[goyo borque]

<p style=”text-align: left;”>Hi there. I am sorry. I am Spanish and I live in Spain. the doctors we have visited are 3 neurologists specialized in neuromotor diseases and a special one in ALS.</p>

[goyo borque]

thanks for the reply.

According to them, they have ruled out everything through analytics and electromyography and magnetic resonance imaging.
I also forgot to comment that it all started when she gave birth to our daughter when she was put the anesthesia and it worked upwards  instead of towards her legs.

I don’t know if I should ask for any analytics or something special to rule out something. The truth as I mentioned we are at a point where they only say that we must wait and it produces so much helplessness to see that time passes that it does not progress and that the doctors do nothing … I am sorry for what I comment and I can only thank you for your experience help and answers. Thank you

[goyo borque]

Thank you very much for the reply. The truth is that I take this uncertainty a little badly, 4 doctors have reviewed it and those who are for private insurance say that it is very rare but they all say that we can only wait for it to evolve. It is rare according to them because it only affects one area and that the bulbar stem is reducing.

[goyo borque]

Thank you very much

[goyo borque]

Thank you. Could you give me the name of the doctor you are commenting on for looking into the future?

[goyo borque]

hello.

They have already carried out the analytical tests for MG and they were negative. ( I don’t know about other possibe test for MG)

I am very sorry for your mother. Thank you very much for your help.