Have a lovely rest Sunshine at the spa. knowing your DS is getting stronger.
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Originally posted by Sunshine View PostHe is still doing well. Hooray!
My DIL is taking my GS to visit him this weekend. They are staying in a premier inn, so they can visit and enjoy a little break too.
Plant, they don’t know who the donor was. There are very strict rules about anonymity. They believe the donor was a man and he was a non smoker. My son will be able to write to the donors family, via the transplant co-ordinator. He is only able to thank the family. He is not allowed to give any details about himself. The rules are very rigid in this regard.
Wee Granny, you are absolutely right. My son is a very determined young man, always has been. When he was a child I saw it as being stubborn, but that stubborn/determined trait has certainly proved beneficial to him.
I am off to a health spa with a friend for a few days. I shall enjoy the relaxation knowing my son is doing so well. I think I need it!
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Well I had a lovely break at the health spa. I really was able to enjoy it knowing my son is on the mend. I came home on Wednesday with every intention of visiting DS at the hospital on Thursday. I spoke to him on Wednesday evening and he said he might be coming home the following day. I think he was going for the Guinness book of records to get out of hospital in record time after a double lung transplant. After much persuasion on his part, they released him on Thursday evening, with the agreement that he would go back again today for a blood test and again on Tuesday for another check up. He told them he wasn’t sleeping well in hospital and not enjoying the food and just wanted to get home to fully recover. He is still very tired, but very happy to be home. I am going over tomorrow to see him and will stay over for childcare while they are at the hospital on Tuesday. My DIL is wonder woman and superwoman all rolled into one, but she is immensely happy and relieved that everything has gone so well. She will never know quite how thankful I am for her care she has shown to my son. Onwards and upwards and everyone is happy.
PS My son was in hospital just over two weeks after his operation. Some of the patients have been in there for two months and more. His determination has really worked in his favour. He is already talking about coaching GS’s football team when he is stronger. They say ‘Where there’s a will, there’s a way.’Always face the sunshine and the shadows fall behind you.
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Sunshine - that is amazing! M is amazing, and so is your DIL. I'm sure his recovery will speed up even more at home where he can be with his family and get proper sleep. I'm sure you and GS will be delighted to see each other as well. His determination is just like Oma's OH when he had his bone marrow transplant.
What a week your family has had!
I'm so glad you enjoyed your spa break - you needed it after so much worry and anxiety."Joy is what happens to us when we allow ourselves to recognise how good things really are. "
(Marianne Williamson)
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Thanks for all the positive comments everyone. My son had a long day at the hospital on Tuesday. They are still pleased with how well he is doing but he does have a chest infection, which they are treating with high dose antibiotics. He also has fluid on his lungs which they will drain today (when he has ANOTHER appointment at Harefield, ) unless the fluid has reduced significantly. He is still extremely tired and VERY cold. I told him yesterday that I am worried and a bit concerned that he left hospital too soon. He reassured me that blips like these are almost guaranteed to happen. Hopefully his check up today will show some improvement. They are keeping a very close eye on him. He will be having regular check up appointments twice a week for some time, until they are confident things will settle down. After that the appointments will be once a week. It is going to be a strain on my DIL too. The journey from their home to Harefield Hospital is an hour and a half each way. It can be much longer if there are problems on the M25. She seems quite relaxed about the travelling. Fortunately she has never been fazed by driving, she actually enjoys driving. This is a real plus.Always face the sunshine and the shadows fall behind you.
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Sunshine - These blips leave you with your heart in your mouth don't they. I'm sure I remember Mr Oma having ups and downs after his bone marrow transplant, too. I hope the fluid has reduced, but they're keeping a very close eye on him which is great. Your DIL is a star and very strong and there is the consolation that it's summer with lots of daylight and no ice or snow to worry about.
Sending you all my love. xx"Joy is what happens to us when we allow ourselves to recognise how good things really are. "
(Marianne Williamson)
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