KevonLem
New member
- Joined
- Feb 7, 2021
- Messages
- 6
- Reason
- Learn about ALS
- Diagnosis
- 00/0000
- Country
- US
- State
- WA
- City
- Seattle
Previous thread
I had posted in this forum in January and February of this year after my covid vaccine where I was experiencing sudden onset widespread for fasciculations and muscle spasms. Subsequently I discovered that fasciculations, muscle weakness, and muscle spasms are all associated with COVID vaccine. I just wanted to post here to update everyone and hopefully help others that are concerned about an ALS diagnosis. During this concerning time when I thought I may have ALS I had two emgs several neurology appointments and a couple of er visits due to a wild set of symptoms. Some people only experience pens and needles tingling and muscle twitches, but some have more dramatic symptoms. We have created a sizable group on Facebook and would be happy to offer some support to those experiencing dramatic delayed symptomology due to the COVID vaccine. I'm not sure if I'm allowed to share the group on this post, but if somebody could let me know it would be appreciated thank you.
P.S. Thank you so much in the past for offering answers and information. It was very useful and kept me sane through a very dark time in my life. I know these ALS inquiries are annoying and a bit tone deaf but I assure you they are extremely helpful thank you again.
I had posted in this forum in January and February of this year after my covid vaccine where I was experiencing sudden onset widespread for fasciculations and muscle spasms. Subsequently I discovered that fasciculations, muscle weakness, and muscle spasms are all associated with COVID vaccine. I just wanted to post here to update everyone and hopefully help others that are concerned about an ALS diagnosis. During this concerning time when I thought I may have ALS I had two emgs several neurology appointments and a couple of er visits due to a wild set of symptoms. Some people only experience pens and needles tingling and muscle twitches, but some have more dramatic symptoms. We have created a sizable group on Facebook and would be happy to offer some support to those experiencing dramatic delayed symptomology due to the COVID vaccine. I'm not sure if I'm allowed to share the group on this post, but if somebody could let me know it would be appreciated thank you.
P.S. Thank you so much in the past for offering answers and information. It was very useful and kept me sane through a very dark time in my life. I know these ALS inquiries are annoying and a bit tone deaf but I assure you they are extremely helpful thank you again.
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