I found this website on my own after reading and reading all over the Internet to find people who could relate to me. I was diagnosed with viral meningitis in August. It is now almost 5 months later and I am really struggling to deal with everything. I have more energy now and don't get headaches very often but my body does ache and my elbows and knees bother me sometimes. I am 26 years old with two young children. If I do not get enough sleep or am really stressed, I feel terrible for a week or more. It is really hard feeling completely normal one day and then the next just feeling like someone just pulled the rug out from under you. Reading other people's post and experiences helps some. This has been a challenge physically, mentally, and definitely emotionally!
Viral meningitis 4 months after : I found... - Meningitis Now
Viral meningitis 4 months after
Some days I feel pretty normal and other days my emotions are all over the place and I just want to cry. I've always been an emotional person but not like this. I just want to be okay again.
Jwire hi,
I'm so very sorry to hear that you've had VM and that you're having a tough time recovering. I am delighted you found this website, as you'll be able to read about other people's experiences and pick up some tips on how to cope and also, it'll help you to see you're not alone 
You don't say if you have talked to your GP about how you're feeling or if you've been in touch with Meningitis Now, who are wonderful with offering help and advice.
I do want to say here that it will take some time for you to feel stronger. You have two young children to look after as well, which doesn't give you a lot of time to rest - 'pacing' yourself is the key here so, you will need to rest. Do you have family nearby who can help you?
I wish you a very Happy New Year, keep well and take each day as it comes (no expectations, OK) and my best wishes to you for 2016
Thank you! I have talked to my dr awhile back but didn't feel like I got much advice. My infectious disease dr just told me it takes time, which I understand but it is so very hard. I am in the U.S. So I have not contacted meningitis now. This website is basically where I've picked up anything I've learned about how it can make you feel afterwards. Thanks for your reply, it's hard to hold things in because I know that people who haven't had meningitis just don't know. I wish you a happy new year Also!
Sorry you have found yourself now in this group, it takes time, and your new " normal" isn't what you were before. I haven't found a lot of help from any doctors, more advice and treatments from this site , writing every thing down for apt with 12 year neurologist. While in hospital dec 8th with another meningitis attack from shingles the doctors wanted to give me shingles vaccine? I refused, this site helped me to see if you are immune compromised (ms) than that is NOT what a person needs. Take it easy , hard to do with small children, I can't imagine what you must be going thru. If you have people in your life maybe sending a few select messages that match what your symptoms are can help them understand. I sent them to my husband, he wasn't clueless, but really opened his eyes to my non exsisting energy levels, and on going ear and headache pain. Wish you the best for the new year, better health, the return of endurance that this condition steals from an individual, joy in your heart for your family. Lower the bar for all tasks, life doesn't measure cleanliness, ask for help even if it's difficult, people really will lend a hand if they know you need it. Take care gramsona
I know how you feel its the same for me.
Hi i know how you feel! I was diagnosed nearly 4 months ago & I still feel as bad as I did when I first got it as I have seizures from inflammation on the brain caused from the virus so its hard especially with having to work as well as my work place though at beginning supported me now just ignore me & have been called a hypercondriac so am getting quite depressed & feel like theres no end in sight to the pain so know there ARE people who understand what you going through xx
Hi jwire,
I am now at the 4 month mark post VM and just came across the post looking through the Meningitis Now archives. I feel very similar - much more energy than 2 months ago, but still lots of difficulty with enough energy to get through a day with 2 young kids.
How are you feeling now that you're 8-9 months post VM? I'm looking for some inspiration for the road ahead that things will get easier/better.
Thanks!
-Mike
I have a lot more good days now but still struggle with soreness in my back and neck going down through my arms. I don't have much strength in my arms which is probably my own fault because I haven't forced myself to try and build some strength back up in that area and I'm a hair stylist so having my arms up all day doesn't really help. Just hoping for complete healing like everyone else on this page is. Thankful for how far I've come but would love to be 95%
Elbows and knees, yes! Mine includes the rest of the limb too. Elbows to the tips of my fingers, knees to the tips of my toes
Hello,
I was diagnosed with Viral Meningitis 6 months ago in July of 2017. I came here looking for answers and somewhat relieved to find others have similar stories and feel the same way I do several months after. All this time I kept wondering if what I was feeling was 'normal' or to be expected.
I kept thinking that I should be better by now. The impression I got from my Doctors was that I would be fine after a couple of weeks- not one Doctor (my GP, neurologist, a few PAs, and multiple ER doctors) even hinted at the fact that this would be several months or years before things are back to normal.
I've tried several medicines over the months and ultimately stopped taking all of them because of the side effects. One medicine simply just didn't work, the other made me lose 15 lbs in 2 two weeks (quite a lot for a 33 yr old, 175lbs healthy man), and the other was Vicodin- which when my headaches would spike I would take 2-3. Taking this many Vicodin wouldn't take my headache pain away and I would still be up all night unable to sleep. The only thing I've found to help ease the pain is marijuana- which was recently legalized here in California and a few other states.
My headaches spiking are fewer are farther between now, although I still have a constant lower grade headache 24/7 that I've just learned to deal with.
I still get tired very easily and want to go to be around 8pm every night. I have severe joint aches that make life pretty hard. I didn't know others experienced this until finding this forum.
I still can't exercise- I usually ride my bike and go surfing several times a week- something I haven't done since before I got sick.
Hopeful that this all goes away soon. Like others, I really wish there was more info on this and what to expect post virus.
Tim
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