Can A Broken Humerus Affect Your Hand And Wrist Long Term?
Sixty-four years ago, my left humerus was broken at school and I don’t think the local hospital fixed it too well. I also don’t think I had the best of physiotherapy, after some of my experiences with physios since my stroke, which have been of a generally very high-quality, from both the NHS and private physiotherapists.
The wrist has not been misbehaving itself recently, so I asked Google AI, the question in the title of this post and received this reply.
Yes, a broken humerus can affect your hand and wrist long-term, especially if a nerve like the radial nerve is injured during the fracture or surgery. This can cause temporary issues like wrist drop, which is the inability to extend the wrist and fingers, often improving with therapy. In rare cases, if nerve recovery is incomplete, surgical procedures may be necessary to restore function, though most fractures have an excellent long-term outlook with proper rehabilitation.
Note.
- I certainly didn’t have proper rehabilitation in 1961 at Highlands Hospital in Winchmore Hill.
- I wonder if I have actually suffered from wrist drop in recent years.
- I suspect that now there are better treatments available.
Google seem to have scraped the article from the respectable Cleveland Clinic.
Why Has My Left Humerus Got Worse In The Last Few Months?
I wonder, if it is new BYD buses on route 141.
- I always sit or stand downstairs, as at 78, I don’t want too risk climbing the stairs.
- The buses are more pokey and the seats are narrower than say a Routemaster or other British bus.
- On Routemasters and other British buses, I usually sit on the far-right seat to protect the humerus.
- It is getting increasingly knocked if I sit in the left-hand seat of a right-sided pair, by peoples’ backpacks.
- The seats are narrow on the BYD buses, and if sitting in a left-hand seat of a left-sided pair, my left humerus rubs against the outside wall of the bus. This is worse with a large person in the right seat.
- If I sit in the right-hand seat of a left-sided pair, it’s usually better, but if there’s a large person in the left seat, because of the narrow seats, the arm get knocked.
- On the BYD buses, there are no forward facing seats downstairs on the right side.
- There are some forward facing seats at the right side at the back, but they are difficult for me to climb into.
- The corridor from the front to the back in the bus is narrow and I sometimes bump the left humerus.
- I met a lady with a pram, who finds the corridor narrow for her pram.
- The step-up and down into the bus is higher and puts strain on my knees, unless I get it right.
I do wonder if the BYD buses were designed around smaller oriental people.
I certainly never had these problems, when I was riding on on Routemasters and other British-designed buses.
For the next few works, I will avoid travelling on the BYD buses unless I can sit in the right-hand seat of a pair, by myself.
I can also stand, if the bus isn’t too full. Looking back, I feel, I don’t mind standing on the buses.
I will now be forwarding this post to those that know me well.
£20 Electronic Ear-Clips Train The Body To Decrease Blood Pressure
The title of this post, is the same as that of this article in The Times.
These two paragraphs outline how the device is used.
A £20 device that delivers “tingling” electric pulses to the ears and can be worn at home could be almost twice as effective as drugs at reducing blood pressure, a neuroscientist has said.
Early trials suggest that wearing the small electrodes clipped to the ears for half an hour per day over two weeks while relaxing, watching TV or eating can reduce blood pressure by up to 15mm of mercury (mm Hg), compared with 8mm Hg to 10mm Hg for drugs such as Ace inhibitors or beta-blockers.
It appears the device has been developed at University College London.
Would I Use Electronic Ear-Clips To Control My Blood Pressure?
Soon after my wife died in 2007, my cholesterol levels rose.
The Ipswich Town Physiotherapist, who was a drinking partner before matches at Portman Road, recommended that I see his dietician.
She identified the following.
- My diet had changed since my my wife’s death, as I was choosing the food and doing the cooking.
- She suspected, that I wasn’t eating enough soluble fibre.
- I was eating enough fruit and vegetables.
Her solution was two-fold.
- Swap butter and other spreads for Benecol.
- Make sure, I eat, at least one small tin of baked beans every week.
Obviously, as I had been found to be coeliac in 1997, I should stay gluten-free.
I’ve seen other dieticians since and none have criticised, what she said.
No doctor has also ever said, that there is something wrong with my cholesterol.
After my stroke in 2010, I was put on Warfarin to thin my blood.
The only addition to my cocktail of drugs, was that after an unexplained collapse, I was put on blood pressure drugs.
So to return to the question I asked at the top of this section.
I may take six or seven drugs and vitamin tablets every day, but swapping one or two for half-an-hour with an electronic device wouldn’t be too much trouble.
That is, if I could tolerate the device, as I’m not keen on headphones.
But it could be an interesting alternative to taking pharmaceutical drugs.
Bonus For GPs If Patients Join Drug Trials In Plan To Lure Firms To NHS
The title of this post, is the same as that of this article on The Times.
This is the sub-heading.
£650m boost for medical research after number of participants slumps
These three paragraphs outline what is to be done.
Tens of thousands more patients will be signed up for clinical trials as ministers promise drug companies better access to the NHS to expand the economy and develop cutting-edge treatments.
Jeremy Hunt, the chancellor, is promising a £650 million package to boost life sciences as he attempts to lure pharmaceutical giants to Britain.
GPs will be offered financial incentives to recruit patients into trials of new treatments and hospitals will be given research targets under plans to reverse a slump in clinical testing while the NHS struggles with the backlog from Covid-19.
It all sounds good to me.
I have been involved in several trials and medical research projects.
- As part of my coeliac disease diagnosis, one endoscopy was performed by Rebecca Fitzgerald at Cambridge, as she was taking samples of bile fluids for her research into Barrett’s esophagus.
- After the death of my wife, I was interviewed by PhD students in the Psychology Department at Liverpool University for their research into widowhood.
- Oxford University interviewed me on diet for their coeliac disease research.
- After my stroke, I spent an entertaining afternoon at the University of East London doing balance tests by computer. Their aim was to develop a reliable balance test for stroke and other patients, that could be carried out by physiotherapists quickly, than by more expensive doctors.
- I have also been on a drug trial at Queen Mary University, but that drug was useless and had no good or bad affects, so the trial was halted. However, it did lead to other enjoyable activities in the field of patient relations with treatment and research.
As a confirmed coward, I should note that with the exception of the drug trial, all of the other projects were low risk.
I should say, that I also sponsor pancreatic cancer research at Liverpool University, in memory of my son, who died from the disease. I wrote about the first Liverpool project in There’s More To Liverpool Than Football And The Beatles!.
A Database Of Projects Open For Volunteers
I believe that this is needed, so that those like me, who like to contribute to research can volunteer.
Perhaps some of the £650 million, that has been promised by Jeremy Hunt, could be used to create the database.
I also believe the database could be used for other non-medical research.