posted
I'm really scared now! My legs have been getting progressively weaker and I was hoping that it was "all in my head". However, when I woke up this morning, I thought I felt pretty good until I stood up and tried to walk. My legs were so weak (particularly left one) that I honestly was afraid they were going to give out on me!!! My hip / butt / lower back feels the same way. I am on Doxy for 10 days ... this is Day 4. What do you think?
posted
Hi, Ok, all I can do is tell you that this happens to me. Leg muscle weakness/spasticity is one of my biggest symptoms. Try and rest them, but also use them, if you can.
Call your dr and let them know what is going on; it's a long weekend. I will be praying for you.
Posts: 113 | From CA | Registered: Jun 2010
| IP: Logged |
Keebler
Honored Contributor (25K+ posts)
Member # 12673
posted
- It's just part of lyme. Happens to most patients. It will get better with treatment. -
Posts: 48021 | From Tree House | Registered: Jul 2007
| IP: Logged |
posted
this happened/happens to me as well. It was one of my first symptoms and I ended up in the ER because I thought I was having a stroke. One of my legs felt weaker too.
I still have very weak legs, my right feels weaker, but doc says left is weaker when he tests. Anyhow, some days I feel strong and others I feel very shaky and weak and uncoordinated. arms are the same. It comes/goes, but overall generalized weakness for sure.
Posts: 618 | From NC | Registered: Oct 2009
| IP: Logged |
posted
Thank you all for responding. It's nice to be reassured that I'm not crazy! I know these symptoms are real no matter how hard I try to convince myself otherwise.
posted
Leg weakness and pain have been the biggest issue with me since I was dx'd two years ago. It is for me as it is for jwall - it comes and goes. I used to be afraid I would be in a wheel chair one morning - now I think, "this too will pass". Hang in there, get treatment and get well.
Posts: 7 | From California | Registered: Oct 2009
| IP: Logged |
littlebit27
Frequent Contributor (1K+ posts)
Member # 24477
posted
Yes, I have this as well. I told my husband before my DX but after my huge avalanche of symptoms that my legs felt like they didn't want to work, they felt like jell-o.
Tricky Tickey
Frequent Contributor (1K+ posts)
Member # 26546
posted
I've had the same symptoms Kim, though not so pronounced. Just recognize it for what it is - a symptom. Keep moving, girl! Make yourself move, even if you have to hold onto things. Refuse to lay down & be defeated, refuse to allow the symptoms to scare you. You know your body better than anyone else. If you feel like something is really wrong, life threatening, you'll know what to do. This makes my own symptoms seem like nothing. I have truly been fortunate to have only been touched by a few discomforts. Compared to everyone else, mine seem mild. I'm now 8 weeks since infection. I think maybe, possibly the reason my symptoms aren't the very worst is because, possibly, I eat lots of antioxidants (berries), take many supplements, try to excercise 3 times per week. I don't know if this means anything or not. I feel like I shouldn't complain at all compared to what most of you are going through...it makes me thankful that I'm hanging on like I am. Kim, don't give up!
-------------------- Early Disseminated LD- 2010. Currently doing acupuncture and yoga. Negative Igenex (IND & Pos Bands) ISSUES AFTER: Tendonitis, letter reversal, Low immune system. PREVENTION:SaltC,Iodine,Humaworm, Chiropractic. Posts: 1013 | From In a van down by the river. | Registered: Jun 2010
| IP: Logged |
dmc
Frequent Contributor (1K+ posts)
Member # 5102
posted
Thank you all so much! This morning was really bad ... I could barely walk ... I was staggering and overstepping my feet and my husband saw it all this time. He helped me back upstairs to my bed. Thank GOD that hubby is home this coming week for vacation ... I just feel bad that he has to worry about me during his time off!
IgG � Igenex Positive; CDC/NYS Negative with 31+; 39 (IND); 41++; 58+ Posts: 339 | From Tennessee | Registered: Jun 2010
| IP: Logged |
Keebler
Honored Contributor (25K+ posts)
Member # 12673
posted
- He does not have to worry about you. I really hate it when people do, I'm sure you do to. It really helps to turn that into action - find out what can help.
This really is just part of what lyme entails. It's not likely to change overnight so being proactive in how you arrange your days will help. Rest when you feel the need. Consider safety measures for getting around, just as you would were you to have a sprained ankle.
For now, magnesium may be your best help in that area for many reasons. Ginger capsules, too. I know you don't have your LLMD appointment for 4 weeks or so, but be sure to read through the links in your collection regarding self-care and support measures.
Good luck. -
Posts: 48021 | From Tree House | Registered: Jul 2007
| IP: Logged |
This was also one of my first really weird and scary symptoms - and I did not know I had Lyme for another 15 months. It would come and go, but one time there was almost a month of it.
What helped me was trying to do whatever I could, not to the point of stress, but a little bit. If I was to weak to stand then leg lifts, if I could stand I would try for little bits at a time. I got a super beginners yoga DVD and just did what I could the way I could. On the days my legs were better I walked -just as far as I felt safe - sometimes down the drive and back, but gradually the distance increased. One key to walking I think is to do it with a friend/or great music - something that will keep you uplifted and not focused entirely on your legs.
Please know it is a symptom of LD and will get better - I am not done with my own treatment, but usually walk about 3 miles a day.
Peace, CalMom
Posts: 29 | From California | Registered: Jan 2010
| IP: Logged |
posted
Thank you, CalMom! That is exactly what I did yesterday .... walk up and down my driveway ... and figured my neighbors thought I have lost my mind!
IgG � Igenex Positive; CDC/NYS Negative with 31+; 39 (IND); 41++; 58+ Posts: 339 | From Tennessee | Registered: Jun 2010
| IP: Logged |
randibear
Honored Contributor (10K+ posts)
Member # 11290
posted
i know this is going to be tough, but you have to walk. or at least get going.
i forced myself to walk a mile every day. i could barely make it the first 25 feet and some days i practically cried doing it. but i dragged my butt out of bed early (cause in texas it gets hot so early) and i drove over to that park and went by myself.
i didn't need to hear all his complaining and it was peaceful with ducks and the lake for me.
some days i stopped at least 4-5 times to get my breath and sometimes i got in the car shaking. i thought i was going to pass out.
but i gradually worked up to where i didn't have to stop, my face didn't get red, and i could make it around in about 20 minutes.
and it strengthened my legs and it really helped a lot.
-------------------- do not look back when the only course is forward Posts: 12262 | From texas | Registered: Mar 2007
| IP: Logged |
posted
yup, i went through it as well. early in treatment and it sucks, you have to push through though. good luck!
-------------------- 3 months Doxy 8 months of Tetra 7 months of Biaxin/Plaq. 4 months Doxy/Biaxin/Plaq. 5 months Biaxin/Plaq. Back on Doxy/Biax/Plaq On the road to recovery. Trying to make people Lyme Aware....... Posts: 289 | From R.I. | Registered: Jun 2009
| IP: Logged |
The Lyme Disease Network is a non-profit organization funded by individual donations. If you would like to support the Network and the LymeNet system of Web services, please send your donations to:
The
Lyme Disease Network of New Jersey 907 Pebble Creek Court,
Pennington,
NJ08534USA http://www.lymenet.org/