Lymph Node Update - Scared

[Carys]

I should be able to tap them basically the same speed on each hand. I can’t. Therefore I have a motor neuron disease. Most people should be able to do this no problem.

Rightho, so let your neurologist know that you definitely have MND. Its a certainty based on your accurate home test (totally unbiased by mental health problems). A home test which came up with the same result in 2016 and on previous occasions. Be sure to come back and let us know when you are recovered from this 'bout of MND'.

Its great news isn't it that the Lymphoma cleared up, from the start of this thread.

[BlueIris]

Congratulations, sounds as though you finally got what you really wanted!

[darkside4k]

I did not sleep tonight I was in so much pain.

[Carys]

Oh, right, are you SURE its MND then ?....as that doesn't cause pain!

Maybe your lymphoma has returned after an untreated remission?

[utrocket09]

I should be able to tap them basically the same speed on each hand. I can’t. Therefore I have a motor neuron disease. Most people should be able to do this no problem.

Actually you are incorrect. Most people cannot do that at the same speed. So glad you were able to diagnosis yourself and hopefully get treatment soon.

[Carys]

Actually you are incorrect. Most people cannot do that at the same speed.

Yeah, you know that, I know that, people have said that......he's had this very 'symptom' at least three times before in the last few years....but none of that matters.

[bin tenn]

What a waste

[Seymour]

Terry and Carys:

I have read your posts and understand how from an outside perspective this might look like a pattern of HA and exaggerating significance of symptoms.

I do however have symptoms and I am suffering and trying to make sense of them and why they don’t improve or go away. My girlfriend says nothing will improve if I don’t make changes but I have a hard time with the concept of bodily symptoms arising spontaneously from anxiety and staying there even outside of acute anxiety attacks.

Since my symptoms match some of those from ALS I have a very hard time letting it go.

[darkside4k]

I now also believe the thumbpad muscles on my hand look smaller than I remember them being. I think they maybe have atrophied from ALS. This is so depressing. I hate it but every new symptom is a fresh arrow pointing at ALS. Intense muscle pain in hands and legs and feet continues. Twitching. Now possibly atrophy visible on my hands.

[Carys]

What a waste indeed bin tenn.

Intense muscle pain in hands and legs and feet continues.

Let me repeat what I said on this page, but louder -

MND does NOT CAUSE PAIN, let alone INTENSE PAIN.