I hadn't intended to take such a long break and the bigger the gap the harder it felt to pop back, but a kind reader left a comment on my last post and it spurred me into action.
Late last year Pip was diagnosed with significant and widespread joint hypermobility which causes pain and partial dislocations in several of her joints. In addition she was complaining of constant dizziness and nausea and then the collapses began occurring and there was a query regarding a Pots diagnosis.
One particular collapse in the middle of May led to yet another hospital admission but in order to transfer her to a trolley the team used a Pat slide and in so doing her right shoulder partially dislocated and when she eventually came too she was screaming in pain. As a result this involved a two week stay in hospital to allow the shoulder to heal but we also had the added complication that every time she tried to sit up she lost consciousness. Finally she stabilised enough for her to be allowed home but within that first week home she collapsed three times and the following week her left elbow partially dislocated! By now we were veterans in pain and collapsing management and thankfully kept her out of hospital!
Pip's consultant is really lovely and knowledgeable and in order to ascertain what is going on he ordered a 7 day ambulatory ECG to track her heart rate during this time. When we returned to clinical investigations on Wednesday to have a 24 hr blood pressure monitored fitted, she lost consciousness whilst sitting down. The team also got their ECG machine on her and her heart rate was 127-156 beats per minute (a normal heart range is between 75-90), her blood pressure shot up and then plummeted as did her oxygen levels - in short she was in a bit of a mess. She was duly taken to the children's ward where the nurses remembered her from last time and after five hours she was allowed home.
The following morning I took some chocolates for the staff on the investigation unit and that is when they sat me down and explained that her heart runs at 127-156 bpm 24/7 even when she is sleeping which is abnormal and therefore the Pots diagnosis isn't looking as likely and there is now a concern that there is something physiologically wrong with her heart. Her case was marked as urgent and the cardiologist on that unit turned his report around in half a day. We are now on a waiting game for the next steps and understandably she is frustrated that she cannot go out on her own or play football at the park. Her consultant had already made a referral to the cardiologist attached to Alder Hey Children's Hospital in Liverpool -they visit our local hospital once a month so hopefully we won't have a long wait.
Thanks for reading, I think we are all caught up and hopefully now that Pip is in her last week at Inter High I might manage to pop in this space more frequently! I'll leave you with two recent photos from Pip's yearly Midsummer Fairy Day with Beth, they had enormous fun following a Harry Potter Scavenger Hunt courtesy of an ETSY download, it was well worth the £5.00 :-)
14 comments:
Dearest San, I so so very sorry to read of Pip's on going and serious health woes. Sorry, too, that there is such a wait for the next specialist consult — have been thru this too both for myself and for my Thomas. Sigh. Praying for strength and courage for you all. And that the peace of Christ will light your way through this thicket. 🙏🏻🕊
I am sorry to hear about all the difficulties you have been having. Such a difficult time to be in this situation. I hope and pray the experts will be able to see and diagnose her soon!x
Your family certainly is no stranger to pain but it must be so difficult to see poor Pip in this place. Thank you so much for the update as I have been so concerned for your family with your blogging silence. Love and prayers to your dear family.
Thanks dear friend for your love and prayers x
Thanks Kezzie 🙂
Thank you for your concern, love and prayers they are appreciated 🙂
Have you gotten any news on her heart? At least she had a wonderful Midsummer day. How are Ben and Dave?
Cardiology at Alder Hey looked at the readings and they believe it is still a Pots thing, so we are now looking for a specialist in this field. We will in all likelihood have to travel South and loads of families on the Pots FB page recommend Dr Nicholas Gall - he is head of cardiology at Kings College Hospital in London and he is the person to see when it comes to Pots. We are doing all the right things but I’m sure some targeted medication would make a huge difference 🙂. Ben and Dave are doing pretty well all things considered and they are pretty good at find distractions to alleviate the stress 😃
Oh goodness me! It sounds like the whole family, but Pip especially have been through the mill. I pray that a diagnosis and treatment can be found soon.
Oh, no! I am so sorry to read about poor Pip. What a terrible time. Thinking of you all. xxx
Praying for a diagnosis an d medicine that can help her.
Hello San! I hadn't realized you had posted. It's nice to read your update, though it's about such a difficult time. I hope you receive more information soon on how to proceed. I send all of you so much love, and I hope things stay quiet for a little while. xoxo
What a time you've had of it! I hope things turn the corner soon and you can enjoy some stress free days. May the Lord bless you, encourage you, and give you strength. xx
Thinking of you all, San! I do hope there has been some improvement this month.Continuing to hold you in my prayers. 🤲🏽🙏🏻🕊
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