Return to Website

Myotonia Congenita Forum

 

This forum has been closed for comments.  You can still search archived messages.

 

Visit  the Non-Dystrophic Myotonias  Facebook Group

Myotonia Congenita Forum
Start a New Topic 
Author
Comment
View Entire Thread
Re: Hopefully I can inspire you.

Jan, the stiffness is always there, I just keep moving all the time and hide the symptoms from others real well. Cold still gets to me real bad.

Type of Myotonia: Thomsen's

Country: Leming, TX

Re: Hopefully I can inspire you.

Hi Garret:

I had military and search and rescue ambitions as well when I was younger but I had to give them up because I have Becker MC, and while the severity of my myotonia has significantly lessened as I got older, I started to have trouble with muscle weakness and stamina issues, that seem to be common in those of us with the recessive form of the disorder.

I have about 6-8 hours of "active time" at the moment, where I feel relatively normal. I try to get my exercise and necessary chores and activities done within this time frame, but at the end of the day my back muscles begin to cramp up and burn and I really just want to go home and let my muscles rest.

Type of Myotonia: Becker

Country: USA

Re: Hopefully I can inspire you.

Hey Garrett, I'm 19 and studying medicine at the moment and was hoping to join the army as a medic, does this mean I won't be able to?
P.S and keep up what your dong it sounds awesome! i've never met anyone else with myotonia, so its really cool to hear what other people are up to! Philippa

Type of Myotonia: Not sure

Country: England

Re: Hopefully I can inspire you.

Philippa, I don't know what the exclusions are in England regarding military service, but in the US if you have confirmed myotonia congenita you would not be allowed to enlist.

Jan

Type of Myotonia: Thomsen's

Country: US

Re: Hopefully I can inspire you.

Hi Garrett....I read your post, and wanted to share with you that I served 12 years in the US Navy, achieving the rank of YN1(SW)(surface warfare specialist), and also served in Operation Desert Storm.....I joined the Navy when I was 20, and had the same types of difficulties with the physical rigors of the military.....my problem was....I didn't know I had MC....had it been diagnosed, I'm sure I would have been discharged. I didn't find out I had MC until I was 50 years old, and was able to see a neurologist at the VA, who diagnosed me....it was quite a relief, knowing that there was something with a name to go along with my symptoms, and that I wasn't just "clumsy"....anyway, wanted to share that, and thank you for signing up to serve our country....and as a Firefighter, you are doing just that!....from a proud Veteran, Thank You!

Type of Myotonia: Beckers

Country: US