About sll : Your near me so I wanted to know if... - CLL Support

CLL Support

23,337 members40,045 posts

About sll

Ironj profile image
13 Replies

Your near me so I wanted to know if we could communicate about sll/cll I’ve been just told I have it and am anxious.

Written by
Ironj profile image
Ironj
To view profiles and participate in discussions please or .
13 Replies
AussieNeil profile image
AussieNeilPartnerAdministrator

Use this site's Private Messaging facility to share addresses/contact details: support.healthunlocked.com/...

Ironj profile image
Ironj in reply toAussieNeil

Ok

Ballyhoo77 profile image
Ballyhoo77

I think that is pretty much normal for all of us. Try not to worry I know it's hard. Could be a long time before you need treatment or ever for that matter. Wishing you the very best.

Ironj profile image
Ironj in reply toBallyhoo77

Thank you for the kind words I really need it and I hope I never need treatments.

MsLockYourPosts profile image
MsLockYourPostsPassed Volunteer

You probably should restrict your posts to community only. For those already up click on the v next to more, then edit and scroll to the bottom of the post and change the setting to community only.

Only the original post can be "locked". The setting on it controls the privacy of all replies to it. You often get more responses to locked posts, because many are careful about their privacy. Anything unlocked can show up on google, Facebook, twitter, etc.

There are other members in your area and there is an in person support group through CLL Society in NYC (look at the top of the home page). I urge you to get to at least one of the meetings. Just being in a room with other CLL patients is very helpful.

MsLockYourPosts profile image
MsLockYourPostsPassed Volunteer

PMs here are called Chat.

Ironj profile image
Ironj in reply toMsLockYourPosts

I’m using an iPhone and it just has a reply , nothing that says chat.

Cllcanada profile image
CllcanadaTop Poster CURE Hero in reply toIronj

On the iPhone it uses symbols... like these..

top menu..

💬💬

annmcgowan profile image
annmcgowan

Hi we are all anxious at first diagnosis you are not alone.

I have used this site to educate and support me emotionally through my difficult times.

You have come to the right place.

Take care

Ann

Ironj profile image
Ironj in reply toannmcgowan

Thank you Ann

annmcgowan profile image
annmcgowan

No problem take care.

Flabal profile image
Flabal

Hi. We all here know how you feel. And we also felt like you feel. But most of them will also be able to give you lessons in strength. I am just going to start treatment and feel just like you do. If you would like to chat please feel free to hit me up. I’m the same age as you.

Ironj profile image
Ironj in reply toFlabal

How long have you had it for ? What is your treatment ? I hope your treatment goes well.

Not what you're looking for?

You may also like...

Question about Sll/CLL

I am trying to figure out what the life expectancy is with Sll and CLL I’m 46 and was told I have...
Ironj profile image

SLL..

Hi i would love to hear from some people with SLL......LYMPHOMA How different is this from CLLas...
Stelladoro profile image

CLL/SLL

Hi got Dx Feb 2017 with CLL/ Sll I know they say it the same , but my oncologist said I had both...
PNall profile image

CLL / SLL

Still new to this SLL/CLL as I was diagnosed two month ago. Doctor said it is more of SLL than CLL...
Egypt58 profile image

Sll questions

I was diagnosed with sll in july 24 and started acalabrutinib in late August. I saw my oncologist...
1reb profile image

Moderation team

See all
AussieNeil profile image
AussieNeilAdministrator
Newdawn profile image
NewdawnAdministrator
CLLerinOz profile image
CLLerinOzAdministrator

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.