on a differnet aspect and you can stand a pot infront or a slab on the ground to help keep the roots cool. If you stand a pot there you will need to water the pot and at the same time think to give the Clematis a drink. Vitecella's are good to start ion they can be quite rampant and will need pruning hard in the early spring but not into old wood only back to where it was shooting on that years growth. Prince Charles and Comptesse de Bouchaud although not vitecella they are treated as such but like Jackmani there flowers are much bigger than many Viteccella.
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Tessa at Blunders with shoots, blossoms 'n roots5 May 2009 at 17:22
Just beautiful Clematis! I wish I had more than one. I have been wanting the Swamp clematis (Clematis Crispa) for years now, but it will have to wait until I move.
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Maureen5 May 2009 at 20:10
Oh Joanne the photography is brilliant. You must be so pleased with them! and I bet your glad that you read the manual ?
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Joanne5 May 2009 at 20:29
Tessa Hi I just googled Clematis Crispa what a lovely bell shaped clematis. How long before your move now?

Maureen Yes I am getting there step by slow step just been trying Irfan View managed to reduce ok but can't sort out the red eye.
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Rob (ourfrenchgarden)5 May 2009 at 21:24
Hi Joanne

Keep at the photography, it's looking good.

Your clematis are really something.

Rob
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Signe6 May 2009 at 07:08
Nice fotos. I love clematis, it realy is beautiful plants.
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Ellie Mae's Cottage6 May 2009 at 17:10
So beautiful! I only have one in my garden but plan on adding more this year. You've inspired me to! -Jackie
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HappyMouffetard6 May 2009 at 19:05
Beautiful photos! I'm eagerly awaiting the first of mine to flower and your photos have made me all the more impatient!
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HappyMouffetard10 May 2009 at 20:23
Beautiful clematis photos - can't wait for mine to start coming out.
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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.

UPDATE

Joanne's Cottage Garden

Monday 4 May 2009

CLEMATIS SEASON BEGINS IN MY GARDEN

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