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# What I Experienced in 2024: I Finally Learned What Really Happened to Me
- URL: https://orange-healing.ghost.io/what-i-experienced-in-2024-i-finally-learned-what-really-happened-to-me/
- Published: 2025-04-28T15:21:04.000Z
- Updated: 2025-04-28T15:21:04.000Z
- Author: Summer
- Tags: My Story

### 

When the new year began, this was my situation:

### **BALANCE**

When I was discharged from the hospital:

- I couldn’t sit upright without falling to the sides.
- I couldn’t stand on my own.
- My torso trembled violently.
- My head constantly shook side to side, back and forth.

**Now:**

- I can sit upright.
- My head tremor has lessened.
- I can stand independently and walk on my own (though I still lose balance).
- I have significantly improved control over my torso tremor — I still tilt to the sides sometimes, but I recover more quickly.
- I used to struggle to take a full step with my right leg; now both legs step more evenly.
- Walking on soft surfaces (balance pads, grass) is still challenging, but there is some improvement.

---

### **COORDINATION**

My hand-eye coordination was almost non-existent.  
For example, I couldn’t catch a ball if it was thrown to me.

**Now:**

- I can sometimes catch a ball, although I still miss it occasionally.
- I can type on a keyboard (hitting the correct keys).
- I can text on my phone (accurately hitting the letters).
- Using both hands at the same time is still difficult.
- Clapping is hard, but if I do it slowly, I can manage.

---

### **SPEECH**

While in the hospital, I couldn't speak at all.  
When I was discharged, only a few words would come out — my voice sounded like a baby’s and was very faint.

**Now:**

- I can pronounce words correctly.
- My voice is deeper. Sometimes I hear glimpses of my real voice.
- My voice sounds louder and stronger.
- I have started using more natural intonation and emphasis.
- I speak faster now, though I am still dysarthric.

---

### **MY HANDS**

My biggest struggle was — and still is — with my dominant hand, my right.  
When I first came home, I couldn’t feed myself, brush my teeth, or even hold a cup. Writing was completely impossible. Showering alone was out of the question.

**Now:**

- Despite persistent tremor, I can feed myself, brush my teeth, and hold a cup.
- I can use my phone and laptop.
- I can write — badly and slowly, but I can.
- I can do some painting and coloring — again, badly, but I can.
- Doing makeup is still very difficult; my hands shake when brought to my face.
- Stirring soup or similar tasks remain tough.

In short: **my hands have shown the least improvement, despite all my efforts**.

---

When lithium was discontinued, I saw noticeable improvement in both my balance and speech within the first month.  
However, because my mood stabilizer changed (I started taking Depakine), I also began to experience increased appetite and emotional detachment. In January alone, I gained 3 kilos — thanks to endless chocolate.

Then, my physiotherapist changed, and I had to adapt to a new program. I was training six days a week, two hours a day — it was exhausting.  
Sometimes I could literally feel my brain burning.

I kept going with stable exercises, but my progress was still painfully slow.

---

In June, I finally dared to walk outside with a cane.  
But one day, as I was leaving a supermarket, an automatic door closed on me, and I fell badly.  
I split open my forehead.  
After that, I developed a severe fear of walking outdoors.  
I stayed at home for months, terrified to walk again.  
It crushed my morale.  
I felt like I wasn’t healing at all.

In desperation, I decided to see one more doctor — a very famous and highly respected neurologist.

He quickly dismissed previous suggestions about FND (Functional Neurological Disorder) and said:

> "Your problem is not psychological. You have **cerebellar dysfunction**."

He reviewed my medical records:

- My lithium level during the initial illness was 1.19.
- Since I hadn’t lost consciousness, he believed it was consistent with **lithium intoxication**.
- Lithium toxicity combined with high fever could cause ataxia — and it was even written in the drug’s prospectus as a known side effect.

---

Researching lithium toxicity shocked me.  
It explained **everything** I had gone through.

The name of the condition?  
**SILENT syndrome** — *Syndrome of Irreversible Lithium-Effectuated Neurotoxicity.*

---

I had been diagnosed with bipolar disorder in 2015 and had started lithium then.  
Now, looking back, I curse that day.

---

Toward the end of the year, I had the chance to travel to Dubai.  
I consulted another neurologist there to get a second opinion.

He reviewed my MRI scans and bloodwork — and he was puzzled:

> "At your age, such severe ataxia shouldn’t happen."

He suspected either **vitamin E deficiency** or **copper excess**, because both can cause ataxia.  
But tests showed neither vitamin E deficiency nor copper excess.

**It was all because of lithium.**

---

\*SILENT syndrome (*Syndrome of Irreversible Lithium-Effectuated Neurotoxicity*) is a rare condition where lithium treatment causes permanent neurological damage even after the drug is stopped.  
Symptoms often include:

- Tremor
- Ataxia (loss of balance and coordination)
- Dysarthria (speech difficulties)
- Cognitive impairment
- Visual disturbances

It typically occurs after lithium toxicity, and symptoms can persist even after blood lithium levels return to normal.