New member : Hello all, I honestly don’t... - My MSAA Community

My MSAA Community

9,432 members21,216 posts

New member

Jimmyspadge profile image
15 Replies

Hello all, I honestly don’t know if I have MS or it is just severe stress/anxiety depression. For the past 5 months I have had blurry vision in my left eye. For the same amount of time I keep getting random pain in the right side of my neck. Since around October of last year I have had bad pain in both my elbows but more so the right elbow. In the past three weeks I have really bad pain in the back of both heels. The pain actually stops me walking, however at other times there is no pain. Today I was walking my dogs and I started getting really sharp pricking pain in both forearms - hands- back of the neck and back of my head. I get very upset at nothing and I just feel the need to cry. I have checked the NHS website as I seem to have some of the symptoms of MS. Any advice greatly appreciated

Written by
Jimmyspadge profile image
Jimmyspadge
To view profiles and participate in discussions please or .
15 Replies
RoyceNewton profile image
RoyceNewton

Go visit a neuroligist and have them diagnose you.

Jimmyspadge profile image
Jimmyspadge in reply toRoyceNewton

Thanks

rjoneslaw profile image
rjoneslaw in reply toRoyceNewton

I completely agree

greaterexp profile image
greaterexp

I'm sorry for all these symptoms. We understand that they are scary. You really need to get to a doctor, at least your primary care doctor, if not a neurologist, as soon as you can. Until you get an accurate diagnosis, you can't begin treatment. The symptoms of MS can also look like many other problems, so you'll need some tests to determine what is causing yours.

We all understand the fears you must be feeling right now, but remember that you can't be sure right now what is causing this. Just getting an accurate diagnosis can be very empowering. But also remember that my MS is not your MS. Every case is different, even with all the similarities. So when you read worst case scenarios, they may not be at all what you'd experience, even if it is MS.

We are here for you while you begin the diagnosis process. So come whenever you need to to ask questions or vent off some steam. MSAA has wonderful resources to help, too.

mymsaa.org/

in reply togreaterexp

Great advise!

Jimmyspadge profile image
Jimmyspadge in reply togreaterexp

Thankyou for your words

greaterexp profile image
greaterexp in reply toJimmyspadge

I hope you'll keep us posted about how you're doing and about your diagnosis progress. We care about one another here.

Jimmyspadge profile image
Jimmyspadge in reply togreaterexp

I will and thanks for your words

Amore55 profile image
Amore55

As has already been said, we are careful to remind everyone that MS can present differently in each person. The only way to know is through a neurologist who specializes in MS. They should do a complete MRI, meaning brain, neck and spine looking for lesions and a lumbar puncture, also known as a spinal tap. That can show if any MS cells are present in spinal fluid. After years of misdiagnoses, the right doctor had my answer in 24 hours. Please let us know. Kelly

goatgal profile image
goatgal

Make an appointment with a neurologist. If you need a referral, see a primary care doctor first. Be prepared to advocate for yourself and be persistent. For many of us here, the road to diagnosis has been long (and occasionally bumpy). Stay strong! I wish you well.

Violonchelo profile image
Violonchelo

And the MR?

JTZES profile image
JTZES

Well I hope it's not. Yes you do have an issue of some kind but internet diagnosis is not the way to figure out what your problem is.

Keep a list of your issues and get into see your primary care doctor and get his reccomendation what to do next.

sashaming1 profile image
sashaming1

MS can be identified by a MRI and spinal tap, or try a steroid to see if the symptoms get better for awhile since that works for MS I understand. These need a Dr.'s (Neurologist) analysis.

mrsmike9 profile image
mrsmike9

I agree with all the above and want to add.... Write all your symptoms and questions before you see the doctor! There is nothing worse than walking out the door and realize you forgot something!!

Best of luck and let us know how you are!

Tazmanian profile image
Tazmanian

Definitely find a neurologist who specialises in MS and write down all your symptoms

Not what you're looking for?

You may also like...

Ms symptoms but mri clear

Wondering if anyone can advise Have intermittent numb foot since April then both feet feeling...
Maura37 profile image

Trying to stay positive with hand issues

Hi Friends, I. Am new here. I have lived with MS for 39 years and have taken many punches and got...
Lulu521 profile image

Upset

Hi everyone,I haven't been on here in a bit. Things seemed to be going ok until they weren't. I had...
Jhayespt profile image

ouch!! Headaches

Back in May I had horrible headaches and extreme spasticity in my shoulders and neck. After a week...
StacyHayward profile image

New member

Just getting used to my MS diagnosis,found out in Jan.Numbness & tingling in feet.Work as...
Curran1970 profile image

Moderation team

See all
johnMSAA profile image
johnMSAAPartner
DanaMSAA profile image
DanaMSAAPartner

Content on HealthUnlocked does not replace the relationship between you and doctors or other healthcare professionals nor the advice you receive from them.

Never delay seeking advice or dialling emergency services because of something that you have read on HealthUnlocked.