Joanne's Cottage Garden: THE PRESIDENT AND FRIENDS

Friday, 15 May 2009

THE PRESIDENT AND FRIENDS

The President can speak for himself. I expected big things but even so he has excelled himself. I am hopeing his namesake will be as successful.

Some of his friends are also doing as well.

Nelly Moser

Marie Boisselot

Josephine

Niobe

HF Young

12 comments:

Carrie15 May 2009 at 20:38
So uber jealous, they are truly gorgeous no wonder you couldn't help taking so many photos - beautiful.
ReplyDelete
Replies
Frances15 May 2009 at 22:07
Hi Joanne, well, both presidents are doing quite well. Your vine is massive! They all look lush and healthy, lot's of rain your way? It has certainly made for a good year here too. :-)
Frances
ReplyDelete
Replies
Signe15 May 2009 at 22:08
Clematis is one of my favorits. Loveley photos.
ReplyDelete
Replies
Catherine@AGardenerinProgress16 May 2009 at 00:53
Joanne, you have such beautiful clematis. I bet it looks so pretty walking through your garden. I just got a call from the nursery to say they are holding 'Josephine' for me :)
I think my 'Nelly Moser' is going to finally bloom for me this year!
ReplyDelete
Replies
Alison16 May 2009 at 02:24
Hi Joanne
Your clematis amaze me!
They are gorgeous
ReplyDelete
Replies
Roses at Wedgwood House and Gardens16 May 2009 at 06:13
Hi Joanne,

Welcome back home. I hope you had a great week and a wonderful time at the wedding. Hope your dad is doing well.
Beautiful clematis here! thanks for sharing the pics.

I think I may have found the coveted geranium I was lusting after. I saw it in many gardens on my morning walks when I was last in England. I was away in Victoria at the weekend and went to a favourite nursery there (a rare occasion as it is out of the way). It also has rare plants, and I saw this low Cranesbill with a label which looks exactly like the one I devoured in England. It is already planted and I am keeping my fingers' crossed. When it is daylight I will read the label and let you know! :) I also purchased another low growing one which was very intriguing also.

In a day or so, I hope to have my weekend in Victoria up on my blog, as the Butchart gardens were so incredible this Spring. I know I am going to have a hard time eliminating pictures to put up on my blog.

Anyhow, glad you are back home safely.

Take good care, Enjoy the summer! I believe the north west is going thought a cold spell right now. I talked to my friend today on the Wirral!
Pauline
ReplyDelete
Replies
Hermes16 May 2009 at 06:25
The President and Nelly Moser are two of my real favourites and grow so well and the flowers are gorgeous.
ReplyDelete
Replies
Joanne16 May 2009 at 10:48
Carrie why not try one or two on your allotment I always enjoyed flowers when I had mine infact the one next to me grew Delphiniums for show it was like gardening in heaven. He also grew pinks and the perfume was also just as intoxicating.

Francis Yes it does sound so. Not that I am prejudiced but I do hope the President does something for Lyme Disease it is a medical scandal of epic proportion. Good news that Conneticut passed their Lyme Bill and hopefully the Bill before the Senate will be just as successful.

Signe Glad you enjoyed them.

Catherine Yes it is easy to enjoy the clematis and not look down at the ground elder. Hope Josephine does well for you and fingers crossed Nelly Noser flowers.

Alison my fellow Canadian Lymie how goes your new treatment? Hope you enjoyed your holiday looking forward to some photos you will have to start blogging especially now the gardening season is about to begin. BTW go visit my friend Pauline from Roses at Wedgewood house and garden she visits in your area Edmondton.

Pauline What a warm welcome. I did have a good trip and have some photos to post from Dad's garden in time. I'm looking forward to your next post. I will also look forward to seeing the geranium and hearing it's name, be funny if it is the one Mary gave me. Yes it was as always a bit chilly North, we have at last been having a bit of rain here in Surrey but more would be good.

Hermes Yes They are good performers but can take a year or two to get gowing. I used to prefer the late flowering vitacella types because they perform well even as new plants but now I am not so sure. I suppose the tendancy is to enjoy what is flowering at that time. I just replaced some clematis I lost so I am back up to nearly 50 again 48 I think to be precise. So hopefully more photos to come I may get a bit of a bore on this subject.
ReplyDelete
Replies
Heather17 May 2009 at 05:29
All of them look so happy to be in your garden. I can't grow clematis to save my life. I love to look at it though. Yours are gorgeous!
ReplyDelete
Replies
Joanne17 May 2009 at 08:44
Heather glad you enjoyed them.
ReplyDelete
Replies
Anonymous17 May 2009 at 16:28
Joanne your Clematis' are doing so wonderful. I just love all of them. I want to get so many more.
Sorry I'm late getting here - we've finally been having some great gardening weather so I've been outside. Headed out again right now!
ReplyDelete
Replies
Joanne17 May 2009 at 20:17
RainGardener You can never have too many clematis in a garden.

I watched the preview of Chelsea flower show tonight and thought when it showed the Clematis stand that although quite nice to see many together you can't beat seeing them growing naturaly in a garden amongst lots of other plants. Even in mine when the bindweed creeps in or should I say runs, it's worse than a Russian vine.
ReplyDelete
Replies

Add comment

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

Friday, 15 May 2009

THE PRESIDENT AND FRIENDS

12 comments:

My Garden

Pageviews from the past week

Translate

My other blogs

Search This Blog

LYME DISEASE

About Me

Visitor numbers starting July 11 2009

Followers

Blog Archive

Popular Posts

LYME LIFE written 2009

My Blog List

LYME DISEASE