Sequela of facial neuritis?

I am a 5-year-old patient with sequelae of facial paralysis. I have tried many methods, such as seeking medical advice, acupuncture, plaster, facial nutrition injection, fire needle and directional neuron repair. It can be said that early correction is still effective, but I think early treatment only treats the symptoms rather than the root cause, and never relieves facial numbness and stiffness. Cold weather or lack of sleep can cause abnormal facial discomfort.

I didn't give up. I searched online, checked in key hospitals in big cities, and treated for two years. I'm not making any progress. I don't expect to recover completely at this time, just want to find a way to relieve my discomfort.

Because, I visited many medical websites, and some doctors directly said that patients with severe facial paralysis, that is, sequelae, have little chance of recovery.

Don't believe that when searching, those medical advertisements that occupy the front page swear that they are fully recovered, and those are liars!

Then I stopped searching for how to treat it. I want to know what caused the sequelae of facial paralysis.

I began to search online for papers on sequelae of facial paralysis, and later found an academic paper on pricking collaterals and cupping and bloodletting. Although the clinic said the effect was very good, I didn't go to the hospital.

However, I am also moved. I have had the experience of facial bloodletting before, and I feel very relaxed after each bloodletting. After reading the paper, I feel that it is a treatment direction.

I'll go to a local doctor who can puncture the collaterals and configure some small transparent cupping cups. When I feel uncomfortable, I will stick needles in my face and cupping. After each time, I feel relaxed and feel much better. Because I haven't been to any hospital mentioned in the report and I haven't received professional treatment, I dare not say what the treatment in the report is like. However, judging from the treatment I have explored myself, stiffness and numbness can be relieved when I feel uncomfortable, and there is a phenomenon of improvement. In addition, every time after pricking and cupping, I take medicine to dredge the meridians and take some supplementary VB.

Many people think that the disease does not eat or drink, and some people just talk with a smile, with their faces and corners of their mouths crooked. In fact, the real pain of this disease is not these, but the cold weather. When I get up in the morning, my face is numb and stiff, which is really unbearable. Sometimes my face hurts faintly. Only by applying hot water and pinching your fingers will you relax a little.

I have been to many QQ groups with sequelae of facial paralysis and met different patients. Most people are completely desperate after seeking medical treatment for a period of time. Despair is not the treatment, but the inability to find a real doctor. It can be said that they are basically cheated!

I put the name of that academic paper here, and people who see it can search it to see if it is useful to them.

Clinical summary of 436 cases of sequela of facial paralysis treated by pricking collaterals and dredging tendons.

You can go and see and find your experience!

Finally, I would like to appeal, can you organize patients with facial nerve sequelae to speak together, so that relevant units can pay attention to it and give this disease a standardized treatment standard and direction?

Or some medical TV programs give us some exclusive interviews and point out a direction?